材料科学
升华(心理学)
钙钛矿(结构)
光伏系统
太阳能电池
能量转换效率
聚结(物理)
纳米技术
化学工程
光电子学
电气工程
心理学
天体生物学
物理
工程类
心理治疗师
作者
Ahmed Ali Said,Erkan Aydın,Esma Ugur,Zhaojian Xu,Caner Değer,Badri Vishal,Aleš Vlk,Pia Dally,Bumın K. Yildırım,Randi Azmi,Jiang Liu,Edward A. Jackson,H. M. Johnson,Manting Gui,Henning Richter,Anil Reddy Pininti,Helen Bristow,Maxime Babics,Arsalan Razzaq,Thomas G. Allen
标识
DOI:10.1038/s41467-024-44974-0
摘要
Abstract Thermally evaporated C 60 is a near-ubiquitous electron transport layer in state-of-the-art p–i–n perovskite-based solar cells. As perovskite photovoltaic technologies are moving toward industrialization, batch-to-batch reproducibility of device performances becomes crucial. Here, we show that commercial as-received (99.75% pure) C 60 source materials may coalesce during repeated thermal evaporation processes, jeopardizing such reproducibility. We find that the coalescence is due to oxygen present in the initial source powder and leads to the formation of deep states within the perovskite bandgap, resulting in a systematic decrease in solar cell performance. However, further purification (through sublimation) of the C 60 to 99.95% before evaporation is found to hinder coalescence, with the associated solar cell performances being fully reproducible after repeated processing. We verify the universality of this behavior on perovskite/silicon tandem solar cells by demonstrating their open-circuit voltages and fill factors to remain at 1950 mV and 81% respectively, over eight repeated processes using the same sublimed C 60 source material. Notably, one of these cells achieved a certified power conversion efficiency of 30.9%. These findings provide insights crucial for the advancement of perovskite photovoltaic technologies towards scaled production with high process yield.
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