Jing Li , Dandan Wang , Xueru Huang , Lu Zhang , Jifeng Guo
{"title":"氧空位促进过氧单硫酸盐在1D/2D CuBi2O4/Bi2MoO6上的激活,以快速去除抗生素和有害的蓝藻失活:双活性位点调控和协同途径的见解","authors":"Jing Li , Dandan Wang , Xueru Huang , Lu Zhang , Jifeng Guo","doi":"10.1016/j.seppur.2025.133650","DOIUrl":null,"url":null,"abstract":"<div><div>Antibiotics exacerbate harmful algal blooms (HABs), seriously threatening water safety. Photocatalytic activation of peroxymonosulfate (PMS) for organic pollutant degradation has emerged as a promising green strategy for environmental remediation. However, developing efficient catalysts with strong interfacial effects and abundant active sites faces significant challenges. Herein, an oxygen vacancy-enriched 1D/2D CuBi<sub>2</sub>O<sub>4</sub>/Bi<sub>2</sub>MoO<sub>6</sub> heterojunction was synthesized for visible-light-driven PMS activation, enabling efficient various antibiotics degradation and <em>Microcystis aeruginosa</em> inactivation. The unique 1D/2D heterostructure, surface OVs, and Cu<sup>2+</sup>/Cu<sup>+</sup> redox cycling facilitated strong interfacial contact and spatial charge separation. Within 30 min, the degradation and mineralization rates of tetracycline (TC) reached 98.9 % and 65.4 %, respectively, while the system rapidly inactivated <em>Microcystis aeruginosa</em>, with an inactivation rate of 88.7 % and chlorophyll <em>a</em> removal rate of 91.3 %. Moreover, t the system overcame the ion leaching issue associated with conventional transition metal activator PMS processes, and the synergy between OVs and Cu dual active sites enhanced material stability, environmental tolerance, and broad applicability. In situ experiments and DFT calculations revealed that the internal electric field and Cu–O-Mo electron bridge triggered the S-scheme charge transport and promoted strong redox reactions. OVs and Cu dual active sites served as additional centers for pollutant adsorption and PMS activation, accelerating electron transfer and O-O bond cleavage, enhancing the synergistic effects at the heterogeneous interface. LC-MS and reactive site identification elucidated degradation pathways and algicidal mechanisms. This work provides valuable insights for designing OVs and metal sites modulated heterojunctions for PMS activation in water purification.</div></div>","PeriodicalId":427,"journal":{"name":"Separation and Purification Technology","volume":"374 ","pages":"Article 133650"},"PeriodicalIF":8.1000,"publicationDate":"2025-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Oxygen vacancies boosting peroxymonosulfate activation on 1D/2D CuBi2O4/Bi2MoO6 for rapid antibiotic removal and harmful cyanobacterial inactivation: Dual active site regulation and synergistic pathway insights\",\"authors\":\"Jing Li , Dandan Wang , Xueru Huang , Lu Zhang , Jifeng Guo\",\"doi\":\"10.1016/j.seppur.2025.133650\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Antibiotics exacerbate harmful algal blooms (HABs), seriously threatening water safety. Photocatalytic activation of peroxymonosulfate (PMS) for organic pollutant degradation has emerged as a promising green strategy for environmental remediation. However, developing efficient catalysts with strong interfacial effects and abundant active sites faces significant challenges. Herein, an oxygen vacancy-enriched 1D/2D CuBi<sub>2</sub>O<sub>4</sub>/Bi<sub>2</sub>MoO<sub>6</sub> heterojunction was synthesized for visible-light-driven PMS activation, enabling efficient various antibiotics degradation and <em>Microcystis aeruginosa</em> inactivation. The unique 1D/2D heterostructure, surface OVs, and Cu<sup>2+</sup>/Cu<sup>+</sup> redox cycling facilitated strong interfacial contact and spatial charge separation. Within 30 min, the degradation and mineralization rates of tetracycline (TC) reached 98.9 % and 65.4 %, respectively, while the system rapidly inactivated <em>Microcystis aeruginosa</em>, with an inactivation rate of 88.7 % and chlorophyll <em>a</em> removal rate of 91.3 %. Moreover, t the system overcame the ion leaching issue associated with conventional transition metal activator PMS processes, and the synergy between OVs and Cu dual active sites enhanced material stability, environmental tolerance, and broad