Functionalized highly electron-rich redox-active electropolymerized 3,4-propylenedioxythiophenes as precursors and targets for bioelectronics and supercapacitors

Research output: Contribution to journalArticleResearchpeer-review

Standard

Functionalized highly electron-rich redox-active electropolymerized 3,4-propylenedioxythiophenes as precursors and targets for bioelectronics and supercapacitors. / Karazehir, Tolga; Sarac, Baran; Gilsing, Hans Detlev et al.
In: Molecular systems design & engineering , Vol. 6.2021, No. 3, 01.03.2021, p. 214-233.

Research output: Contribution to journalArticleResearchpeer-review

Vancouver

Bibtex - Download

@article{6c7f5ecf13284c49afc6d5a307f285ed,
title = "Functionalized highly electron-rich redox-active electropolymerized 3,4-propylenedioxythiophenes as precursors and targets for bioelectronics and supercapacitors",
abstract = "In order to combine capacitive properties with processability, e.g. solubility in organic solvents, poly(3,4-propylenedioxythiophene) derivatives containing different functional groups like oxyphenyl methanol (–OPhCH2OH), oxybenzyl (–OBz), bromide (–Br) and tosyl (–OTs) were synthesized and electropolymerized as thin films from acetonitrile (ACN) using Et4NBF4 as an electrolyte. Multifunctionality in the substitution pattern of the polymer exhibits a similar trend between monomer oxidation potentials and specific capacitance (Csp) vs. crystal size. The presence of π–π stacking interactions in the polymer structures plays an important role in building the crystal structures. The same order of flat band potential and Csp values are observed for –OBz < –Br < –OTs < –OPhCH2OH substitutions. The structures of PProDOT–OBz and PProDOT–OPhCH2OH resemble each other much more than those of PProDOT–Br and PProDOT–OTs. Impedance measurements were conducted at different applied biases in order to define a Mott–Schottky analysis revealing the dependence of the semiconducting properties on the type of substituent present in the PProDOT derivative.",
author = "Tolga Karazehir and Baran Sarac and Gilsing, {Hans Detlev} and Selin Gumrukcu and J{\"u}rgen Eckert and Sarac, {A. Sezai}",
note = "Publisher Copyright: {\textcopyright} The Royal Society of Chemistry.",
year = "2021",
month = mar,
day = "1",
doi = "10.1039/d0me00126k",
language = "English",
volume = "6.2021",
pages = "214--233",
journal = "Molecular systems design & engineering ",
issn = "2058-9689",
publisher = "Royal Society of Chemistry",
number = "3",

}

RIS (suitable for import to EndNote) - Download

TY - JOUR

T1 - Functionalized highly electron-rich redox-active electropolymerized 3,4-propylenedioxythiophenes as precursors and targets for bioelectronics and supercapacitors

AU - Karazehir, Tolga

AU - Sarac, Baran

AU - Gilsing, Hans Detlev

AU - Gumrukcu, Selin

AU - Eckert, Jürgen

AU - Sarac, A. Sezai

N1 - Publisher Copyright: © The Royal Society of Chemistry.

PY - 2021/3/1

Y1 - 2021/3/1

N2 - In order to combine capacitive properties with processability, e.g. solubility in organic solvents, poly(3,4-propylenedioxythiophene) derivatives containing different functional groups like oxyphenyl methanol (–OPhCH2OH), oxybenzyl (–OBz), bromide (–Br) and tosyl (–OTs) were synthesized and electropolymerized as thin films from acetonitrile (ACN) using Et4NBF4 as an electrolyte. Multifunctionality in the substitution pattern of the polymer exhibits a similar trend between monomer oxidation potentials and specific capacitance (Csp) vs. crystal size. The presence of π–π stacking interactions in the polymer structures plays an important role in building the crystal structures. The same order of flat band potential and Csp values are observed for –OBz < –Br < –OTs < –OPhCH2OH substitutions. The structures of PProDOT–OBz and PProDOT–OPhCH2OH resemble each other much more than those of PProDOT–Br and PProDOT–OTs. Impedance measurements were conducted at different applied biases in order to define a Mott–Schottky analysis revealing the dependence of the semiconducting properties on the type of substituent present in the PProDOT derivative.

AB - In order to combine capacitive properties with processability, e.g. solubility in organic solvents, poly(3,4-propylenedioxythiophene) derivatives containing different functional groups like oxyphenyl methanol (–OPhCH2OH), oxybenzyl (–OBz), bromide (–Br) and tosyl (–OTs) were synthesized and electropolymerized as thin films from acetonitrile (ACN) using Et4NBF4 as an electrolyte. Multifunctionality in the substitution pattern of the polymer exhibits a similar trend between monomer oxidation potentials and specific capacitance (Csp) vs. crystal size. The presence of π–π stacking interactions in the polymer structures plays an important role in building the crystal structures. The same order of flat band potential and Csp values are observed for –OBz < –Br < –OTs < –OPhCH2OH substitutions. The structures of PProDOT–OBz and PProDOT–OPhCH2OH resemble each other much more than those of PProDOT–Br and PProDOT–OTs. Impedance measurements were conducted at different applied biases in order to define a Mott–Schottky analysis revealing the dependence of the semiconducting properties on the type of substituent present in the PProDOT derivative.

UR - http://www.scopus.com/inward/record.url?scp=85102582980&partnerID=8YFLogxK

U2 - 10.1039/d0me00126k

DO - 10.1039/d0me00126k

M3 - Article

AN - SCOPUS:85102582980

VL - 6.2021

SP - 214

EP - 233

JO - Molecular systems design & engineering

JF - Molecular systems design & engineering

SN - 2058-9689

IS - 3

ER -