材料科学
钙钛矿(结构)
失真(音乐)
光电子学
工程物理
化学工程
放大器
CMOS芯片
工程类
作者
Wenya Zhao,Ruijing Fu,Jiayi Yang,Guanjun Xiao,Bo Zou
标识
DOI:10.1002/adom.202401732
摘要
Abstract Building an explicit structure‐property relationship for two‐dimensional (2D) hybrid perovskites is critical to guide the synthesis of highly luminescent materials. However, traditional studies are limited to the deviation of individual intra‐octahedron, which fails to well reflect collective lattice distortion. Here, a set of new structural distortion descriptors associated with inter‐octahedra is introduced for 2D perovskite (C 7 H 10 N) 2 PbBr 4, that is,(PMA) 2 PbBr 4 through pressure engineering. An experimental conclusion is reached that adjacent Pb displacement, as the inter‐octahedron distortion, is an effective parameter in determining the structural distortion and emission behavior of (PMA) 2 PbBr 4 under high pressure. Under high pressure, 2D perovskite (PMA) 2 PbBr 4 exhibits two emission behaviors, free excitons (FEs) emission and self‐trapped excitons (STEs) emission. Different types of four‐Pb‐shaped quadrilateral correspond to different emissions: square‐type (only FEs emission), parallelogram‐type (coexistence of FEs emission and STEs emission), kite‐type (only STEs emission). Moreover, an enhanced violet emission at ≈431 nm is achieved under a mild pressure of 1.0 GPa, which is a crucial light source of medical sterilization. The underlying structure‐property relationship is clarified fundamentally deepens the photophysical mechanism of (PMA) 2 PbBr 4 , thus facilitating the design of high‐efficiency perovskite luminophores.
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