JP2001059062A - Photoelectric conversion element, photoelectrochemical battery or cell and metal complex coloring matter - Google Patents

Abstract

PROBLEM TO BE SOLVED: To obtain the subject element capable of exhibiting an excellent light absorptive power even in a long wavelength region and further a high photoelectric conversion efficiency and providing a good photoelectrochemical battery or cell by using a specific metal complex coloring matter. SOLUTION: This photoelectric conversion element comprises semiconductor fine particles (preferably titanium oxide fine particles or the like) sensitized with a metal complex coloring matter represented by formula I [M is a metal atom; LL1 is a bidentate ligand represented by formula II (R1 and R2 are each carboxyl or the like; R3 and R4 are each a substituent group; a1 and a2 are each 0-4; b1 is 0-3; b2 is 0-5); LL2 is a bi- or a tridentate ligand represented by formula III (Za to Zc are each a nonmetallic atom group capable of forming a five- or a six-membered ring; c is 0 or 1); X is a mono- or a bidentate ligand or the like coordinated with a group selected from the group consisting of an acyloxy or the like; m1 is 1-3; m2 is 0-2; m3 is 0-3; CI is a counterion when the counterion is required to neutralize an electric charge]. The photoelectric conversion element is capable of exhibiting high photoelectric conversion characteristics in a visible light to an infrared regions.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a metal complex dye having high light absorption even in a long wavelength region, a photoelectric conversion element using semiconductor fine particles sensitized by such a metal complex dye, and a photoelectrochemical cell comprising the same. About.

[0002]

2. Description of the Related Art As a solar cell used for photovoltaic power generation, a solar cell made of single-crystal silicon, polycrystalline silicon, amorphous silicon, or a compound such as cadmium telluride or indium copper selenide has been put into practical use or has been mainly used for research and development. Although it is a target, in order to spread it widely to household power sources, there are problems such as high production cost, difficulty in securing raw materials, long energy payback time, etc. There is a need. On the other hand, many solar cells using an organic material have been proposed for the purpose of increasing the area and reducing the cost, but generally have the problems of low conversion efficiency and poor durability.

[0003] Under such circumstances, Nature (Vol. 353,
737-740, 1991), and U.S. Pat.
O 94/04497, etc., have proposed a wet photoelectric conversion element and a solar cell using a titanium dioxide porous thin film spectrally sensitized with a ruthenium complex dye as a working electrode, and materials and manufacturing techniques for producing the same. . The first advantage of this wet photoelectric conversion element is that an inexpensive oxide semiconductor such as titanium dioxide can be used without purification to a high degree of purity, so that an inexpensive photoelectric conversion element can be provided. Is that the absorption of the dye used is broad, so that light in almost all wavelength regions of visible light can be converted into electricity.

[0004] However, although known ruthenium complex dyes absorb visible light, they hardly absorb infrared light having a wavelength longer than 700 nm, and thus have a problem of low photoelectric conversion ability in the infrared region. Therefore, in order to further increase the conversion efficiency, it is desired to develop a dye having an absorptivity in a wide wavelength range from visible light to an infrared region and exhibiting a high photoelectric conversion ability.

[0005]

SUMMARY OF THE INVENTION An object of the present invention is to provide a metal complex which has a high light absorption capacity not only in the visible light region but also in the infrared region and which can efficiently sensitize semiconductor fine particles to a long wavelength region. An object of the present invention is to provide a dye, a photoelectric conversion element having high photoelectric conversion efficiency by using such a metal complex dye, and a photoelectrochemical cell including the same.

[0006]

Means for Solving the Problems As a result of intensive studies in view of the above object, a specific ligand capable of bidentate coordination with a metal atom at a nitrogen atom and, if necessary, a 5- or 6-membered ring have been completed. Having a non-metallic atom necessary for
A metal complex dye obtained by coordinating a monodentate or bidentate ligand coordinating with a ligand capable of coordinating and a thiocyanate group has excellent light absorbing ability even in a long wavelength region, and Semiconductor fine particles sensitized by such a metal complex dye,
The present inventors have found that a high photoelectric conversion efficiency suitable as a photoelectric conversion element and a good photoelectrochemical cell are obtained, and the present invention has been reached.

That is, the photoelectric conversion element of the present invention has the following general formula (I): M (LL ₁ ) _m1 (LL ₂ ) _m2 (X) _m3 · CI (I) (where M is a metal atom And LL ₁ represents the following general formula (I
I):

Embedded image (Provided that R ₁ and R ₂ are independently a carboxyl group, a sulfonic acid group, a hydroxyl group, a hydroxamic acid group, represents a phosphoryl group or a phosphonyl group, R ₃ and
R ₄ each independently represents a substituent, a1 and a2 each represents independently an integer of 0 to 4, b1 represents an integer of 0 to 3, b2 represents an integer of 0 to 5. When a1 is 2 or more, R ₁ may be the same or different; when a2 is 2 or more, R ₂ may be the same or different; when b1 is 2 or more, R ₃ may be the same or different They may be linked to each other to form a ring, and when b2 is 2 or more, R ₄ may be the same or different, and may be linked to each other to form a ring. b1 and
b2 may form a ring wherein R ₃ and R ₄ together one or more time. ) Represents a bidentate ligand represented by, LL ₂ the following general formula (III):

Embedded image (However, Za, Zb and Zc are each independently 5 or 6
Represents a group of non-metallic atoms capable of forming a membered ring, and c is 0 or 1
Represents X represents an acyloxy group, an acylthio group, a thioacyloxy group, a thioacylthio group, an acylaminooxy group, a thiocarbamate group, a dithiocarbamate group, a thiocarbonate group, A group selected from the group consisting of dithiocarbonate, trithiocarbonate, acyl, thiocyanate, isothiocyanate, cyanate, isocyanate, cyano, alkylthio, arylthio, alkoxy, and aryloxy groups Coordinate with 1
A bidentate or bidentate ligand, or a monodentate or bidentate ligand consisting of a halogen atom, carbonyl, dialkyl ketone, 1,3-diketone, carbonamide, thiocarbonamide, thiourea or isothiourea; 1 to
When m1 is 2 or 3, LL ₁ may be the same or different; m2 represents an integer of 0 to 2;
, LL ₂ may be the same or different, and m3 is 0-3
And when m3 is 2 or 3, Xs may be the same or different, and Xs may be linked to each other, and CI
Represents a counter ion when a counter ion is required to neutralize the charge. ), Characterized by containing semiconductor fine particles sensitized by the metal complex dye represented by the formula (1).

A photoelectrochemical cell according to the present invention is characterized by using the above-mentioned photoelectric conversion element.

According to the present invention, a photovoltaic cell and a photoelectrochemical cell containing semiconductor fine particles sensitized by a metal complex dye having more excellent light absorbing ability in a long wavelength region can be obtained by satisfying the following conditions.

(1) M in the general formula (I) is Ru, Fe, Os, C
u, W, Cr, Mo, Ni, Pd, Pt, Co, Ir, Rh, Re, Mn or
It is preferably Zn, more preferably Ru, Fe, Os or Cu, and particularly preferably Ru.

(2) The sum of a1 and a2 in the general formula (II) is 1 to 4
Is preferably an integer.

(3) a1 in the general formula (II) preferably represents 0 or 1, and a2 preferably represents 1 or 2.

(4) R ₁ and R ₂ in the general formula (II) are preferably each independently a carboxyl group or a phosphonyl group.

(5) In the general formula (II), b1 is preferably an integer of 0 to 2, and b2 is preferably an integer of 1 to 4.

(6) The sum of b1 and b2 in the general formula (II) is from 1 to 6
R ₃ and R ₄ are each independently an alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group,
It is preferably a hydroxyl group, an alkoxy group, an aryloxy group, an amino group or an acylamino group.

(7) The 5- or 6-membered ring formed by Za, Zb and Zc in the general formula (III) is preferably a pyridine ring or an imidazole ring. These rings may be monocyclic or condensed.

(8) c in the general formula (III) is preferably 0. That is, LL ₂ is preferably a bidentate ligand.

(9) In the general formula (I), m1 is 1 or 2, m2
Is preferably 0 or 1, and m3 is preferably an integer of 0 to 2,
In particular, when m1 is 1, m2 is preferably 1 and m3 is preferably 1 or 2, and when m1 is 2, m2 is 0 and m3 is preferably 1 or 2.

(10) LL ₂ in the general formula (I) is represented by the following general formula (IV)
-1) to (IV-8):

Embedded image(However, R₁₁~ R₁₈Is independently a carboxyl group,
Sulfonic acid group, hydroxyl group, hydroxamic acid group, e
Represents a phoryl or phosphonyl group, R₁₉~ R₂₆Is it
Each independently represents a substituent, R₂₇~ R₃₁Are each independently water
Represents an alkyl, alkenyl, or aryl group.
Then R₁₁~ R₂₆May be bonded to any position on the ring,
d1 to d8, d13, d14 and d16 are each independently 0 to 4
Represents an integer, and d9 to d12 and d15 are each independently 0 to 6
And when d1 to d8 are 2 or more, R ₁₁~ R₁₈Is the same
May be different, and when d9 to d16 are 2 or more, R₁₉~ R
₂₆May be the same or different and are linked together to form a ring
It may be formed. ) Is represented by either
Preferably, the compound represented by the general formula (IV-1), (IV-2), (IV-4) or (IV
-6), more preferably represented by the general formula (IV-1)
Or (IV-2).

(11) R _{11 to} R in the general formulas (IV-1) to (IV-8)
Preferably, ₁₈ is each independently a carboxyl group or a phosphonyl group.

(12) R _{19 to} R in the general formulas (IV-1) to (IV-8)
₂₆ are each independently an alkyl group, an alkenyl group, a cycloalkyl group, an aryl group, a heterocyclic group, an alkoxy group,
Aryloxy group, acyloxy group, alkoxycarbonyl group, carbamoyl group, acylamino group, amino group,
It is preferably an acyl group, a sulfonamide group, a cyano group or a halogen atom.

(13) The semiconductor fine particles are preferably titanium oxide fine particles.

In the metal complex dye according to a preferred embodiment of the present invention, M in the general formula (I) is Ru, and LL ₁ is a bidentate ligand represented by the general formula (II). , LL ₂ is a bidentate or tridentate ligand represented by any of formulas (IV-1) to (IV-8), X is an acyloxy group,
Acylthio, thioacyloxy, thioacylthio, acylaminooxy, thiocarbamate, dithiocarbamate, thiocarbonate, dithiocarbonate, trithiocarbonate, acyl, thiocyanate, isothiocyanate, cyanate A monodentate or bidentate ligand coordinated with a group selected from the group consisting of a group, an isocyanate group, a cyano group, an alkylthio group, an arylthio group, an alkoxy group and an aryloxy group;
Or a monodentate or bidentate ligand consisting of a halogen atom, carbonyl, dialkyl ketone, 1,3-diketone, carbonamide, thiocarbonamide, thiourea or isothiourea, m1 is 1 or 2, and m1 is 2
When LL ₁ may be the same or different, m2 is 0 or 1, m3 represents an integer of 0 to 2, and when m3 is 2, X
May be the same or different, and X may be linked to each other, m2 and m3 are not simultaneously 0, and CI is a counter ion when a counter ion is necessary to neutralize the charge. is there.

In the metal complex dye according to this preferred embodiment, the sum of a1 and a2 in the general formula (II) is preferably an integer of 1 to 4. Further, the sum of b1 and b2 in the general formula (II) is an integer of 1 to 6, and R ₃ and R ₄ are each independently an alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, a hydroxyl group, an alkoxy group , An aryloxy group, an amino group or an acylamino group.

[0025]

DETAILED DESCRIPTION OF THE INVENTION [1] Metal Complex Dye The metal complex dye used in the photoelectric conversion device of the present invention has the following general formula (I): M (LL ₁ ) _m1 (LL ₂ ) _m2 (X) _m3 · CI... (I). Hereinafter, each component will be described in detail.

(A) The metal atom MM represents a metal atom. M is preferably a metal capable of four or six coordination, more preferably Ru, Fe, Os, Cu,
W, Cr, Mo, Ni, Pd, Pt, Co, Ir, Rh, Re, Mn or Zn
And particularly preferably Ru, Fe, Os or Cu, and most preferably Ru.

(B) Ligands LL ₁ LL ₁ represents a bidentate ligand. M1 representing the number of LL ₁ is an integer of 1 to 3, is preferably 1 or 2, and more preferably 2. m1 is LL ₁ when 2 or 3 may be the same or different.

