期刊
SEPARATION AND PURIFICATION TECHNOLOGY
卷 284, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.seppur.2021.120263
关键词
ZnFe2O4/AgBr; Magnetoresistance; Photodegradation; Magnetic field
资金
- Tianjin Natural Science Foundation [19JCQNJC06200, 18JCZDJC99800]
- National Nat-ural Science Foundation of China [52071183, 51871122, 61804108]
In this study, a ZnFe2O4/AgBr magnetic photocatalyst was constructed to simplify the structure of the Z-scheme photocatalyst and enhance its photocatalytic activity using the magnetoresistance effect and an external magnetic field. The photocurrent density of ZnFe2O4/AgBr was higher than that of pure ZnFe2O4, and showed a notable increase under a magnetic field. The magnetic field-enhanced effect also improved the photodegradation activity of ZnFe2O4/AgBr for organic pollutants.
A ZnFe2O4/AgBr magnetic photocatalyst was constructed to simply the structure of the Z-scheme photocatalyst, and further enhance the photocatalytic activity using the magnetoresistance (MR) effect of the system and an external magnetic field. The photocurrent density of ZnFe2O4/AgBr was 75.1 mu A/cm(2), which was higher than that of pure ZnFe2O4 (47.6 mu A/cm(2)). Whereas the photocurrent density of pure ZnFe2O4 did not notably change under a magnetic field, that of ZnFe2O4/AgBr clearly increased to 151.8 mu A/cm(2) under a magnetic field of 1000 Oe. The MR results demonstrated that ZnFe2O4/AgBr had a more negative MR than ZnFe2O4 did, therefore, the transfer of photogenerated carriers for ZnFe2O4/AgBr was quicker under the magnetic field. The existence of this magnetic field-enhanced effect can replace the role of the electron transfer bridge, and simply the Z-scheme structure. In addition, the photodegradation activity of ZnFe2O4/AgBr for organic pollutants also got obvious enhancement under the magnetic field.
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