材料科学
钙钛矿(结构)
碘化物
光伏
化学工程
相变
溶解过程
真空蒸发
退火(玻璃)
蒸发
光伏系统
纳米技术
薄膜
无机化学
光电子学
化学
复合材料
热力学
物理
工程类
生物
量子力学
生态学
作者
Jiahao Wang,Yuan Zhou,Wei Ai,Dexin Pu,Hongyi Fang,Shiqiang Fu,Hongling Guan,Wenlong Shao,Guoyi Chen,Weiwei Meng,Guojia Fang,Weijun Ke
标识
DOI:10.1002/aenm.202404954
摘要
Abstract Perovskite solar cells (PSCs) represent a promising technology for next‐generation photovoltaics, yet scaling up from laboratory to industrial production via the solution spin‐coating method encounters significant challenges. Vacuum deposition offers a potential alternative but struggles with controlling perovskite phases and ensuring sufficient precursor reactions. Here, the study presents a hybrid evaporation‐solution approach using a large cation‐based pseudo‐halogen anion salt (guanidine thiocyanate) and a compensating cation salt (methylammonium iodide) as co‐additives to finely modulate the phase transition process. This approach eliminates the need for intermediate‐phase transitions, promotes sufficient precursor reactions, and facilitates the formation of highly oriented α‐phase perovskites prior to annealing. Consequently, it prevents detrimental δ‐phase formation, yielding enlarged, homogeneous perovskite grains with significantly reduced defects. The resulting p‐i‐n‐structured PSCs achieve a maximum efficiency of 24.72% and a low open‐circuit voltage loss of 0.377 V, coupled with significantly improved stability. The work integrates the advantages of vacuum deposition and solution processing, providing new insights into perovskite phase transitions and paving the way for the efficient, scalable production of high‐performance PSCs.
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