The ligand LL ₁ has the following general formula (II):

Embedded image Is represented by

R ₁ and R ₂ in the general formula (II) each independently represent a carboxyl group, a sulfonic acid group, a hydroxyl group, or a hydroxamic acid group (preferably having 1 to 20 carbon atoms, for example,
-CONHOH, -CONCH ₃ OH, etc.), phosphoryl group (for example, -OP (O)
(OH) ₂ etc.) and a phosphonyl group (eg -P (O) (OH) ₂ etc.)
And is preferably a carboxyl group, a phosphoryl group or a phosphonyl group, more preferably a carboxyl group or a phosphonyl group, and most preferably a carboxyl group.

R ₃ and R ₄ in the formula (II) each independently represent a substituent, preferably an alkyl group (preferably having 1 to 20 carbon atoms, for example, a methyl group, an ethyl group, an isopropyl group, a t- Butyl, pentyl, heptyl, 1-ethylpentyl, benzyl, 2-ethoxyethyl, 1-carboxymethyl, etc., alkenyl (preferably having 2 to 20 carbon atoms, for example, vinyl, allyl) Oleyl group), alkynyl group (preferably having 2 to 20 carbon atoms, such as ethynyl group, butadiynyl group, phenylethynyl group, etc.), cycloalkyl group (preferably having 3 to 2 carbon atoms).
0, for example, a cyclopropyl group, a cyclopentyl group, a cyclohexyl group, a 4-methylcyclohexyl group, etc.), a hydroxyl group, an aryl group (preferably having 6 to 26 carbon atoms,
For example, phenyl group, 1-naphthyl group, 4-methoxyphenyl group, 2-chlorophenyl group, 3-methylphenyl group, etc., heterocyclic group (preferably having 2 to 20 carbon atoms, for example, 4-pyridyl group, 1-imidazolyl) Group, 2-benzimidazolyl group,
2-thiazolyl group, 2-oxazolyl group, etc.), alkoxy group (preferably having 1 to 20 carbon atoms, for example, methoxy group, ethoxy group, isopropyloxy group, benzyloxy group, etc.), and aryloxy group (preferably having carbon atom number) 6-2
6, for example, phenoxy group, 1-naphthyloxy group, 3-methylphenoxy group, 4-methoxyphenoxy group, etc., alkoxycarbonyl group (preferably having 2 to 20 carbon atoms, for example, ethoxycarbonyl group, 2-ethylhexyloxycarbonyl group) Etc.), an amino group (preferably having 0 to 2 carbon atoms)
0, for example, amino group, N, N-dimethylamino group, N, N-diethylamino group, N-ethylamino group, anilino group, etc., acyl group (preferably having 1 to 20 carbon atoms, for example, acetyl group, benzoyl group) Etc.), a sulfonamide group (preferably having 0 to 20 carbon atoms such as N, N-dimethylsulfonamide group, N-phenylsulfonamide group and the like), an acyloxy group (preferably having 1 to 20 carbon atoms such as acetyloxy group) Group, benzoyloxy group, etc.), carbamoyl group (preferably having 1 to 20 carbon atoms, such as N, N-dimethylcarbamoyl group, N-phenylcarbamoyl group, etc.), acylamino group (preferably having 1 to 20 carbon atoms, e.g., Acetylamino group, benzoylamino group, etc.), cyano group, or halogen atom (eg, fluorine atom, chlorine atom, bromine atom, iodine atom, etc.).

In the general formula (II), R ₃ and R ₄ are more preferably an alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, a hydroxyl group, an alkoxy group, an aryloxy group, an amino group or an acylamino group, More preferably, an alkyl group, an alkenyl group, an alkoxy group,
It is an amino group or an acylamino group, particularly preferably an alkyl group, an alkoxy group or an amino group.

[0032] Incidentally, when LL ₁ comprises an alkyl group, an alkenyl group or the like, they may be linear or branched, may be either unsubstituted substituted. When LL ₁ contains an aryl group, a heterocyclic group, or the like, they may be monocyclic or condensed, and may be substituted or unsubstituted.

In the general formula (II), a1 and a2 each independently represent an integer of 0 to 4. When a1 is 2 or more, R ₁ may be the same or different. When a2 is 2 or more, R ₂ may be R _2. May be the same or different. R ₁ may be substituted on any carbon atom on the pyridine ring, and R ₂ may be substituted on any carbon atom on the quinoline ring. Preferably, a1 represents an integer of 0 to 2, more preferably 0 or 1. a2 is preferably 1 or 2. The sum of a1 and a2 is preferably 1 to 4,
More preferably, it is 1 or 2.

B1 in the general formula (II) represents an integer of 0 to 3,
b2 represents an integer of 0 to 5. When b1 is 2 or more, R ₃ may be the same or different and may be connected to each other to form a ring, and when b2 is 2 or more, R ₄ may be the same or different and may be connected to each other to form a ring. It may be formed. When both b1 and b2 are 1 or more, R ₃ and R ₄ may be linked to form a ring,
The ring formed is preferably a benzene ring, a cyclohexane ring or a cyclopentane ring. R ₃ may be substituted on any carbon atom on the pyridine ring, and R ₄ may be substituted on any carbon on the quinoline ring.

B1 preferably represents an integer of 0 to 2;
Or it is more preferably 1. Further, b2 preferably represents an integer of 1 to 4, and more preferably 1 or 2. The sum of b1 and b2 is preferably 1 to 6,
More preferably, it is 3.

[0036] While specific examples of LL ₁ in the general formula (I) of the present invention described below, the present invention is not limited thereto.

[0037]

[Formula 10]

[0038]

[Formula 11]

[0039]

Embedded image

[0040]

Embedded image

[0041]

Embedded image

(C) Ligands LL ₂ LL ₂ represents a bidentate or tridentate ligand. M2 representing the number of LL ₂
Is an integer of 0 to 2, and is preferably 0 or 1. m2 is LL ₂ when the two may be the same or different.

The ligand LL ₂ has the following general formula (III):

Embedded image Is represented by

Za, Zb and Zc in the general formula (III) each independently represent a group of non-metallic atoms capable of forming a 5- or 6-membered ring. It may be substituted, monocyclic or condensed. Za, Zb and Zc are preferably composed of a carbon atom, a hydrogen atom, a nitrogen atom, an oxygen atom, a sulfur atom, a phosphorus atom and / or a halogen atom, and preferably form an aromatic ring.
In the case of a 5-membered ring, it is preferable to form an imidazole ring, an oxazole ring, a thiazole ring or a triazole ring, and in the case of a 6-membered ring, it is preferable to form a pyridine ring, a pyrimidine ring, a pyridazine ring or a pyrazine ring. Among them, it is more preferable to form an imidazole ring or a pyridine ring.

In the general formula (III), c represents 0 or 1. c
Is preferably 0, ie LL ₂ is preferably a bidentate ligand.

The ligand LL ₂ has the following general formulas (IV-1) to (IV-
8):

Embedded image Preferably, it is represented by any of

R _{11 to} R ₁₈ in the general formulas (IV-1) to (IV-8) each independently represent a carboxyl group, a sulfonic acid group, a hydroxyl group, or a hydroxamic acid group (preferably having 1 to carbon atoms).
20, for example, -CONHOH, -CONCH ₃ OH, etc., phosphoryl groups (for example, -OP (O) (OH) _2, etc.) and phosphonyl groups (for example, -P (O)
(OH) ₂ or the like, preferably a carboxyl group, a phosphoryl group or a phosphonyl group, more preferably a carboxyl group or a phosphonyl group, and most preferably a carboxyl group.

R _{19 to} R ₂₆ in formulas (IV-1) to (IV-8) each independently represent a substituent, preferably an alkyl group, an alkenyl group, a cycloalkyl group, an aryl group, or a heterocyclic group. , An alkoxy group, an aryloxy group, an acyloxy group, an alkoxycarbonyl group, a carbamoyl group, an acylamino group, an amino group, an acyl group, a sulfonamide group, a cyano group, or a halogen atom (the preferred examples are those of R ₃
And R ₄ ), more preferably an alkyl group, an alkenyl group, an aryl group, a heterocyclic group, an alkoxy group, an alkoxycarbonyl group, an acylamino group, an amino group or a halogen atom, and particularly preferably an alkyl group Alkenyl group, alkoxy group, alkoxycarbonyl group, acylamino group or amino group.

In the general formulas (IV-1) to (IV-8), R _{27 to} R ₃₁ each independently represent a hydrogen, an alkyl group, an alkenyl group or an aryl group (the preferred examples are the same as R ₃ and R ₄₎ ), And is preferably an alkyl group substituted with an alkyl group or a carboxyl group. When LL ₂ contains an alkyl group, an alkenyl group, or the like, they may be linear or branched, and may be substituted or unsubstituted. Also, LL ₂
Includes an aryl group, a heterocyclic group, etc., they may be monocyclic or condensed, and may be substituted or unsubstituted.

In formulas (IV-1) to (IV-8), R _{11 to} R ₂₆ may be bonded to any position on the ring, and d 1 to d 6 each independently represent an integer of 0 to 4. And preferably represents an integer of 0 to 2, d7 and d8 each independently represent an integer of 0 to 4, and preferably represents an integer of 0 to 3. d9-d12 and d15
Each independently represents an integer of 0 to 6, d13, d14 and
d16 each independently represents an integer of 0 to 4, and d9 to d16 preferably each represent an integer of 0 to 3.

[0051] d1~d8 well be the R ₁₁ to R ₁₈ when two or more the same or different from each other, R ₁₉ to R ₂₆ when d9~d16 is 2 or more
May be the same or different, and may be linked to each other to form a ring. Particularly d10 it is preferable to form a further pyridine ring R ₁₀ mutually connected on the pyridine ring of 2 or more time.

The ligand LL ₂ has the general formula (IV-1), (IV-2),
It is more preferably represented by (IV-4) or (IV-6), and particularly preferably represented by general formula (IV-1) or (IV-2).

[0053] Specific examples of ligands LL ₂ of the present invention are shown below, but the invention is not limited thereto.

[0054]

Embedded image

[0055]

Embedded image

[0056]

Embedded image

[0057]

Embedded image

[0058]

Embedded image

[0059]

Embedded image

[0060]

Embedded image

[0061]

Embedded image

[0062]

Embedded image

[0063]

Embedded image

[0064]

Embedded image

[0065]

Embedded image

[0066]

Embedded image

[0067]

Embedded image

[0068]

Embedded image

(D) Ligand X In the general formula (I), X represents a monodentate or bidentate ligand, and m3 representing the number of ligands X represents an integer of 0 to 3, preferably Is 0 to 2, more preferably 1 or 2. In particular, when X is a monodentate ligand, m3 is preferably 2, and when X is a bidentate ligand, m3 is preferably 1. When m3 is 2 or 3, X may be the same or different, and Xs may be connected to each other.

The ligand X is an acyloxy group (preferably having 1 to 20 carbon atoms, for example, acetyloxy group, benzoyloxy group, salicylic acid group, glycyl group, N, N-dimethylglycyl group, oxalylene group (-OC (O) C (O) O-), etc.), acylthio group (preferably having 1 to 20 carbon atoms, such as acetylthio group, benzoylthio group and the like), and thioacyloxy group (preferably having 1 to 20 carbon atoms, such as thiol) Acetyloxy group (CH ₃ C (S) O—) and the like, thioacylthio group (preferably having 1 to 20 carbon atoms, for example, thioacetylthio group (CH ₃ C (S) S—), thiobenzoylthio group (PhC (S) S-)
Etc.), an acylaminooxy group (preferably having 1 carbon atom)
-20, for example, N-methylbenzoylaminooxy group (PhC
(O) N (CH ₃ ) O-), acetylaminooxy group (CH ₃ C (O) NHO
-) Etc.), thiocarbamate group (preferably having 1 to 20 carbon atoms, for example, N, N-diethylthiocarbamate group and the like),
Dithiocarbamate group (preferably having 1 to 20 carbon atoms,
For example, N-phenyldithiocarbamate group, N, N-dimethyldithiocarbamate group, N, N-diethyldithiocarbamate group, N, N-dibenzyldithiocarbamate group, etc.), thiocarbonate group (preferably having 1 to 20, for example such as ethyl thiocarbonate group), dithiocarbonate group (preferably having 1 to 20 carbon atoms, for example ethyl dithiocarbonate group _{(C 2 H 5 OC (S} ) S-) and the like), trithiocarbonate group (preferably having 1 to 20 carbon atoms, for example ethyl trithiocarbonate group _{(C 2 H 5 SC (S} ) S-) and the like), an acyl group (preferably having 1 to 20 carbon atoms such as acetyl group, benzoyl Group), thiocyanate group, isothiocyanate group, cyanate group, isocyanate group, cyano group, alkylthio group (preferably having 1 to 20 carbon atoms, for example, methanethio group, ethylenedithio group ), An arylthio group (preferably having 6 to 20 carbon atoms such as benzenethio group, 1,2-phenylenedithio group and the like), an alkoxy group (preferably having 1 to 20 carbon atoms such as methoxy group and the like) and an aryloxy group ( A monodentate or bidentate ligand coordinated by a group preferably having 6 to 20 carbon atoms, for example, a phenoxy group, a quinoline-8-hydroxyl group and the like, or a halogen atom (preferably chlorine) atom, a bromine atom or an iodine atom), carbonyl (... CO), dialkyl ketones (preferably 3 to 20 carbon atoms, such as acetone _{((CH 3) 2 CO ...} ) (... represents a coordinate bond), etc.), 1,3-
Diketone (preferably 3 to 20 carbon atoms, such as acetylacetone _{(CH 3 C (O-) CH} = C (O ...) CH 3), trifluoroacetylacetone _{(CF 3 C (O-) CH} = C (O ...) CH _3), dipivaloylmethane _{(tC 4 H 9 C (O-} ) CH = C (O ...) -tC 4 H 9), dibenzoylmethane (PhC (O-) CH = C (O ...) Ph ), 3-chloro-acetylacetone _{(CH 3 C (O-) CCl} = C (O ...) CH 3) , etc.) carboxamide (preferably having 1 to 20 carbon atoms, e.g.
_{CH 3 N = C (CH 3} ) O -, - OC (= NH) -C (= NH) O- , etc.), thio carbonamido (preferably having 1 to 20 carbon atoms, for example, CH ₃ N = C (C
H ₃₎ S-, etc.), thiourea (preferably having a carbon atom 1-2
0, for example, _{... NH 2 -C (S ...)} NH 2, ... N (CH 3) 2 -C (S ...) N (CH 3) 2
Etc.) or isothiourea (preferably having 1 carbon atom)
20, for example, ... NH = C (S-) NH 2, ... N (CH 3) = C (S-) NHCH 3 , etc.)
Represents a ligand consisting of

