Thermoelectric Performances of Free-Standing Polythiophene and Poly(3-Methylthiophene) Nanofilms

被引:64
作者
Lu Bao-Yang [1 ]
Liu Cong-Cong [1 ]
Lu Shan [2 ]
Xu Jing-Kun [1 ]
Jiang Feng-Xing [1 ]
Li Yu-Zhen [1 ]
Zhang Zhuo [3 ]
机构
[1] Jiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Peoples R China
[2] Zhejiang Univ, Dept Control Sci & Engn, Hangzhou 310027, Peoples R China
[3] BOE Technol Grp Co Ltd, Beijing 100016, Peoples R China
基金
中国国家自然科学基金;
关键词
ELECTROCHEMICAL POLYMERIZATION; ORGANIC SEMICONDUCTOR; HIGH-CONDUCTIVITY; DERIVATIVES; POLYMERS; FILMS; POWER;
D O I
10.1088/0256-307X/27/5/057201
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Thermoelectric performances of free-standing polythiophene ( PT) and poly(3-methylthiophene) (PMeT) nanofilms with high tensile strength electrosynthesized from boron trifluoride diethyl etherate (BFEE) are systematically investigated. They display decent electric conductivity (47 and 73 S.cm(-1)), high Seebeck coefficient (130 and 76 mu V.K-1) and low thermal conductivity (0.17 and 0.15W.m(-1).K-1) at room temperature. Their figure of merit can reach 3.0 x 10(-2) at 250 K, higher than that of many other conducting polymers. The decrease of charge carrier concentration resulting from volatile and water-sensitive dopants from BFEE leads to the decrease of electrical conductivity but a substantial increase of the Seebeck coefficient, making their figure-of-merit values maintained at more than 10(-2) even after prolonged storage ( two months). Moreover, free-standing PT and PMeT exhibit much better thermoelectric performances than those in pressed pellets due to the good arrangement of the polymer chains and preferably oriented structure in films. It therefore provides a way to improve the thermoelectric performances of conducting polymers by controlling regularity of the extended conjugated chain structure and/or the chain packing to achieve high charge mobility.
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页数:4
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