钝化
光电流
材料科学
薄膜
钙钛矿(结构)
化学工程
碘化物
降级(电信)
微晶
相(物质)
成核
无机化学
纳米技术
化学
图层(电子)
光电子学
冶金
电子工程
有机化学
工程类
作者
Sumin Han,Seok‐Ki Hyeong,Seoung‐Ki Lee,Naechul Shin
标识
DOI:10.1016/j.cej.2022.135715
摘要
Understanding the correlation between surface passivation and degradation kinetics in vapor-deposited organic–inorganic hybrid perovskite thin films is crucial for developing strategies to enhance their structural integrity for long-term operational stability. Here, we demonstrate that the sequential introduction of vapor-phase phenethylammonium iodide (PEAI) and methylammonium (MAI) into methylammonium lead iodide (MAPbI3) thin films, which is obtained from PbI2, suppresses their degradation and enhances the ambient stability. Compared with the simultaneous PEAI introduction during the conversion of PbI2 to MAPbI3, the MAPbI3 films with sequential treatment exhibited higher PEAI surface coverage, which imparts superior resistance to degradation. Combined analyses of the exposure-time-dependent crystal structure evolution, photoemission profiles, and photocurrent generation characteristics of the films reveal that conformal PEAI passivation suppresses the volatile release of methylammonium (MA) species and the inclusion of O2/H2O molecules. This study highlights the importance of developing a vapor-phase passivation strategy for innate polycrystalline perovskite thin films and their optoelectronic applications with long-term stability.
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