Muhammad Usman, Hamza Khaliq, Muhammad Ibrahim, Saeed Anwar, Muhammad Adnan, Ghulam Abbas Ashraf, Mutabar Latipova, Doniyor Jumanazarov, N. Sfina, Ahlem Guesmi
{"title":"Cu-N-TiO₂/g-C3N4 photocathode-driven sediment microbial fuel cells for azithromycin degradation and enhanced bioelectricity generation","authors":"Muhammad Usman, Hamza Khaliq, Muhammad Ibrahim, Saeed Anwar, Muhammad Adnan, Ghulam Abbas Ashraf, Mutabar Latipova, Doniyor Jumanazarov, N. Sfina, Ahlem Guesmi","doi":"10.1016/j.dwt.2025.101564","DOIUrl":null,"url":null,"abstract":"The widespread occurrence of antibiotic pollutants such as azithromycin (AZI) in aquatic habitats needs the development of efficient and long-term cleanup solutions. This study looks into the use of photocatalysis in conjunction with sediment microbial fuel cells (SMFCs) to degrade AZI and generate bioelectricity. We developed and analyzed a novel heterojunction photocatalyst, Cu-N-TiO₂/g-C₃N₄, coated onto a graphene conductive material (GCM), which serves as an effective photocathode. Comprehensive characterization (XRD, XPS, UV-Vis, and SEM) confirmed successful heterojunction production, with XPS revealing important impurity states from N and Cu co-doping. The improved heterostructure had a dramatically narrower bandgap of 1.02 eV, which increased its visible-light absorption capability. The Cu-N-TiO₂/g-C₃N₄ photocathode outperformed pure g-C₃N₄ (70.95%), Cu-N-TiO₂ (65.64%), and the control (49.21%) in SMFCs using natural sunshine, attaining 84.73% AZI degradation. While AZI stress reduced microbial diversity and hence hindered energy generation, the improved photocathodes enabled sustained bioelectricity production. This study identifies sunlight-driven SMFCs with customized heterojunction photocathodes as a potential, synergistic technique for the effective cleanup of antibiotic-contaminated water.","PeriodicalId":11260,"journal":{"name":"Desalination and Water Treatment","volume":"324 1","pages":"101564-101564"},"PeriodicalIF":3.4000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Desalination and Water Treatment","FirstCategoryId":"0","ListUrlMain":"https://doi.org/10.1016/j.dwt.2025.101564","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The widespread occurrence of antibiotic pollutants such as azithromycin (AZI) in aquatic habitats needs the development of efficient and long-term cleanup solutions. This study looks into the use of photocatalysis in conjunction with sediment microbial fuel cells (SMFCs) to degrade AZI and generate bioelectricity. We developed and analyzed a novel heterojunction photocatalyst, Cu-N-TiO₂/g-C₃N₄, coated onto a graphene conductive material (GCM), which serves as an effective photocathode. Comprehensive characterization (XRD, XPS, UV-Vis, and SEM) confirmed successful heterojunction production, with XPS revealing important impurity states from N and Cu co-doping. The improved heterostructure had a dramatically narrower bandgap of 1.02 eV, which increased its visible-light absorption capability. The Cu-N-TiO₂/g-C₃N₄ photocathode outperformed pure g-C₃N₄ (70.95%), Cu-N-TiO₂ (65.64%), and the control (49.21%) in SMFCs using natural sunshine, attaining 84.73% AZI degradation. While AZI stress reduced microbial diversity and hence hindered energy generation, the improved photocathodes enabled sustained bioelectricity production. This study identifies sunlight-driven SMFCs with customized heterojunction photocathodes as a potential, synergistic technique for the effective cleanup of antibiotic-contaminated water.
期刊介绍:
The journal is dedicated to research and application of desalination technology, environment and energy considerations, integrated water management, water reuse, wastewater and related topics.