[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Li et al., 2010 - Google Patents

Polythiophenes with carbazole side chains: design, synthesis and their application in organic solar cells

Li et al., 2010

Document ID
3367996693375882454
Author
Li W
Han Y
Chen Y
Li C
Li B
Bo Z
Publication year
Publication venue
Macromolecular Chemistry and Physics

External Links

Snippet

A series of polythiophene derivatives P1‐P5 containing carbazole side chains were designed and synthesized via the Stille polymerization. All carbazole containing polymers showed broad absorption in the visible region. The power conversion efficiencies of solar …
Continue reading at onlinelibrary.wiley.com (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
    • 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
    • H01L51/0034Organic polymers or oligomers
    • H01L51/0035Organic polymers or oligomers comprising aromatic, heteroaromatic, or arrylic chains, e.g. polyaniline, polyphenylene, polyphenylene vinylene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/12Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
    • C08G61/122Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
    • C08G61/123Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
    • 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
    • H01L51/0034Organic polymers or oligomers
    • H01L51/0043Copolymers
    • 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
    • H01L51/0045Carbon containing materials, e.g. carbon nanotubes, fullerenes
    • H01L51/0046Fullerenes, e.g. C60, C70
    • H01L51/0047Fullerenes, e.g. C60, C70 comprising substituents, e.g. PCBM
    • 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
    • H01L51/4253Solid 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 comprising bulk hetero-junctions, e.g. interpenetrating networks
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/32Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
    • C08G2261/322Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed
    • C08G2261/3223Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed containing one or more sulfur atoms as the only heteroatom, e.g. thiophene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/34Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain
    • C08G2261/344Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain containing heteroatoms
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/90Applications
    • C08G2261/91Photovoltaic applications
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/40Polymerisation processes
    • C08G2261/41Organometallic coupling reactions
    • C08G2261/411Suzuki reactions
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10Definition of the polymer structure

Similar Documents

Publication Publication Date Title
Najari et al. Synthesis and characterization of new thieno [3, 4‐c] pyrrole‐4, 6‐dione derivatives for photovoltaic applications
Wang et al. Extending π-conjugation system with benzene: an effective method to improve the properties of benzodithiophene-based polymer for highly efficient organic solar cells
Zhou et al. Tuning energy levels of low bandgap semi-random two acceptor copolymers
Huo et al. Alkylthio‐substituted polythiophene: absorption and photovoltaic properties
Chen et al. Synthesis and characterization of a narrow‐bandgap polymer containing alternating cyclopentadithiophene and diketo‐pyrrolo‐pyrrole units for solar cell applications
Wen et al. Synthesis of 4, 7-diphenyl-2, 1, 3-benzothiadiazole-based copolymers and their photovoltaic applications
Zhou et al. Low band gap copolymers consisting of porphyrins, thiophenes, and 2, 1, 3‐benzothiadiazole moieties for bulk heterojunction solar cells
Agneeswari et al. Synthesis of polymers containing 1, 2, 4‐oxadiazole as an electron‐acceptor moiety in their main chain and their solar cell applications
Hu et al. Synthesis and photovoltaic properties of ester group functionalized polythiophene derivatives
Wang et al. Very‐Low‐Bandgap Metallopolyynes of Platinum with a Cyclopentadithiophenone Ring for Organic Solar Cells Absorbing Down to the Near‐Infrared Spectral Region
Song et al. Synthesis of the 2H-benzimidazole-based conjugated polymers with various thiophene units and their application in photovoltaic
Karakawa et al. Near‐Infrared Photovoltaic Performance of Conjugated Polymers Containing Thienoisoindigo Acceptor Units
Zhang et al. Synthesis and photovoltaic properties of copolymers based on bithiophene and bithiazole
Kim et al. Low-bandgap poly (4H-cyclopenta [def] phenanthrene) derivatives with 4, 7-dithienyl-2, 1, 3-benzothiadiazole unit for photovoltaic cells
Du et al. Ethynylene‐containing donor–acceptor alternating conjugated polymers: Synthesis and photovoltaic properties
KR101142206B1 (en) Conducting polymer incorporating with dithiophene-thiazolothiazole derivatives, organic photoelectric device using it and organic solar cell
Baek et al. Synthesis of new alternating conjugated copolymers consisting of tetrazine/carbazole or tetrazine/fluorene derivatives along with thiophene spacers for photovoltaic applications
Zhou et al. Synthesis and Photovoltaic Properties of a Poly (2, 7‐carbazole) Derivative Based on Dithienosilole and Benzothiadiazole
Kim et al. Effect of side chains on phenanthrene based DA type copolymers for polymer solar cells
Tamilavan et al. Synthesis of three new 1‐(2, 6‐diisopropylphenyl)‐2, 5‐di (2‐thienyl) pyrrole‐based donor polymers and their bulk heterojunction solar cell applications
Jang et al. Synthesis and characterization of low-band-gap poly (thienylenevinylene) derivatives for polymer solar cells
Alqurashy et al. Pyrene–benzothiadiazole‐based copolymers for application in photovoltaic devices
Tamilavan et al. Benzodithiophene‐Based Broad Absorbing Random Copolymers Incorporating Weak and Strong Electron Accepting Imide and Lactam Functionalized Pyrrolo [3, 4‐c] pyrrole Derivatives for Polymer Solar Cells
Zhang et al. Synthesis and Photovoltaic Properties of Conjugated Copolymers with Benzo [1, 2‐b: 4, 5‐b′] dithiophene and Bis (thiophene) phthalimide Units
Lee et al. Random copolymers based on 3‐hexylthiophene and benzothiadiazole with induced π‐conjugation length and enhanced open‐circuit voltage property for organic photovoltaics