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Tunable inverted gap in monolayer quasi-metallic MoS(2) induced by strong charge-lattice coupling
Polymorphism of two-dimensional transition metal dichalcogenides such as molybdenum disulfide (MoS(2)) exhibit fascinating optical and transport properties. Here, we observe a tunable inverted gap (~0.50 eV) and a fundamental gap (~0.10 eV) in quasimetallic monolayer MoS(2). Using spectral-weight tr...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589873/ https://www.ncbi.nlm.nih.gov/pubmed/28883392 http://dx.doi.org/10.1038/s41467-017-00640-2 |
Sumario: | Polymorphism of two-dimensional transition metal dichalcogenides such as molybdenum disulfide (MoS(2)) exhibit fascinating optical and transport properties. Here, we observe a tunable inverted gap (~0.50 eV) and a fundamental gap (~0.10 eV) in quasimetallic monolayer MoS(2). Using spectral-weight transfer analysis, we find that the inverted gap is attributed to the strong charge–lattice coupling in two-dimensional transition metal dichalcogenides (2D-TMDs). A comprehensive experimental study, supported by theoretical calculations, is conducted to understand the transition of monolayer MoS(2) on gold film from trigonal semiconducting 1H phase to the distorted octahedral quasimetallic 1T’ phase. We clarify that electron doping from gold, facilitated by interfacial tensile strain, is the key mechanism leading to its 1H–1T’ phase transition, thus resulting in the formation of the inverted gap. Our result shows the importance of charge–lattice coupling to the intrinsic properties of the inverted gap and polymorphism of MoS(2), thereby unlocking new possibilities for 2D-TMD-based device fabrication. |
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