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WO2002005294A1 - Electrically conductive ink - Google Patents

Electrically conductive ink Download PDF

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Publication number
WO2002005294A1
WO2002005294A1 PCT/GB2001/002912 GB0102912W WO0205294A1 WO 2002005294 A1 WO2002005294 A1 WO 2002005294A1 GB 0102912 W GB0102912 W GB 0102912W WO 0205294 A1 WO0205294 A1 WO 0205294A1
Authority
WO
WIPO (PCT)
Prior art keywords
electrically conductive
fibres
conductive ink
ink
carbon
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/GB2001/002912
Other languages
French (fr)
Inventor
Robert John Potter
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Johnson Matthey PLC
Original Assignee
Johnson Matthey PLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Johnson Matthey PLC filed Critical Johnson Matthey PLC
Priority to AU2001266213A priority Critical patent/AU2001266213A1/en
Publication of WO2002005294A1 publication Critical patent/WO2002005294A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10FINORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F77/00Constructional details of devices covered by this subclass
    • H10F77/20Electrodes
    • H10F77/206Electrodes for devices having potential barriers
    • H10F77/211Electrodes for devices having potential barriers for photovoltaic cells
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00Inks
    • C09D11/52Electrically conductive inks
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/20Conductive material dispersed in non-conductive organic material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/20Conductive material dispersed in non-conductive organic material
    • H01B1/22Conductive material dispersed in non-conductive organic material the conductive material comprising metals or alloys
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/20Conductive material dispersed in non-conductive organic material
    • H01B1/24Conductive material dispersed in non-conductive organic material the conductive material comprising carbon-silicon compounds, carbon or silicon
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10FINORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F77/00Constructional details of devices covered by this subclass
    • H10F77/20Electrodes
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K71/00Manufacture or treatment specially adapted for the organic devices covered by this subclass
    • H10K71/60Forming conductive regions or layers, e.g. electrodes
    • H10K71/611Forming conductive regions or layers, e.g. electrodes using printing deposition, e.g. ink jet printing
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K1/00Printed circuits
    • H05K1/02Details
    • H05K1/09Use of materials for the conductive, e.g. metallic pattern
    • H05K1/092Dispersed materials, e.g. conductive pastes or inks
    • H05K1/095Dispersed materials, e.g. conductive pastes or inks for polymer thick films, i.e. having a permanent organic polymeric binder
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K30/00Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
    • H10K30/50Photovoltaic [PV] devices
    • H10W20/4473
    • 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 GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/40Solar thermal energy, e.g. solar towers
    • Y02E10/46Conversion of thermal power into mechanical power, e.g. Rankine, Stirling or solar thermal engines
    • 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 GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/549Organic PV cells

