光催化
异质结
制氢
材料科学
光电子学
生产(经济)
锌
氢
化学工程
冶金
化学
工程类
催化作用
生物化学
有机化学
经济
宏观经济学
作者
Asif Raza,Shumail Farhan,Zhixian Yu,Yan Wu
标识
DOI:10.3866/pku.whxb202406020
摘要
This work illustrates the novelty of double S-scheme ZnS/ZnO/CdS ternary heterojunction photocatalyst with efficient photocatalytic activity . The sample with optimal CdS content, ZnS/ZnO/CdS-14% (ZZC14%), displayed the maximum H 2 evolution rate of 4.1 mmol·g ‒1 ·h ‒1 . The maximum photocatalytic performance was approximately 2 and 13 times higher than their corresponding counterparts, ZnS/CdS and ZnO/ZnS, respectively. A high AQE of 19.8% under 420 nm was obtained. Additionally, the slight changes in H 2 evolution activities and retentions of crystal structures after six successive cycles indicate the stability of the photocatalyst. In accordance with the theoretical calculations and experimental results, the remarkable enhancement in photocatalytic activity is attributed to fast electron transfer and separation as well as the intimate contact due to mutual interaction between S-scheme. This work highlights an innovative approach to constructing a dual S-scheme photocatalytic system with high separation and fast migration capabilities of photogenerated charge carriers for splitting water to produce hydrogen. This work highlights an innovative approach to constructing a dual S-scheme ZnS/ZnO/CdS photocatalytic system with high separation and fast migration capabilities of photogenerated charge carriers for splitting water to produce hydrogen.
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