[go: up one dir, main page]

Ponder Jr et al., 2023 - Google Patents

Metal‐like Charge Transport in PEDOT (OH) Films by Post‐processing Side Chain Removal from a Soluble Precursor Polymer

Ponder Jr et al., 2023

View PDF
Document ID
3993113722031839604
Author
Ponder Jr J
Gregory S
Atassi A
Advincula A
Rinehart J
Freychet G
Su G
Yee S
Reynolds J
Publication year
Publication venue
Angewandte Chemie International Edition

External Links

Snippet

Herein, a route to produce highly electrically conductive doped hydroxymethyl functionalized poly (3, 4‐ethylenedioxythiophene)(PEDOT) films, termed PEDOT (OH) with metal‐like charge transport properties using a fully solution processable precursor polymer is reported …
Continue reading at onlinelibrary.wiley.com (PDF) (other versions)

Classifications

    • HELECTRICITY
    • H01BASIC ELECTRIC 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
    • H01B1/06Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
    • H01B1/12Organic substances
    • H01B1/124Intrinsically conductive polymers
    • H01B1/125Intrinsically conductive polymers comprising aliphatic main chains, e.g. polyactylenes
    • HELECTRICITY
    • H01BASIC ELECTRIC 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
    • H01B1/06Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
    • H01B1/12Organic substances
    • H01B1/124Intrinsically conductive polymers
    • H01B1/127Intrinsically conductive polymers comprising five-membered aromatic rings in the main chain, e.g. polypyrroles, polythiophenes
    • 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
    • Y02E60/00Enabling technologies or technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage
    • Y02E60/13Ultracapacitors, supercapacitors, double-layer capacitors
    • 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
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/02Polyamines
    • C08G73/026Wholly aromatic polyamines
    • C08G73/0266Polyanilines or derivatives thereof
    • 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

Similar Documents

Publication Publication Date Title
Ponder Jr et al. Metal‐like Charge Transport in PEDOT (OH) Films by Post‐processing Side Chain Removal from a Soluble Precursor Polymer
Pei et al. Li− N interaction induced deep eutectic gel polymer electrolyte for high performance lithium‐metal batteries
Wang et al. Solution‐processable thermally crosslinked organic radical polymer battery cathodes
Jones et al. Branched oligo (ether) side chains: a path to enhanced processability and elevated conductivity for polymeric semiconductors
CN103987735B (en) Improved methods and related compositions for the synthesis of conjugated polymers by oxidative polymerization
Meng et al. Solid-state synthesis of a conducting polythiophene via an unprecedented heterocyclic coupling reaction
Li et al. Side‐Chain Engineering for High‐Performance Conjugated Polymer Batteries
Ryu et al. Polyaniline doped with dimethyl sulfate as a nucleophilic dopant and its electrochemical properties as an electrode in a lithium secondary battery and a redox supercapacitor
Ho et al. Synthesis, Morphology, and Optical and Electrochemical Properties of Poly (3-hexylthiophene)-b-poly (3-thiophene hexylacetate)
Li et al. Electropolymerized polythiophenes bearing pendant nitroxide radicals
Yu et al. Mixed ionic and electronic conduction in radical polymers
Liu et al. Fluorinated polyimide tunneling layer for efficient and stable perovskite photovoltaics
CN108165140B (en) Electroactive coating and composition for forming the same
Merkle et al. Mixed conductivity of polythiophene-based ionic polymers under controlled conditions
Sarang et al. Poly (fluorene-alt-naphthalene diimide) as n-Type Polymer Electrodes for Energy Storage
WO2012121417A1 (en) Conducting polymer / redox polymer blends via in-situ oxidative polymerization - preparation methods and application as an electro-active polymeric materials
Xue et al. Crosslinked network solid polymer electrolyte with self‐healing ability and high stability for lithium metal battery
Schmode et al. A Solution‐Processable Pristine PEDOT Exhibiting Excellent Conductivity, Charge Carrier Mobility, and Thermal Stability in the Doped State
Luo et al. Self‐doped conjugated polymers with electron‐deficient quinone units for enhanced electron transport in highly efficient organic solar cells
Hochgesang et al. Highly Efficient n‐Doping via Proton Abstraction of an Acceptor1‐Acceptor2 Alternating Copolymer toward Thermoelectric Applications
Jeon et al. Water/Alcohol‐Processable Low‐Cost Dihydropyrazine‐Based Polymers for Highly Sensitive, Stable and Flexible Temperature Sensors
Zhao et al. High Efficiency n‐Type Doping of Organic Semiconductors by Cation Exchange
Khawas et al. Highly Water‐Soluble Rod–Coil Conjugated Block Copolymer for Efficient Humidity Sensor
Li et al. Scalable Synthesis and Multi‐Electron Transfer of Aniline/Fluorene Copolymer for Solution‐Processable Battery Cathodes
Pasker et al. Photovoltaic response to structural modifications on a series of conjugated polymers based on 2‐aryl‐2H‐benzotriazoles