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Unraveling of cocatalysts photodeposited selectively on facets of BiVO(4) to boost solar water splitting
Bismuth vanadate (BiVO(4)) has been widely investigated as a photocatalyst or photoanode for solar water splitting, but its activity is hindered by inefficient cocatalysts and limited understanding of the underlying mechanism. Here we demonstrate significantly enhanced water oxidation on the particu...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789891/ https://www.ncbi.nlm.nih.gov/pubmed/35079003 http://dx.doi.org/10.1038/s41467-022-28146-6 |
Sumario: | Bismuth vanadate (BiVO(4)) has been widely investigated as a photocatalyst or photoanode for solar water splitting, but its activity is hindered by inefficient cocatalysts and limited understanding of the underlying mechanism. Here we demonstrate significantly enhanced water oxidation on the particulate BiVO(4) photocatalyst via in situ facet-selective photodeposition of dual-cocatalysts that exist separately as metallic Ir nanoparticles and nanocomposite of FeOOH and CoOOH (denoted as FeCoO(x)), as revealed by advanced techniques. The mechanism of water oxidation promoted by the dual-cocatalysts is experimentally and theoretically unraveled, and mainly ascribed to the synergistic effect of the spatially separated dual-cocatalysts (Ir, FeCoO(x)) on both interface charge separation and surface catalysis. Combined with the H(2)-evolving photocatalysts, we finally construct a Z-scheme overall water splitting system using [Fe(CN)(6)](3−/4−) as the redox mediator, whose apparent quantum efficiency at 420 nm and solar-to-hydrogen conversion efficiency are optimized to be 12.3% and 0.6%, respectively. |
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