Energy harvesting and temperature sensing thermoelectric devices based on the carbon template method

被引:3
|
作者
Jiang, Nan [1 ]
Qu, Meijie [1 ]
Wang, Hai [1 ]
Bin, Yuezhen [1 ]
Zhang, Rui [1 ]
Tang, Ping [1 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, Dept Polymer Sci & Engn, 2 Linggong Rd, Dalian 116024, Peoples R China
基金
中国国家自然科学基金;
关键词
carbon materials; morphological structure; PEDOT; PSS; thermoelectric generators; INDUCED ELECTRICITY; CONDUCTING POLYMER; COMPOSITE FILM; ENHANCEMENT; PERFORMANCE;
D O I
10.1002/app.53336
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A series of self-supporting carbon nanomaterial films with different morphologies were employed as conductive templates for n-junction after polyethyleneimine (PEI) doping by taking advantages of the entanglement between carbon nanotubes. With the assistance of dimethyl sulfoxide (DMSO)-treated poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT:PSS) films as p-junction, flexible and light-weight thermoelectric generators (TEGs) were assembled. The effect of the morphology of the carbon nanomaterial, including multi-walled carbon nanotube (MWCNT), whisker carbon nanotube (WSCNT), and graphene on the electrical conductivity, mechanical properties and morphology of n-junction was investigated, on basis of which thermoelectric properties of TEG were evaluated. The properties of the three carbon-based self-supporting films show significant differences. The MWCNT/PEI film exhibits a tensile strength of up to 36.23 +/- 0.57 MPa due to the high entanglement network density of MWCNT. The entanglement of WSCNT/MWCNT/PEI provides an ideal conductive template for PEI to prepare n-junction material. TEGs with PEDOT:PSS-DMSO and WSCNT/MWCNT/PEI as p- and n-junctions show high power generation performance and cyclability. The output power density is up to 4.6 nW/cm(2) at Delta T = 42.0 K, matched to a suitable load. With its fast response and slow recovery, this TEG is expected to be used for human health monitoring and energy storage.
引用
收藏
页数:11
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