异质结
激子
钙钛矿(结构)
光致发光
皮秒
超快激光光谱学
超短脉冲
材料科学
扩散
化学物理
光电子学
载流子
相(物质)
电荷(物理)
吸收(声学)
凝聚态物理
化学
光学
物理
结晶学
热力学
量子力学
复合材料
有机化学
激光器
作者
Fabiola Faini,Yaiza Asensio,Federico Visentin,Lucía Olano‐Vegas,Martin Hörmann,Luis E. Hueso,Giulio Cerullo,Franco V. A. Camargo,Beatriz Martín‐García,Giulia Grancini
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-12-13
卷期号:10 (1): 120-127
被引量:12
标识
DOI:10.1021/acsenergylett.4c02786
摘要
Addressing interface physics and related photoinduced dynamics is crucial to understand charge carrier paths and losses and ultimately design efficient optoelectronic devices. However, such dynamics are often masked when bulky systems are investigated. In this work, we combine photoluminescence with ultrafast transient absorption microscopy to map charge transfer processes in few-layers-thick heterostructures made of low-dimensional (C 6 H 5 CH 2 CH 2 NH 3 ) 2 (CH 3 NH 3 ) n-1 Pb n I 3n+1 perovskite flakes of different dimensionalities ( n = 3) and ( n = 1). We observe that the hole transfer process from the ( n = 3) to the ( n = 1) phase happens after exciton diffusion on a time scale of tens of picoseconds, whereas electron transfer is hindered by the high exciton binding energy and low diffusion coefficient within the ( n = 1) phase. This study sets the stage for a deeper understanding needed for the smart development of new heterostructure combinations with different dimensionalities and band alignments.
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