Nothing Special   »   [go: up one dir, main page]

Handoko et al., 2020 - Google Patents

Effect of cyano substituent on photovoltaic properties of quinoxaline-based polymers

Handoko et al., 2020

Document ID
159932585940096758
Author
Handoko S
Jin H
Whang D
Kim J
Chang D
Publication year
Publication venue
Journal of Industrial and Engineering Chemistry

External Links

Snippet

Three donor-acceptor type quinoxaline-based conjugated polymers, in which electron- donating indacenodithiophene (IDT) and indacenodithieno [3, 2-b] thiophene (IDTT) were connected to the electron-accepting 2, 3-diphenylquinoxaline (DPQ) derivatives, were …
Continue reading at www.sciencedirect.com (other versions)

Classifications

    • 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
    • C08G61/124Macromolecular 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 with a five-membered ring containing one nitrogen atom in the ring
    • 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
    • C08G2261/30Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/31Monomer units or repeat units incorporating structural elements in the main chain incorporating aromatic structural elements in the main chain
    • 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
    • C08G2261/10Definition of the polymer structure
    • 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
    • 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
    • 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
    • H01L51/0043Copolymers

Similar Documents

Publication Publication Date Title
Handoko et al. Synthesis of quinoxaline-based polymers with multiple electron-withdrawing groups for polymer solar cells
Data et al. Unusual properties of electropolymerized 2, 7-and 3, 6-carbazole derivatives
Putri et al. Step-by-step improvement in photovoltaic properties of fluorinated quinoxaline-based low-band-gap polymers
Xu et al. Side‐Chain engineering of Benzodithiophene‐fluorinated Quinoxaline low‐band‐gap co‐polymers for high‐performance polymer solar cells
Handoko et al. Effect of cyano substituent on photovoltaic properties of quinoxaline-based polymers
Sakthivel et al. Synthesis and characterization of new indeno [1, 2-b] indole-co-benzothiadiazole-based π-conjugated ladder type polymers for bulk heterojunction polymer solar cells
Tamilavan et al. Synthesis of conjugated polymers with broad absorption bands and photovoltaic properties as bulk heterojuction solar cells
Hwang et al. Synthesis, characterization, and photovoltaic applications of dithienogermole-dithienylbenzothiadiazole and-dithienylthiazolothiazole copolymers
Sun et al. Improved bulk-heterojunction polymer solar cell performance through optimization of the linker groupin donor–acceptor conjugated polymer
Gao et al. An all small molecule organic solar cell based on a porphyrin donor and a non-fullerene acceptor with complementary and broad absorption
Wang et al. Synthesis and photovoltaic properties of low-bandgap polymers based on N-arylcarbazole
Shen et al. Side chain effect on photovoltaic properties of D–A copolymers based on benzodithiophene and thiophene-substituted bithiazole
Pola et al. Synthesis of fluorinated benzotriazole (BTZ)-and benzodithiophene (BDT)-based low-bandgap conjugated polymers for solar cell applications
Hou et al. Synthesis, characterization, and photovoltaic performance of the polymers based on thiophene-2, 5-bis ((2-ethylhexyl) oxy) benzene-thiophene
Tamilavan et al. Synthesis of N-[4-Octylphenyl] dithieno [3, 2-b: 2′, 3′-d] pyrrole-based broad absorbing polymers and their photovoltaic applications
Chan et al. Synthesis of indolo [3, 2-b] carbazole-based random copolymers for polymer solar cell applications
Xiang et al. B← N bridged polymer acceptors with 900 nm absorption edges enabling high-performance all-polymer solar cells
Ameen et al. Solution processed bulk heterojunction organic solar cells using small organic semiconducting materials based on fluorene core unit
Cevher et al. Effect of substituent groups on quinoxaline-based random copolymers on the optoelectronic and photovoltaic properties
Li et al. Synthesis and photovoltaic properties of D-π-A copolymers based on thieno [3, 2-b] thiophene bridge unit
Hu et al. Benzothiadiazole [1, 2-b: 4, 3-b′] dithiophene, a new ladder-type multifused block: Synthesis and photovoltaic application
Yu et al. Structure-performance correlation of indacenodithiophene-based narrow band-gap polymers with pendant diketopyrrolopyrrole units
Goker et al. Incorporation of different conjugated linkers into low band gap polymers based on 5, 6‐Bis (octyloxy)‐2, 1, 3 benzooxadiazole for tuning optoelectronic properties
Bathula et al. Selenophene based benzodithiophene polymers as potential candidates for optoelectronic applications
Hu et al. An easily available near-infrared absorbing non-fullerene photovoltaic electron acceptor with indeno [1, 2-b] indole as the central core