Mild solution-processed metal-doped TiO2 compact layers for hysteresis-less and performance-enhanced perovskite solar cells

被引:65
|
作者
Liang, Chao [1 ]
Li, Pengwei [1 ]
Zhang, Yiqiang [1 ]
Gu, Hao [1 ]
Cai, Qingbin [1 ]
Liu, Xiaotao [1 ]
Wang, Jiefei [1 ]
Wen, Hua [1 ]
Shao, Guosheng [1 ]
机构
[1] Zhengzhou Univ, SCICDLCEM, Sch Mat Sci & Engn, Zhengzhou 450001, Henan, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Rutile TiO2; Doping chemistry; Metal chloride; Hysteresis effect; Perovskite solar cell; ELECTRON-TRANSPORT LAYER; PHOTOVOLTAIC PERFORMANCE; BAND ALIGNMENT; EFFICIENCY; STABILITY; TRIHALIDE; INJECTION; NANORODS; BEHAVIOR; WATER;
D O I
10.1016/j.jpowsour.2017.10.079
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
TiO2 is extensively used as electron-transporting material on perovskite solar cells (PSCs). However, traditional TiO2 processing method needs high annealing temperature (> 450 degrees C) and pure TiO2 suffers from low electrical mobility and poor conductivity. In this study, a general one-pot solution-processed method is devised to grow uniform crystallized metal-doped TiO2 thin film as large as 15 x 15 cm(2). The doping process can be controlled effectively via a series of doping precursors from niobium (V), tin (IV), tantalum (V) to tungsten (VI) chloride. As far as we know, this is so far the lowest processing temperature for metal-doped TiO2 compact layers, as low as 70 degrees C. The overall performance of PSCs employing the metal-doped TiO2 layers is significantly improved in term of hysteresis effect, short circuit current, open-circuit voltage, fill factor, power conversion efficiency, and device stability. With the insertion of metal ions into TiO2 lattice, the corresponding CH3NH3PbI3 PSC leads to a similar to 25% improved PCE of over 16% under irradiance of 100 mW cm(-2) AM1.5G sunlight, compared with control device. The results indicate that this mild solution-processed metal-doped TiO2 is an effective industry-scale way for fabricating hysteresis-less and high-performance PSCs.
引用
收藏
页码:235 / 244
页数:10
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