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

IF 8.1 1区 工程技术 Q1 ENGINEERING, CHEMICAL
Jing Li , Dandan Wang , Xueru Huang , Lu Zhang , Jifeng Guo
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引用次数: 0

摘要

抗生素加剧有害藻华,严重威胁水体安全。光催化活化过氧单硫酸盐(PMS)降解有机污染物已成为一种有前景的绿色环境修复策略。然而,开发具有强界面效应和丰富活性位点的高效催化剂面临着重大挑战。本文合成了一种富氧空位的1D/2D CuBi2O4/Bi2MoO6异质结,用于可见光驱动PMS激活,可有效降解各种抗生素并灭活铜绿微囊藻。独特的1D/2D异质结构、表面OVs和Cu2+/Cu+氧化还原循环促进了强界面接触和空间电荷分离。在30 min内,四环素(TC)的降解率和矿化率分别达到98.9 %和65.4 %,同时该系统快速灭活了铜绿微囊藻(Microcystis aeruginosa),灭活率为88.7 %,叶绿素a去除率为91.3 %。此外,该系统克服了与传统过渡金属活化剂PMS工艺相关的离子浸出问题,OVs和Cu双活性位点之间的协同作用增强了材料的稳定性、环境耐受性和广泛的适用性。原位实验和DFT计算表明,内部电场和Cu-O-Mo电子桥触发了S-scheme电荷输运,促进了强氧化还原反应。OVs和Cu双活性位点作为污染物吸附和PMS活化的附加中心,加速了电子转移和O-O键的裂解,增强了非均相界面的协同效应。LC-MS和活性位点鉴定阐明了降解途径和杀藻机制。这项工作为设计用于水净化中PMS激活的OVs和金属位点调制异质结提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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.
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来源期刊
Separation and Purification Technology
Separation and Purification Technology 工程技术-工程:化工
CiteScore
14.00
自引率
12.80%
发文量
2347
审稿时长
43 days
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.
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