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Constructing Co(3)O(4)/g-C(3)N(4) Ultra-Thin Nanosheets with Z-Scheme Charge Transfer Pathway for Efficient Photocatalytic Water Splitting
Photocatalytic water splitting for hydrogen generation is a significant pathway for sustainable energy conversion and production. The photocatalysts with a Z-scheme water splitting charge transfer pathway is superior due to the good separation and migration ability of photoexcited charge carriers. H...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8706009/ https://www.ncbi.nlm.nih.gov/pubmed/34947689 http://dx.doi.org/10.3390/nano11123341 |
Sumario: | Photocatalytic water splitting for hydrogen generation is a significant pathway for sustainable energy conversion and production. The photocatalysts with a Z-scheme water splitting charge transfer pathway is superior due to the good separation and migration ability of photoexcited charge carriers. Herein, Co(3)O(4)/g-C(3)N(4) photocatalysts with Z-scheme charge transfer pathway were successfully constructed by an electrostatic interaction-annealing method. The as-prepared Co(3)O(4)/g-C(3)N(4) ultra-thin nanosheets were tested and analyzed by XRD, EA, ICP, SEM, TEM, AFM, XPS, UV-Vis DRS, PL and photoelectrochemical measurements. Moreover, the influences of fabrication parameters on performance of Co(3)O(4)/g-C(3)N(4) catalysts were investigated, and 0.5% Co(3)O(4)/g-C(3)N(4) exhibited the optimal activity. Based on the characterization and catalytic performance, the Z-scheme charge transfer pathway of Co(3)O(4)/g-C(3)N(4) was established and put forward. To further improve the catalytic performance of Co(3)O(4)/g-C(3)N(4), 0.5% Pt was added as a co-catalyst. The obtained Pt/0.5% Co(3)O(4)/g-C(3)N(4) was recyclable and remained the original catalytic water splitting performance within 20 h. The modification of Co(3)O(4) and Pt improved the separation and migration of e(−) and h(+), and induced the increased hydrogen evolution rate of g-C(3)N(4). |
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