The ligand X is preferably an acyloxy group, a thioacylthio group, an acylaminooxy group, a dithiocarbamate group, a dithiocarbonate group, a trithiocarbonate group, a thiocyanate group, an isothiocyanate group, a cyanate group, an isocyanate group, a cyano group. Group, an alkylthio group, an arylthio group, a ligand coordinated with a group selected from the group consisting of an alkoxy group and an aryloxy group, or a ligand consisting of a halogen atom, carbonyl, 1,3-diketone or thiourea. More preferably, an acyloxy group, an acylaminooxy group, a dithiocarbamate group, a thiocyanate group, an isothiocyanate group, a cyanate group, an isocyanate group, a ligand coordinated with a group selected from the group consisting of a cyano group and an arylthio group, Or a halogen atom, 1, A ligand comprising a 3-diketone or thiourea, more preferably a ligand coordinated with a group selected from the group consisting of a dithiocarbamate group, a thiocyanate group, an isothiocyanate group, a cyanate group and an isocyanate group, or halogen Atom or 1,
A ligand consisting of a 3-diketone, particularly preferably a ligand coordinated with a group selected from the group consisting of a dithiocarbamate group, a thiocyanate group and an isothiocyanate group, or a ligand consisting of a 1,3-diketone I am a child. The ligand X is an alkyl group, an alkenyl group, an alkynyl group,
When an alkylene group or the like is contained, they may be linear or branched, and may be substituted or unsubstituted. When containing an aryl group, a heterocyclic group, a cycloalkyl group, and the like,
They may be substituted or unsubstituted, and may be monocyclic or condensed.

In the general formula (I), when X is a bidentate ligand, X represents an acyloxy group, an acylthio group, a thioacyloxy group,
Thioacylthio, acylaminooxy, thiocarbamate, dithiocarbamate, thiocarbonate, dithiocarbonate, trithiocarbonate,
A ligand coordinated with a group selected from the group consisting of an acyl group, an alkylthio group, an arylthio group, an alkoxy group and an aryloxy group, or a ligand composed of 1,3-diketone, carbonamide, thiocarbonamide or thiourea It is preferred that When X is a monodentate ligand, X is a ligand coordinated with a group selected from the group consisting of a thiocyanate group, an isothiocyanate group, a cyanate group, an isocyanate group, a cyano group, an alkylthio group and an arylthio group, or It is preferably a ligand consisting of a halogen atom, carbonyl, 1,3-diketone or thiourea.

Specific examples of the ligand X of the present invention are shown below, but the present invention is not limited to these. It should be noted that the structural formula shown here is only one of the limit structures of a number of possible resonance structures, and the distinction between a covalent bond (represented by-) and a coordination bond (represented by ...) is formal. It does not represent a distinction.

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When M in the general formula (I) is a metal such as Cu, Pd, or Pt that favors four coordination, m1 is preferably 1 or 2, and m2 is preferably 0. In this case, when m1 is 1, m3 is preferably 1 or 2, and when m1 is 2, m3 is preferably 0. When M is a metal that prefers 6 coordination, m1 is 1 or 2
Is preferably, and more preferably 2. In this case, when m1 is 1, m2 is preferably 1 or 2, and more preferably 1. Here, when m2 is 1,
m3 is preferably 1 or 2, and when m2 is 2, m3
Is preferably 0. When m1 is 2, m2 is 0
Or, it is preferably 1, and more preferably 0. Here, when m2 is 0, m3 is preferably 1 or 2, and when m2 is 1, m3 is preferably 0. When m1 is 3, both m2 and m3 are preferably 0.

(E) Counter ion CI CI in the general formula (I) represents a counter ion when a counter ion is required to neutralize the charge. Whether a dye is a cation or anion, or has a net ionic charge, depends on the metal, ligand, and substituents in the dye. When the substituent has a dissociable group, it may dissociate and have a negative charge, and in this case also, the charge of the entire molecule is neutralized by CI.

[0082] Typical positive counterions are inorganic or organic ammonium ions (eg, tetraalkylammonium ions, pyridinium ions, etc.), alkali metal ions and protons. On the other hand, the negative counter ion may be any of an inorganic anion and an organic anion, for example, a halogen anion (for example, a fluoride ion, a chloride ion, a bromide ion, an iodide ion), a substituted arylsulfonate ion (for example, p-toluenesulfonic acid ion, p-chlorobenzenesulfonic acid ion, etc.), aryl disulfonic acid ion (eg, 1,3-benzenedisulfonic acid ion, 1,5-naphthalenedisulfonic acid ion, 2,6-naphthalenedisulfonic acid ion, etc.) Alkyl sulfate ion (for example, methyl sulfate ion), sulfate ion, thiocyanate ion, perchlorate ion, tetrafluoroborate ion, hexafluorophosphate ion, picrate ion, acetate ion, trifluoromethanesulfonate ion and the like. Can be Furthermore, as a charge balancing counter ion,
An ionic polymer or another dye having a charge opposite to that of the dye may be used, and a metal complex ion (for example, bisbenzene-1,2-dithiolatonickel (III) or the like) may also be used.

(F) Bonding Group The dye represented by the general formula (I) has at least one suitable interlocking group for the surface of the semiconductor fine particles, and preferably has 1 to 6 and preferably 1 to 6.
It is more preferable to have 4 to 4. Preferred linking groups are
Carboxyl group, sulfonic acid group, hydroxyl group, hydroxamic acid group (eg, -CONHOH), phosphoryl group (eg, -OP (O) (OH) _2, etc.), phosphonyl group (eg, -P (O) (OH)
₂ ) etc. (substituents having a dissociable proton)
It is.

[0084] The acidic groups, LL ₁ in the general formula (I) has at least one or more, LL ₂ also preferably has at least one more.

(G) Specific Examples of Metal Complex Dyes Among the above metal complex dyes, particularly preferred are the following formulas (V): Ru (LL ₁ ) _m1 (LL ₂ ) _m2 (X) _m3 · CI (V) (where LL ₁ represents a bidentate ligand represented by the above general formula (II), and LL ₂ represents a compound represented by any of the above general formulas (IV-1) to (IV-8). Represents a bidentate or tridentate ligand to be
X is an acyloxy group, an acylthio group, a thioacyloxy group, a thioacylthio group, an acylaminooxy group, a thiocarbamate group, a dithiocarbamate group, a thiocarbonate group, a dithiocarbonate group, a trithiocarbonate group, an acyl group, a thiocyanate group, Monodentate or bidentate ligand coordinated by a group selected from the group consisting of isothiocyanate group, cyanate group, isocyanate group, cyano group, alkylthio group, arylthio group, alkoxy group and aryloxy group, or halogen atom , Carbonyl, dialkyl ketone, 1,3-diketone, carbonamide, thiocarbonamide, thiourea or isothiourea, represents a monodentate or bidentate ligand, m1 is 1 or 2, and when m1 is 2, LL ₁ may be the same or different, m2 is 0 or 1 Ri, m3 represents an integer of 0 to 2, X when m3 is 2 may be the same or different,
In addition, X may be connected to each other, m2 and m3 are not simultaneously 0, and CI represents a counter ion when a counter ion is required to neutralize the charge. ) Is a ruthenium complex dye represented by

Specific examples of the metal complex dye of the present invention are shown below, but the present invention is not limited thereto.

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The synthesis of the metal complex dye represented by formula (I) of the present invention is described in Chem. Phys. Lett., 85, 309 (1982).
Chem. Phys. Lett., 71, 220 (1980), J. Am. Che
m. Soc., 115, 6382 (1993) and the methods cited therein. Each ligand is described in Synth. Commun., 27, 2165 (1997), Aust. JC
hem., 25, 1631 (1972).

[2] Photoelectric conversion element The photoelectric conversion element of the present invention has semiconductor fine particles sensitized by the above metal complex dye in the photosensitive layer. Preferably, as shown in FIG. 1, the conductive layer 10, the photosensitive layer 20, the charge transfer layer 30, and the counter electrode conductive layer 40 are laminated in this order, and the photosensitive layer 20 is sensitized by the metal complex dye 22 of the present invention. 21 and a charge transporting material 23 filled in a space between the semiconductor fine particles 21. The charge transport material 23 is composed of the same components as the materials used for the charge transfer layer 30. Further, a substrate 50 may be provided on the conductive layer 10 side and / or the counter electrode conductive layer 40 side in order to impart strength to the photoelectric conversion element. Hereinafter, in the present invention, a layer composed of the conductive layer 10 and the optional substrate 50 is referred to as a “conductive support”, and a layer composed of the counter electrode conductive layer 40 and the optional substrate 50 is referred to as a “counter electrode”. A photoelectrochemical cell in which the photoelectric conversion element is connected to an external circuit to perform a work is provided. Note that the conductive layer 10, the counter electrode conductive layer 40, and the substrate 50 in FIG. 1 may be a transparent conductive layer 10a, a transparent counter electrode conductive layer 40a, and a transparent substrate 50a, respectively.

In the photoelectric conversion device of the present invention shown in FIG. 1, the light incident on the photosensitive layer 20 containing the semiconductor fine particles 21 sensitized by the metal complex dye 22 excites the dye 22, etc., and the excited dye 22, etc. High-energy electrons inside are semiconductor fine particles 21
And reaches the conductive layer 10 by diffusion. At this time, molecules such as the dye 22 are oxidized. In the photoelectrochemical cell, the electrons in the conductive layer 10 return to an oxidant such as the dye 22 via the counter electrode conductive layer 40 and the charge transfer layer 30 while working in an external circuit, and the dye 22 is regenerated. Photosensitive layer
20 works as a negative electrode. At the boundary of each layer (for example, the boundary between the conductive layer 10 and the photosensitive layer 20, the boundary between the photosensitive layer 20 and the charge transfer layer 30, the boundary between the charge transfer layer 30 and the counter electrode conductive layer 40, etc.)
The constituent components of each layer may be mutually diffused and mixed.
Hereinafter, each layer will be described in detail.

(A) Conductive Support The conductive support comprises (1) a single layer of a conductive layer, or (2) two layers of a conductive layer and a substrate. A substrate is not necessarily required if a conductive layer that maintains sufficient strength and sealing properties is used.

In the case of (1), a conductive layer having sufficient strength, such as metal, and having conductivity is used.

In the case of (2), a conductive agent is contained on the photosensitive layer side.
A substrate having a conductive layer can be used. Preferred conductive agents are metals (for example, platinum, gold, silver, copper, aluminum, rhodium, indium, etc.), carbon, or conductive metal oxides (indium-tin composite oxide, tin oxide doped with fluorine, etc.). Is mentioned. The thickness of the conductive layer is preferably about 0.02 to 10 μm.

The lower the surface resistance of the conductive support, the better. The preferred range of the surface resistance is 100 Ω / □ or less, more preferably 40 Ω / □ or less. The lower limit of the surface resistance is not particularly limited, but is usually about 0.1Ω / □.

In the case where light is irradiated from the conductive support side, the conductive support is preferably substantially transparent.
Substantially transparent means that the light transmittance is 10% or more, preferably 50% or more, and particularly preferably 70% or more.

