Activated H2O2 on Ag/SiO2-SrWO4 surface for enhanced dark and visible-light removal of methylene blue and p-nitrophenol

被引:48
作者
El-Sheshtawy, Hamdy S. [1 ]
Ghubish, Zaynab [2 ]
Shoueir, Kamel R. [2 ]
El-Kemary, Maged [2 ]
机构
[1] Kafrelsheikh Univ, Fac Sci, Chem Dept, Kafrelsheikh, Egypt
[2] Kafrelsheikh Univ, Inst Nanosci & Nanotechnol, Kafrelsheikh, Egypt
关键词
Activated H2O2; Ag/SiO2/SrWO4; Catalytic; Photocatalytic; DFT calculations; PHOTOCATALYTIC ACTIVITY; SILVER NANOPARTICLES; GREEN SYNTHESIS; MWO4; M; OXIDATION; REDUCTION; DEGRADATION; PHOTOLUMINESCENCE; CATALYST; KINETICS;
D O I
10.1016/j.jallcom.2020.155848
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
Activated H2O2 on the surface of nanostructures for advanced oxidation process attracts the interest for energy consumption, time saving rather than Fenton reaction process. Here, we introduce Ag/SiO2 NPs immobilized on SrWO4 surface for enhanced catalytic and photocatalytic oxidation of methylene blue and reduction of p-nitrophenol by H2O2 surface activation. Both theoretical calculations (rwb97xd/LANL2DZ) and experimental (FT-IR and XRD) show that the catalytic enhancement was due to the surface interaction between Ag/SiO2 and SrWO4 that activate H2O2 surface molecules in absence of light. The photocatalytic enhancement was interpreted by the hot electrons ejected from Ag NPs to the SrWO4 rather than the p-n junction created by Ag/SiO2 and SrWO4 mechanism. Different spectroscopic techniques such as SEM, TEM, XRD were used for the catalysts characterizations. The optical measurements such as UV-Vis and photoluminescence were incorporated to further support the mechanism. The catalyst posses high catalytic activity over wide pH range (4-10). (C) 2020 Elsevier B.V. All rights reserved.
引用
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页数:12
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