Synergistic conductivity increase in polypyrrole/molybdenum disulfide composite

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F18%3A10439665" target="_blank" >RIV/00216208:11320/18:10439665 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/61389013:_____/18:00491295

Výsledek na webu

<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=nMg4kfvQl-" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=nMg4kfvQl-</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.polymer.2018.07.004" target="_blank" >10.1016/j.polymer.2018.07.004</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Synergistic conductivity increase in polypyrrole/molybdenum disulfide composite

Popis výsledku v původním jazyce

Polypyrrole/molybdenum disulfide (PPy/MoS2) composites were synthesized by in situ chemical polymerization of pyrrole in the presence of MoS2 flakes. The conductivity of the composite with a moderate content of PPy (15-30 wt%) reached 13 S cm(-1) , which is markedly higher than the conductivity of both the pristine PPy and MoS2 ,1 and 10(-6) S cm(-1) , respectively. The improved conductivity was explained by the formation of ordered thin PPy films with high conductivity at the MoS2 surface. At higher pyrrole content, globular PPy was formed in the bulk of the composite resulting in an increase of a disordered polymer fraction, and the conductivity decreased. The composite conductivity is thus controlled not only by content of PPy but also by the proportions between ordered and disordered PPy phases. The structural and morphological characterization of composite materials is based on Fourier-transform infrared and Raman spectroscopies, wide-angle X-ray diffraction, and scanning and transmission electron microscopies. The charge-carrier transport in the composites fits the Mott variable-range hopping mechanism. (C) 2018 Elsevier Ltd. All rights reserved.

Název v anglickém jazyce

Synergistic conductivity increase in polypyrrole/molybdenum disulfide composite

Popis výsledku anglicky

Polypyrrole/molybdenum disulfide (PPy/MoS2) composites were synthesized by in situ chemical polymerization of pyrrole in the presence of MoS2 flakes. The conductivity of the composite with a moderate content of PPy (15-30 wt%) reached 13 S cm(-1) , which is markedly higher than the conductivity of both the pristine PPy and MoS2 ,1 and 10(-6) S cm(-1) , respectively. The improved conductivity was explained by the formation of ordered thin PPy films with high conductivity at the MoS2 surface. At higher pyrrole content, globular PPy was formed in the bulk of the composite resulting in an increase of a disordered polymer fraction, and the conductivity decreased. The composite conductivity is thus controlled not only by content of PPy but also by the proportions between ordered and disordered PPy phases. The structural and morphological characterization of composite materials is based on Fourier-transform infrared and Raman spectroscopies, wide-angle X-ray diffraction, and scanning and transmission electron microscopies. The charge-carrier transport in the composites fits the Mott variable-range hopping mechanism. (C) 2018 Elsevier Ltd. All rights reserved.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10301 - Atomic, molecular and chemical physics (physics of atoms and molecules including collision, interaction with radiation, magnetic resonances, Mössbauer effect)

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2018

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Polymer

ISSN

0032-3861

e-ISSN

—

Svazek periodika

150

Číslo periodika v rámci svazku

15 August

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

8

Strana od-do

130-137

Kód UT WoS článku

000442535600013

EID výsledku v databázi Scopus

2-s2.0-85049777746