The transparent conductive support is preferably a transparent substrate made of a conductive metal oxide formed on the surface of a transparent substrate such as glass or plastic by coating or vapor deposition. Of these, conductive glass in which a conductive layer made of tin dioxide doped with fluorine is deposited on a transparent substrate made of low-cost soda-lime float glass is preferable. For a low-cost and flexible photoelectric conversion element or solar cell, a transparent polymer film provided with a conductive layer is preferably used. Transparent polymer film materials include tetraacetyl cellulose (TAC),
Polyethylene terephthalate (PET), polyethylene naphthalate (PEN), syndiotactic polysterene (SPS), polyphenylene sulfide (PPS), polycarbonate (PC), polyarylate (PAr), polysulfone (PSF), polyester sulfone (PES) , Polyetherimide (PEI), cyclic polyolefin, brominated phenoxy and the like. To ensure sufficient transparency,
The coating amount of the conductive metal oxide is preferably a support 1 m ² per 0.01~100g of glass or plastic.

It is preferable to use a metal lead for the purpose of lowering the resistance of the transparent conductive support. The material of the metal lead is preferably a metal such as aluminum, copper, silver, gold, platinum, and nickel, and particularly preferably aluminum and silver. The metal lead is preferably provided on a transparent substrate by vapor deposition, sputtering, or the like, and a transparent conductive layer made of tin oxide doped with fluorine or an ITO film is preferably provided thereon. It is also preferable to provide a metal lead on the transparent conductive layer after providing the transparent conductive layer on the transparent substrate. The decrease in the amount of incident light due to the installation of the metal leads is preferably within 10%, more preferably 1 to 5%.

(B) Photosensitive Layer In the photosensitive layer containing the semiconductor fine particles sensitized by the metal complex dye of the present invention, the semiconductor fine particles act as a so-called photoreceptor, absorb light to separate electric charges, and form electrons and positive electrons. Creates a hole. In the dye-sensitized semiconductor fine particles, light absorption and the resulting generation of electrons and holes mainly occur in the dye, and the semiconductor fine particles have a role of receiving and transmitting the electrons.

(1) Semiconductor Fine Particles Semiconductor fine particles include a simple semiconductor such as silicon or germanium, a III-V compound semiconductor, a metal chalcogenide (eg, oxide, sulfide, selenide, etc.), or a perovskite structure. Compounds (for example, strontium titanate, calcium titanate, sodium titanate, barium titanate, potassium niobate, etc.) can be used.

Preferred chalcogenides of metals include titanium, tin, zinc, iron, tungsten, zirconium, hafnium, strontium, indium, cerium, yttrium, lanthanum, vanadium, oxides of niobium or tantalum, cadmium, zinc, lead, silver, Examples include antimony or bismuth sulfide, cadmium or lead selenide, and cadmium telluride. Other compound semiconductors include phosphides such as zinc, gallium, indium and cadmium, selenides of gallium-arsenic or copper-indium, and sulfides of copper-indium.

Preferred specific examples of the semiconductor used in the present invention are Si, TiO ₂ , SnO ₂ , Fe ₂ O ₃ , WO ₃ , ZnO, Nb ₂ O ₅ , CdS, Z
nS, PbS, Bi ₂ S ₃ , CdSe, CdTe, GaP, InP, GaAs, CuIn
S ₂ , CuInSe ₂ or the like, more preferably TiO ₂ , ZnO, Sn
O ₂ , Fe ₂ O ₃ , WO ₃ , Nb ₂ O ₅ , CdS, PbS, CdSe, InP, GaAs,
CuInS ₂ or CuInSe ₂ , particularly preferably TiO ₂ or Nb ₂ O ₅ , most preferably TiO ₂ .

The semiconductor used in the present invention may be single crystal or polycrystal. From the viewpoint of conversion efficiency, a single crystal is preferable,
Polycrystal is preferred from the viewpoints of production cost, securing of raw materials, energy payback time and the like.

Although the particle size of the semiconductor fine particles is generally on the order of nm to μm, the average particle size of the primary particles obtained from the diameter when the projected area is converted into a circle is preferably from 5 to 200 nm, and from 8 to 200 nm. 100 nm is more preferred. The average particle size of the semiconductor fine particles (secondary particles) in the dispersion is preferably 0.01 to 100 μm.

Two or more types of fine particles having different particle size distributions may be mixed. In this case, the average size of the small particles is 5 nm.
It is preferred that: For the purpose of improving the light capture rate by scattering incident light, semiconductor particles having a large particle size, for example, about 300 nm may be mixed.

As a method for producing semiconductor fine particles, "Science of Sol-Gel Method" by Agio Sakuhana (Agne Shofusha, 1998) and "Thin Film Coating Technology by Sol-Gel Method" by Technical Information Association (1995) ), Tadao Sugimoto, "Synthesis of Monodisperse Particles and Size Morphology Control by New Synthetic Gel-Sol Method", Materia, Vol. 35, No. 9, 1012-1018.
The gel-sol method described on page (1996) is preferred. Also
A method developed by Degussa to produce an oxide by high-temperature hydrolysis of a chloride in an oxyhydrogen salt is also preferable.

When the semiconductor fine particles are titanium oxide, any of the above-mentioned sol-gel method, gel-sol method, and high-temperature hydrolysis method in chloride oxyhydrogen salt are preferred. Applied Technology "Gihodo Publishing (1997)
The sulfuric acid method and the chlorine method described in (1) can also be used. Further, the sol-gel method is described in Barb et al., Journal of American Ceramic Society, Vol.
No. 12, pages 3157-3171 (1997), and Burnside et al., Chemical Materials, Vol. 10, No. 9,
The method described on pages 2419 to 2425 is also preferred.

(2) Semiconductor fine particle layer In order to coat the semiconductor fine particles on the conductive support, in addition to the method of applying a dispersion or colloid solution of the semiconductor fine particles on the conductive support, the above-mentioned sol-gel A method can also be used. In consideration of mass production of photoelectric conversion elements, physical properties of semiconductor fine particle liquid, flexibility of a conductive support, and the like, a wet film forming method is relatively advantageous. As a wet film forming method, a coating method and a printing method are typical.

As a method for preparing a dispersion of semiconductor fine particles, in addition to the above-mentioned sol-gel method, a method of grinding in a mortar, a method of dispersing while pulverizing using a mill, or a method of preparing a solvent when synthesizing a semiconductor. A method of precipitating fine particles in the solution and using it as it is, may be mentioned.

Examples of the dispersion medium include water and various organic solvents (eg, methanol, ethanol, isopropyl alcohol, dichloromethane, acetone, acetonitrile, ethyl acetate, etc.). At the time of dispersion, a polymer, a surfactant, an acid, a chelating agent, or the like may be used as a dispersing aid, if necessary.

The application method includes a roller method and a dipping method as an application system, an air knife method and a blade method as a metering system, and a method in which the application and the metering can be the same part.
No. 589, the wire bar method disclosed in U.S. Pat.
The slide hopper method, extrusion method, curtain method and the like described in JP-A Nos. 94, 2761419, 2761791 and the like are preferable. As a general-purpose machine, a spin method or a spray method is also preferable. As the wet printing method, intaglio printing, rubber printing, screen printing, and the like are preferable, including three major printing methods of letterpress, offset and gravure. From these, a preferable film forming method is selected according to the liquid viscosity and the wet thickness.

The viscosity of the dispersion of semiconductor fine particles greatly depends on the type and dispersibility of the semiconductor fine particles, the type of solvent used, and additives such as a surfactant and a binder. For a high viscosity liquid (for example, 0.01 to 500 Poise), an extrusion method, a casting method, a screen printing method, or the like is preferable. For a low-viscosity liquid (for example, 0.1 Poise or less), a slide hopper method, a wire bar method, or a spin method is preferable, and a uniform film can be formed. If a certain amount of coating is used, application by the extrusion method is possible even in the case of a low-viscosity liquid. As described above, a wet film forming method may be appropriately selected according to the viscosity of the coating solution, the coating amount, the support, the coating speed, and the like.

The layer of semiconductor fine particles is not limited to a single layer, but a multi-layer coating of a dispersion of semiconductor fine particles having different particle diameters, or a coating layer containing semiconductor fine particles of different types (or different binders and additives) may be formed in multiple layers. It can also be applied. Multilayer coating is effective even when the film thickness is insufficient by one coating. The extrusion method or the slide hopper method is suitable for multilayer coating. In the case of multi-layer coating, multi-layer coating may be performed at the same time, or several to dozens of times may be sequentially applied. Furthermore, a screen printing method can also be preferably used in the case of successive coating.

In general, as the thickness of the semiconductor fine particle layer (same as the thickness of the photosensitive layer) becomes larger, the amount of dye carried per unit projected area increases, so that the light capture rate increases, but the diffusion distance of generated electrons increases. Therefore, the loss due to charge recombination also increases. Therefore, the preferred thickness of the semiconductor fine particle layer is
It is 0.1-100 μm. When used in a photoelectrochemical cell, the thickness of the semiconductor fine particle layer is preferably 1 to 30 μm, and 2 to 25 μm.
Is more preferred. The coating amount of the semiconductor fine particles per m ² of the support is preferably 0.5 to 400 g, more preferably 5 to 100 g.

After the semiconductor fine particles are coated on the conductive support, the semiconductor fine particles are brought into electronic contact with each other,
Heat treatment is preferably performed to improve the strength of the coating film and the adhesion to the support. A preferred heating temperature range is from 40 ° C to less than 700 ° C, more preferably from 100 ° C to 600 ° C. The heating time is about 10 minutes to 10 hours. When a support having a low melting point or softening point such as a polymer film is used, high-temperature treatment is not preferable because it causes deterioration of the support. It is preferable that the temperature be as low as possible from the viewpoint of cost. The lowering of the temperature can be attained by the above-mentioned combined use of small semiconductor particles of 5 nm or less, heat treatment in the presence of a mineral acid, and the like.

For the purpose of increasing the surface area of the semiconductor fine particles after the heat treatment, increasing the purity in the vicinity of the semiconductor fine particles, and increasing the efficiency of electron injection from the dye to the semiconductor particles, for example, chemical plating using an aqueous solution of titanium tetrachloride or trichloride. Electrochemical plating using an aqueous titanium solution may be performed.

It is preferable that the semiconductor fine particles have a large surface area so that many dyes can be adsorbed. Therefore, the surface area in a state where the layer of semiconductor fine particles is coated on the support is preferably 10 times or more the projected area,
Further, it is preferably 100 times or more. The upper limit is not particularly limited, but is usually about 1000 times.

(3) Adsorption of Metal Complex Dye on Semiconductor Fine Particles The metal complex dye is adsorbed on the semiconductor fine particles by dipping a conductive support having a well-dried semiconductor fine particle layer in a solution of the metal complex dye. Alternatively, a method of applying a solution of a metal complex dye to the semiconductor fine particle layer can be used. In the former case, a dipping method, a dipping method, a roller method, an air knife method, or the like can be used. In the case of the immersion method, the adsorption of the metal complex dye may be performed at room temperature, or may be performed by heating and refluxing as described in JP-A-7-249790. The latter coating method includes a wire bar method, a slide hopper method, an extrusion method, a curtain method, a spin method, a spray method and the like, and a printing method includes letterpress, offset, gravure, screen printing and the like. The solvent can be appropriately selected according to the solubility of the metal complex dye. For example, alcohols (methanol, ethanol, t-butanol, benzyl alcohol, etc.), nitriles (acetonitrile, propionitrile, 3-methoxypropionitrile, etc.), nitromethane, halogenated hydrocarbons (dichloromethane, dichloroethane, chloroform, chlorobenzene) ), Ethers (diethyl ether, tetrahydrofuran, etc.), dimethyl sulfoxide, amides (N, N-
Dimethylformamide, N, N-dimethylacetamide, etc.)
N-methylpyrrolidone, 1,3-dimethylimidazolidinone,
3-methyloxazolidinone, esters (ethyl acetate,
Butyl acetate, etc.), carbonates (diethyl carbonate, ethylene carbonate, propylene carbonate, etc.), ketones (acetone,
Examples thereof include 2-butanone, cyclohexanone, etc.), hydrocarbons (hexane, petroleum ether, benzene, toluene, etc.), water, and a mixed solvent thereof.

As for the viscosity of the solution of the metal complex dye, a high viscosity liquid (for example, 0.01
~ 500 Poise), various printing methods other than the extrusion method are suitable, and low viscosity liquids (for example, 0.1 Poise or less)
In this case, a slide hopper method, a wire bar method or a spin method is suitable, and any of them can form a uniform film.

As described above, the viscosity of the coating solution of the metal complex dye,
The dye adsorption method may be appropriately selected according to the amount of application, the conductive support, the application speed, and the like. The time required for dye adsorption after coating should be as short as possible in consideration of mass production.

