[go: up one dir, main page]

Zhao et al., 2014 - Google Patents

Thieno [2, 3-a] carbazole-based donor–π–acceptor organic dyes for efficient dye-sensitized solar cells

Zhao et al., 2014

View PDF
Document ID
3835088742321074298
Author
Zhao J
Jin T
Islam A
Kwon E
Akhtaruzzaman M
Asao N
Han L
Alamry K
Kosa S
Asiri A
Yamamoto Y
Publication year
Publication venue
Tetrahedron

External Links

Snippet

New donor–π–acceptor organic dyes K-1 and K-2 containing thieno [2, 3-a] carbazole as an electron donor were designed and synthesized for dye-sensitized solar cells (DSCs). Photophysical and electrochemical properties of K-dyes were investigated. DSCs based on …
Continue reading at www.sciencedirect.com (PDF) (other versions)

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GASES [GHG] EMISSION, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/54Material technologies
    • Y02E10/549Material technologies organic PV cells
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GASES [GHG] EMISSION, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/54Material technologies
    • Y02E10/542Dye sensitized solar cells
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/005Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
    • H01L51/0062Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S
    • H01L51/0071Polycyclic condensed heteroaromatic hydrocarbons
    • H01L51/0072Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ringsystem, e.g. phenanthroline, carbazole
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/005Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
    • H01L51/0062Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S
    • H01L51/0071Polycyclic condensed heteroaromatic hydrocarbons
    • H01L51/0073Polycyclic condensed heteroaromatic hydrocarbons comprising only oxygen in the heteroaromatic polycondensed ringsystem, e.g. cumarine dyes
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/0077Coordination compounds, e.g. porphyrin
    • H01L51/0084Transition metal complexes, e.g. Ru(II)polypyridine complexes
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/005Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
    • H01L51/0052Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G9/00Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/20Light-sensitive devices
    • H01G9/2059Light-sensitive devices comprising an organic dye as the active light absorbing material, e.g. adsorbed on an electrode or dissolved in solution
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/42Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof specially adapted for sensing infra-red radiation, light, electro-magnetic radiation of shorter wavelength or corpuscular radiation and adapted for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation using organic materials as the active part, or using a combination of organic materials with other material as the active part; Multistep processes for their manufacture

Similar Documents

Publication Publication Date Title
Luo et al. Co-sensitization of dithiafulvenyl-phenothiazine based organic dyes with N719 for efficient dye-sensitized solar cells
Gupta et al. Carbazole based A-π-D-π-A dyes with double electron acceptor for dye-sensitized solar cell
Gao et al. Oligothiophene-linked D–π–A type phenothiazine dyes for dye-sensitized solar cells
Yang et al. Efficient and stable organic DSSC sensitizers bearing quinacridone and furan moieties as a planar π-spacer
Zhang et al. Triphenylamine-based dyes for dye-sensitized solar cells
Wang et al. Influence of the terminal electron donor in D–D–π–A phenothiazine dyes for dye-sensitized solar cells
Shen et al. Effects of aromatic π-conjugated bridges on optical and photovoltaic properties of N, N-diphenylhydrazone-based metal-free organic dyes
Fernandes et al. Synthesis and characterization of novel thieno [3, 2-b] thiophene based metal-free organic dyes with different heteroaromatic donor moieties as sensitizers for dye-sensitized solar cells
Qian et al. T-shaped (D) 2–A–π–A type sensitizers incorporating indoloquinoxaline and triphenylamine for organic dye-sensitized solar cells
Jia et al. Synthesis of dendritic triphenylamine derivatives for dye-sensitized solar cells
Zang et al. Molecular design of the diketopyrrolopyrrole-based dyes with varied donor units for efficient dye-sensitized solar cells
Zhang et al. Novel metal-free organic dyes containing linear planar 11, 12-dihydroindolo [2, 3-a] carbazole donor for dye-sensitized solar cells: Effects of π spacer and alkyl chain
Akhtaruzzaman et al. Donor–acceptor dyes incorporating a stable dibenzosilole π-conjugated spacer for dye-sensitized solar cells
Qian et al. 6H-Indolo [2, 3-b] quinoxaline-based organic dyes containing different electron-rich conjugated linkers for highly efficient dye-sensitized solar cells
Qin et al. Panchromatic donor–acceptor–acceptor sensitizers based on 4H-cyclopenta [2, 1-b: 3, 4-b′] dithiophen-4-one as a strong acceptor for dye-sensitized solar cells
Shi et al. New efficient dyes containing tert-butyl in donor for dye-sensitized solar cells
Yan et al. Ethynylene-linked planar rigid organic dyes based on indeno [1, 2-b] indole for efficient dye-sensitized solar cells
Qian et al. Triazatruxene-based organic dyes containing a rhodanine-3-acetic acid acceptor for dye-sensitized solar cells
Hong et al. Synthesis of double D–A branched organic dyes employing indole and phenoxazine as donors for efficient DSSCs
Singh et al. Fluorene-based organic dyes containing acetylene linkage for dye-sensitized solar cells
Liu et al. Triazine dyes as photosensitizers for dye-sensitized solar cells
Li et al. Organic dyes incorporating N-functionalized pyrrole as conjugated bridge for dye-sensitized solar cells: convenient synthesis, additional withdrawing group on the π-bridge and the suppressed aggregation
Knyazeva et al. Dye-sensitized solar cells: Investigation of DA-π-A organic sensitizers based on [1, 2, 5] selenadiazolo [3, 4-c] pyridine
Fan et al. The position effect of electron-deficient quinoxaline moiety in porphyrin based sensitizers
Maglione et al. Tuning optical absorption in pyran derivatives for DSSC