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Polypyrrole salts and bases: Superior conductivity of nanotubes and their stability towards the loss of conductivity by deprotonation

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22340%2F16%3A43902002" target="_blank" >RIV/60461373:22340/16:43902002 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/61389013:_____/16:00462628 RIV/00216208:11320/16:10330000

  • Výsledek na webu

    <a href="http://pubs.rsc.org/en/Content/ArticleLanding/2016/RA/C6RA19461C#!divAbstract" target="_blank" >http://pubs.rsc.org/en/Content/ArticleLanding/2016/RA/C6RA19461C#!divAbstract</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/c6ra19461c" target="_blank" >10.1039/c6ra19461c</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Polypyrrole salts and bases: Superior conductivity of nanotubes and their stability towards the loss of conductivity by deprotonation

  • Popis výsledku v původním jazyce

    Polypyrrole nanotubes exhibit conductivity of tens S cm-1 which is one of the highest among the current conducting polymers. They are thus superior to the common globular form with the conductivity of units of S cm-1 or lower. The conductivity of both forms is reduced after treatment with alkalis but still remains high, units of S cm-1 and 10-2 S cm-1, respectively. The deprotonation, which is responsible for conductivity reduction, is discussed on the basis of salt-base transition in polypyrrole. It is not fully reversible, and the reprotonation with acids recovers the conductivity only in part. The role of methyl orange, which was used to support the formation of nanotubes, is proposed to be similar to that of surfactants. FTIR and Raman spectroscopies prove that methyl orange is strongly bound to polypyrrole in its acid form, and an "insertion" mechanism is proposed to explain the resistance towards the deprotonation of nanotubes. The spectra also illustrate that the molecular structure of nanotubular polypyrrole is preserved even under highly alkaline conditions at a pH close to 14, where the globular form becomes damaged. Polypyrrole, especially in its nanotubular form, is of promise in applications requiring electrical conduction even under neutral or alkaline conditions, where other conducting polymers, such as polyaniline, lose their exploitable conductivity.

  • Název v anglickém jazyce

    Polypyrrole salts and bases: Superior conductivity of nanotubes and their stability towards the loss of conductivity by deprotonation

  • Popis výsledku anglicky

    Polypyrrole nanotubes exhibit conductivity of tens S cm-1 which is one of the highest among the current conducting polymers. They are thus superior to the common globular form with the conductivity of units of S cm-1 or lower. The conductivity of both forms is reduced after treatment with alkalis but still remains high, units of S cm-1 and 10-2 S cm-1, respectively. The deprotonation, which is responsible for conductivity reduction, is discussed on the basis of salt-base transition in polypyrrole. It is not fully reversible, and the reprotonation with acids recovers the conductivity only in part. The role of methyl orange, which was used to support the formation of nanotubes, is proposed to be similar to that of surfactants. FTIR and Raman spectroscopies prove that methyl orange is strongly bound to polypyrrole in its acid form, and an "insertion" mechanism is proposed to explain the resistance towards the deprotonation of nanotubes. The spectra also illustrate that the molecular structure of nanotubular polypyrrole is preserved even under highly alkaline conditions at a pH close to 14, where the globular form becomes damaged. Polypyrrole, especially in its nanotubular form, is of promise in applications requiring electrical conduction even under neutral or alkaline conditions, where other conducting polymers, such as polyaniline, lose their exploitable conductivity.

Klasifikace

  • Druh

    J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

  • CEP obor

    CD - Makromolekulární chemie

  • OECD FORD obor

Návaznosti výsledku

  • Projekt

    Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Ostatní

  • Rok uplatnění

    2016

  • Kód důvěrnosti údajů

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

Údaje specifické pro druh výsledku

  • Název periodika

    RSC Advances

  • ISSN

    2046-2069

  • e-ISSN

  • Svazek periodika

    6

  • Číslo periodika v rámci svazku

    91

  • Stát vydavatele periodika

    GB - Spojené království Velké Británie a Severního Irska

  • Počet stran výsledku

    10

  • Strana od-do

    88382-88391

  • Kód UT WoS článku

    000384571800066

  • EID výsledku v databázi Scopus

    2-s2.0-84988422336