Electrospun FeS nanorods with enhanced stability as counter electrodes for dye-sensitized solar cells

被引:45
作者
Zhang, Chenle [1 ,2 ]
Deng, Libo [1 ]
Zhang, Peixin [1 ,2 ]
Ren, Xiangzhong [1 ]
Li, Yongliang [1 ]
He, Tingshu [2 ,3 ]
机构
[1] Shenzhen Univ, Coll Chem & Environm Engn, Shenzhen 518060, Guangdong, Peoples R China
[2] Shenzhen Univ, Shenzhen Key Lab Environm Chem & Ecol Remediat, Coll Chem & Environm Engn, Shenzhen, Guangdong, Peoples R China
[3] Xian Univ Architecture & Technol, Sch Mat & Mineral Resources, Xian 710055, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrospinning; counter electrode; FeS; catalytic activity; durability; IN-SITU GROWTH; LOW-COST; IRON; PERFORMANCE; EFFICIENCY; NANOFIBERS; SPECTROSCOPY; ELECTROLYTES; MORPHOLOGY; CAPACITORS;
D O I
10.1016/j.electacta.2017.01.148
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The performance of dye-sensitized solar cells (DSSCs) is strongly influenced by the catalytic performance of counter electrode (CE) materials. Platinum (Pt) is extensively used as the CE for DSSC, but the high cost and low resistance to corrosion of Pt-based CE material restricts its practical application. Herein, we prepared alpha-Fe2O3 and FeS nanorods (NRs) through electrospinning and investigated their valence states using Mossbauer spectroscopy and also assessed their catalytic performances as CE materials. It was found that upon the conversion of n-type semiconductor alpha-Fe2O3 into p-type semiconductor FeS through the sulfurization process, the photoenergy conversion efficiency (PCE) was increased from 3.79% to 6.47% which is comparable with Pt. This increment might be related to the higher amount of electron-hole pairs and higher electrical conductivity, as well as the mixed valence of Fe element in the iron sulfide which can facilitate the transfer of electrons to the electrolyte. Furthermore, the FeS NRs show a much better longterm stability than Pt due to the interconnected conductive paths and excellent mechanical stability endowed by the one-dimensional morphology. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:229 / 238
页数:10
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