Since the presence of unadsorbed metal complex dye causes disturbance of device performance, it is preferable to remove the dye by washing immediately after adsorption. It is preferable to perform washing with a polar solvent such as acetonitrile and an organic solvent such as an alcohol solvent using a wet washing tank. In order to increase the amount of dye adsorbed,
It is preferable to perform a heat treatment before the adsorption. After the heat treatment, it is preferable that the dye be quickly adsorbed at a temperature of 40 to 80 ° C. without returning to room temperature in order to avoid the adsorption of water on the surface of the semiconductor fine particles.

The total amount of the metal complex dye used is preferably 0.01 to 100 mmol per unit surface area (1 m ² ) of the conductive support. The amount of the dye adsorbed on the semiconductor fine particles is preferably 0.01 to 1 mmol per 1 g of the semiconductor fine particles. By setting the adsorption amount of the metal complex dye as described above, a sufficient sensitizing effect in the semiconductor can be obtained. On the other hand, if the amount of the dye is too small, the sensitizing effect becomes insufficient, and if the amount of the dye is too large, the dye not adhering to the semiconductor floats and causes a reduction in the sensitizing effect.

In order to widen the wavelength range of the photoelectric conversion as much as possible and to increase the conversion efficiency, two or more dyes can be mixed. In this case, it is preferable to select the dyes to be mixed and the ratio thereof so as to match the wavelength range and the intensity distribution of the light source. Specifically, the metal complex dye of the present invention is
It is possible to use more than one kind in combination, or to use the metal complex dye of the present invention in combination with a conventional metal complex dye and / or polymethine dye.

For the purpose of reducing the interaction between metal complex dyes such as association, a colorless compound may be co-adsorbed on the semiconductor fine particles. Examples of the hydrophobic compound to be co-adsorbed include a steroid compound having a carboxyl group (for example, chenodeoxycholic acid). Further, an ultraviolet absorber can be used in combination.

For the purpose of promoting the removal of excess metal complex dye, the surface of the semiconductor fine particles may be treated with an amine after adsorbing the metal complex dye. Preferred amines include pyridine, 4-t-butylpyridine, polyvinylpyridine and the like. When these are liquids, they may be used as they are, or may be used after being dissolved in an organic solvent.

(C) Charge Transfer Layer The charge transfer layer is a layer having a function of replenishing the oxidized metal complex dye with electrons. Typical materials that can be used for the charge transfer layer include a liquid (electrolytic solution) in which a redox couple is dissolved in an organic solvent, a so-called gel electrolyte in which a liquid in which a redox couple is dissolved in an organic solvent is impregnated in a polymer matrix,
Molten salts containing a redox couple may be mentioned. Further, a solid electrolyte or a hole transporting material can be used.

The electrolytic solution used in the present invention preferably comprises an electrolyte, a solvent and an additive. As the electrolyte,
(A) I ₂ and an iodide (a metal iodide such as LiI, NaI, KI, CsI, and CaI ₂ , or an iodide salt of a quaternary ammonium compound such as a tetraalkylammonium iodide, a pyridinium iodide, an imidazolium iodide, and the like) ), And (b) Br ₂ and bromide (LiBr, NaBr, KBr, CsBr, C
a bromide such as aBr ₂ or a bromide salt of a quaternary ammonium compound such as tetraalkylammonium bromide and pyridinium bromide); Metal complexes, (d) sodium polysulfide, sulfur compounds such as alkylthiol-alkyldisulfide, (e) viologen dyes, hydroquinone-quinone and the like can be used. Among them, I ₂ and LiI or pyridinium iodide, electrolyte obtained by combining the iodine salt of imidazolium iodide quaternary ammonium compounds such as id are preferred. The above electrolytes may be used as a mixture. The electrolyte is EP718288, WO95 / 18456, J. Electrochem. So
c., Vol. 143, No. 10, 3099 (1996), Inorg. Chem., 35,
The salt in a molten state at room temperature (molten salt) described in 1168 to 1178 (1996) can also be used. When a molten salt is used as an electrolyte, a solvent need not be used.

The preferred electrolyte concentration is 0.1 to 15M, more preferably 0.2 to 10M. The preferred concentration of iodine when adding iodine to the electrolyte is 0.01 to 0.5 M.
It is.

As the solvent for the electrolyte, a compound that can exhibit excellent ionic conductivity because it has low viscosity and high ion mobility, or has high dielectric constant and high effective carrier concentration, or both is used. It is desirable. Examples of such solvents include, for example, the following.

(A) Carbonates Esters such as ethylene carbonate, propylene carbonate, vinylene carbonate, butylene carbonate, dimethyl carbonate, diethyl carbonate, methyl ethyl carbonate and dipropyl carbonate are preferred.

(B) Lactones For example, γ-butyrolactone, γ-valerolactone, γ-caprolactone, crotlactone, γ-caprolactone, δ-valerolactone and the like are preferable.

(C) Ethers For example, ethyl ether, 1,2-dimethoxyethane, diethoxyethane, trimethoxymethane, ethylene glycol dimethyl ether, polyethylene glycol dimethyl ether, 1,3-dioxolan, 1,4-dioxane and the like are preferable.

(D) Alcohols For example, methanol, ethanol, ethylene glycol monomethyl ether, propylene glycol monoethyl ether, polyethylene glycol monoalkyl ether, polypropylene glycol monoalkyl ether and the like are preferable.

(E) Glycols For example, ethylene glycol, propylene glycol, polyethylene glycol, polypropylene glycol, glycerin and the like are preferable.

(F) Glycol ethers Preferred are, for example, ethylene glycol dialkyl ether, propylene glycol dialkyl ether, polyethylene glycol dialkyl ether, polypropylene glycol dialkyl ether and the like.

(G) Tetrahydrofurans For example, tetrahydrofuran, 2-methyltetrahydrofuran and the like are preferable.

(H) Nitriles For example, acetonitrile, glutarodinitrile, propionitrile, methoxyacetonitrile, benzonitrile and the like are preferable.

(I) Carboxylic esters Esters such as methyl formate, methyl acetate, ethyl acetate and methyl propionate are preferred.

(J) Phosphoric acid triesters For example, trimethyl phosphate, triethyl phosphate and the like are preferable.

(K) Heterocyclic compounds For example, N-methylpyrrolidone, 4-methyl-1,3-dioxane, 2-methyl-1,3-dioxolan, 3-methyl-2-oxazolidinone, 1,3-propanesal Ton, sulfolane and the like are preferred.

(L) Other aprotic organic solvents such as dimethyl sulfoxide, formamide, N, N-dimethylformamide, nitromethane, etc.
Water and the like are preferred.

Of these, carbonate-based, nitrile-based and heterocyclic compound-based solvents are preferred. These solvents may be used as a mixture of two or more as necessary.

In the present invention, J. Am. Ceram. Soc., 80
(12), 3157-3171 (1997).
Basic compounds such as butylpyridine, 2-picoline and 2,6-lutidine can also be added. A preferred concentration range when adding a basic compound is 0.05 to 2M.

The electrolyte can be gelled (solidified) by a method such as addition of a polymer or an oil gelling agent, polymerization of coexisting polyfunctional monomers, and crosslinking reaction with the polymer. When gelling by adding a polymer, use "Polymer Electrolyte Reviews-1,2" (JR Mac
ELSEIVER APPLIED SCIE co-edited by CaLLum and CA Vincent
NCE) can be used,
In particular, it is preferable to use polyacrylonitrile and polyvinylidene fluoride. When gelation is performed by adding an oil gelling agent, use J. Chem. Soc. Japan, Ind. Chem. Se.
c., 46, 779 (1943), J. Am. Chem. Soc., 111, 5542.
(1989), J. Chem. Soc., Chem. Commun., 1993, 390, A
ngew. Chem. Int. Ed. Engl., 35, 1949 (1996), Chem.
Lett., 1996, 885; J. Chem. Soc., Chem. Commun., 5
45 (1997) and the like can be used. Among these, preferred are compounds having an amide structure in the molecular structure.

When a gel electrolyte is formed by polymerization of polyfunctional monomers coexisting in the electrolyte, a solution is prepared from the polyfunctional monomers, a polymerization initiator, an electrolyte and a solvent,
Coating is performed on the dye-sensitized semiconductor fine particle layer (photosensitive layer 20) by a method such as a casting method, a coating method, a dipping method, and an impregnation method. FIG.
As shown in (2), it is preferable to fill the voids between the dye-sensitized semiconductor fine particles 21 with a sol-like electrolyte, form a sol-like electrolyte layer on the photosensitive layer 20, and then gel it by radical polymerization.

The polyfunctional monomer is preferably a compound having two or more ethylenically unsaturated groups, for example, divinylbenzene, ethylene glycol dimethacrylate,
Preferred are ethylene glycol diacrylate, ethylene glycol dimethacrylate, diethylene glycol diacrylate, diethylene glycol dimethacrylate, triethylene glycol diacrylate, triethylene glycol dimethacrylate, pentaerythritol triacrylate, trimethylolpropane triacrylate, and the like.

The gel electrolyte may contain a monofunctional monomer in addition to the above polyfunctional monomer. Examples of the monofunctional monomer include esters or amides derived from acrylic acid or α-alkylacrylic acid (eg, methacrylic acid) (eg, N-isopropylacrylamide, acrylamide, 2-acrylamido-2-methylpropanesulfonic acid, Derived from acrylamidopropyltrimethylammonium chloride, methyl acrylate, hydroxyethyl acrylate, N-propyl acrylate, N-butyl acrylate, 2-methoxyethyl acrylate, cyclohexyl acrylate, etc., vinyl esters (eg vinyl acetate), maleic acid or fumaric acid Esters (eg, dimethyl maleate, dibutyl maleate, diethyl fumarate, etc.) and organic acid salts (eg, sodium salt of maleic acid, fumaric acid or p-styrenesulfonic acid) ), A nitrile (acrylonitrile,
Methacrylonitrile, etc.), dienes (eg, butadiene, cyclopentadiene, isoprene, etc.), aromatic vinyl compounds (eg, styrene, p-chlorostyrene, sodium styrenesulfonate, etc.), vinyl compounds having a nitrogen-containing heterocyclic ring, Vinyl compounds having a quaternary ammonium salt, N-vinylformamide, N-vinyl-N-methylformamide, vinylsulfonic acid, sodium vinylsulfonate, vinylidene fluoride, vinylidene chloride, vinyl alkyl ethers (eg, methyl vinyl ether) , Olefins (ethylene, propylene, 1-
Butene, isobutene, etc.), N-phenylmaleimide and the like. The ratio of the polyfunctional monomer to the total amount of the monomers is preferably 0.5 to 70% by weight, more preferably
1.0 to 50% by weight.

The above-mentioned monomers for gel electrolytes are described in Takatsu Otsu,
Masayoshi Kinoshita, "Experimental Methods for Polymer Synthesis" (Chemical Doujin)
Alternatively, the polymerization can be carried out by a radical polymerization method which is a general polymer synthesis method described in “Lecture Polymerization Theory 1 Radical Polymerization (I)” by Takayuki Otsu (Chemical Doujinshi). Radical polymerization of monomers for gel electrolyte is performed by heating, light,
It can be carried out by ultraviolet rays, electron beams or the like or electrochemically, but it is particularly preferable to carry out radical polymerization by heating.

When a crosslinked polymer is formed by heating, preferred polymerization initiators are, for example, 2,2′-azobis (isobutyronitrile), 2,2′-azobis (dimethylvaleronitrile), dimethyl 2,2 ′ Azo initiators such as azobis (2-methylpropionate) and peroxide initiators such as benzoyl peroxide. The preferable addition amount of the polymerization initiator is 0.01 to 20% by weight, more preferably 0.1 to 10% by weight, based on the total amount of the monomers.

The weight composition range of the monomers in the gel electrolyte is preferably from 0.5 to 70% by weight, more preferably from 1.0 to 50% by weight.

When the electrolyte is gelled by a crosslinking reaction of the polymer, it is desirable to use a polymer having a crosslinking reactive group and a crosslinking agent together. Preferred crosslinkable reactive groups are
It is a nitrogen-containing heterocyclic ring (for example, a pyridine ring, an imidazole ring, a thiazole ring, an oxazole ring, a triazole ring, a morpholine ring, a piperidine ring, a piperazine ring, etc.), and a preferable crosslinking agent is capable of electrophilic reaction with a nitrogen atom. Reagents having two or more functionalities (eg, alkyl halides, aralkyl halides, sulfonic acid esters, acid anhydrides, acid chlorides, isocyanates, etc.).

Organic and / or inorganic hole transporting materials can be used in place of the electrolyte. Examples of the organic hole transporting material that can be preferably used in the present invention include the following.

