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Department of Energy Science and Engineering
CMMM Lab(Curious Minds Molecular Modeling Laboratory)
1. Journal Articles
Hard-Cation-Soft-Anion Ionic Liquids for PEDOT:PSS Treatment
Choi, Changwon
;
Izarra, Ambroise de
;
Han, Ikhee
;
Jeon, Woojin
;
Lansac, Yves
;
Jang, Yun Hee
Department of Energy Science and Engineering
CMMM Lab(Curious Minds Molecular Modeling Laboratory)
1. Journal Articles
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Title
Hard-Cation-Soft-Anion Ionic Liquids for PEDOT:PSS Treatment
Issued Date
2022-02
Citation
Choi, Changwon. (2022-02). Hard-Cation-Soft-Anion Ionic Liquids for PEDOT:PSS Treatment. Journal of Physical Chemistry B, 126(7), 1615–1624. doi: 10.1021/acs.jpcb.1c09001
Type
Article
Keywords
PARTICLE MESH EWALD
;
MOLECULAR-DYNAMICS
;
ELECTRICAL-CONDUCTIVITY
;
TRANSPARENT ELECTRODE
;
HYDROIODIC ACID
;
FORCE-FIELD
;
BASES HSAB
;
FILMS
;
POLY(3,4-ETHYLENEDIOXYTHIOPHENE)
;
ENHANCEMENT
ISSN
1520-6106
Abstract
A promising conducting polymer poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) experiences significant conductivity enhancement when treated with proper ionic liquids (ILs). Based on the hard-soft-acid-base principle, we propose a combination of a hydrophilic hard cation A+ (instead of the commonly used 1-ethyl-3-methyl imidazolium, EMIM+) and a hydrophobic soft anion X- (such as tetracyanoborate, TCB-) as the best ILs for this purpose. Such ILs would decouple hydrophilic-but-insulating PSS- from conducting-but-hydrophobic PEDOT+ most efficiently by strong interactions with hydrophilic A+ and hydrophobic X-, respectively. Such a favorable ion exchange between PEDOT+:PSS- and A+:X- ILs would allow the growth of conducting PEDOT+ domains decorated by X-, not disturbed by PSS- or A+. Using density functional theory calculations and molecular dynamics simulations, we demonstrate that a protic cation- (aliphatic N-alkyl pyrrolidinium, in particular) combined with the hydrophobic anion TCB- indeed outperforms EMIM+ by promptly leaving hydrophobic TCB- and strongly binding to hydrophilic PSS-. © 2022 American Chemical Society.
URI
http://hdl.handle.net/20.500.11750/16432
DOI
10.1021/acs.jpcb.1c09001
Publisher
American Chemical Society
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