{"title":"Rationally designed ZnFe1.2Co0.8O4/BiVO4 S-scheme heterojunction with spin-polarization for the elimination of antibiotic","authors":"Jinwang Wu , Qijing Xie , Chengliang Zhang , Haifeng Shi","doi":"10.1016/j.actphy.2025.100050","DOIUrl":null,"url":null,"abstract":"<div><div>Recently, the regulation of electronic spin polarization has attracted considerable interest as an effective strategy to mitigate the rapid recombination of photo-generated charges. However, current research predominantly targets individual photocatalysts, where the efficiency of charge separation still has significant room for improvement. Herein, a ZnFe<sub>1.2</sub>Co<sub>0.8</sub>O<sub>4</sub> (ZFCO) and BiVO<sub>4</sub> (BVO) S-scheme heterojunction was developed, which synergistically promoted charge separation through the S-scheme heterojunction and spin polarization, and further enhanced the photocatalytic performance in removing organic pollutants under an external magnetic field. Experimental results revealed that under sole light irradiation, ZB-1.5 (ZFCO : BVO = 3 : 2) demonstrated optimal performance, with a reaction rate constant (<em>k</em>) for tetracycline (TC) degradation of 0.0146 min<sup>−1</sup>. Under light irradiation and magnetic field conditions, the reaction rate constant (<em>k</em>) of ZB-1.5 for TC degradation increased to 0.0175 min<sup>−1</sup>, indicating enhanced photocatalytic performance. DFT calculations indicated that ZFCO exhibited the spin polarization. Photoluminescence measurements demonstrated that the S-scheme heterojunction structure improved the charge separation efficiency. In addition, possible degradation pathways and toxicity were assessed, indicating successful detoxification. This work provides some useful insights into utilizing S-scheme heterojunctions to develop photocatalysts with efficient separation of photo-generated charges.</div></div>","PeriodicalId":6964,"journal":{"name":"物理化学学报","volume":"41 5","pages":"Article 100050"},"PeriodicalIF":10.8000,"publicationDate":"2025-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"物理化学学报","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1000681825000062","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Recently, the regulation of electronic spin polarization has attracted considerable interest as an effective strategy to mitigate the rapid recombination of photo-generated charges. However, current research predominantly targets individual photocatalysts, where the efficiency of charge separation still has significant room for improvement. Herein, a ZnFe1.2Co0.8O4 (ZFCO) and BiVO4 (BVO) S-scheme heterojunction was developed, which synergistically promoted charge separation through the S-scheme heterojunction and spin polarization, and further enhanced the photocatalytic performance in removing organic pollutants under an external magnetic field. Experimental results revealed that under sole light irradiation, ZB-1.5 (ZFCO : BVO = 3 : 2) demonstrated optimal performance, with a reaction rate constant (k) for tetracycline (TC) degradation of 0.0146 min−1. Under light irradiation and magnetic field conditions, the reaction rate constant (k) of ZB-1.5 for TC degradation increased to 0.0175 min−1, indicating enhanced photocatalytic performance. DFT calculations indicated that ZFCO exhibited the spin polarization. Photoluminescence measurements demonstrated that the S-scheme heterojunction structure improved the charge separation efficiency. In addition, possible degradation pathways and toxicity were assessed, indicating successful detoxification. This work provides some useful insights into utilizing S-scheme heterojunctions to develop photocatalysts with efficient separation of photo-generated charges.