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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...

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Detalles Bibliográficos
Autores principales: Qi, Yu, Zhang, Jiangwei, Kong, Yuan, Zhao, Yue, Chen, Shanshan, Li, Deng, Liu, Wei, Chen, Yifan, Xie, Tengfeng, Cui, Junyan, Li, Can, Domen, Kazunari, Zhang, Fuxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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
Descripción
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.