Synergistic effect of oxygen vacancies and Ni particles over the ZnWO4/CdS heterostructure for enhanced photocatalytic reduction and oxidation activities

Optimization of charge-transfer pathway is of great significance in a capable photocatalytic system with a heterostructure for ensuring excellent reducibility and oxidizability. Herein, we synthesized well-built photocatalysts of oxygen vacancy decorated ZnWO4 (Vo-ZnWO4) nanorods coupled with CdS mi...

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Veröffentlicht in:Catalysis science & technology 2023-02, Vol.13 (4), p.1196-1207
Hauptverfasser: Zhang, Houfeng, Gan, Shenglong, Hou, Dongfang, Xiu-qing Qiao, Ruan Chi, Dong-Sheng, Li
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Sprache:eng
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Zusammenfassung:Optimization of charge-transfer pathway is of great significance in a capable photocatalytic system with a heterostructure for ensuring excellent reducibility and oxidizability. Herein, we synthesized well-built photocatalysts of oxygen vacancy decorated ZnWO4 (Vo-ZnWO4) nanorods coupled with CdS microspheres and Ni particles via a hydrothermal and photochemical deposition method, which may result in a change in the interface charge-transfer pathway from the traditional type-II to the Z-scheme mechanism. The Vo-ZnWO4/CdS–Ni Z-scheme heterojunction presented significant enhancements in photocatalytic activities and stability for H2 evolution, and the rate was up to 22.84 mmol g−1 h−1, approximately 2284 and 7 times higher than those of pure Vo-ZnWO4 and CdS, respectively. In addition, it showed excellent activities in the photocatalytic reduction of CO2 and in the oxidative degradation of tetracycline (TC) under visible-light irradiation. Benefiting from the introduction of oxygen vacancies and Ni particles with the dual function of an electron medium and cocatalyst, a feasible and efficient Z-scheme band alignment was constructed to steer the carriers in a predictable direction, addressing two major issues associated with the poor activity and stability. This work could appeal to researchers in designing an effective strategy to carry out multi-directional modification for enhancing photocatalytic reduction and oxidation activities.
ISSN:2044-4753
2044-4761
DOI:10.1039/d2cy01872a