Improved air stability of perovskite solar cells via solution-processed metal oxide transport layers

被引:0
|
作者
You, Jingbi [1 ]
Meng, Lei [1 ]
Song, Tze-Bin [1 ]
Guo, Tzung-Fang [2 ]
Yang, Yang [1 ]
Chang, Wei-Hsuan [1 ]
Hong, Ziruo [1 ]
Chen, Huajun [1 ]
Zhou, Huanping [1 ]
Chen, Qi [1 ]
Liu, Yongsheng [1 ]
De Marco, Nicholas [1 ]
Yang, Yang [1 ]
机构
[1] Univ Calif Los Angeles, Dept Mat Sci & Engn, Los Angeles, CA 90095 USA
[2] Natl Cheng Kung Univ, Adv Optoelect Technol Ctr, Dept Photon, Tainan 701, Taiwan
基金
美国国家科学基金会;
关键词
INORGANIC HOLE CONDUCTOR; HIGH-PERFORMANCE; THIN-FILM; ANOMALOUS HYSTERESIS; HALIDE PEROVSKITES; EFFICIENT; INTERFACE; CONTACTS; TIN;
D O I
10.1038/NNANO.2015.230
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Lead halide perovskite solar cells have recently attracted tremendous attention because of their excellent photovoltaic efficiencies. However, the poor stability of both the perovskite material and the charge transport layers has so far prevented the fabrication of devices that can withstand sustained operation under normal conditions. Here, we report a solution-processed lead halide perovskite solar cell that has p-type NiOx and n-type ZnO nanoparticles as hole and electron transport layers, respectively, and shows improved stability against water and oxygen degradation when compared with devices with organic charge transport layers. Our cells have a p-i-n structure (glass/indium tin oxide/NiOx/perovskite/ZnO/Al), in which the ZnO layer isolates the perovskite and Al layers, thus preventing degradation. After 60 days storage in air at room temperature, our all-metal-oxide devices retain about 90% of their original efficiency, unlike control devices made with organic transport layers, which undergo a complete degradation after just 5 days. The initial power conversion efficiency of our devices is 14.6 +/- 1.5%, with an uncertified maximum value of 16.1%.
引用
收藏
页码:75 / +
页数:8
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