Functionalized highly electron-rich redox-active electropolymerized 3,4-propylenedioxythiophenes as precursors and targets for bioelectronics and supercapacitors
Publikationen: Beitrag in Fachzeitschrift › Artikel › Forschung › (peer-reviewed)
Standard
in: Molecular systems design & engineering , Jahrgang 6.2021, Nr. 3, 01.03.2021, S. 214-233.
Publikationen: Beitrag in Fachzeitschrift › Artikel › Forschung › (peer-reviewed)
Harvard
APA
Vancouver
Author
Bibtex - Download
}
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 -