Co(SxSe1-x)2 Nanorods Arrays with Rhombus Cross-section Exhibiting High Catalytic Activity for Quantum dot Sensitized Solar Cells

被引:11
作者
Wang, Hongju [1 ]
Wu, Dapeng [1 ,3 ]
Cao, Kun [1 ,2 ]
Wang, Fujuan [1 ,2 ]
Gao, Zhiyong [1 ,3 ]
Xu, Fang [1 ,3 ]
Jiang, Kai [1 ,2 ]
机构
[1] Henan Normal Univ, Sch Chem & Chem Engn, Collaborat Innovat Ctr Henan Prov Green Mfg Fine, Key Lab Green Chem Media & React,Minist Educ, Xinxiang 453007, Henan, Peoples R China
[2] Henan Normal Univ, Sch Environm, Xinxiang 453007, Henan, Peoples R China
[3] Henan Normal Univ, Henan Key Lab Boron Chem & Adv Energy Mat, Xinxiang 453007, Henan, Peoples R China
关键词
Nanorod arrays; Growth mechanism; Counter electrode; Reflectivity; Quantum-dot sensitized solar cells; EFFICIENT COUNTER ELECTRODE; CARBON NANOTUBE; THIN-FILM; PERFORMANCE; DEPOSITION; NANOCRYSTALS; FABRICATION; PHOTOANODE; NANOSHEETS; ROBUST;
D O I
10.1016/j.electacta.2017.08.134
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Unique Co(SxSe1-x)(2) nanorod arrays (NRAs) with rhombus cross-section were grown on FTO by a Solid-Gas-Solid process and used for quantum-dot sensitized solar cells (QDSSCs). The composition of S/Se of the Co(SxSe1-x)(2) products could be facilely controlled by changing the molar ratios of S and Se powders. The as-prepared Co(SxSe1-x)(2) NRAs have high porosity, root mean square (27.3 nm) and small water contact angle (39.6 degrees), which benefits the electrolyte penetration and provides large active areas, leading to higher electrocatalytic activity and lower charge transfer resistance toward the reduction of S-n(2-) ions compared with Pt. In addition, the Co(SxSe1-x)(2) NRAs exhibits high reflectivity, which helps to improve the light-harvesting efficiency of the photoanode. Thanks to these structural advantages, when used as counter electrode, a high J(sc) of 16.37 mA cm(-2) was demonstrated, which leads to maximum power conversion efficiency (PCE) of 4.72% indicating similar to 55% improvement compared with the Pt based device (2.62%). (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:378 / 387
页数:10
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