钝化
钙钛矿(结构)
材料科学
甲脒
化学工程
可控性
薄膜
碘化物
曲面(拓扑)
纳米技术
无机化学
过程(计算)
溶剂
光电子学
载流子寿命
图层(电子)
能量转换效率
表面改性
表面状态
溶解过程
作者
Mengjun Liu,Shenghan Hu,Xinyu Deng,Changyu Duan,Yichen Dou,Tiancan Zhang,Meichen Liu,Yuanbo Song,Ya Chen,Xuyang Chen,Jinyi Lian,Zhiliang Ku
标识
DOI:10.1021/acsami.6c00384
摘要
Perovskite films grown by a vapor–solid reaction are highly attractive due to their exceptional process controllability and industrial potential. A key feature of the vapor–solid approach is that the reaction initiates at the surface and progressively penetrates the film, often yielding an excess of surface formamidinium cations (FA + ) and disrupting the stoichiometry. This imbalance hinders subsequent surface passivation and ultimately constrains device performance. Here, we introduce a solvent-cleaning–assisted vapor-phase passivation strategy with synergistic surface engineering. First, isopropanol washing selectively removes excess surface FA + to tailor the surface chemistry, followed by vapor-phase passivation using phenethylammonium iodide (PEAI). This coordinated process promotes the reconstruction of the perovskite surface and effectively passivates surface defects, producing high-quality films. Working with these films, inverted-structure perovskite solar cells show a notable efficiency boost from 18.17% to 20.70% (0.148 cm 2 ), with larger-area devices (1 × 1 cm 2 ) achieving 18.42%. Additionally, unencapsulated devices retain over 90% of their initial efficiency after 1500 h, indicating strong interfacial stability. This study demonstrates a practical route to actively regulate the surface chemical environment of vapor–solid-grown perovskite films and offers a reference point for the future development of vapor-phase passivation strategies in perovskite technology.
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