光催化
异质结
磷化物
材料科学
可见光谱
催化作用
氧化还原
载流子
氧化物
光化学
辐照
金属
密度泛函理论
化学工程
光电子学
化学
计算化学
有机化学
工程类
物理
核物理学
冶金
作者
Yi-Shan Ouyang,Qing‐Yuan Yang
标识
DOI:10.1016/j.jcis.2023.04.078
摘要
Photocatalyst systems generally consist of catalysts and cocatalysts to realize light capture, charge carrier migration, and surface redox reactions. Developing a single photocatalyst that performs all functions while minimizing efficiency loss is extremely challenging. Herein, rod-shaped photocatalysts Co3O4/CoO/Co2P are designed and prepared using Co-MOF-74 as a template, which displays an outstanding H2 generation rate of 6.00 mmol·g-1·h-1 when exposed to visible light irradiation. It is 12.8 times higher than pure Co3O4. Under light excitation, the photoinduced electrons migrate from the catalysts of Co3O4 and CoO to the cocatalyst Co2P. The trapped electrons can subsequently undergo a reduction reaction to produce H2 on the surface. Density functional theory calculations and spectroscopic measurements reveal that enhanced performance results from the extended lifetime of photogenerated carriers and higher charge transfer efficiency. The ingenious structure and interface design presented in this study may guide the general synthesis of metal oxide/metal phosphide homometallic composites for photocatalysis.
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