钙钛矿(结构)
材料科学
光电子学
纳米技术
过程(计算)
化学工程
计算机科学
工程类
操作系统
作者
Matthew R. Leyden,Viktor Škorjanc,Aleksandra Miaskiewicz,Stefanie Severin,Suresh Maniyarasu,Thomas W. Gries,Johannes M. Beckedahl,Florian Scheler,Maxim Simmonds,Philippe Holzhey,Jona Kurpiers,Lars Korte,Marcel Roß,Steve Albrecht
标识
DOI:10.1002/solr.202400575
摘要
Organo‐lead‐halide perovskites are promising materials for solar cell applications with efficiencies now exceeding 26% for single junction, and over 33% for silicon tandem devices. Evaporation has proven viable for industrial scale‐up but presents challenges for perovskite materials. Perovskite precursor is introduced into self‐assembling MeO‐2PACz hole transport layers for application to 4 source perovskite coevaporation. This allows precursors that can be difficult to add via evaporation, like methylammonium chloride. These precursor molecules influence growth during evaporation, film behavior during annealing as measured by photoluminescence, and aid the conversion to perovskite as shown by X‐Ray diffraction. Devices have improved power conversion efficiency and stability compared to a control sample within the same evaporation. The best cells reach ≈21% efficiency and comparable performing ≈20% cells maintain their original efficiency after 1000 h of maximum power tracking at 25 °C. This process provides significant process flexibility for perovskite evaporation and requires no additional steps.
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