Definitions

  • the present invention relates to the use of conductive inks to form electrically conductive layers, especially in optoelectronic devices.
  • Particulate materials such as e.g. carbon
  • WO 94/15344 discloses a conductive ink comprising carbon particulate materials.
  • Particulate carbon has also been used as part of the counter-electrode in dye-sensitised solar cells (so called Graetzel cells), often applied to substrates in the form of a paste or as an ink.
  • electrical conductivity in the carbon layer or film produced under these circumstances relies on point-to-point contact between small, frequently micro-sized, carbon particles.
  • the electrical pathway is both tortuous and very sensitive to the physical and chemical nature of the carbon particle surfaces.
  • the present invention provides for the use of an electrically conductive ink comprising an electrically conductive powder and electrically conductive fibres wherein the aspect ratio of the fibres is greater than 2:1, to form an electrically conductive layer.
  • the electrically conductive powder suitably comprises one or more conductive particulate materials such as carbon, nickel, tungsten and F-doped tin oxide, but is preferably carbon powder.
  • conductive particulate materials such as carbon, nickel, tungsten and F-doped tin oxide
  • Specific examples of carbon powder that can be used include, but are not limited to, Nulcan XC72R (Cabot Carbon Limited, Stanlow, Ellesmere Port, South Wirral, L65 4HT, UK) and TIMREX KS15 Graphite (Timcal Ltd, CH-6743, Bodio, Switzerland).
  • the electrically conductive powder suitably has a surface area in the range from 5 to 1000m 2 /g, preferably from 20 to 250m 2 /g.
  • the electrically conductive fibres have an aspect ratio of greater than 2:1, preferably greater than 10:1.
  • the fibres may be any electrically conductive fibres, including carbon, nickel, tungsten and F-doped tin oxide, but are preferably carbon fibres.
  • the fibres must be chosen to ensure that they are chemically compatible with the other components.
  • the fibres are suitably of a length of at least 1 micron, preferably greater than 1mm.
  • the conducting fibres preferably have a thickness of not more than 100 microns, preferably not more than 50 microns.
  • the relative ratio by weight of fibres to powder is suitably in the range from
  • the electrically conductive layer may be a film, an electrode or an electrically conductive track.
  • the ink may be used to form a track wherein the majority of the fibres are oriented along the direction of the track. It is possible that this will increase conductivity in the direction of the track.
  • the component fibres and powders may be mixed together using the following technique. An ink is made-up by hand, eg using the proportions 28.4wt% carbon powder, 17% Disperbyk 164 surfactant (Byk, Holland) and 54.6% pine oil, followed by triple-roll milling to ensure even mixing.
  • This 'base' ink typically has a viscosity of approximately 100 Pa.
  • the desired weight of fibre, pre-cut to the required length, is added to the base ink with manual stirring or for instance using a paddle-stirrer. After stirring for several minutes to ensure adequate mixing, the ink is ready for use.
  • Such mixtures are suitably converted into films or tracks by applying the mixture to a substrate surface, preferably a smooth surface, by e.g. screen-printing or some similar technique and allowing the same to dry followed by suitable firing in an air or nitrogen atmosphere between 300-500°C.
  • the ink used in the present invention is particularly useful for making electrodes in optoelectronic devices such as solar cells (including photovoltaic cells). For instance in a solar cell, such electrodes are used for the purpose of transporting the electrical current generated by the photo-active components away to an external circuit or the next cell in a series or parallel configuration etc.
  • the film may also serve to protect the internals of the cell from the external environment.
  • the present invention provides a solar cell comprising an electrically conductive layer formed by the use of an electrically conductive ink according to the present invention.
  • the present invention provides a photovoltaic cell comprising an electrically conductive layer formed by the use of an electrically conductive ink according to the present invention.
  • Carbon fibres, of length 1 mm were mixed in with a 'base' carbon powder ink made as described hereinbefore, by continuously stirring with a spatula for 5 minutes.
  • the weight ratio of carbon fibre to ink was 1:3.
  • the fibre-containing ink was then used to form thin films of 1 x 5 cm dimension on float glass substrates by screen-printing through a nylon mesh of 150 holes per inch.
  • a single or double-pass print was normally sufficient to produce a coherent strip approximately 100 microns thick before drying. After printing of the film, the piece was fired in an air oven at 450°C for 16 minutes in air.
  • the conductivity of the film was measured using a standard '4-point probe' technique using a Jandel scientific commercial instrument. This technique is widely used in industry for measuring electrical conductivities.
  • Test samples were prepared as 1 x 5cm strips on clear float glass substrates as described previously. Electrical contact was made either end of the longer side by coating silver-paint (Agar Scientific) overlays onto the samples with an overlap of 2mm each end. One current-driving and one potential-sensing lead were then connected to each end of the strip and the conductivity read directly on a Hewlett Packard high-impedance systems meter. All tests were done at room temperature and humidity. The results of this test are shown in Table 1 below:

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  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Dispersion Chemistry (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Manufacturing & Machinery (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

The invention relates to the use of electrically conductive inks, said inks comprising electrically conductive powder and electrically conducting fibres, wherein the aspect ratio of the fibres is greater than 2:1. The inks are used to form electrically conductive layers, especially in optoelectronic devices such as solar cells. The layers have considerably reduced electrical resistance than if the electrically conductive powder were used alone.

