光催化
纳米片
材料科学
氢氧化物
硫化镉
镍
化学工程
催化作用
纳米结构
纳米技术
硫化物
光化学
化学
有机化学
冶金
工程类
作者
Zhiyong Zhao,Xuemei Diao,Peng Wang,Hongyi Gao,John T. S. Irvine,Rong Liu,Xiaowei Zhang,Ge Wang
标识
DOI:10.1016/j.cej.2024.149184
摘要
The controllable hollow sphere, serving as an excellent light-trapping cavity, represents one of the most appealing structures in photocatalytic CO2 reduction but is plagued by limited catalytic active sites. Herein, we report an in situ self-assembly strategy to decorate cadmium sulfide hollow spheres (CdS HS) with ultrathin nickel hydroxide (Ni(OH)2) nanosheets to boost CO2 photoreduction. The as-grown CdS@Ni(OH)2 photocatalyst affords a higher CO yield of 3.12 mmol g-1h−1 and a good apparent quantum efficiency (AQE) of 2.05 % compared with the pristine CdS HS (0.38 mmol g-1h−1). The superior performance could be assigned to the unique hollow nanostructure and the synergistic effect between CdS HS and Ni(OH)2 nanosheets. The interior CdS HS strengthens the multiple light reflections that leads to optimized light harvesting. The ultrathin Ni(OH)2 nanosheet shell effectively prevents photocorrosion of CdS while providing a suitable local chemical environment that promotes CO2 adsorption and activation. Additionally, the close contact interface of CdS@Ni(OH)2 facilitates efficient separation and migration of photoinduced electrons and holes, thus boosting photocatalytic kinetics. This study presents a facile route for the controllable engineering of hollow microreactors toward CO2 photoreduction and sheds light on the structure-dependent photocatalytic mechanisms.
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