Dong Jiansheng, Ouyang Gang
Key Laboratory of Low-Dimensional Quantum Structures and Quantum Control of Ministry of Education, Synergetic Innovation Center for Quantum Effects and Applications (SICQEA), Hunan Normal University, Changsha 410081, China.
ACS Omega. 2019 May 16;4(5):8641-8649. doi: 10.1021/acsomega.9b00507. eCollection 2019 May 31.
Layered two-dimensional transition-metal dichalcogenide (TMD) alloys with strong intralayer ionic-covalent bonds and weak interlayer van der Waals bonds have been extensively studied in recent years owing to their tunable electronic and optoelectronic properties. However, the relationship among atomic bond identities, band offset, and related semiconductor-to-metal transition in ternary alloys of TMDs with different thicknesses under hydrostatic pressure at the atomic level remains largely unexplored, despite the fact that it plays an important role in the functionality of TMD-based devices. In this work, we investigate the thickness-dependent band offset and semiconductor-to-metal transition in MoW S with different thicknesses under hydrostatic pressure based on the atomic-bond-relaxation correlation mechanism. It was found that the compression ratio in the out-of-plane direction is significantly higher than that of in-plane, and the band shift and semiconductor-to-metal transition are significantly modulated by the hydrostatic pressure, number of layers, and composition. The theoretical predictions are consistent with the experimental observations and calculations, suggesting that our approach can be suitable for other layered TMDs.
近年来,具有强层内离子共价键和弱层间范德华键的层状二维过渡金属二硫属化物(TMD)合金因其可调谐的电子和光电特性而受到广泛研究。然而,尽管原子键特性、带隙偏移以及相关的半导体到金属的转变在基于TMD的器件功能中起着重要作用,但在静水压力下不同厚度的TMD三元合金中,这些因素在原子水平上的关系在很大程度上仍未得到探索。在这项工作中,我们基于原子键弛豫相关机制,研究了静水压力下不同厚度的MoW S中与厚度相关的带隙偏移和半导体到金属的转变。结果发现,面外方向的压缩率明显高于面内方向,并且带移和半导体到金属的转变受到静水压力、层数和成分的显著调制。理论预测与实验观察和计算结果一致,表明我们的方法适用于其他层状TMD。