scispace - formally typeset
Search or ask a question
Topic

Conductive polymer

About: Conductive polymer is a research topic. Over the lifetime, 21817 publications have been published within this topic receiving 692491 citations. The topic is also known as: intrinsically conducting polymer & ICP.


Papers
More filters
Journal ArticleDOI
TL;DR: In this paper, highly conductive and stretchable polymer films were prepared by blending a conductive polymer, poly(3,4-ethylenedioxythiophene):polystyrenesulfonate (PEDOT:PSS), with highly stretchable waterborne polyurethane (WPU).
Abstract: Fast-growing flexible and stretchable electronics, such as robots, portable electronics and wearable devices, are regarded as the next-generation electronic devices. Flexible or even stretchable electromagnetic interference (EMI) shielding materials with high performance are needed to avoid the adverse effects of electromagnetic radiation produced by these devices. In this work, highly conductive and stretchable polymer films were prepared by blending a conductive polymer, poly(3,4-ethylenedioxythiophene):polystyrenesulfonate (PEDOT:PSS), with highly stretchable waterborne polyurethane (WPU). The two polymers have good miscibility at a wide range of blending ratios. The conductivity of the composite films increases while the stretchability decreases with the increase of PEDOT:PSS loading. At a 20 wt% PEDOT:PSS loading, the composite films show a conductivity of 77 S cm−1 and an elongation at break of about 32.5%. More interestingly, they exhibit a high EMI shielding effectiveness (SE) of about 62 dB over the X-band frequency range at a film thickness of only 0.15 mm.

163 citations

Journal ArticleDOI
TL;DR: Poly(3,4-ethylenedioxythiophene)/poly(styrene-4-sulfonate) (PEDOT/PSS) composites have been prepared from aqueous and acetonitrile solutions of EDOT and NaPSS by oxidation using Fe(III) salts as mentioned in this paper.
Abstract: Poly(3,4-ethylenedioxythiophene)/poly(styrene-4-sulfonate) (PEDOT/PSS) composites have been prepared from aqueous and aqueous acetonitrile solutions of EDOT and NaPSS by oxidation using Fe(III) salts. Powders with PEDOT to PSS ratios ranging from 0.3 to 4.2 and electronic conductivities as high as 10 S cm-1 have been obtained in good yields. The PEDOT/PSS blends are cation exchangers and exhibit facile eletrochemistry in both aqueous and acetonitrile media. Impedance measurements have shown that 30 μm thick PEDOT/PSS layers have proton conductivities as high as 0.03 S cm-1.

162 citations

Journal ArticleDOI
TL;DR: In this paper, partial benzene-ring sulfonation has been proposed to explain the wide range in conductivity of PANI bases, 10−11−10−7 S cm−1.
Abstract: Polyaniline (PANI) was prepared by the oxidation of aniline in the presence of various inorganic and organic acids at 20 °C and −50 °C. When strong acids were used, the conductivity of the protonated PANI was typically 1–10 S cm−1. The results indicate that the protonation of PANI in media containing carboxylic acids was achieved with the help of sulfuric acid produced during the reaction with ammonium peroxydisulfate. The conductivity of PANI prepared under such conditions was reduced. Partial benzene-ring sulfonation has been proposed to explain the wide range in conductivity of PANI bases, 10−11–10−7 S cm−1. The densities of the samples reflect the nature of the acid used. The densities of the corresponding PANI bases exhibit much less variation. Molecular weight and degree of crystallinity of PANI are higher when the polymerization is carried out at −50 °C. The conductivity of the PANI is determined mainly by way of protonation. The effects of molecular weight and of crystallinity on PANI conductivity are marginal. Copyright © 2004 Society of Chemical Industry

162 citations

Journal ArticleDOI
TL;DR: In this paper, the thermal conductivities of various protonic acid-doped polyaniline films were measured by combination of a laser flash method and a differential scanning calorimeter in relation with electrical conductivity.
Abstract: Thermal transporting properties of electrically conductive polyaniline films were first investigated in wide range of temperatures above room temperature as organic thermoelectric materials. Thermal conductivities of various protonic acid-doped polyaniline films were measured by combination of a laser flash method and a differential scanning calorimeter in relation with electrical conductivity and a kind of dopant. The thermal conductivities thus measured are in the range of conventional organic polymers, indicating that the doped polyaniline films have extremely low thermal conductivities among electrically conductive materials, and have correlation with neither electrical conductivity, nor a kind of dopant. Consequently the polyaniline film, which shows very high electrical conductivity, has comparable thermoelectric figure-of-merit (ZT) with feasible inorganic thermoelectric materials such as iron silicide.

162 citations

Journal ArticleDOI
TL;DR: A new polymer blend formed by poly(3-hexylthiophene)-poly(4-vinylpyridine) block copolymers and [6,6]-phenyl-C61-butyric acid methyl ester is reported, which exhibits microphase separated morphologies of electron-donor and electron-acceptor rich domains.
Abstract: A new polymer blend formed by poly(3-hexylthiophene)-poly(4-vinylpyridine) (P3HT-P4VP) block copolymers and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) is reported. The P4VP and PCBM are mixed together by weak supramolecular interactions, and the resulting materials exhibit microphase separated morphologies of electron-donor and electron-acceptor rich domains. The properties of the blend, used in photovoltaic devices as active layers, are also discussed.

162 citations


Network Information
Related Topics (5)
Carbon nanotube
109K papers, 3.6M citations
92% related
Graphene
144.5K papers, 4.9M citations
91% related
Oxide
213.4K papers, 3.6M citations
90% related
Polymerization
147.9K papers, 2.7M citations
88% related
Thin film
275.5K papers, 4.5M citations
88% related
Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023347
2022701
2021738
2020845
2019942
2018934