applicability. In situ experiments and DFT calculations revealed that the internal electric field and Cu–O-Mo electron bridge triggered the S-scheme charge transport and promoted strong redox reactions. OVs and Cu dual active sites served as additional centers for pollutant adsorption and PMS activation, accelerating electron transfer and O-O bond cleavage, enhancing the synergistic effects at the heterogeneous interface. LC-MS and reactive site identification elucidated degradation pathways and algicidal mechanisms. This work provides valuable insights for designing OVs and metal sites modulated heterojunctions for PMS activation in water purification.</div></div>\",\"PeriodicalId\":427,\"journal\":{\"name\":\"Separation and Purification Technology\",\"volume\":\"374 \",\"pages\":\"Article 133650\"},\"PeriodicalIF\":8.1000,\"publicationDate\":\"2025-05-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Separation and Purification Technology\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1383586625022476\",\"RegionNum\":1,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, CHEMICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Separation and Purification Technology","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1383586625022476","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
Oxygen vacancies boosting peroxymonosulfate activation on 1D/2D CuBi2O4/Bi2MoO6 for rapid antibiotic removal and harmful cyanobacterial inactivation: Dual active site regulation and synergistic pathway insights
Antibiotics exacerbate harmful algal blooms (HABs), seriously threatening water safety. Photocatalytic activation of peroxymonosulfate (PMS) for organic pollutant degradation has emerged as a promising green strategy for environmental remediation. However, developing efficient catalysts with strong interfacial effects and abundant active sites faces significant challenges. Herein, an oxygen vacancy-enriched 1D/2D CuBi2O4/Bi2MoO6 heterojunction was synthesized for visible-light-driven PMS activation, enabling efficient various antibiotics degradation and Microcystis aeruginosa inactivation. The unique 1D/2D heterostructure, surface OVs, and Cu2+/Cu+ redox cycling facilitated strong interfacial contact and spatial charge separation. Within 30 min, the degradation and mineralization rates of tetracycline (TC) reached 98.9 % and 65.4 %, respectively, while the system rapidly inactivated Microcystis aeruginosa, with an inactivation rate of 88.7 % and chlorophyll a removal rate of 91.3 %. Moreover, t the system overcame the ion leaching issue associated with conventional transition metal activator PMS processes, and the synergy between OVs and Cu dual active sites enhanced material stability, environmental tolerance, and broad applicability. In situ experiments and DFT calculations revealed that the internal electric field and Cu–O-Mo electron bridge triggered the S-scheme charge transport and promoted strong redox reactions. OVs and Cu dual active sites served as additional centers for pollutant adsorption and PMS activation, accelerating electron transfer and O-O bond cleavage, enhancing the synergistic effects at the heterogeneous interface. LC-MS and reactive site identification elucidated degradation pathways and algicidal mechanisms. This work provides valuable insights for designing OVs and metal sites modulated heterojunctions for PMS activation in water purification.
期刊介绍:
Separation and Purification Technology is a premier journal committed to sharing innovative methods for separation and purification in chemical and environmental engineering, encompassing both homogeneous solutions and heterogeneous mixtures. Our scope includes the separation and/or purification of liquids, vapors, and gases, as well as carbon capture and separation techniques. However, it's important to note that methods solely intended for analytical purposes are not within the scope of the journal. Additionally, disciplines such as soil science, polymer science, and metallurgy fall outside the purview of Separation and Purification Technology. Join us in advancing the field of separation and purification methods for sustainable solutions in chemical and environmental engineering.