光电探测器
激子
材料科学
钙钛矿(结构)
光电子学
紫外线
载流子
三元运算
Crystal(编程语言)
紫外线
化学
结晶学
凝聚态物理
物理
计算机科学
程序设计语言
作者
Mingda Li,Chensi Cao,Wenbo Liu,Nana Wang,Chang Yi,Renzhi Li,Jianpu Wang
标识
DOI:10.1021/acs.jpclett.2c01715
摘要
Ternary copper halides with a formula of CsCu2X3 (X = Cl, Br, I) have been considered as prospective materials for ultraviolet (UV) photodetectors, due to their suitable band gaps, environmental stability, eco-friendliness, and low cost. However, the crystal orientation of one-dimensional (1D) CsCu2X3 perovskites significantly affects the exciton/carrier transport in the films and thus the photodetector performance. Here, we tune the crystal orientation and exciton/charge transport of 1D CsCu2I3 perovskite films by using antisolvents during the film formation process. Compared to the randomly oriented film treated by ethyl acetate, the CsCu2I3 film using toluene as antisolvent exhibits preferential (221)-oriented growth, which induces enhanced vertical exciton diffusion/charge transport and suppressed nonradiative recombination. On the basis of this strategy, we demonstrate a self-powered, stable, and visible-blind UV photodetector with significantly enhanced response speed and detectivity. Our work clarifies that tuning the crystal orientation of 1D CsCu2X3 perovskites is the key to achieve efficient exciton diffusion/charge transport and thus high-performance lead-free perovskite optoelectronic devices.
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