Unconventional solution-phase epitaxial growth of organic-inorganic hybrid perovskite nanocrystals on metal sulfide nanosheets

材料科学 外延 异质结 覆盖层 纳米晶 纳米技术 成核 钙钛矿(结构) 化学工程 光电子学 物理化学 有机化学 工程类 化学 图层(电子)
作者
Zhipeng Zhang,Fangfang Sun,Zhaohua Zhu,Jie Dai,Kai Gao,Qi Wei,Xiaotong Shi,Qian Sun,Yan Yan,Hai Li,Hai‐Dong Yu,Guichuan Xing,Xiao Huang,Wei Huang
出处
期刊:Science China. Materials [Springer Science+Business Media]
卷期号:62 (1): 43-53 被引量:22
标识
DOI:10.1007/s40843-018-9274-y
摘要

Epitaxial heterostructures based on organic-inorganic hybrid perovskites and two-dimensional materials hold great promises in optoelectronics, but they have been prepared only via solid-state methods that restricted their practical applications. Herein, we report cubic-phased MAPbBr3 (MA=CH3NH3+) nanocrystals were epitaxially deposited on trigonal/hexagonal-phased MoS2 nanosheets in solution by facilely tuning the solvation conditions. In spite of the mismatched lattice symmetry between the square MAPbBr3 (001) overlayer and the hexagonal MoS2 (001) substrate, two different aligning directions with lattice mismatch of as small as 1% were observed based on the domainmatching epitaxy. This was realized most likely due to the flexible nature and absence of surface dangling bonds of MoS2 nanosheets. The formation of the epitaxial interface affords an effective energy transfer from MAPbBr3 to MoS2, and as a result, paper-based photodetectors facilely fabricated from these solution-dispersible heterostructures showed better performance compared to those based on MoS2 or MAPbBr3 alone. In addition to the improved energy transfer and light adsorption, the use of MoS2 nanosheets provided flexible and continuous substrates to connect the otherwise discrete MAPbBr3 nanocrystals and achieved the better film forming ability. Our work suggests that the scalable preparation of heterostructures based on organic-inorganic hybrid perovskites and 2D materials via solution-phase epitaxy may bring about more opportunities for expanding their optoelectronic applications.
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