光电探测器
钙钛矿(结构)
响应度
材料科学
光电子学
单晶
正交晶系
带隙
卤化物
Crystal(编程语言)
成核
异质结
半导体
结晶学
晶体结构
化学
无机化学
有机化学
程序设计语言
计算机科学
作者
Jianxu Ding,Songjie Du,Zhiyuan Zuo,Ying Zhao,Hongzhi Cui,Xiaoyuan Zhan
标识
DOI:10.1021/acs.jpcc.7b01171
摘要
Band gap tunable hybrid organic–inorganic lead halide perovskites (APbX3, A = CH3NH3+ and NH2CH═NH2+, and X = Cl, Br, or I) have attracted significant attention in optoelectronic- and photovoltaic-related fields on account of their outstanding optoelectronic properties. Single crystals of hybrid perovskites, such as CH3NH3PbI3 and CH3NH3PbBr3, were certified to be advantageous over thin films as photodetectors. However, their resistance toward heat and moisture hinders their future development. Fully inorganic perovskite CsPbBr3 stands a chance to fill the gap as a novel photodetector with perovskite structure. We revealed the growth of CsPbBr3 single crystal was of a 2D nucleation mechanism. Similarities of d values and octahedra arrangements along [101] and [020] orientations restricted single-crystal growth. Under optimized conditions, orthorhombic CsPbBr3 single crystals with (101) crystallographic facets were grown by using methyl alcohol as antisolvent from saturated DMSO solution. The optoelectronic properties of the single crystal were explored through a metal–semiconductor–metal photodetector device. Meanwhile, their steady and transient performances were also investigated. A highest responsivity of 0.028 A/W and a response time of <100 ms were achieved.
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