杰纳斯
硫族元素
拉曼光谱
材料科学
密度泛函理论
替代(逻辑)
化学物理
过渡金属
兴奋剂
结晶学
电子
偶极子
化学
工作(物理)
纳米技术
电子结构
金属
半导体
光化学
光电子学
超晶格
电子传输链
堆积
原子电子跃迁
紫外线
晶体管
石墨烯
作者
Dingkun Bi,Tianyishan Sun,Weizi Lu,Hiroto Ogura,Yanlin Gao,Mina Maruyama,Susumu Okada,Toshiaki Kato
标识
DOI:10.1021/acsmaterialslett.6c00018
摘要
High Resolution Image Download MS PowerPoint Slide Understanding atomic substitution in Janus transition metal dichalcogenides (TMDs) is crucial for controlling intrinsic out-of-plane dipoles and electronic asymmetry. Although room-temperature Janus conversion has been reported, the microscopic origin of selective chalcogen replacement remains unclear. Here, we develop an in situ optical–electrical platform enabling correlated Raman and field-effect transistor measurements during plasma-assisted atomic-layer substitution under vacuum. We identify a plasma-electron-assisted room-temperature topotactic reaction, in which electrons accumulate near the TMD surface and at the MoSe 2 /SiO 2 interface, weaken metal–chalcogen bonds, and facilitate hydrogen-assisted substitution. Density functional theory calculations show that excess electron doping lowers bond formation energies. Ultraviolet illumination further enhances electron accumulation and accelerates substitution kinetics. This work experimentally verifies a charge-mediated topotactic substitution mechanism and establishes plasma-electron-assisted synthesis as a route for room-temperature Janus TMD formation.
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