异质结
材料科学
硫系化合物
堆积
成核
化学气相沉积
光电子学
纳米电子学
纳米技术
凝聚态物理
化学
物理
有机化学
作者
Yecheng Cheng,Pengtao Tang,Pei Liang,Xueyin Liu,Dan Cao,Xiaoshuang Chen,Haibo Shu
标识
DOI:10.1021/acs.jpcc.0c09101
摘要
The rational control of the nucleation and growth kinetics to enable the high-quality growth of two-dimensional (2D) semiconducting metal chalcogenide heterostructures is a key step for the realization of their applications in nanoelectronics and optoelectronics. Here, we report a facile one-step chemical vapor deposition synthesis of 2D SnS–SnS 2 heterostructures with controlled interfacial structures and stacking configurations via tuning S-precursor concentration during the growth. We demonstrate that the change of S-precursor concentration can drive growth transition from vertically stacking SnS 2 /SnS van der Waals heterostructures to SnS/SnS 2 core–shell structures with both the lateral and vertical interfaces. Such a transition originates from a delicate competition between the nucleation of SnS and SnS 2 . High-resolution spectroscopy measurements and density functional theory (DFT) calculations reveal these SnS–SnS 2 heterostructures with the type-II band alignment, and the measured valence and conduction band offsets are 1.33 and 0.34 eV for vertical SnS 2 /SnS heterostructures and 1.43 and 0.54 eV for SnS/SnS 2 core–shell ones, respectively. This work provides an efficient strategy to control the growth of 2D SnS–SnS 2 heterostructures for optoelectronic applications, such as photodetectors and solar cells.
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