Green low-temperature-solution-processed in situ HI modified TiO2/SnO2 bilayer for efficient and stable planar perovskite solar cells build at ambient air conditions

被引:21
|
作者
Deng, Yaxin
Li, Shuxian
Li, Xuandong
Wang, Rui
Li, Xin
机构
基金
中国国家自然科学基金;
关键词
TiO2/SnO2; Electron transfer layer; Ambient condition; Perovskite solar cell; ELECTRON-TRANSPORT LAYER; PERFORMANCE; TIO2; STABILITY; CH3NH3PBI3; DEPOSITION; MORPHOLOGY; ROUTE; CU2O;
D O I
10.1016/j.electacta.2019.134924
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Planar structures for halide perovskite solar cells with the high efficiencies typically use high-temperature processed TiO2 as the electron transporting layers (ETLs). Here, we demonstrate that an in-situ passivation strategy for TiO2 film through the introduction of HI during low-temperature preparation process. HI not only controls hydrolysis of TiO2 precursor but also eliminates defects and suppresses trap states in TiO2 film. Meanwhile, the double-layer architecture is constructed by coating TiO2 with SnO2 layer, the double ETLs can improve the photovoltaic performance of methylamine lead iodide (MAPbI(3)) perovskite solar cells. The TiO2(HI)/SnO2 ETL can effectively reduce the interfacial charge recombination and facilitate electron transfer. More importantly, the preparation of TiO2 and SnO2 are totally performed at low-temperature (150 degrees C) and the devices are fabricated in uncontrolled ambient conditions. Our best-performing planar perovskite cell using such a TiO2(HI)/SnO2 ETL has achieved a maximum power conversion efficiency (PCE) of 16.74%, and the devices exhibit good stability which maintaining 85% and 83% of their initial efficiency after heating at 100 degrees C for 22 h and under illuminating upon 1 sun irradiation for 6 h, respectively. Our results suggest a new approach for further improving the stability of PSCs fabricated in the air condition. (C) 2019 Elsevier Ltd. All rights reserved.
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页数:9
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