ZnCdS/CoMoOS Photocatalyst with High Electron Flux at the Ternary Interface Enhances H2 production

被引:5
作者
Liu, Qian [1 ]
Zhang, Chao [1 ]
Li, Weiping [1 ]
Ming, Shujun [2 ]
Li, Lu [3 ,4 ]
Lv, Zhiguo [1 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem Engn, State Key Lab Base Ecochem Engn, Qingdao 266042, Peoples R China
[2] Huanggang Normal Univ, Sch Chem & Chem Engn, Hubei Key Lab Proc & Applicat Catalyt Mat, Huangzhou 438000, Peoples R China
[3] Shaanxi Univ Sci & Technol, Key Lab Auxiliary Chem & Technol Chem Ind, Minist Educ, Xian 710021, Peoples R China
[4] Shaanxi Univ Sci & Technol, Shaanxi Collaborat Innovat Ctr Ind Auxiliary Chem, Xian 710021, Peoples R China
基金
中国国家自然科学基金;
关键词
ternary interface; ZnCdS; CoMoOS; high electron flux; H-2; evolution; HYDROGEN-PRODUCTION; CONSTRUCTION; NANORODS;
D O I
10.1021/acsanm.4c01243
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In this paper, CoMoOx-CoMoSx-CoSx (CoMoOS) were employed as cocatalysts for the first time to fabricate a ZnCdS/CoMoOS photocatalyst featuring a high electron flux ternary interface. The photocatalytic hydrogen production rate reached 52.31 mmol h(-1) g(-1), which is 6.4 times that of ZnCdS (8.147 mmol h(-1) g(-1)). Furthermore, owing to the presence of the CoMoOS/ZnCdS ternary interface, ZnCdS is capable of transferring electrons to CoMoOS through this interface, thus accelerating the separation of electron-hole pairs. The close contact at the ternary interface can significantly shorten the transmission path between electronically excited photosensitive sites (ZnCdS) and the water splitting active site (CoMoOS). From the calculation of DFT, CoSx and CoMoSx exhibit the optimal Gibbs free energy (-0.14 eV) and water adsorption energy (-10.30 eV), respectively, thereby deducing that CoMoOx, CoMoSx, and CoSx serve as e(-) auxiliary shunt, H2O adsorption, and H* combination functions, respectively.
引用
收藏
页码:8278 / 8288
页数:11
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