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In Situ ESR/UV-vis-NIR and ATR-FTIR Spectroelectrochemical Studies on the p-Doping of Copolymers of 3-Methylthiophene and 3-Hexylthiophene
被引:19
作者:
Chazaro-Ruiz, Luis F.
[1
]
Kellenberger, Andrea
[1
,2
]
Dunsch, Lothar
[1
]
机构:
[1] Leibniz Inst Festkorper & Werkstofforschung, Abt Elektrochem & Leitfahige Polymere, D-01069 Dresden, Germany
[2] Univ Politehn Timisoara, Fac Ind Chem & Environm Engn, RO-300006 Timisoara, Romania
关键词:
CHARGE-CARRIERS;
CONDUCTING POLYMERS;
OPTICAL-PROPERTIES;
MOBILITIES;
POLY(3-ALKYLTHIOPHENES);
POLYTHIOPHENE;
POLY(3-METHYLTHIOPHENE);
POLARONS;
FILMS;
ELECTROPOLYMERIZATION;
D O I:
10.1021/jp806810r
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 combined spectroelectrochemical study by ESR/UV-vis-NIR as well as FTIR spectroscopy on the influence of the copolymer composition on the stabilization of charges upon electrochemical p-doping is presented. As compared to the parent homopolymers 3-hexylthiophene (3-HeTh) and 3-methylthiophene (3-MeTh) which seems to be irregular, FTIR studies of the copolymer of both monomers (copMeHeTh) point to a regioregular structure. The in situ ESR and UV-vis-NIR spectroelectrochemistry at higher doping levels of the polymeric materials proves bipolarons and polaron pairs as stable charged states in poly(3-hexylthiophene) as well as the copolymer copMeHeTh. During the p-doping of poly(3-methylthiophene) bipolarons are the dominating species at higher doping levels. It is demonstrated that only the simultaneous use of both the ESR and the UV-vis-NIR spectroscopy enables the differentiation of polarons (paramagnetic) and polaron pairs (diamagnetic) in a conducting polymer.
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页码:2310 / 2316
页数:7
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