Pseudo metallic (1T) molybdenum disulfide for efficient photo/electrocatalytic water splitting
2D-layered metallic molybdenum disulfide i.e. 1T MoS2 possess prominent electronic conductivity and abundant electrochemically active sites. However, tuning its metastable crystal structure for promoting catalytic performance is a big technical challenge. Here, we reveal the role of the intercalated...
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Veröffentlicht in: | Applied catalysis. B, Environmental Environmental, 2022-06, Vol.307, p.121156, Article 121156 |
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Sprache: | eng |
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Zusammenfassung: | 2D-layered metallic molybdenum disulfide i.e. 1T MoS2 possess prominent electronic conductivity and abundant electrochemically active sites. However, tuning its metastable crystal structure for promoting catalytic performance is a big technical challenge. Here, we reveal the role of the intercalated reducible -NH and -NH2 species as structural stabilizers in supporting the lamellar structure of 1T MoS2, and then propose a novel H2O2-cleaning strategy to reduce the amount of reducible -NH and -NH2 species for modulating the crystallinity and layer thickness of 1T MoS2 without degrading to 2H MoS2. The resultant pseudo-1T MoS2 exhibits larger specific surface area (up by 1.6 times) and higher electron mobility compared to original 1T MoS2, leading to excellent photo/electrocatalytic HER activity. Impressively, pseudo-1T MoS2 achieves high visible-light-driven photocatalytic HER rate of 235.0 mmol·h−1·g−1 in combination with CdS. This work offers an extendable crystal structural fine-tuning approach to promote the catalytic activity of metallic transition metal dichalcogenides.
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•A facile H2O2-cleaning strategy for preparing pseudo-1T MoS2 is proposed.•Pseudo-1T MoS2 evolved by partially removing -NH and -NH2 species in 1T MoS2.•Compared with 1T MoS2, pseudo-1T MoS2 has low crystallinity and less thickness.•Pseudo-1T MoS2 exhibits improved electrocatalytic HER activity in acidic medium.•Pseudo-1T MoS2/CdS shows outstanding visible-light photocatalytic HER activity. |
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ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2022.121156 |