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Ultra-small Rh nanoparticles supported on WO(3−x) nanowires as efficient catalysts for visible-light-enhanced hydrogen evolution from ammonia borane

Hydrolysis of ammonia borane (AB) is a safe and convenient means of H(2) production when efficient catalysts are used. Here we report a facile one-pot solvothermal method to synthesize Rh/WO(3−x) hybrid nanowires. Ultra-small Rh nanoparticles with an average size of ∼1.7 nm were tightly anchored on...

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Detalles Bibliográficos
Autores principales: Li, Xiao, Yan, Yucong, Jiang, Yi, Wu, Xingqiao, Li, Shi, Huang, Jingbo, Li, Junjie, Lin, Yangfan, Yang, Deren, Zhang, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9416929/
https://www.ncbi.nlm.nih.gov/pubmed/36132115
http://dx.doi.org/10.1039/c9na00424f
Descripción
Sumario:Hydrolysis of ammonia borane (AB) is a safe and convenient means of H(2) production when efficient catalysts are used. Here we report a facile one-pot solvothermal method to synthesize Rh/WO(3−x) hybrid nanowires. Ultra-small Rh nanoparticles with an average size of ∼1.7 nm were tightly anchored on WO(3−x) nanowires. Rh/WO(3−x) catalysts exhibited substantially enhanced activity for hydrolytic dehydrogenation of AB under both dark and visible light irradiation conditions relative to mixed Rh nanoparticles and WO(3−x) nanowires (Rh + WO(3−x)), and Rh/C and WO(3−x) nanowires. X-ray photoelectron spectroscopy (XPS) analysis indicated that the synergistic effect between Rh nanoparticles and WO(3−x) nanowires was responsible for such an enhancement in activity. Specifically, Rh/WO(3−x) achieved the highest turnover frequency (TOF) with a value of 805.0 mol(H(2)) mol(Rh)(−1) min(−1) at room temperature under visible light irradiation. The H(2) release rate as a function of reaction time exhibited a volcano plot under visible light irradiation, indicating that a self-activation process occurred in the hydrolytic dehydrogenation of AB due to additional oxygen vacancies arising from in situ reduction of WO(3−x) nanowires by AB, and thus an enhanced localized surface plasmon resonance (LSPR). Such a self-activation process was responsible for the enhanced catalytic activity under visible light irradiation relative to that under dark conditions, which was supported by the lower activation energy (45.2 vs. 50.5 kJ mol(−1)). In addition, Rh/WO(3−x) catalysts were relatively stable with only little loss in activity after five cycles due to the tight attachment between two components.