A new carbon nanotubes (CNTs)-poly acrylonitrile (PAN) composite electrolyte for solid state dye sensitized solar cells

被引:32
作者
Akhtar, M. Shaheer [1 ,2 ,3 ]
Li, Zhen Yu [1 ,2 ]
Park, Dong Min [1 ,2 ]
Oh, Dea Woong [1 ,2 ]
Kwak, Do-Hwan [1 ,2 ]
Yang, O-Bong [1 ,2 ,3 ]
机构
[1] Chonbuk Natl Univ, Sch Semicond & Chem Engn, Jeonju 561756, Jeonbuk, South Korea
[2] Chonbuk Natl Univ, Solar Energy Res Ctr, Jeonju 561756, Jeonbuk, South Korea
[3] Chonbuk Natl Univ, New & Renewable Energy Mat Dev Ctr NewREC, Jeonju 561756, Jeonbuk, South Korea
基金
新加坡国家研究基金会;
关键词
Carbon nanotubes; Poly acrylonitrile; Composite electrolyte; Dye sensitized solar cells; Short circuit current density; TRANSPORT; POLYACRYLONITRILE; PERFORMANCE; MORPHOLOGY; STABILITY; DIFFUSION;
D O I
10.1016/j.electacta.2011.08.082
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A new carbon nanotube (CNTs)-poly acrylonitrile (PAN) composite electrolyte was prepared by the thermal polymerization of acrylonitrile (AN) with CNTs for solid-state dye sensitized solar cells (DSSCs). It was found that the uniform CNT-PAN composite was formed due to the thermal polymerization of AN on CNTs. The strong bonding between CNTs and PAN could be confirmed by the characterization of XPS and Raman spectroscopy, resulting in the lowering of crystallinity and the increasing the ionic conductivity of composite electrolytes. On comparison with bare CNTs and the other composite electrolytes, the formation of triiodide (I-3(-)) ions in CNT-PAN composite electrolytes was drastically increased which was expected from the high ionic conductivity of electrolyte via I-3(-)/I- redox couple. DSSCs fabricated with CNT-PAN composite electrolytes achieved relatively high conversion efficiency of 3.9% with an open circuit voltage (V-OC) of 0.57 V. short circuit current density (J(SC)) of 10.9 mA/cm(2) and fill factor of 63.6%, which attributed to supply the higher extent of I-3(-) ions from CNT-PAN composite electrolyte during the charge transport process. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:9973 / 9979
页数:7
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