Investigation of Diazinon degradation via advanced photocatalysis of CoWO4/g-C3N4 Z scheme heterojunction with addition of H2O2

被引:8
作者
Anh, Tran Minh [1 ]
Pham, Thanh-Dong [1 ]
Viet, Nguyen Minh [2 ]
Anh, Dao Thi Ngoc [1 ]
Cam, Nguyen Thi Dieu [3 ]
Noi, Nguyen Van [1 ,2 ]
Nhiem, Dao Ngoc [5 ]
Chau, Chu Ngoc [1 ]
Ha, Tran Thi Viet [4 ]
Phuong, Nguyen Minh [1 ]
机构
[1] Vietnam Natl Univ, Univ Sci, Fac Chem, Hanoi, Vietnam
[2] VNU Univ Sci, Key Lab Adv Mat Green Growth, Hanoi, Vietnam
[3] Quy Nhon Univ, Binh Dinh, Vietnam
[4] Vietnam Acad Sci & Technol, Inst Mat Sci, Hanoi, Vietnam
[5] Vietnam Japan Univ, Hanoi, Vietnam
关键词
CoWO4; Z-scheme; Photocatalysis; Diazinon degradation; WASTE-WATER; SEPARATION;
D O I
10.1016/j.chemphys.2023.112166
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
CoWO4, a relatively positive valence band semiconductor, has been coupled with g-C3N4, a relatively negative conduction band semiconductor, to establish a Z -scheme heterojunction. The photocatalytic tests indicated that the Diazinon removal efficiency of the heterojunction was 71.6 %, which was remarkably higher than those of the pristine CoWO4 (63.0 %) and g-C3N4 (61.1 %). This was because of Z -scheme mechanism, which photoexcited e- at the CoWO4 Cband migrated to the g-C3N4 Vband to preserve e- at the g-C3N4 Cband and h+ in the CoWO4 Vband. Then, remained e- and h+ with strong re-dox ability respectively reacted with O2 and H2O to generate O2 center dot- and center dot OH radicals to degrade Diazinon. The study also investigated that H2O2 effectively acted as electron acceptor for hydroxyl radical production to completely degrade Diazinon. Finally, the photocatalysis of the CoWO4/g-C3N4 was remained after three recycling runs implying that the heterojunction was relatively stable.
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页数:7
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