光催化
制氢
材料科学
三元运算
异质结
纳米棒
化学工程
分解水
电子转移
贵金属
复合数
固溶体
纳米颗粒
化学
纳米技术
催化作用
氢
光化学
金属
光电子学
复合材料
冶金
工程类
有机化学
生物化学
程序设计语言
计算机科学
作者
Junwen Wang,Tao Song,Lei Su,Haoyang Xu,Xiaoyu Bai,Lina Zhou,Weixia Tu
出处
期刊:Langmuir
[American Chemical Society]
日期:2021-10-20
卷期号:37 (43): 12654-12662
被引量:8
标识
DOI:10.1021/acs.langmuir.1c02025
摘要
Photocatalytic reactions over effective photocatalysts are attractive to explore clean hydrogen energy from water with the utilization of solar energy. Ternary Co 1– x S@ZnCoS/CdS (ZCS/CdS) composites are constructed as photocatalysts through the hydrothermal formation of Co 1– x S and ZnCoS nanoparticles on CdS nanorods. Superior to the binary Co 1– x S/CdS composite, ZCS/CdS shows the improved photocatalytic activity with a hydrogen production rate of 58.4 mmol·g –1 ·h –1, which is 31.4 and 2.1 times higher than those of CdS and Co 1– x S/CdS, respectively. Different from binary Co 1– x S/CdS, the participation of a small amount of zinc favors the formation of ZnCoS solid solution in ZCS/CdS. A synergistic promotion effect of ZnCoS and Co 1– x S is confirmed due to tight heterojunctions among Co 1– x S, ZnCoS, and CdS in ZCS/CdS. The unique heterostructure of ZCS/CdS benefits its enhanced absorption ability of visible light, accelerating the separation of photoinduced electron–hole pairs and the electron transfer. ZCS/CdS exhibits the strong reduction ability and superior photocatalytic stability due to the role of double Z-scheme electron transfer pathways in the ternary composite. This work provides a suitable way to tune noble metal-free composite photocatalysts for efficient H 2 production.
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