钙钛矿(结构)
锡
材料科学
卤化物
太阳能电池
能量转换效率
氧化铟锡
带隙
串联
铟
氧化锡
光电子学
异质结
化学工程
纳米技术
图层(电子)
无机化学
兴奋剂
化学
复合材料
冶金
工程类
作者
Rohit Prasanna,Tomas Leijtens,Sean P. Dunfield,James A. Raiford,Eli J. Wolf,Simon A. Swifter,Jérémie Werner,Giles E. Eperon,Camila de Paula,Axel F. Palmstrom,Caleb C. Boyd,Maikel F. A. M. van Hest,Stacey F. Bent,Glenn Teeter,Joseph J. Berry,Michael D. McGehee
出处
期刊:Nature Energy
[Nature Portfolio]
日期:2019-10-07
卷期号:4 (11): 939-947
被引量:319
标识
DOI:10.1038/s41560-019-0471-6
摘要
Low bandgap tin–lead iodide perovskites are key components of all-perovskite tandem solar cells, but can be unstable because tin is prone to oxidation. Here, to avoid a reaction with the most popular hole contact, we eliminated polyethylenedioxythiophene:polystyrenesulfonate as a hole transport layer and instead used an upward band offset at an indium tin oxide–perovskite heterojunction to extract holes. To suppress oxidative degradation, we improved the morphology to create a compact and large-grained film. The tin content was kept at or below 50% and the device capped with a sputtered indium zinc oxide electrode. These advances resulted in a substantially improved thermal and environmental stability in a low bandgap perovskite solar cell without compromising the efficiency. The solar cells retained 95% of their initial efficiency after 1,000 h at 85 °C in air in the dark with no encapsulation and in a damp heat test (85 °C with 85% relative humidity) with encapsulation. The full initial efficiency was maintained under operation near the maximum power point and near 1 sun illumination for over 1,000 h. Low bandgap tin–lead perovskites are crucial to making efficient all-perovskite tandem solar cells but have so far shown poor stability. By removing the hole transport layer and improving film morphology, Prasanna et al. demonstrate a low-gap perovskite solar cell that is stable for 1,000 h under heat, light and atmospheric conditions.
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