(A) Aromatic amines N, N'-diphenyl-N, N'-bis (4-methoxyphenyl)-(1,
1'-biphenyl) -4,4'-diamine (J. Hagen et al., Syn
thetic Metal, 89, 2153-220, (1997)), 2,2 ', 7,7'-
Tetrakis (N, N-di-p-methoxyphenylamine) 9,9'-spirobifluorene (Nature, Vol. 395, 8 Oct. 1998, p
p.583-585 and WO97 / 10617), aromatic diamine compounds in which tertiary aromatic amine units of 1,1-bis [4- (di-p-tolylamino) phenyl] cyclohexane are linked (Japanese Unexamined Patent Publication No. 59-1)
No. 94393) and 4,4′-bis [(N-1-naphthyl) -N-phenylamino] biphenyl containing two or more tertiary amines and two or more fused aromatic rings having a nitrogen atom , An aromatic triamine having a starburst structure with a derivative of triphenylbenzene (US Pat. No. 4,923,774, JP-A-4-308688), N, N'-
Aromatic diamines such as diphenyl-N, N′-bis (3-methylphenyl)-(1,1′-biphenyl) -4,4′-diamine (US Pat. No. 4,764,625), α, α, α ′, α'-tetramethyl-α, α'-
Bis [4- (di-p-tolylamino) phenyl] -p-xylene (JP-A-3-269084), a p-phenylenediamine derivative, and a triphenylamine derivative whose whole molecule is sterically asymmetric (JP-A-4-129271) ), A compound in which a pyrenyl group is substituted with a plurality of aromatic diamino groups (JP-A-4-175395), an aromatic diamine in which a tertiary aromatic amine unit is linked by an ethylene group (JP-A-4-264189), styryl Aromatic diamines having a structure (Japanese Patent Application Laid-Open No. 4-290851), benzylphenyl compounds (Japanese Patent Application Laid-Open No. 4-364153), tertiary amines linked by a fluorene group (Japanese Patent Application Laid-Open No. 5-25473), and triamine compounds (JP-A-5-25473) Kaihei 5-239455), bis (dipyridylamino) biphenyl (JP-A-5-320634), N, N, N-triphenylamine derivatives (JP-A-6-1972), and aromatic diamines having a phenoxazine structure Kaihei 7-138562), diaminophenylfe Ntorijin derivatives (JP-A-7-252474) and the like.

(B) Oligothiophene compounds α-octylthiophene and α, ω-dihexyl-α-octylthiophene (Adv. Mater., Vol. 9, No. 7, 5578)
(1997)), hexadodecyldodecithiophene (Angew. C
hem. Int. Ed. Engl., 34, No. 3, 303-307 (1995)),
2,8-dihexyl anthra [2,3-b: 6,7-b '] dithiophene (JACS, Vol. 120, No. 4, 664-672 (1998)) and the like.

(C) Conducting Polymer Polypyrrole (K. Murakoshi et al., Chem. Lett., 19
97, p. 471), and polyacetylene and its derivatives, poly (p-phenylene) and its derivatives, poly (p-phenylenevinylene) and its derivatives, polythienylenevinylene and its derivatives, polythiophene and its derivatives, polyaniline and its Derivatives and polytoluidine and its derivatives (each described in the Handbook of
Organic Conductive Molecules and Polymers, ”Vol.
1-4 (written by NALWA, WILEY Publishing)).

Organic, hole-transporting materials include Nature,
As described in Vol. 395, 8 Oct. 583-585 (1998), a compound containing a cation radical such as tris (4-bromophenyl) aminium hexachloroantimonate is used to control the dopant level. Alternatively, a salt such as Li [(CF ₃ SO ₂ ) ₂ N] may be added in order to control the potential of the oxide semiconductor surface (compensate for the space charge layer).

The organic hole transporting material can be introduced into the inside of the electrode by a method such as a vacuum evaporation method, a casting method, a coating method, a spin coating method, an immersion method, an electrolytic polymerization method and a photoelectrolytic polymerization method. When a hole transport material is used instead of an electrolyte, use Electorochim. Acta, 40, 643-6 to prevent short circuits.
It is preferable to apply a thin layer of titanium dioxide as an undercoat layer by using a technique such as spray pyrolysis described in JP 52 (1995).

When an inorganic solid compound is used in place of the electrolyte, copper iodide (p-CuI) (J. Phys. D: Appl. Phys.,
31, 1492-1496 (1998)), copper thiocyanate (Thin Sol
id Films, 261 (1995), 307-310, J. Appl. Phys., 80
(8), 15 October 1996, 4749-4754, Chem. Mater., 19
98, 10, 1501-1509, SemiCond.Sci. Technol., 10,16
89 to 1693) can be introduced into the electrode by a method such as a casting method, a coating method, a spin coating method, a dipping method, and an electrolytic plating method.

To form the charge transfer layer, the following two methods can be used. One is to attach a counter electrode via a spacer on the dye-sensitized semiconductor fine particle layer,
This is a method in which the open ends of both are immersed in an electrolyte solution to allow the electrolyte solution to penetrate into the semiconductor fine particle layer and the gap between the semiconductor fine particle layer and the counter electrode. The other is a method in which an electrolyte solution is applied to the semiconductor fine particle layer so that the electrolyte solution penetrates into the semiconductor fine particle layer, a charge transfer layer is formed on the semiconductor fine particle layer, and finally a counter electrode is provided.

In the former case, as a method for infiltrating the electrolyte solution into the gap between the semiconductor fine particle layer and the counter electrode, a normal pressure method utilizing a capillary phenomenon, and an upper open end of the semiconductor fine particle layer and the counter electrode (when immersed in the electrolyte solution). There is a decompression method that sucks from the open end that does not exist.

In the latter case, in the case of a wet type charge transfer layer, a counter electrode is provided while it is not dried, and measures are taken to prevent liquid leakage at the edge portion. In the case of a gel electrolyte, a counter electrode may be provided after being wet-coated and solidified by a method such as polymerization, or a solid may be provided after the counter electrode is provided. As a method of forming a layer of a wet organic hole transport material or a gel electrolyte in addition to the electrolytic solution, as in the case of forming a semiconductor fine particle layer and dye adsorption, a dipping method, a roller method, a dipping method, an air knife method, An extrusion method, a slide hopper method, a wire bar method, a spin method, a spray method, a casting method, various printing methods and the like can be used. In the case of a solid electrolyte or a solid hole (hole) transport material, the charge transfer layer may be formed by a dry film forming process such as a vacuum evaporation method or a CVD method, and then a counter electrode may be provided.

In the case of an electrolyte which cannot be solidified or a wet hole transporting material, it is preferable to seal the edge portion immediately after coating, and in the case of a solidifying hole transporting material, it is preferable that the hole transport material be wetted. After forming the hole transport layer, it is preferable to solidify the film by a method such as photopolymerization or thermal radical polymerization. As described above, the film application method may be appropriately selected depending on the physical properties of the electrolyte and the process conditions.

The amount of water in the charge transfer layer was 10,000 ppm.
The following is preferred, more preferably 2,000 ppm or less, and particularly preferably 100 ppm or less.

(D) Counter electrode When the photoelectric conversion element is a photoelectrochemical cell, the counter electrode functions as a positive electrode of the photoelectrochemical cell. The counter electrode may have a single-layer structure of a counter electrode conductive layer made of a conductive material, or may be composed of a counter electrode conductive layer and a support substrate, similarly to the above-described conductive support. Examples of the conductive material used for the counter electrode conductive layer include metals (for example, platinum, gold, silver, copper, aluminum, rhodium, indium, etc.), carbon, and conductive metal oxides (indium-tin composite oxide, tin oxide doped with fluorine). And the like). Preferred examples of the supporting substrate for the counter electrode are glass and plastic, to which the above-described conductive material is applied or vapor-deposited. The thickness of the counter electrode conductive layer is not particularly limited, but is preferably 3 nm to 10 μm. When the counter electrode conductive layer is made of metal, its thickness is preferably 5 μm or less, more preferably 5 nm to 3 μm.
Range.

Since light may be irradiated from one or both of the conductive support and the counter electrode, at least one of the conductive support and the counter electrode is substantially transparent in order for the light to reach the photosensitive layer. I just need. From the viewpoint of improving power generation efficiency,
It is preferable that the conductive support is made transparent and light is incident from the conductive support side. In this case, the counter electrode preferably has a property of reflecting light. As such a counter electrode, glass or plastic on which a metal or a conductive oxide is deposited, or a metal thin film can be used.

The procedure for providing the counter electrode support is as follows:
Providing a charge transfer layer after forming it,
(B) There are two cases in which a counter electrode is disposed on a layer of dye-sensitized semiconductor fine particles via a spacer, and then the space is filled with an electrolyte solution. In the case of (a), a conductive material is applied directly on the charge transfer layer, plated or vapor-deposited (PVD, CVD), or the conductive layer side of the substrate having the conductive layer is attached. In the case of (b), a counter electrode is assembled and fixed on the dye-sensitized semiconductor fine particle layer via a spacer, and the open end of the obtained assembly is immersed in an electrolyte solution, and utilizing capillary action or decompression. An electrolyte solution is made to penetrate into the gap between the dye-sensitized semiconductor fine particle layer and the counter electrode. In this case, if the electrolyte is a polymer electrolyte or the like, crosslinking is performed by heating or the like as necessary.
Further, similarly to the case of the conductive support, it is preferable to use a metal lead for the purpose of reducing the resistance of the counter electrode, particularly when the counter electrode is transparent. Note that the preferable material and the installation method of the metal lead, the decrease in the amount of incident light due to the installation of the metal lead, and the like are the same as those of the conductive support.

(E) Other Layers A functional layer such as a protective layer or an antireflection layer may be provided on one or both of the conductive support serving as an electrode and the counter electrode. When such a functional layer is formed in multiple layers, a simultaneous multilayer coating method or a sequential coating method can be used, but from the viewpoint of productivity, the simultaneous multilayer coating method is preferable. In the simultaneous multi-layer coating method, a slide hopper method or an extrusion method is suitable in consideration of productivity and uniformity of a coating film. In forming these functional layers, an evaporation method, a sticking method, or the like can be used depending on the material.

(F) Specific Example of Internal Structure of Photoelectric Conversion Element As described above, the internal structure of the photoelectric conversion element can take various forms according to the purpose. When roughly divided into two, a structure in which light can enter from both sides and a structure in which light can be entered only from one side are possible. 2 to 9 exemplify an internal structure of a photoelectric conversion element which can be preferably applied to the present invention.

FIG. 2 shows the transparent conductive layer 10a and the transparent counter electrode conductive layer 4.
The photosensitive layer 20 and the charge transfer layer 30 are interposed between the photosensitive layer 20a and the light transfer layer 0a, and have a structure in which light enters from both sides.
FIG. 3 shows that a metal lead 11 is partially provided on a transparent substrate 50a, a transparent conductive layer 10a is further provided, an undercoat layer 60, a photosensitive layer 20, a charge transfer layer 30, and a counter electrode conductive layer 40 are provided in this order. The substrate 50 is arranged, and has a structure in which light is incident from the conductive layer side. FIG. 4 shows that the conductive layer 10 is provided on the support substrate 50, the photosensitive layer 20 is provided via the undercoat layer 60, the charge transfer layer 30 and the transparent counter electrode conductive layer 40a are provided, and the metal leads 11 are partially provided. The provided transparent substrate 50a is arranged with the metal lead 11 side inside, and has a structure in which light enters from the counter electrode side. FIG. 5 shows that a metal lead 11 is provided on each of two transparent substrates 50a and a transparent conductive layer 10a or a transparent counter electrode conductive layer 40a is provided, respectively, and an undercoat layer 60, a photosensitive layer 20, and a charge transfer layer 30 are interposed therebetween. This is a structure in which light is incident from both sides. 6 has a transparent conductive layer 10a on a transparent substrate 50a, provides a photosensitive layer 20 via an undercoat layer 60, further provides a charge transfer layer 30 and a counter electrode conductive layer 40,
A support substrate 50 is disposed thereon, and has a structure in which light is incident from the conductive layer side. FIG. 7 shows that the conductive layer 10 is provided on the supporting substrate 50, the photosensitive layer 20 is provided via the undercoat layer 60, the charge transfer layer 30 and the transparent counter electrode conductive layer 40a are provided, and the transparent substrate 50a is disposed thereon. This is a structure in which light is incident from the counter electrode side. FIG. 8 has a transparent conductive layer 10a on a transparent substrate 50a, a photosensitive layer 20 is provided via an undercoat layer 60, a charge transfer layer 30 and a transparent counter electrode conductive layer 40a are further provided, and the transparent substrate 50a is provided thereon. They are arranged so that light enters from both sides. FIG. 9 shows a supporting substrate.
A conductive layer 10 is provided on 50, a photosensitive layer 20 is provided via an undercoat layer 60, a solid charge transfer layer 30 is further provided, and a counter electrode conductive layer 40 or a metal lead 11 is partially provided thereon,
Light is incident from the counter electrode side.

