{"title":"Preparation of Ag@Ag2O/AgCl composite photocatalytic material and degradation performance for SD I under sunlight","authors":"Daxiang Gao","doi":"10.1007/s13201-025-02405-5","DOIUrl":null,"url":null,"abstract":"<div><p>The photocatalytic material Ag@Ag<sub>2</sub>O/AgCl was successfully prepared using GO and CA gel as carriers, through chemical coupling, in situ deposition, and photo-induced reduction. The performance of the composite photocatalytic material, its photodegradation performance, mechanism, and pathways of Sudan I (SD I) in APG aqueous solution were explored. The results showed that the prepared composite photocatalytic material was loaded with a large amount of irregular nano-Ag<sub>2</sub>O, AgCl, and silver nanoparticles (AgNPs). In the material, the mass fraction of Ag element is the highest (36.41 wt%). The photocatalytic material showed a significant broad absorption in both the UV and visible light regions, and under visible light irradiation, it can generate a stable and reversible photocurrent, with a small resistance to photogenerated electron transfer, exhibiting good photocatalytic performance. SD I exhibits good solubility in APG (7 mL/1000 mL) aqueous solution after ultrasonic and heating (100 ℃) treatment for 30 min. At a certain concentration of SD I, acidic solution and lower temperature are conducive to the photocatalytic degradation of SD I, and the catalytic degradation process conforms to the pseudo-first-order reaction kinetic relationship. Through five cycles of experiments, the stability of the material was demonstrated to be good. Superoxide radicals (·O<sub>2</sub><sup>−</sup>) and holes (h<sup>+</sup>) generated during the photocatalytic degradation are the main active species responsible for degrading SD I. SD I molecules were decolorized by N=N and C-N bond cleavage, and the benzene and naphthalene ring were opened under the action of active substances (h<sup>+</sup>, ·O<sub>2</sub><sup>−</sup>) and finally mineralized into CO<sub>2</sub>, H<sub>2</sub>O and inorganic ions.</p></div>","PeriodicalId":8374,"journal":{"name":"Applied Water Science","volume":"15 4","pages":""},"PeriodicalIF":5.7000,"publicationDate":"2025-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s13201-025-02405-5.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Water Science","FirstCategoryId":"93","ListUrlMain":"https://link.springer.com/article/10.1007/s13201-025-02405-5","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"WATER RESOURCES","Score":null,"Total":0}
引用次数: 0
Abstract
The photocatalytic material Ag@Ag2O/AgCl was successfully prepared using GO and CA gel as carriers, through chemical coupling, in situ deposition, and photo-induced reduction. The performance of the composite photocatalytic material, its photodegradation performance, mechanism, and pathways of Sudan I (SD I) in APG aqueous solution were explored. The results showed that the prepared composite photocatalytic material was loaded with a large amount of irregular nano-Ag2O, AgCl, and silver nanoparticles (AgNPs). In the material, the mass fraction of Ag element is the highest (36.41 wt%). The photocatalytic material showed a significant broad absorption in both the UV and visible light regions, and under visible light irradiation, it can generate a stable and reversible photocurrent, with a small resistance to photogenerated electron transfer, exhibiting good photocatalytic performance. SD I exhibits good solubility in APG (7 mL/1000 mL) aqueous solution after ultrasonic and heating (100 ℃) treatment for 30 min. At a certain concentration of SD I, acidic solution and lower temperature are conducive to the photocatalytic degradation of SD I, and the catalytic degradation process conforms to the pseudo-first-order reaction kinetic relationship. Through five cycles of experiments, the stability of the material was demonstrated to be good. Superoxide radicals (·O2−) and holes (h+) generated during the photocatalytic degradation are the main active species responsible for degrading SD I. SD I molecules were decolorized by N=N and C-N bond cleavage, and the benzene and naphthalene ring were opened under the action of active substances (h+, ·O2−) and finally mineralized into CO2, H2O and inorganic ions.