Oxygen vacancies-enriched Cu/Co bimetallic oxides catalysts for high-efficiency peroxymonosulfate activation to degrade TC: Insight into the increase of Cu+ triggered by Co doping

双金属片 催化作用 电子顺磁共振 氧气 化学 激进的 降级(电信) 双金属 密度泛函理论 碳纤维 电子转移 猝灭(荧光) 光化学 材料科学 多相催化 化学工程 无机化学 物理化学 荧光 有机化学 计算化学 计算机科学 电信 工程类 物理 核磁共振 量子力学 复合数 复合材料
作者
Lei Liu,Chunjiang Han,Guofang Ding,Meiying Yu,Yunfei Li,Shengnan Liu,Yunxuan Xie,Jia Liu
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:450: 138302-138302 被引量:136
标识
DOI:10.1016/j.cej.2022.138302
摘要

Bimetallic CuCo-doped graphene-like carbon nanosheets ([email protected]) were synthesized via a facile and efficient process using agarose as carbon templates to activate peroxymonosulfate (PMS) for tetracycline (TC) degradation. In this study, [email protected]/PMS system exhibited excellent TC removal efficiency (0.182 min−1), which was unaffected by various water matrices and applicable to a wide pH range (3.44–8.44). Radicals (SO4•−, •OH, and O2•−) and non-radical (1O2) pathways collectively contributed to catalytic TC oxidation based on quenching experiments and electron paramagnetic resonance (EPR) analysis. Density functional theory (DFT) calculations revealed that the mechanism of PMS molecules activated on the surface of [email protected], in which CoO provided more catalytic sites while Cu2O further enhanced electron transfer. Moreover, the synergistic effect of CuCo bimetal could accelerate redox cycles of Cu+/Cu2+ and Co2+/Co3+, inducing the generation of abundant oxygen vacancies (OVs), thus enhancing PMS activation performance. Three potential TC degradation pathways were proposed according to fifteen possible intermediates detected by liquid chromatography-mass spectrometry (LC-MS). In brief, this work provides an efficient [email protected] heterogeneous catalyst and a new insight into PMS activation, which extends the application of bimetallic materials for environmental remediation.
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