Description

ELECTRICALLY CONDUCTIVE INK
The present invention relates to the use of conductive inks to form electrically conductive layers, especially in optoelectronic devices.
In any form of electrical power generation device, power conversion losses due to ohmic resistance of internal conductive pathways is usually undesirable and must be kept to a minimum. In conventional solid-state solar cells that convert light energy into electrical energy, such as those based on silicon, printed tracks made e.g. from silver pastes are commonly used to carry the electrical current from the active part of the cell to the external environment. Silver or similar metals are used due to their low electrical resistance. Newer types of solar cells incorporating e.g. solid polymer electrolytes and/or dye-sensitised semi-conductor powders may or may not be able to use conducting tracks based on metal pastes depending upon the chemical environment within the cells and also upon cost considerations. There is therefore a need to develop alternative conducting track and/or electrode materials for use in these types of cells that are more chemically resistant and/or are cheaper.
Particulate materials, such as e.g. carbon, are well-established electrical conductors that have been used as track and electrode material in solar cells. WO 94/15344 discloses a conductive ink comprising carbon particulate materials. Particulate carbon has also been used as part of the counter-electrode in dye-sensitised solar cells (so called Graetzel cells), often applied to substrates in the form of a paste or as an ink. However, electrical conductivity in the carbon layer or film produced under these circumstances relies on point-to-point contact between small, frequently micro-sized, carbon particles. Thus the electrical pathway is both tortuous and very sensitive to the physical and chemical nature of the carbon particle surfaces.
It has now been found that if such particulate conductive materials, such as e.g. carbon, are partially replaced by conductive fibres in inks, the resultant conductive inks or layers produced therefrom are significantly more conductive than an equivalent volume of particulate materials. Thus, in the first aspect the present invention provides for the use of an electrically conductive ink comprising an electrically conductive powder and electrically conductive fibres wherein the aspect ratio of the fibres is greater than 2:1, to form an electrically conductive layer.
The electrically conductive powder suitably comprises one or more conductive particulate materials such as carbon, nickel, tungsten and F-doped tin oxide, but is preferably carbon powder. Specific examples of carbon powder that can be used include, but are not limited to, Nulcan XC72R (Cabot Carbon Limited, Stanlow, Ellesmere Port, South Wirral, L65 4HT, UK) and TIMREX KS15 Graphite (Timcal Ltd, CH-6743, Bodio, Switzerland). The electrically conductive powder suitably has a surface area in the range from 5 to 1000m2/g, preferably from 20 to 250m2/g.
The electrically conductive fibres have an aspect ratio of greater than 2:1, preferably greater than 10:1. The fibres may be any electrically conductive fibres, including carbon, nickel, tungsten and F-doped tin oxide, but are preferably carbon fibres. The fibres must be chosen to ensure that they are chemically compatible with the other components. The fibres are suitably of a length of at least 1 micron, preferably greater than 1mm. The conducting fibres preferably have a thickness of not more than 100 microns, preferably not more than 50 microns. Specific examples of conductive carbon fibres that may be used in the compositions of the present invention include, but are not limited to, Toray M40B 6000 50B (Toray Industries, Japan) and Graphil 34-700 12 K (Grafil Europe, Sutherland House, Matlock Road, Coventry, CV1 4JQ, UK).
The relative ratio by weight of fibres to powder is suitably in the range from
10E-04 to 1, preferably from 0.01 to 0.5.
The electrically conductive layer may be a film, an electrode or an electrically conductive track. There may be a preferred orientation of the electrically conductive fibres within the layer because this may enhance conductivity in a particular direction. For example, the ink may be used to form a track wherein the majority of the fibres are oriented along the direction of the track. It is possible that this will increase conductivity in the direction of the track. The component fibres and powders may be mixed together using the following technique. An ink is made-up by hand, eg using the proportions 28.4wt% carbon powder, 17% Disperbyk 164 surfactant (Byk, Holland) and 54.6% pine oil, followed by triple-roll milling to ensure even mixing. This 'base' ink typically has a viscosity of approximately 100 Pa. The desired weight of fibre, pre-cut to the required length, is added to the base ink with manual stirring or for instance using a paddle-stirrer. After stirring for several minutes to ensure adequate mixing, the ink is ready for use. Such mixtures are suitably converted into films or tracks by applying the mixture to a substrate surface, preferably a smooth surface, by e.g. screen-printing or some similar technique and allowing the same to dry followed by suitable firing in an air or nitrogen atmosphere between 300-500°C.
The ink used in the present invention is particularly useful for making electrodes in optoelectronic devices such as solar cells (including photovoltaic cells). For instance in a solar cell, such electrodes are used for the purpose of transporting the electrical current generated by the photo-active components away to an external circuit or the next cell in a series or parallel configuration etc. The film may also serve to protect the internals of the cell from the external environment.
In a second aspect the present invention provides a solar cell comprising an electrically conductive layer formed by the use of an electrically conductive ink according to the present invention.
In a final aspect, the present invention provides a photovoltaic cell comprising an electrically conductive layer formed by the use of an electrically conductive ink according to the present invention.
The present invention is illustrated with reference to the following Example:
EXAMPLE 1
Carbon fibres, of length 1 mm were mixed in with a 'base' carbon powder ink made as described hereinbefore, by continuously stirring with a spatula for 5 minutes. The weight ratio of carbon fibre to ink was 1:3. The fibre-containing ink was then used to form thin films of 1 x 5 cm dimension on float glass substrates by screen-printing through a nylon mesh of 150 holes per inch. A single or double-pass print was normally sufficient to produce a coherent strip approximately 100 microns thick before drying. After printing of the film, the piece was fired in an air oven at 450°C for 16 minutes in air.
The conductivity of the film was measured using a standard '4-point probe' technique using a Jandel scientific commercial instrument. This technique is widely used in industry for measuring electrical conductivities. Test samples were prepared as 1 x 5cm strips on clear float glass substrates as described previously. Electrical contact was made either end of the longer side by coating silver-paint (Agar Scientific) overlays onto the samples with an overlap of 2mm each end. One current-driving and one potential-sensing lead were then connected to each end of the strip and the conductivity read directly on a Hewlett Packard high-impedance systems meter. All tests were done at room temperature and humidity. The results of this test are shown in Table 1 below:
TABLE 1
Figure imgf000005_0001
These results show that the combination of a carbon powder ink with carbon fibres results in a considerable reduction in the resistance of the resultant product.

