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0D/2D heterojunction photocatalysts for improved full-spectrum-light-driven hydrogen evolution
Enhancing the full-spectrum light-driven hydrogen evolution of water splitting continues to be a pivotal challenge in the pursuit of advanced photocatalysts. In this study, the instability of MXene under light illumination has been effectively countered by affixing ultra-minor nanoparticles ZnO quan...
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Published in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2024-10, Vol.12 (42), p.29278-29287 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Enhancing the full-spectrum light-driven hydrogen evolution of water splitting continues to be a pivotal challenge in the pursuit of advanced photocatalysts. In this study, the instability of MXene under light illumination has been effectively countered by affixing ultra-minor nanoparticles ZnO quantum dots (QDs) onto the surface of the two-dimensional (2D) MXene substrate. This process ensures the high electronic conductivity of MXene, thereby enhancing its photocatalytic stability and maintaining hydrogen production efficiency. The loading of a small amount of ZnO QDs enables MXene to realize a 10-fold improvement under full-spectrum excitation. Combined with density functional theory (DFT) calculations, the results confirm that such excellent photocatalytic performance is mainly attributed to the increase of reactive active sites for hydrogen-extraction reaction (HER) on the surface of MXene, the fast carrier migration at the interface of heterostructure, and the improvement of the electron-hole pairs separation, thus resulting in the efficient full-spectrum solar catalytic activity and kinetic processes.
Enhancing the full-spectrum light-driven hydrogen evolution of water splitting continues to be a pivotal challenge in the pursuit of advanced photocatalysts. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d4ta06179a |