卤化物
异质结
材料科学
亚稳态
钙钛矿(结构)
相(物质)
八面体
化学物理
化学工程
结晶学
光电子学
无机化学
晶体结构
化学
有机化学
工程类
作者
Min Xiong,Wenjun Zou,Ke Fan,Chaochao Qin,Sibo Li,Linfeng Fei,Jizhong Jiang,Haitao Huang,Liang Shen,Feng Gao,Alex K.‐Y. Jen,Kai Yao
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2022-01-04
卷期号:7 (1): 550-559
被引量:33
标识
DOI:10.1021/acsenergylett.1c02580
摘要
Although the fabrication of two-dimensional (2D)/three-dimensional (3D) halide perovskite heterostructures has been employed to balance the long-term stability and high efficiency of perovskite solar cells, the formation of metastable quasi-2D perovskites remains the most serious challenge. Here, we demonstrate that large lattice mismatch derived from halide and cation differences between 2D and 3D perovskites are key to avoiding the formation of unintended 2D phases in the preparation of 2D/3D bulk heterostructure because the phase transformation becomes less thermodynamically favorable. Specifically, by employing chloride 2D perovskite (PYA)2PbCl4 (PYA = propargylammonium) crystals into a 3D precursor solution, we achieve a phase-pure 2D/3D heterojunction with clean type-I band alignment, which exhibits greatly reduced charge recombination. Furthermore, the incorporation of alkyne perovskites is also shown to suppress iodine diffusion and formation due to their exceptional iodine capture capacity. The resultant 2D/3D heterostructured devices exhibited enhanced efficiencies and stabilities compared with their 3D counterparts.
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