Claims

1. The use of an electrically conductive ink comprising an electrically conductive powder and electrically conductive fibres wherein the aspect ratio of the fibres is greater than 2: 1, to form an electrically conductive layer.
2. The use of an electrically conductive ink as claimed in claim 1 wherein the electrically conductive powder comprises one or more of carbon, nickel, tungsten and F-doped tin oxide.
3. The use of an electrically conductive ink as claimed in claim 1 wherein the electrically conductive powder is carbon powder.
4. The use of an electrically conductive ink as claimed in any one preceding claims wherein the electrically conductive powder has a surface area in the range from 5 to
1000 m2/g.
5. The use of an electrically conductive ink as claimed any one of the preceding claims wherein the electrically conducting fibres are selected from carbon, nickel, tungsten and F-doped tin oxide.
6. The use of an electrically conductive ink as claimed in claim 5 wherein the electrically conducting fibres are carbon fibres.
7. The use of an electrically conductive ink as claimed in any one of the preceding claims wherein the electrically conductive fibres have a length of at least 1 micron.
8. The use of an electrically conductive ink as claimed in any one preceding claims wherein the electrically conductive fibres have a thickness of not more than 100 microns.
9. The use of an electrically conductive ink as claimed in any one of the preceding claims wherein the relative ratio by weight of electrically conductive fibres to electrically conductive powder is in the range from 10E-04 to 1.
10. A solar cell comprising an electrically conductive layer formed by the use of an electrically conductive ink as claimed in any one of the preceding claims.
11. A photovoltaic cell comprising an electrically conductive layer formed by the use of an electrically conductive ink as claimed in any of claims 1 -9.
PCT/GB2001/002912 2000-07-08 2001-06-29 Electrically conductive ink Ceased WO2002005294A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2001266213A AU2001266213A1 (en) 2000-07-08 2001-06-29 Electrically conductive ink

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0016747.8A GB0016747D0 (en) 2000-07-08 2000-07-08 Ink
GB0016747.8 2000-07-08

Publications (1)

Publication Number Publication Date
WO2002005294A1 true WO2002005294A1 (en) 2002-01-17

