High intrinsic phase stability of ultrathin 2M WS2
Metallic 2M or 1T′-phase transition metal dichalcogenides (TMDs) attract increasing interests owing to their fascinating physicochemical properties, such as superconductivity, optical nonlinearity, and enhanced electrochemical activity. However, these TMDs are metastable and tend to transform to the...
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Veröffentlicht in: | Nature communications 2024-02, Vol.15 (1), p.1263-1263, Article 1263 |
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Sprache: | eng |
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Zusammenfassung: | Metallic 2M or 1T′-phase transition metal dichalcogenides (TMDs) attract increasing interests owing to their fascinating physicochemical properties, such as superconductivity, optical nonlinearity, and enhanced electrochemical activity. However, these TMDs are metastable and tend to transform to the thermodynamically stable 2H phase. In this study, through systematic investigation and theoretical simulation of phase change of 2M WS
2
, we demonstrate that ultrathin 2M WS
2
has significantly higher intrinsic thermal stabilities than the bulk counterparts. The 2M-to-2H phase transition temperature increases from 120 °C to 210 °C in the air as thickness of WS
2
is reduced from bulk to bilayer. Monolayered 1T′ WS
2
can withstand temperatures up to 350 °C in the air before being oxidized, and up to 450 °C in argon atmosphere before transforming to 1H phase. The higher stability of thinner 2M WS
2
is attributed to stiffened intralayer bonds, enhanced thermal conductivity and higher average barrier per layer during the layer(s)-by-layer(s) phase transition process. The observed high intrinsic phase stability can expand the practical applications of ultrathin 2M TMDs.
Metallic 2M or 1T′-phase transition metal dichalcogenides (TMDs) are characterized by interesting properties, but they are metastable. Here, the authors demonstrate that the thermal and oxidation stability of 2M WS
2
significantly increases as the thickness is reduced down to monolayer, expanding the potential applications of 2M TMDs. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-024-45676-3 |