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Heterolayered 2D nanohybrids of uniformly stacked transition metal dichalcogenide–transition metal oxide monolayers with improved energy-related functionalities
Heterolayered 2D nanohybrids of uniformly stacked transition metal dichalcogenide (TMD)–transition metal oxide (TMO) monolayers are synthesized by a self-assembly of exfoliated nanosheets (NSs) with charge-balancing cations. This is the first example of a layer-by-layer-ordered 2D nanohybrid of exfo...
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Published in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2018, Vol.6 (31), p.15237-15244 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Heterolayered 2D nanohybrids of uniformly stacked transition metal dichalcogenide (TMD)–transition metal oxide (TMO) monolayers are synthesized by a self-assembly of exfoliated nanosheets (NSs) with charge-balancing cations. This is the first example of a layer-by-layer-ordered 2D nanohybrid of exfoliated TMD and TMO nanosheets. The homogeneous incorporation of MnO
2
NSs into restacked MoS
2
NSs is quite effective in improving the multifunctionality of MoS
2
as an electrocatalyst for the hydrogen evolution reaction (HER) and electrode for Li-ion batteries, underscoring the universal merit of layer-by-layer ordering of TMD and TMO NSs.
In situ
spectroscopic analysis of the present TMD–TMO nanohybrid during the electrocatalytic reaction highlights the efficient interfacial charge transfer of the restacked nanosheets with enhanced porosity. The beneficial effect of incorporated TMO NSs on the performance of TMD NSs is attributable to an efficient interfacial charge transfer and increased porosity with depressed self-stacking of NSs and the stabilization of the metallic 1T TMD phase, resulting in the improvement of charge transfer kinetics, the enhancement of reactivity, and the provision of many reaction sites upon hybridization. Density functional theory (DFT) calculations further support the stabilization of the 1T TMD structure over the 2H TMD one
via
the interaction with neighboring TMO NSs. The present study clearly demonstrates that the restacking of the colloidal mixtures of TMO and TMD NSs can provide an effective way to explore novel multifunctional heterostructures. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/C8TA04167A |