TY - JOUR
T1 - Facile fabrication of Z-scheme Ag2WO4/BiOBr heterostructure with oxygen vacancies for improved visible-light photocatalytic performance
AU - Fu, Shuai
AU - Du, Yanqiang
AU - Bie, Junhong
AU - Huang, Zhiquan
AU - Hu, Hai
AU - Huang, Qiang
AU - Zhu, Huijie
AU - Yuan, Wei
AU - Li, Leicheng
AU - Liu, Bo
PY - 2023
Y1 - 2023
N2 - Z-scheme Ag2WO4/BiOBr heterojunction with rich oxygen vacancies was successfully synthesized by the simplest hydrothermal method, which was systematically characterized in the structural, optical and electronic properties. The photocatalytic applications of Z-scheme Ag2WO4/BiOBr heterostructure with different weight percentages of Ag2WO4 were studied. The optimized Ag2WO4(20%)/BiOBr heterostructure exhibited superior photodegradation efficiencies (98%) towards Lanasol Red 5 B (LR5B), which was 4.67- and 3.38-fold higher than pristine BiOBr and Ag2WO4, respectively. The principal reason for the elevated photocatalytic property of Ag2WO4/BiOBr was ascribed to the formation of oxygen vacancies and intimate Z-scheme heterostructure between Ag2WO4 and BiOBr, improving the light trapping capability and facilitating separation of photo-induced charge. Moreover, the removal efficiencies of Ag2WO4/BiOBr heterostructure towards TC (tetracycline), CIP (ciprofloxacin) and RhB (rhodamine B) were 74%, 23%, and 13%, respectively. The simultaneous degradation experiment confirmed the competitiveness between LR5B and CIP for active species, leading to the inferior degradation efficiency for LR5B, along with the experimental factor towards LR5B was researched. The probable Z-scheme mechanism and the significant role of hydroxyl radical and superoxide radicals were demonstrated by the radical capture experiment and electron spin resonance (ESR). The Z-scheme mechanism has resulted in prominent improvement in charge separation, along with higher redox properties, which were responsible for the excellent photocatalytic activity.& COPY; 2023 Vietnam National University, Hanoi. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
AB - Z-scheme Ag2WO4/BiOBr heterojunction with rich oxygen vacancies was successfully synthesized by the simplest hydrothermal method, which was systematically characterized in the structural, optical and electronic properties. The photocatalytic applications of Z-scheme Ag2WO4/BiOBr heterostructure with different weight percentages of Ag2WO4 were studied. The optimized Ag2WO4(20%)/BiOBr heterostructure exhibited superior photodegradation efficiencies (98%) towards Lanasol Red 5 B (LR5B), which was 4.67- and 3.38-fold higher than pristine BiOBr and Ag2WO4, respectively. The principal reason for the elevated photocatalytic property of Ag2WO4/BiOBr was ascribed to the formation of oxygen vacancies and intimate Z-scheme heterostructure between Ag2WO4 and BiOBr, improving the light trapping capability and facilitating separation of photo-induced charge. Moreover, the removal efficiencies of Ag2WO4/BiOBr heterostructure towards TC (tetracycline), CIP (ciprofloxacin) and RhB (rhodamine B) were 74%, 23%, and 13%, respectively. The simultaneous degradation experiment confirmed the competitiveness between LR5B and CIP for active species, leading to the inferior degradation efficiency for LR5B, along with the experimental factor towards LR5B was researched. The probable Z-scheme mechanism and the significant role of hydroxyl radical and superoxide radicals were demonstrated by the radical capture experiment and electron spin resonance (ESR). The Z-scheme mechanism has resulted in prominent improvement in charge separation, along with higher redox properties, which were responsible for the excellent photocatalytic activity.& COPY; 2023 Vietnam National University, Hanoi. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
U2 - 10.1016/j.jsamd.2023.100561
DO - 10.1016/j.jsamd.2023.100561
M3 - Article
SN - 2468-2284
VL - 8
JO - Journal of Science: Advanced Materials and Devices
JF - Journal of Science: Advanced Materials and Devices
IS - 2
ER -