Strategic Side-Chain Engineering Approach for Optimizing Thermoelectric Properties of Isoindigo-Based Conjugated Polymers

被引:19
作者
Yoon, Sang Eun [1 ]
Shin, So Jeong [1 ]
Lee, Sang Yeon [3 ]
Jeon, Gyeong G. [1 ]
Kang, Hyunwoo [3 ]
Seo, Hyungtak [3 ]
Zheng, Jian [1 ,2 ]
Kim, Jong H. [1 ]
机构
[1] Ajou Univ, Dept Mol Sci & Technol, Suwon 16499, South Korea
[2] Lingnan Normal Univ, Sch Chem & Chem Engn, Zhanjiang 524048, Peoples R China
[3] Ajou Univ, Dept Mat Sci & Engn, Dept Energy Syst Res, Suwon 16499, South Korea
基金
新加坡国家研究基金会;
关键词
organic thermoelectric; conjugated polymer; sequential doping; side-chain engineering; dopant diffusion; FIELD-EFFECT MOBILITY; CARRIER MOBILITY; TRANSISTORS; LENGTH; DESIGN; TRANSPORT; DONOR; SIZE;
D O I
10.1021/acsapm.0c00332
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Strategic side-chain engineering has led to an increase in the power factor of isoindigo-based conjugated polymers (CPs) by an order of magnitude. We investigated the effect of side chains on the electrical properties of doped isoindigo-based CPs and gained insight into structure-electrical property-thermoelectric transport intercorrelation for optimization of thermoelectric CPs. For this study, we designed and synthesized four isoindigo-based polymers having different types of alkyl chains. The size of the alkyl chains significantly affected the crystallinity of the films, which subsequently resulted in different charge carrier mobilities and diffusion efficiencies of the molecular dopant. Amorphous polymers with bulkier alkyl chains promoted efficient dopant diffusion while their carrier mobility was relatively lower than that of crystalline CPs. Systematic characterizations on the structural, electrical, and thermoelectrical properties of the CP films showed a trade-off effect for these side-chain structures for optimization of the thermoelectric effect, and with the optimized structure, we obtained a significantly improved power factor up to 37.8 mu W.m(-1).K-2. This study suggests that exercising fine control of crystallinity through side-chain modification of the fixed polymer backbone can be a simple but very effective approach to maximizing organic thermoelectric effects of CPs.
引用
收藏
页码:2729 / 2735
页数:7
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