Direct Z-scheme composite of CdS and oxygen-defected CdWO4: An efficient visible-light-driven photocatalyst for hydrogen evolution

被引:194
作者
Jia, Xu [1 ,2 ]
Tahir, Muhammad [1 ,2 ]
Pan, Lun [1 ,2 ]
Huang, Zhen-Feng [1 ,2 ]
Zhang, Xiangwen [1 ,2 ]
Wang, Li [1 ,2 ]
Zou, Ji-Jun [1 ,2 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Key Lab Green Chem Technol, Minist Educ, Tianjin 300072, Peoples R China
[2] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
CdS/CdWO4; Photocatalysis; Hydrogen evolution; Direct Z-scheme; Oxygen defects; STATE Z-SCHEME; NEAR-INFRARED ABSORPTION; IN-SITU SYNTHESIS; ELECTRONIC-STRUCTURES; TUNGSTEN-OXIDE; TIO2; NANOPARTICLES;
D O I
10.1016/j.apcatb.2016.05.046
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Direct Z-scheme photocatalyst, which enables efficient charge separation and retains high redox ability, is promising material for visible-light-driven hydrogen evolution. Here we developed a one-step solvothermal method to fabricate direct Z-scheme CdS/CdWO4 composite via treating W18O49 with CH3CSNH2 and Cd(CH3COO)(2). By controlling the dosage of Cd(CH3COO)(2), CdS nanoparticles decorated CdWO4 nanowires (CS-2) is synthesized. UV-vis DRS and XPS spectra demonstrate that the CdWO4 possesses a large amount of oxygen vacancies, which help to form ohmic contact and broaden light absorption. Compared with CdS, CS-2 Exhibits 18 times higher visible-light H-2 evolution activity using lactic acid as sacrificial agent and shows 7.8-fold higher photocurrent density. Moreover, photoelectrochemical test manifests the efficient separation of the photo-induced charge carriers. Radical-trapping experiments along with in-situ Pt photodeposition further prove that the charge transfer and separation follows Z-scheme mechanism. This work highlights the critical role of defects in the formation of direct Z-scheme composite. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:154 / 161
页数:8
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