[3] Photoelectrochemical Battery The photoelectrochemical battery of the present invention is one in which the above-mentioned photoelectric conversion element is made to work in an external circuit. It is preferable that the side surface of the photoelectrochemical cell is sealed with a polymer, an adhesive, or the like in order to prevent deterioration of components and volatilization of the contents. The external circuit itself connected to the conductive support and the counter electrode via the lead may be a known one.

[4] Dye-Sensitized Solar Cell When the photoelectric conversion device of the present invention is applied to a so-called solar cell, the structure inside the cell is basically the same as the structure of the above-described photoelectric conversion device. Hereinafter, a module structure of a solar cell using the photoelectric conversion element of the present invention will be described.

The dye-sensitized solar cell of the present invention can have a module structure basically similar to a conventional solar cell module. The solar cell module generally has a structure in which cells are formed on a supporting substrate such as a metal and a ceramic, and the cells are covered with a filling resin or a protective glass or the like, and light is taken in from the opposite side of the supporting substrate. It is also possible to adopt a structure in which a transparent material such as tempered glass is used for the support substrate, a cell is formed thereon, and light is taken in from the transparent support substrate side. Specifically, a module structure called a superstrate type, a substrate type, or a potting type, a substrate-integrated module structure used in an amorphous silicon solar cell, and the like are known. The module structure of the dye-sensitized solar cell of the present invention can be appropriately selected depending on the purpose of use, the place of use, and the environment.

In a typical superstrate type or substrate type module, cells are arranged at regular intervals between supporting substrates which are transparent on one or both sides and have been subjected to antireflection treatment, and adjacent cells are made of metal leads or flexible. It is connected by wiring or the like, and a current collecting electrode is arranged on the outer edge, so that generated power is taken out to the outside. Between the substrate and the cell, various kinds of plastic materials such as ethylene vinyl acetate (EVA) may be used in the form of a film or a filling resin, depending on the purpose, in order to protect the cell and improve current collection efficiency. Also,
When used in places where it is not necessary to cover the surface with a hard material, such as places where there is little external impact, the surface protective layer is made of a transparent plastic film, or a protective function is provided by curing the above-mentioned filling resin. It is possible to eliminate the support substrate on one side. The periphery of the support substrate is fixed in a sandwich shape with a metal frame in order to secure the inside sealing and the rigidity of the module, and the space between the support substrate and the frame is hermetically sealed with a sealing material. Also,
If a flexible material is used for the cell itself, the supporting substrate, the filling material, and the sealing material, a solar cell can be formed on a curved surface.

In the super straight type solar cell module, for example, while a front substrate sent from a substrate supply device is conveyed by a belt conveyor or the like, a cell is formed thereon with a sealing material-cell connection lead wire, a back surface sealing. After laminating sequentially with materials and the like, a back substrate or a back cover can be placed, and a frame can be set on the outer edge to produce.

On the other hand, in the case of the substrate type, while the support substrate sent out from the substrate supply device is transported by a belt conveyor or the like, the cells are sequentially laminated thereon with the inter-cell connection lead wires, the sealing material, and the like. It can be manufactured by placing a front cover and setting a frame on the periphery.

FIG. 10 shows an example of a structure in which the photoelectric conversion element of the present invention is formed into a module integrated with a substrate. 10 has one face transparent conductive layer 10a on the transparent substrate 50a, further photosensitive layer 20 containing a dye-adsorbed TiO ₂ thereon, the solid charge transfer layer 30 and the metal counter electrically conductive layer 40 Is provided as a module, and an antireflection layer 70 is provided on the other surface of the substrate 50a.
Represents a structure provided with. In the case of such a structure, it is preferable to increase the area ratio of the photosensitive layer 20 (the area ratio when viewed from the substrate 50a which is the light incident surface) in order to increase the utilization efficiency of incident light.

In the case of the module having the structure shown in FIG. 10, selective plating, selective etching, and CVD are performed so that the transparent conductive layer, the photosensitive layer, the charge transfer layer, the counter electrode, and the like are arranged three-dimensionally at regular intervals on the substrate. , PVD and other semiconductor process technologies, laser scribing after pattern coating or wide coating, plasma CVM (Solar Energy Materials and Sola)
r Cells, 48, pp. 373-381), and a desired module structure can be obtained by patterning with a mechanical method such as grinding.

Hereinafter, other members and steps will be described in detail.

Examples of the sealing material include liquid EVA (ethylene vinyl acetate), depending on the purpose of imparting weather resistance, imparting electrical insulation, improving light collection efficiency, and improving cell protection (impact resistance).
Various materials such as a film-like EVA and a mixture of a vinylidene fluoride copolymer and an acrylic resin can be used. It is preferable to use a sealing material having high weather resistance and moisture resistance between the outer edge of the module and the frame surrounding the periphery. In addition, the strength and light transmittance can be increased by mixing a transparent filler into the sealing material.

When the sealing material is fixed on the cell, a method suitable for the physical properties of the material is used. In the case of film-like materials, various methods such as roll pressing, bar coating, spray coating, screen printing, etc. are possible. is there.

When a flexible material such as PET or PEN is used as a support substrate, a roll-shaped support is drawn out to form a cell thereon, and then a sealing layer is continuously laminated by the above-described method. Can be highly productive.

In order to increase the power generation efficiency, the surface of the substrate (generally tempered glass) on the light intake side of the module is subjected to an antireflection treatment. As the anti-reflection treatment method,
There are a method of laminating an antireflection film, a method of coating an antireflection layer, and the like.

Further, by treating the surface of the cell by a method such as grooving or texturing, it is possible to increase the utilization efficiency of incident light.

In order to increase the power generation efficiency, it is most important that the light is taken into the module without loss. However, the light that has passed through the photoelectric conversion layer and has reached the inside thereof is reflected to improve the efficiency toward the photoelectric conversion layer side. It is also important to return well. As a method of increasing the light reflectance, after mirror polishing the surface of the supporting substrate, a method of depositing or plating Ag or Al, etc., an alloy layer such as Al-Mg, Al-Ti at the bottom layer of the cell as a reflective layer. There are a method of providing a texture structure and a method of forming a texture structure in the lowermost layer by annealing.

In order to increase the power generation efficiency, it is important to reduce the connection resistance between cells from the viewpoint of suppressing the internal voltage drop. As a method of connecting the cells, wire bonding and connection using a conductive flexible sheet are generally used.However, a method of fixing the cells using a conductive adhesive tape or a conductive adhesive and simultaneously electrically connecting the cells, There is also a method of pattern-coating a conductive hot melt at a desired position.

In the case of a solar cell using a flexible support such as a polymer film, cells are sequentially formed by the above-described method while the roll-shaped support is being sent out, cut into a desired size, and the peripheral portion is made flexible and moisture-proof. The battery body can be manufactured by sealing with a material having a property.
Also, Solar Energy Materials and Solar Cells, 48,
A module structure called “SCAF” described in p383-391 can also be used. Further, a solar cell using a flexible support can be used by being adhered and fixed to a curved glass or the like.

As described in detail above, solar cells having various shapes and functions can be manufactured according to the purpose of use and environment of use.

[0204]

EXAMPLES The present invention will be described in more detail with reference to the following Examples, but it should not be construed that the present invention is limited thereto.

1. Synthesis of Metal Complex Dye Hereinafter, the metal complex dyes D-8, D-75, D-1, D-71, D-
3 and 3 show methods for synthesizing D-73.

[0206]

Embedded image

[0207]

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[0208]

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(A) Synthesis of D-8 24.6 g (0.2 mol) of p-anisidine 1 and 20 ml of concentrated hydrochloric acid were dissolved in 150 ml of water, and 39.7 g (0.24 mol) of chloral hydrate 2 and 250 g of sulfuric acid were added thereto. An aqueous solution in which sodium was dissolved in 850 ml of water was added, and an aqueous solution in which 49.7 g (0.71 mol) of hydroxylamine hydrochloride was dissolved in 600 ml of water was added, followed by refluxing for 10 minutes. The aqueous solution was cooled, and the crystals were separated by filtration and washed with water to obtain 33.7 g of brown crystals of oxime 3 (yield 8
7%).

17.5 g (90 mmol) of oxime 3 was added to 90% sulfuric acid 1
The mixture was dissolved in 00 ml and heated and stirred at 80 ° C. for 10 minutes. After cooling,
The mixture was stirred in 2 liters of water, and the resulting crystals were separated by filtration and washed with water to obtain 5.0 g of methoxyisatin 4 crystals (yield 31).
%).

1.95 g (11 mmol) of methoxyisatin 4
5.5 g in a mixture of 1.21 g (10 mmol) of acetylpyridine 5
NaOH 33% aqueous solution was added dropwise at 5 ° C, and 60 ° C for 1 hour at 5 ° C.
Stirred at C for 1 hour. Add 10 ml of ice water to this and filter.
After washing with ice water and acetone, 1.12 g of pyridylquinoline 6 crystals were obtained (yield 31%).

Dry 0.60 g (2 mmol) of pyridylquinoline 6 and 0.26 g (1 mmol) of ruthenium chloride trihydrate
It was dissolved in 15 ml of N, N-dimethylformamide and refluxed for 8 hours in a dark place under a nitrogen atmosphere. After concentration under reduced pressure, the residue was dispersed in acetonitrile and separated by filtration to obtain 0.77 g of crystals of ruthenium complex 7 (yield: 99%).

0.143 g (0.2 mmol) of ruthenium complex 7,
0.18 g (2.2 mmol) of sodium thiocyanate was dissolved in a mixed solvent of 10 ml of N, N-dimethylformamide / 3 ml of water, and the mixture was refluxed for 6 hours in a dark place under a nitrogen atmosphere. After concentrating under reduced pressure, dissolve in water, add dilute nitric acid to precipitate crystals, filter, wash with water,
Sephadex column LH-20 (Developing solvent: methanol)
To give 0.072 g of a metal complex dye D-8 (yield 5
0%). The structure was confirmed by an NMR spectrum.

(B) Synthesis of D-75 0.12 g (0.2 mmol) of ruthenium complex 8 and 0.032 g of sodium thiocyanate (2.4%) synthesized with reference to the method described in J. Chem. Soc., Dalton, 1973, 204. mmol) was dissolved in a mixed solvent of 30 ml of N, N-dimethylformamide / 10 ml of water, and the mixture was refluxed under a nitrogen atmosphere in a dark place for 2 hours. 0.06g to this
(0.2 mmol) of pyridylquinoline 6 was added and refluxed for 6 hours. Further, 15 ml of triethylamine was added and the mixture was refluxed for 6 hours. The reaction solution was concentrated, dissolved in methanol, purified by Sephadex column LH-20 (developing solvent: methanol), concentrated, dissolved in water, and diluted with nitric acid to precipitate crystals. Complex dye D-75 was obtained (yield 41
%). The structure was confirmed by an NMR spectrum.

(C) Synthesis of D-1 and D-71 Pyridylquinoline 10 was synthesized in the same manner as in the synthesis of pyridylquinoline 6, except that equimolar commercial isatin 9 was used instead of methoxyisatin 4. did. Using this pyridylquinoline 10 instead of pyridylquinoline 6, metal complex dyes D-1 and D-71 were synthesized in exactly the same manner as in the synthesis of D-8 and D-75, respectively. The structure is NMR
The spectrum was confirmed.

(D) Synthesis of D-3 and D-73 The above D-1 and D-7 were used except that 1/2 mol of sodium dithiocarbamate 11 was used instead of sodium thiocyanate.
Metal complex dyes D-3 and D-73 were synthesized in exactly the same manner as in the synthesis of 1. The structure was confirmed by an NMR spectrum.

(E) Synthesis of Other Dyes Other metal complex dyes used in the following examples can be synthesized in the same manner as the above synthesis examples by appropriately combining specific examples of each ligand. Each ligand can be easily obtained as a commercial product or can be obtained from Synth. Commun., 2
7, 2165 (1997), Aust. J. Chem., 25, 1631 (1972) and the like, or can be synthesized with reference to these references.

[0219] 2. Measurement of Absorption Spectra Absorption spectra in methanol of D-1, D-3, D-8, D-71, D-73, D-75 and Comparative Dye 1 were measured.
Table 1 shows the absorption maximum wavelength and the long wavelength end.

[0219]

[Table 1]

As is clear from Table 1, the maximum absorption wavelength of the metal complex dye of the present invention was longer and broader than that of Comparative Dye 1. Therefore, it is very preferable to use the metal complex dye of the present invention in a photoelectrochemical cell because it can spectrally sensitize even longer wavelength light and convert it into a photocurrent.

