光催化
异质结
三元运算
金属
载流子
可见光谱
化学
光化学
材料科学
氧化还原
光电子学
催化作用
无机化学
冶金
生物化学
计算机科学
程序设计语言
作者
Md Moniruddin,Ellis Oppong,David J. Stewart,Christopher McCleese,Ajit K. Roy,Juliusz Warzywoda,Nurxat Nuraje
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2019-09-04
卷期号:58 (18): 12325-12333
被引量:35
标识
DOI:10.1021/acs.inorgchem.9b01854
摘要
Heterostructure formation is an effective method used for designing photocatalysts that solve problems caused by photoexcited charge recombination phenomena associated with the photocatalytic water redox reaction. This work reports a new Co-metal-incorporated ternary heterostructured photocatalyst, CdS/CoOx/Co-metal, which enhanced charge separation to increase photocatalytic H2 evolution 30.5-fold in comparison to pure CdS under visible light. This work demonstrates for the first time the effect of the Co metal on photocatalytic H2 evolution using the CdS/CoOx/Co-metal ternary heterostructure. In the ternary heterostructure, Co metal and CoOx act as photogenerated electron- and hole-capturing cocatalysts, respectively. Results from photoelectrochemical studies along with photocatalytic H2 evolution data proved the enhancement of charge transfer and separation in the CdS/CoOx/Co-metal heterostructure due to the addition of Co metal and CoOx. Hence, the synergistic charge separation improvement achieved by the combination of CoOx and the Co metal with CdS produced a photocatalytic H2 evolution rate of 9.54 μmol/h, which is the highest reported H2 evolution rate for a CdS-based system under l sun solar irradiance (>420 nm) to the best of our knowledge.
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