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Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004093180A1 (en) * 2003-04-15 2004-10-28 California Institute Of Technology Flexible carbon-based ohmic contacts for organic transistors
WO2005012445A3 (en) * 2003-06-30 2005-04-14 Trustees Of The University Of Illinois Conducting inks
US6951666B2 (en) 2001-10-05 2005-10-04 Cabot Corporation Precursor compositions for the deposition of electrically conductive features
US6964861B1 (en) 1998-11-13 2005-11-15 Invitrogen Corporation Enhanced in vitro recombinational cloning of using ribosomal proteins
US7198924B2 (en) 2000-12-11 2007-04-03 Invitrogen Corporation Methods and compositions for synthesis of nucleic acid molecules using multiple recognition sites
US7223576B2 (en) 1995-06-07 2007-05-29 Invitrogen Corporation Recombinational cloning using engineered recombination sites
US7244560B2 (en) 2000-05-21 2007-07-17 Invitrogen Corporation Methods and compositions for synthesis of nucleic acid molecules using multiple recognition sites
US7282326B2 (en) 1995-06-07 2007-10-16 Invitrogen Corporation Recombinational cloning using engineered recombination sites
US7351578B2 (en) 1999-12-10 2008-04-01 Invitrogen Corp. Use of multiple recombination sites with unique specificity in recombinational cloning
US7393632B2 (en) 1999-12-10 2008-07-01 Invitrogen Corp. Use of multiple recombination sites with unique specificity in recombinational cloning
US7408049B2 (en) 1997-10-24 2008-08-05 Invitrogen Corporation Recombinational cloning using nucleic acids having recombination sites
EP2003941A2 (en) 2007-06-14 2008-12-17 manroland AG Printed functional components
US7524528B2 (en) 2001-10-05 2009-04-28 Cabot Corporation Precursor compositions and methods for the deposition of passive electrical components on a substrate
US7533361B2 (en) 2005-01-14 2009-05-12 Cabot Corporation System and process for manufacturing custom electronics by combining traditional electronics with printable electronics
US7553512B2 (en) 2001-11-02 2009-06-30 Cabot Corporation Method for fabricating an inorganic resistor
US7575621B2 (en) 2005-01-14 2009-08-18 Cabot Corporation Separation of metal nanoparticles
US7621976B2 (en) 1997-02-24 2009-11-24 Cabot Corporation Coated silver-containing particles, method and apparatus of manufacture, and silver-containing devices made therefrom
US7629017B2 (en) 2001-10-05 2009-12-08 Cabot Corporation Methods for the deposition of conductive electronic features
WO2012044281A1 (en) * 2010-09-28 2012-04-05 E. I. Du Pont De Nemours And Company Conductive paste for solar cell electrode
US8167393B2 (en) 2005-01-14 2012-05-01 Cabot Corporation Printable electronic features on non-uniform substrate and processes for making same
US8334464B2 (en) 2005-01-14 2012-12-18 Cabot Corporation Optimized multi-layer printing of electronics and displays
US8338091B2 (en) 2003-08-08 2012-12-25 Life Technologies Corporation Methods and compositions for seamless cloning of nucleic acid molecules
US8597397B2 (en) 2005-01-14 2013-12-03 Cabot Corporation Production of metal nanoparticles
US8883988B2 (en) 1999-03-02 2014-11-11 Life Technologies Corporation Compositions for use in recombinational cloning of nucleic acids
US9534252B2 (en) 2003-12-01 2017-01-03 Life Technologies Corporation Nucleic acid molecules containing recombination sites and methods of using the same
WO2025005889A1 (en) * 2023-06-28 2025-01-02 National University Of Singapore Electrodes for halide perovskite devices

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US7282326B2 (en) 1995-06-07 2007-10-16 Invitrogen Corporation Recombinational cloning using engineered recombination sites
US7714116B2 (en) 1995-06-07 2010-05-11 Life Technologies Corporation Recombinational cloning using nucleic acids having recombination sites
US7304130B2 (en) 1995-06-07 2007-12-04 Invitrogen Corporation Recombinational cloning using engineered recombination sites
US7223576B2 (en) 1995-06-07 2007-05-29 Invitrogen Corporation Recombinational cloning using engineered recombination sites
US7621976B2 (en) 1997-02-24 2009-11-24 Cabot Corporation Coated silver-containing particles, method and apparatus of manufacture, and silver-containing devices made therefrom
US7408049B2 (en) 1997-10-24 2008-08-05 Invitrogen Corporation Recombinational cloning using nucleic acids having recombination sites
US6964861B1 (en) 1998-11-13 2005-11-15 Invitrogen Corporation Enhanced in vitro recombinational cloning of using ribosomal proteins
US8883988B2 (en) 1999-03-02 2014-11-11 Life Technologies Corporation Compositions for use in recombinational cloning of nucleic acids
US7393632B2 (en) 1999-12-10 2008-07-01 Invitrogen Corp. Use of multiple recombination sites with unique specificity in recombinational cloning
US7351578B2 (en) 1999-12-10 2008-04-01 Invitrogen Corp. Use of multiple recombination sites with unique specificity in recombinational cloning
US7244560B2 (en) 2000-05-21 2007-07-17 Invitrogen Corporation Methods and compositions for synthesis of nucleic acid molecules using multiple recognition sites
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