化学
胺气处理
碘化物
甲脒
结晶
钙钛矿(结构)
X射线光电子能谱
薄膜
苯
化学工程
有机化学
无机化学
材料科学
纳米技术
工程类
作者
Blake P. Finkenauer,Yiyuan Zhang,Ke Ma,Jonathan W. Turnley,Jacob F. Schulz,Martin Gómez-Domínguez,Aidan H. Coffey,Dewei Sun,Jiaonan Sun,Rakesh Agrawal,Libai Huang,Letian Dou
标识
DOI:10.1021/acs.jpcc.2c06967
摘要
Controlling the crystallization of perovskites is imperative to reduce defect densities in perovskite thin films and extend device lifetimes. In this work, combinations of amine and chalcogenide ligands were introduced in the sequential deposition method to fabricate highly crystalline and orientated formamidinium lead iodide thin films with reduced defect densities and increased charge carrier lifetimes. The dual additives can tune the perovskite intermediate state and control the crystallization leading to devices with improved efficiencies and stabilities. While thiophenol failed to prevent the amine ligand from degrading the perovskite precursors, benzene selenol combinations with amine-ligands drastically changed the solution chemistry to increase the PbI<sub>2</sub> conversion to highly crystalline and orientated α-FAPbI<sub>3</sub> films with lower defect densities. X-ray photoelectron spectroscopy studies reveal benzene selenol evaporates from the thin film leaving behind a modified surface, which is associated with the amine additive. These results indicate the amine selection can be used to tune the surface properties. Lastly, we propose a highly tunable I<sub>2</sub> reduction strategy using chalcogenide chemistry to help enable the realization of perovskite solar cells with high performance and stability.
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