甲胺
成核
材料科学
钙钛矿(结构)
结晶度
结晶
粒度
化学工程
气相
相(物质)
薄膜
化学物理
纳米技术
复合材料
化学
物理化学
有机化学
工程类
作者
Jifei Wang,Shiqiang Luo,Xianglan Tang,Si Xiao,Zhihui Chen,Shuping Pang,Zhang Lin,Yun Lin,Jun He,Yongbo Yuan
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2021-09-21
卷期号:6 (10): 3634-3642
被引量:24
标识
DOI:10.1021/acsenergylett.1c01771
摘要
Perovskites with grain size comparable to film thickness are intensively pursued for high-efficiency solar cells. Geometrically, large grains with high crystallinity tend to form polyhedral shapes that have difficulty forming compact and smooth films. When quasi-two-dimensional RP perovskite films adopt a downward growth mode, defective contacts tend to form at their bottom interfaces with many nanocavities. This is attributed to the angular growing fronts of RP perovskite grains adopting [111] (or/and [101]) growth directions. Self-generated methylamine gas, by a replacement reaction in solution, is introduced to in situ heal these irregular nanocavities that are deeply buried in perovskite films during crystallization processes. The amount of self-generated methylamine gas should be adequately controlled to avoid the homogeneous nucleation of perovskites from a liquid perovskite-amine intermediate phase, which is a key to avoid ruining the grain size and film composition. This in situ healing strategy offers significantly enhanced charge collection efficiency and device working stability.
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