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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.


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Journal ArticleDOI
TL;DR: In this paper, the authors used time-domain flectance measurements of thermal conductivity along multiple directions of thin drop-cast PEDOT films to show that the thermal conductivities can be highly anisotropic (Λ∥ ≈ 1.0 W m −1 K −1 and Λ⊥ 0.3 W m−1 K−1 −1 for the in-plane and through-plane directions, respectively) when the electrical conductivity in the inplane direction is large (σ ≈ 500 S cm −1 ).
Abstract: Mixtures of poly(3,4-ethylenedioxythiophene) and polystyrenesulfonate (PEDOT:PSS) have high electrical conductivity when cast from aqueous suspensions in combination with a high boiling-point cosolvent dimethyl sulfoxide (DMSO). The electronic component of the thermal conductivity of these highly conducting polymers is of interest for evaluating their potential for thermoelectric cooling and power generation. We find, using time-domain thermore- flectance measurements of thermal conductivity along multiple directions of thick (>20 μm) drop-cast PEDOT films, that the thermal conductivity can be highly anisotropic (Λ∥ ≈ 1.0 W m −1 K −1 and Λ⊥ ≈ 0.3 W m −1 K −1 for the in-plane and through- plane directions, respectively) when the electrical conductivity in the in-plane direction is large (σ ≈ 500 S cm −1 ). We relate the increase in thermal conductivity to the estimated electronic component of the thermal conductivity using the Wiedemann−Franz law, and find that our data are consistent with conventional Sommerfeld value of the Lorenz number. We use measurements of the elastic constants (C11 ≈ 11 GPa and C44 ≈ 17 GPa) of spin-cast PEDOT films and through-plane thermal conductivity (Λ⊥ ≈ 0.3 W m −1 K −1 ) of drop-cast and spin-cast films to support our assumption that the phonon contribution to the thermal conductivity does not change significantly with DMSO composition.

253 citations

Journal ArticleDOI
29 Aug 2012-ACS Nano
TL;DR: It is demonstrated that the anisotropic growth of PANI at the nanometer scale can be kinetically controlled by employing a polymeric stabilizer, poly(N-vinylpyrrolidone), and it is believed that the stabilizer sterically restricts the directional fiber growth mechanism governing PANI chain growth in aqueous solution.
Abstract: Polyaniline (PANI) is one of the most widely investigated conducting polymers and is considered to be of practical use for many future applications. Here, we first demonstrate that the anisotropic growth of PANI at the nanometer scale can be kinetically controlled by employing a polymeric stabilizer, poly(N-vinylpyrrolidone). The polymerization rate became slower in the presence of the stabilizer (the rate constants calculated at the initial stage decreased with increasing concentration of the stabilizer), yielding PANI nanostructures with lower aspect ratios. Therefore, it is believed that the stabilizer sterically restricts the directional fiber growth mechanism governing PANI chain growth in aqueous solution. Three PANI nanostructures, specifically nanospheres, nanorods, and nanofibers, were fabricated and their oxidation/protonation levels were investigated systematically. It was found that the nanofibers had the most outstanding oxidation/protonation level accompanied by structural ordering (note that the only difference between the polymerization conditions in each case was the concentration of the stabilizer). We also examine the electrochemical properties of PANI nanostructure electrodes in three-electrode and two-electrode (actual capacitor cell) configurations. The intrinsic charge-transport ability of individual nanostructures strongly affected the electrochemical properties of the electrodes. Briefly, the nanofiber electrode had faster electrode kinetics and better capacitance than the nanorods and nanospheres. Lastly, an extrinsic factor, the interparticle contact resistance, also turned out to noticeably influence the capacitances of the electrodes.

253 citations

Journal ArticleDOI
TL;DR: The APTES-BNNS/epoxy composite prepared in this paper has excellent thermal management capability and can be applied to the packaging of high-power electronic devices.
Abstract: The effective dissipation of heat is critical to the performance and longevity of high-power electronics, so it is important to prepare highly thermally conductive polymer-based packaging materials for efficient thermal management. Due to the excellent thermal conductivity of boron nitride nanosheets (BNNSs), the hexagonal boron nitride (hBN) powder was dissolved in a mixed solution of isopropanol and deionized water for ultrasonic exfoliation to obtain hydroxylated BN nanosheets. Then, the prepared BNNS was functionalized with (3-aminopropyl)triethoxysilane (APTES) to enhance its dispersibility and interfacial compatibility in the epoxy resin, which play an important role in the improvement of the thermal conductivity of the composites. Finally, APTES-BNNS was uniformly dispersed in the epoxy resin by solvent mixing, and the oriented APTES-BNNS/epoxy composites were prepared through spin-coating and hot-pressing methods. It was found that APTES-BNNS/epoxy composites prepared herein exhibited significant anisotropic thermal conductivity. The results show that the thermal conductivity of APTES-BNNS/epoxy composites reached 5.86 W/mK at a filler content of 40 wt % and these composites have favorable thermal stability and mechanical properties. The APTES-BNNS/epoxy composite prepared in this paper has excellent thermal management capability and can be applied to the packaging of high-power electronic devices.

252 citations

Journal ArticleDOI
TL;DR: In this article, the application of conjugated polymers in potentiometric ion sensors (ion-selective electrodes, ISEs) is reviewed, which is related to the unique electrical, electrochemical and optical properties of polymers that can be used to convert chemical information into electrical or optical signals in the solid state.
Abstract: Conducting polymers (electroactive conjugated polymers, ECPs) have emerged as one of the most promising transducers for chemical sensors. This is related to the unique electrical, electrochemical and optical properties of conjugated polymers that can be used to convert chemical information (concentration, activity, partial pressure) into electrical or optical signals in the solid state. Application of conjugated polymers in potentiometric ion sensors (ion-selective electrodes, ISEs) is reviewed.

251 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023347
2022701
2021738
2020845
2019942
2018934