二硫化钼
单层
材料科学
X射线光电子能谱
兴奋剂
基质(水族馆)
石墨烯
光致发光
锰
化学气相沉积
钼
过渡金属
惰性
纳米技术
化学工程
光电子学
化学
冶金
催化作用
工程类
有机化学
生物化学
地质学
海洋学
作者
Kehao Zhang,Simin Feng,Junjie Wang,Angelica Azcatl,Ning Lü,Rafik Addou,Nan Wang,Chanjing Zhou,Jordan O. Lerach,Vincent Bojan,Moon J. Kim,Long‐Qing Chen,Robert M. Wallace,Mauricio Terrones,Jun Zhu,Joshua A. Robinson
出处
期刊:Nano Letters
[American Chemical Society]
日期:2015-09-09
卷期号:15 (10): 6586-6591
被引量:377
标识
DOI:10.1021/acs.nanolett.5b02315
摘要
Substitutional doping of transition metal dichalcogenides (TMDs) may provide routes to achieving tunable p-n junctions, bandgaps, chemical sensitivity, and magnetism in these materials. In this study, we demonstrate in situ doping of monolayer molybdenum disulfide (MoS2) with manganese (Mn) via vapor phase deposition techniques. Successful incorporation of Mn in MoS2 leads to modifications of the band structure as evidenced by photoluminescence and X-ray photoelectron spectroscopy, but this is heavily dependent on the choice of substrate. We show that inert substrates (i.e., graphene) permit the incorporation of several percent Mn in MoS2, while substrates with reactive surface terminations (i.e., SiO2 and sapphire) preclude Mn incorporation and merely lead to defective MoS2. The results presented here demonstrate that tailoring the substrate surface could be the most significant factor in substitutional doping of TMDs with non-TMD elements.
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