The Role of Ordering on the Thermoelectric Properties of Blends of Regioregular and Regiorandom Poly(3-hexylthiophene)

被引:82
|
作者
Lim, Eunhee [1 ]
Glaudell, Anne M. [1 ]
Miller, Rachel [2 ]
Chabinyc, Michael L. [1 ]
机构
[1] Univ Calif Santa Barbara, Dept Mat, Santa Barbara, CA 93106 USA
[2] Cornell Univ, Dept Mat Sci & Engn, Ithaca, NY 14850 USA
基金
美国国家科学基金会;
关键词
organic thermoelectric; poly(3-hexylthiophene); semiconducting polymer; CHARGE-TRANSPORT; CONJUGATED POLYMERS; REVERSIBLE CRYSTALLIZATION; ORGANIC SEMICONDUCTORS; POWER-FACTOR; FILMS; P3HT; AGGREGATION; DISORDER; MOBILITY;
D O I
10.1002/aelm.201800915
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The thermoelectric properties of semiconducting polymers are influenced by both the carrier concentration and the morphology that sets the pathways for charge transport. A combination of optical, morphological, and electrical characterization is used to assess the effect of the role of disorder on the thermoelectric properties of thin films of poly(3-hexylthiophene) (P3HT) doped with 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane (F(4)TCNQ). Controlled morphologies are formed by casting blends of regioregular (RR-P3HT) and regiorandom (RRa-P3HT) and then subsequently doped with F(4)TCNQ from the vapor phase. Optical spectroscopy and X-ray scattering show that vapor phase doping induces order in the disordered regions of thin films and increases the long-range connectivity of the film. The thermoelectric properties are assessed as a function of composition and it is shown that while the Seebeck coefficient is affected by structural ordering, the electrical conductivity and power factor are more strongly correlated with the long-range connectivity of ordered domains.
引用
收藏
页数:11
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