钙钛矿(结构)
材料科学
卤化物
能量转换效率
氧化铟锡
降级(电信)
氧化物
制作
铟
化学工程
光活性层
太阳能电池
钙钛矿太阳能电池
光伏系统
金属
纳米技术
光电子学
图层(电子)
无机化学
化学
聚合物太阳能电池
冶金
生物
生态学
计算机科学
替代医学
病理
工程类
电信
医学
作者
Jingbi You,Lei Meng,Tze‐Bin Song,Tzung‐Fang Guo,Yang Yang,Wei‐Hsuan Chang,Ziruo Hong,Huajun Chen,Huanping Zhou,Qi Chen,Yongsheng Liu,Nicholas De Marco,Yang Yang
标识
DOI:10.1038/nnano.2015.230
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 NiO(x) 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/NiO(x)/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%.
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