共 91 条
Hard-Cation-Soft-Anion Ionic Liquids for PEDOT:PSS Treatment
被引:16
作者:
Choi, Changwon
[1
]
de Izarra, Ambroise
[1
,2
]
Han, Ikhee
[1
]
Jeon, Woojin
[1
]
Lansac, Yves
[1
,2
,3
]
Jang, Yun Hee
[1
]
机构:
[1] DGIST, Dept Energy Sci & Engn, Daegu 42988, South Korea
[2] Univ Tours, GREMAN, CNRS, UMR 7347, F-37200 Tours, France
[3] Univ Paris Saclay, Lab Phys Solides, CNRS, UMR 8502, F-91405 Orsay, France
基金:
新加坡国家研究基金会;
关键词:
PARTICLE MESH EWALD;
MOLECULAR-DYNAMICS;
ELECTRICAL-CONDUCTIVITY;
TRANSPARENT ELECTRODE;
HYDROIODIC ACID;
FORCE-FIELD;
BASES HSAB;
FILMS;
POLY(3,4-ETHYLENEDIOXYTHIOPHENE);
ENHANCEMENT;
D O I:
10.1021/acs.jpcb.1c09001
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
A promising conducting polymer poly(3,4ethylenedioxythiophene):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-.
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页码:1615 / 1624
页数:10
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