Synergistic effects of ZnO compact layer and TiCl4 post-treatment for dye-sensitized solar cells

被引:50
作者
Huang, Niu [2 ]
Liu, Yumin [2 ]
Peng, Tao [2 ]
Sun, Xiaohua [2 ]
Sebo, Bobby [2 ]
Tai, Qidong [2 ]
Hu, Hao [2 ]
Chen, Bolei [2 ]
Guo, Shi-shang [1 ,2 ]
Zhao, Xingzhong [1 ,2 ]
机构
[1] Wuhan Univ, Minist Educ, Key Lab Artificial Micro Nanostruct, Wuhan 430072, Hubei, Peoples R China
[2] Wuhan Univ, Sch Phys Sci & Technol, Wuhan 430072, Hubei, Peoples R China
关键词
Dye sensitized solar cells; Zinc oxide compact layer; Titanium tetrachloride post-treatment; Electrical transport; Charge recombination; NB-DOPED TIO2; PERFORMANCE IMPROVEMENT; ENHANCED EFFICIENCY; CHARGE-TRANSFER; LOW-COST; FILMS; ELECTRODES; OXIDE; CONVERSION; LIGHT;
D O I
10.1016/j.jpowsour.2011.12.027
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
The interaction between ZnO compact layer and TiCl4 post-treatment on TiO2 photoelectrode for dye sensitized solar cell (DSSC) is investigated. Photoelectrode combined the two modifications is designated as ZnO+2I+TiCl4. It is found that after the TiCl4 treatment the ZnO compact layer transforms to a hi-functional layer, which suppresses back electrons transfer from FO to electrolyte and reduces the FTO/TiO2 interfacial resistance. In addition, the newly formed TiO2 coating generated by TiCl4 post-treatment contains abundant and well dispersed Zn element, which further facilitates electron transfer at TiO2 layer. Meanwhile, the electron lifetime in ZnO+2I+TiCl4 is the longest. Consequently, the overall energy conversion efficiency of the cell with ZnO+2I+TiCl4 is significantly enhanced to 8.9%, which is 8.8% higher than that with pure TiCl4 post-treatment and 17.7% higher than that without any treatment. These results are verified by material characterization and corresponding opto-electrical properties measurements. Experimental results demonstrate this facile method is a more promising alternative to the conventional interface and surface modification in high efficient DSSCs. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:257 / 264
页数:8
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