Highly stretchable organic thermoelectrics with an enhanced power factor due to extended localization length

被引:18
|
作者
Jo, Junhyeon [1 ]
Oh, Inseon [1 ]
Jin, Mi-Jin [1 ]
Park, Jungmin [1 ]
Son, Jae Sung [1 ]
An, Ki-Seok [2 ]
Yoo, Jung-Woo [1 ]
机构
[1] Ulsan Natl Inst Sci & Technol Ulsan, Sch Mat Sci & Engn, Low Dimens Carbon Mat Ctr, Ulsan 44919, South Korea
[2] Korea Res Inst Chem Technol, Thin Film Mat Res Grp, Daejeon 34114, South Korea
基金
新加坡国家研究基金会;
关键词
Organic thermoelectrics; Stretchable thermoelectrics; Conducting polymer; Electron delocalization; Hopping transport; LOW-TEMPERATURE CONDUCTIVITY; WEARABLE ELECTRONICS; HOPPING CONDUCTION; CHARGE-TRANSPORT; PEDOT; FILMS; PERFORMANCE; SOLVENT; POLY(3,4-ETHYLENEDIOXYTHIOPHENE); SEMICONDUCTORS;
D O I
10.1016/j.orgel.2017.08.013
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Wearable electronics, as a new form of ubiquitous technology, require a sustainable self-powering system with an enhanced mechanical durability. In this report, we demonstrate a conducting polymer based stretchable thermoelectric performance with a synergetic effect of an enhanced power factor due to electron delocalization. The fluorosurfactant treatment of poly(3,4-ethylene dioxythiophene): poly(styrenesulphonate) (PEDOT: PSS) films induced a significant dedoping effect with an enhanced Seebeck coefficient and a morphological change into an elongated lamellar structure. Such structural transformation led to a reduced transport dimensionality with strongly extended electron delocalization yielding a simultaneous enhancement of the electron mobility and the Seebeck coefficient, which produced an improved thermoelectric power factor. Most notably, the mechanical durability of the PEDOT: PSS film was greatly improved tolerating up to a 60% static strain and over several hundred cycles of 50% strain. The demonstrated concomitant enhancement of the mechanical stretchability and thermoelectric performance inspires a promising approach for improving shape-adjustable self-powering devices. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:367 / 375
页数:9
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