Enhanced thermoelectric properties of CNT/PANI composite nanofibers by highly orienting the arrangement of polymer chains

被引:231
作者
Wang, Qun [1 ]
Yao, Qin [1 ]
Chang, Jiang [2 ]
Chen, Lidong [1 ]
机构
[1] Chinese Acad Sci, CAS Key Lab Mat Energy Convers, Shanghai Inst Ceram, Shanghai 200050, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Ceram, Biomat & Tissue Engn Res Ctr, Shanghai 200050, Peoples R China
基金
中国国家自然科学基金;
关键词
CARBON NANOTUBE NETWORKS; ELECTRICAL-PROPERTIES; DOPED POLYANILINE; FILMS; POLY(3,4-ETHYLENEDIOXYTHIOPHENE); ACID; CSA;
D O I
10.1039/c2jm32750c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Carbon nanotube (CNT)/Polyaniline (PANI) thermoelectric composite nanofibers were prepared by a combination of in situ polymerization and electro-spinning processes. The obtained composite nanofibers were macroscopically aligned, while the CNTs were embedded in the nanofibers and oriented along the fiber axis. Polarized Raman spectra and X-ray diffraction (XRD) studies verified that the PANI backbone chains were orientated along the CNT axis and therefore along the fiber axis due to the strong chemical interactions between PANI and CNTs. The highly ordered arrangement of the PANI backbone chains not only reduces the pi-pi conjugated defects in the polymer backbone, but also increases the effective degree of electron delocalization and therefore enhances the carrier mobility in PANI, which results in the anisotropic thermoelectric properties especially with more than a doubled improvement of power factor in the orientation direction. This study not only provides an effective route to orient the conducting polymer chains at the molecular level but also demonstrates a possibility to design a conducting polymer with high thermoelectric performance through constructing a highly extended and orderly aligned backbone chain structure by chemical routes.
引用
收藏
页码:17612 / 17618
页数:7
相关论文
共 27 条
  • [1] Bubnova O, 2011, NAT MATER, V10, P429, DOI [10.1038/NMAT3012, 10.1038/nmat3012]
  • [2] Conductive polypyrrole nanofibers via electrospinning: Electrical and morphological properties
    Chronakis, IS
    Grapenson, S
    Jakob, A
    [J]. POLYMER, 2006, 47 (05) : 1597 - 1603
  • [3] Cochet M, 2000, J RAMAN SPECTROSC, V31, P1041, DOI 10.1002/1097-4555(200012)31:12<1041::AID-JRS641>3.0.CO
  • [4] 2-R
  • [5] A comparative study of m-cresol treated polyaniline and Langmuir Blodgett films
    da Silva, JEP
    de Torresi, SIC
    Temperini, MLA
    Gonçalves, D
    Oliveira, ON
    [J]. SYNTHETIC METALS, 1999, 101 (1-3) : 691 - 691
  • [6] da Silva JEP, 2000, MACROMOLECULES, V33, P3077
  • [7] X-ray scattering study of CSA protonated polyaniline films and powders
    Djurado, D
    Nicolau, YF
    Dalsegg, I
    Samuelsen, EJ
    [J]. SYNTHETIC METALS, 1997, 84 (1-3) : 121 - 122
  • [8] Du Y., 2011, PROG POLYM IN PRESS
  • [9] Large-scale fabrication of aligned single-walled carbon nanotube array and hierarchical single-walled carbon nanotube assembly
    Gao, JB
    Yu, AP
    Itkis, ME
    Bekyarova, E
    Zhao, B
    Niyogi, S
    Haddon, RC
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (51) : 16698 - 16699
  • [10] Evaluation of Thermoelectric Properties of Polythiophene Films Synthesized by Electrolytic Polymerization
    Hiraishi, Kentaro
    Masuhara, Akito
    Nakanishi, Hachiro
    Oikawa, Hidetoshi
    Shinohara, Yosikazu
    [J]. JAPANESE JOURNAL OF APPLIED PHYSICS, 2009, 48 (07)