异质结
材料科学
化学气相沉积
成核
光电子学
纳米技术
光电探测器
化学
有机化学
作者
Wei Li,Qiuyin Qin,Xin Li,Ying Huangfu,Dingyi Shen,Jialing Liu,Jia Li,Bo Li,Ruixia Wu,Xidong Duan
标识
DOI:10.1002/adma.202408367
摘要
Abstract Two dimension (2D) transition metal dichalcogenides (TMD) heterostructures have opened unparalleled prospects for next‐generation electronic and optoelectronic applications due to their atomic‐scale thickness and distinct physical properties. The chemical vapor deposition (CVD) method is the most feasible approach to prepare 2D TMD heterostructures. However, the synthesis of 2D vertical heterostructures faces competition between in‐plane and out‐of‐plane growth, which makes it difficult to precisely control the growth of vertical heterostructures. Here, a universal and controllable strategy is reported to grow various 2D TMD vertical heterostructures through an ammonium‐assisted CVD process. The ammonium‐assisted strategy shows excellent controllability and operational simplicity to prevent interlayer diffusion/alloying and thermal decomposition of the existed TMD templates. Ab initio simulations demonstrate that the reaction between NH 4 Cl and MoS 2 leads to the formation of MoS 3 clusters, promoting the nucleation and growth of 2D MoS 2 on existed 2D WS 2 layer, thereby leading to the growth of vertical heterostructure. The resulting 2D WSe 2 /WS 2 vertical heterostructure photodetectors demonstrate an outstanding optoelectronic performance, which are comparable to the performances of photodetectors fabricated from mechanically exfoliated and stacked vertical heterostructures. The ammonium‐assisted strategy for robust growth of high‐quality vertical van der Waals heterostructures will facilitate fundamental physics investigations and device applications in electronics and optoelectronics.
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