材料科学
格子(音乐)
卤化物
电致伸缩
激发
半导体
凝聚态物理
晶体结构
单晶
光子学
光学
光电子学
级联
光子晶体
谐振器
结构稳定性
同种类的
结晶学
单晶硅
化学物理
分子物理学
作者
Mansha Dubey,Bekir Türedi,Andrii Kanak,Maksym V Kovalenko,Marina S. Leite
标识
DOI:10.1002/adma.202521800
摘要
The unique characteristics of soft-lattice halide perovskites (HPs) have motivated extensive research into their application in semiconductor devices. Mechanically and chemically modulated strain in monocrystalline HPs improves stability and phase purity. However, a comprehensive understanding of the photoexcitation-driven lattice distortions arising from the strong electron-phonon coupling paired with the dynamics of the A-site cation remains underdeveloped. Here, we present the transient lattice distortions occurring in single crystal MAPbBr3, FAPbBr3, and CsPbBr3 in response to above-bandgap light excitation. Using an X-ray probe, we uncover reversible and hysteresis-free photoinduced lattice distortion. We find that the photoinduced distortion in the HPs is a function of the pump power, with CsPbBr3 showing the highest resilience against lattice deformation with a 0.062% change in its out-of-plane lattice parameter. Conversely, the organic HPs unveil a stronger interaction with photocarriers resulting in more significant yet elastic distortion, with MAPbBr3 exhibiting up to 0.3% change. We demonstrate the modality of this distortion by varying the excitation power over 20 distinct states and cycles, highlighting the suitability of HPs as building blocks for electrostriction devices. Our findings represent a key step toward establishing HPs as ideal platforms for optical and strain-driven switchable photonic devices.
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