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