3. Preparation of titanium dioxide dispersion liquid Titanium dioxide (made by Nippon Aerosil Co., Ltd.)
15 g of Degussa P-25), 45 g of water, 1 g of a dispersant (Triton X-100, manufactured by Aldrich), and 30 g of zirconia beads (manufactured by Nikkato) having a diameter of 0.5 mm, and using a sand grinder mill (manufactured by Imex). The dispersion treatment was performed at 1500 rpm for 2 hours. Zirconia beads were removed from the obtained dispersion by filtration. The average particle size of the titanium dioxide fine particles in the obtained dispersion was 2.5 μm. The particle size was measured with a master sizer manufactured by MALVERN.

[0222] 4. Preparation of dye-adsorbed TiO ₂ electrode Conductive glass with tin oxide layer doped with fluorine (TCO glass-U manufactured by Asahi Glass Co., Ltd. cut into a size of 20 mm x 20 mm, surface resistance about 30 Ω / □ The above dispersion was applied to the conductive surface side of ( ² ) using a glass rod (the applied amount of semiconductor fine particles was 20 g / m ² ). At this time, a part of the conductive surface side (3 from the end)
mm) to form a spacer, and glass was arranged side by side so that the adhesive tape was positioned at both ends, and applied eight at a time. After application, the adhesive tape was peeled off and air-dried at room temperature for one day. Next, the glass was placed in an electric furnace (muffle furnace FP-32 type, manufactured by Yamato Scientific Co., Ltd.), and baked at 450 ° C. for 30 minutes.
To give an O ₂ electrode. After the electrode was taken out and cooled, it was immersed in a methanol solution of the metal complex dye of the present invention and the comparative dye 1 (each 3 × 10 ⁻⁴ mol / l) for 15 hours. The dyed TiO ₂ electrode was immersed in 4-t-butylpyridine for 15 minutes, washed with ethanol, and air-dried. The thickness of the obtained photosensitive layer was 10 μm.

[0223] 5. Fabrication of photoelectrochemical cell Dye-sensitized TiO ₂ electrode substrate (20 mm
× 20 mm) was overlaid with a platinum-deposited glass of the same size. Next, an electrolytic solution (3-methoxypropionitrile was used as an electrolyte to form a 1-
Iodine salt of methyl-3-hexylimidazolium (0.65mol
/ l) and iodine (0.05 mol / l) were impregnated and introduced into a TiO ₂ electrode to obtain a photoelectrochemical cell.
According to the present embodiment, a conductive support layer made of conductive glass (a conductive layer 10a provided on a transparent substrate 50a made of glass), a photosensitive layer 20 of dye-sensitized TiO ₂ shown in FIG. A photoelectrochemical cell in which the charge transfer layer 30 made of the electrolytic solution, the counter electrode conductive layer 40 made of platinum, and the transparent substrate 50a made of glass were laminated in this order and sealed with an epoxy-based sealant was produced.

[0224] 6. Measurement of Photoelectric Conversion Wavelength and Photoelectric Conversion Efficiency The photoelectric conversion efficiency at 800 nm of the obtained photoelectric conversion element was measured using an IPCE (Incident Photon to Current Con
version Efficiency). Table 2 shows the photoelectric conversion efficiency of the photoelectrochemical cell using each metal complex dye.

[0225]

[Table 2]

From Table 2, it can be seen that the comparative dyes do not exhibit photoelectric conversion ability for light at 800 nm because they have no absorption ability, whereas the metal complex dyes of the present invention exhibit good photoelectric conversion ability. Understand. As described above, all of the dyes of the present invention have high photoelectric conversion ability not only in visible light but also in infrared region.

[0227]

As described in detail above, the metal complex dye of the present invention has good light absorption in a wide wavelength range from visible light to infrared light, and therefore contains semiconductor fine particles adsorbing such a metal complex dye. The photoelectric conversion element has high photoelectric conversion characteristics over a range from visible light to infrared light. A photoelectrochemical cell comprising such a photoelectric conversion element is extremely effective as a solar cell.

[Brief description of the drawings]

FIG. 1 is a partial sectional view showing the structure of a preferred photoelectric conversion element of the present invention.

FIG. 2 is a partial sectional view showing the structure of a preferred photoelectric conversion element of the present invention.

FIG. 3 is a partial sectional view showing the structure of a preferred photoelectric conversion element of the present invention.

FIG. 4 is a partial sectional view showing the structure of a preferred photoelectric conversion element of the present invention.

FIG. 5 is a partial sectional view showing the structure of a preferred photoelectric conversion element of the present invention.

FIG. 6 is a partial sectional view showing the structure of a preferred photoelectric conversion element of the present invention.

FIG. 7 is a partial sectional view showing the structure of a preferred photoelectric conversion element of the present invention.

FIG. 8 is a partial sectional view showing the structure of a preferred photoelectric conversion element of the present invention.

FIG. 9 is a partial sectional view showing the structure of a preferred photoelectric conversion element of the present invention.

FIG. 10 is a partial cross-sectional view illustrating an example of the structure of a substrate-integrated solar cell module using the metal complex dye of the present invention.

[Description of Signs] 10: Conductive layer 10a: Transparent conductive layer 11: Metal lead 20: Photosensitive layer 21: Semiconductor fine particles 22: Metal complex dye 23: Charge transport material 30 ・ ・ ・ Charge transfer layer 40 ・ ・ ・ Counter conductive layer 40a ・ ・ ・ Transparent counter conductive layer 50 ・ ・ ・ Substrate 50a ・ ・ ・ Transparent substrate 60 ・ ・ ・ Undercoat layer 70 ・ ・ ・ Anti-reflective layer

Claims (11)

[Claims] 1. The following general formula (I): M (LL ₁ ) _m1 (LL ₂ ) _m2 (X) _m3 · CI (I) (where M represents a metal atom and LL ₁ represents the following general formula: Formula (II): (Provided that R ₁ and R ₂ are independently a carboxyl group, a sulfonic acid group, a hydroxyl group, a hydroxamic acid group, represents a phosphoryl group or a phosphonyl group, R ₃ and
R ₄ each independently represents a substituent, a1 and a2 each represents independently an integer of 0 to 4, b1 represents an integer of 0 to 3, b2 represents an integer of 0 to 5. When a1 is 2 or more, R ₁ may be the same or different; when a2 is 2 or more, R ₂ may be the same or different; when b1 is 2 or more, R ₃ may be the same or different They may be linked to each other to form a ring, and when b2 is 2 or more, R ₄ may be the same or different, and may be linked to each other to form a ring. b1 and
b2 may form a ring wherein R ₃ and R ₄ together one or more time. ) Represents a bidentate ligand represented by, LL ₂ the following general formula (III): ## STR2 ## (However, Za, Zb and Zc are each independently 5 or 6
Represents a group of non-metallic atoms capable of forming a membered ring, and c is 0 or 1
Represents X represents an acyloxy group, an acylthio group, a thioacyloxy group, a thioacylthio group, an acylaminooxy group, a thiocarbamate group, a dithiocarbamate group, a thiocarbonate group, A group selected from the group consisting of dithiocarbonate, trithiocarbonate, acyl, thiocyanate, isothiocyanate, cyanate, isocyanate, cyano, alkylthio, arylthio, alkoxy, and aryloxy groups Or a bidentate or bidentate ligand consisting of a halogen atom, carbonyl, dialkylketone, 1,3-diketone, carbonamide, thiocarbonamide, thiourea or isothiourea And m1 represents an integer of 1 to 3, and m1 is 2 or LL ₁ when 3 may be the same or different, m2 represents an integer of 0 to 2, the LL ₂ when m2 is 2 may be the same or different, m3 represents an integer of 0 to 3, When m3 is 2 or 3, Xs may be the same or different, and Xs may be linked to each other, and CI represents a counterion when a counterion is required to neutralize the charge. A photoelectric conversion element comprising semiconductor fine particles sensitized by a metal complex dye represented by the formula (1). 2. The photoelectric conversion device according to claim 1, wherein M in the general formula (I) is Ru, Fe, Os, or Cu. 3. The photoelectric conversion device according to claim 2, wherein M in the general formula (I) is Ru. 4. The photoelectric conversion device according to claim 1, wherein the sum of a1 and a2 in the general formula (II) is 1 to 4.
A photoelectric conversion element, characterized in that: 5. The photoelectric conversion device according to claim 1, wherein the sum of b1 and b2 in the general formula (II) is 1 to 6.
Wherein R ₃ and R ₄ are each independently an alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, a hydroxyl group, an alkoxy group, an aryloxy group, an amino group or an acylamino group. . 6. The photoelectric conversion device according to claim 1,
In the replacement element, LL in the general formula (I)_TwoIs the following general formula (I
V-1) to (IV-8):(However, R₁₁~ R₁₈Is independently a carboxyl group,
Sulfonic acid group, hydroxyl group, hydroxamic acid group, e
Represents a phoryl or phosphonyl group, R₁₉~ R₂₆Is it
Each independently represents a substituent, R₂₇~ R₃₁Are each independently water
Represents an alkyl, alkenyl, or aryl group.
Then R₁₁~ R₂₆May be bonded to any position on the ring,
d1 to d8, d13, d14 and d16 are each independently 0 to 4
Represents an integer, and d9 to d12 and d15 are each independently 0 to 6
And when d1 to d8 are 2 or more, R ₁₁~ R₁₈Is the same
May be different, and when d9 to d16 are 2 or more, R₁₉~ R
₂₆May be the same or different and are linked together to form a ring
It may be formed. )
A photoelectric conversion element characterized by the above-mentioned. 7. The photoelectric conversion device according to claim 1, wherein said semiconductor fine particles are titanium oxide fine particles. 8. A photoelectrochemical cell using the photoelectric conversion element according to claim 1. 9. The following general formula (I): M (LL₁)_m1(LL_Two)_m2(X)_m3・ CI ・ ・ ・ (I) (where M is Ru and LL₁Is the following general formula (II):(However, R₁And R_TwoAre independently carboxyl
Group, sulfonic acid group, hydroxyl group, hydroxamic acid
Group, phosphoryl group or phosphonyl group, R_Threeand
R_FourEach independently represents a substituent, a1 and a2 are each
Independently represent an integer of 0 to 4; b1 represents an integer of 0 to 3
And b2 represents an integer of 0 to 5. R when a1 is 2 or more₁Is the same
May be the same or different, and when a2 is 2 or more, R_TwoIs the same
But may be different, and when b1 is 2 or more, R_ThreeIs the same
May be different from each other to form a ring
If b2 is 2 or more, R_FourAre the same or different
They may be connected to each other to form a ring. b1 and
R when b2 is 1 or more_ThreeAnd R_FourAre linked to form a ring
Good. ) Represents a bidentate ligand represented by_TwoAre the following general formulas (IV-1) to (IV-8):(However, R₁₁~ R₁₈Is independently a carboxyl group,
Sulfonic acid group, hydroxyl group, hydroxamic acid group, e
Represents a phoryl or phosphonyl group, R₁₉~ R₂₆Is it
Each independently represents a substituent, R₂₇~ R₃₁Are each independently water
Represents an alkyl, alkenyl, or aryl group.
Then R₁₁~ R₂₆May be bonded to any position on the ring,
d1 to d8, d13, d14 and d16 are each independently 0 to 4
Represents an integer, and d9 to d12 and d15 are each independently 0 to 6
And when d1 to d8 are 2 or more, R ₁₁~ R₁₈Is the same
May be different, and when d9 to d16 are 2 or more, R₁₉~ R
₂₆May be the same or different and are linked together to form a ring
It may be formed. 2) represented by either of
Or a tridentate ligand, X is an acyloxy group, an acylthio group, a thioacyloxy
Group, thioacylthio group, acylaminooxy group, thioca
Rubamate group, dithiocarbamate group, thiocarbonate
G, dithiocarbonate, trithiocarbonate
Group, acyl group, thiocyanate group, isothiocyanate
Group, cyanate group, isocyanate group, cyano group,
Kirthio, arylthio, alkoxy and ant
Monodentate coordinated with a group selected from the group consisting of
Or bidentate ligand, or halogen atom, carbon
, Dialkyl ketone, 1,3-diketone, carboxamide
Thiocarbonamide, thiourea or isothiour
Represents a monodentate or bidentate ligand consisting of rare, m1 is 1 or 2, and when m1 is 2, LL₁Are the same but different
M2 is 0 or 1, m3 represents an integer of 0 to 2, and when m3 is 2, X is the same or different.
X and X may be linked to each other, m2 and m3 are not simultaneously 0, and CI is a counter ion when a counter ion is necessary to neutralize the charge.
Indicates ON. Metal complex characterized by being represented by
Body pigment. 10. The metal complex dye according to claim 9, wherein the sum of a1 and a2 in the general formula (II) is from 1 to 4. 11. The metal complex dye according to claim 9, wherein the sum of b1 and b2 in the general formula (II) is 1 to 6, and R ₃ and R ₄ are each independently an alkyl group or an alkenyl group. A metal complex dye, which is a group, an alkynyl group, a cycloalkyl group, a hydroxyl group, an alkoxy group, an aryloxy group, an amino group or an acylamino group.