Coupling ultrafine plasmonic Co3O4 with thin-layer carbon over SiO2 nanosphere for dual-functional PMS activation and solar interfacial water evaporation

被引:27
作者
Du, Rongrong [1 ]
Zhu, Hongyang [1 ]
Zhao, Hongyao [1 ]
Lu, Hao [1 ]
Dong, Chang [1 ]
Liu, Mengting [1 ]
Yang, Fu [1 ]
Yang, Jun [3 ]
Wang, Jun [2 ]
Pan, Jianming [4 ]
机构
[1] Jiangsu Univ Sci & Technol, Sch Environm & Chem Engn, Zhenjiang 212003, Peoples R China
[2] Anhui Polytech Univ, Sch Biol & Food Engn, Wuhu 241000, Peoples R China
[3] Jiangsu Univ Sci & Technol, Sch Mat Sci & Engn, Zhenjiang 212003, Peoples R China
[4] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
基金
中国博士后科学基金;
关键词
Advanced oxidation process; Ultrafine plasmonic Co 3 O 4; Photothermal conversion; Solar water evaporation; Core-shell; PEROXYMONOSULFATE ACTIVATOR; ORGANIC POLLUTANTS; DEGRADATION; REMOVAL; PERFORMANCE; ENVIRONMENT; CONTAMINANTS; CATALYSTS;
D O I
10.1016/j.jallcom.2023.168816
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photothermal materials afford growing interest in environmental governance, especially for addressing complicated environmental issues including the purification of wastewater and regeneration of freshwater together. Here, we constructed a dual-functional photothermal nanosphere by integrating ultrafine plas-monic Co3O4 (similar to 10 nm) into an N-doping carbon layer over silica nanosphere (SiO2@Co/C). Biocompatible dopamine coating induces the incorporation of Co precursor and activity optimization of metal species over the SiO2 nanosphere during the synthetic process. In this way, the SiO2 nanosphere maintains the stable configuration of the carbon coating thin layer to accommodate the local interfacial Co3O4 catalytic active substances. Impressively, this catalyst also owns a well-developed interconnecting N-containing network structure, unconventional redox cycle pair of Co(II)/Co(III), and significant metal-carbon interaction. A controlled thermal procedure (500-800 degrees C) was implemented to tune the optimized activity state of the catalyst. Under these merits, advanced oxidation process (AOPs) through activating persulfate by the ob-tained materials to degrade organic pollutants was performed in the presence/absence of sunlight, further validating the appreciable photothermal effect to improve the catalytic thermodynamic behavior. The re-action parameters ad anion interference were studied in detail, and SiO2@Co/C-60 0 can completely degrade bisphenol A (BPA) (30 mg L-1) with a high reaction rate constant of 0.722 min -1 and a low reaction activation energy of Ea (19.4 kJ/mol), and also shows superior mineralization activity for some stubborn pollutants, including oxytetracycline (OTC), 2,4-dichlorophenol and tetracycline (TC) through the reinforced photo -thermal approach. Besides, SiO2@Co/C-60 0 shows multiple functions in interfacial solar water evaporation application (1.36 kg m-2 h-1, 81.59 %), revealing great potential value of purification and regeneration of water in the complex pollution condition. This work gives the possibility for the next-generation versatile and competitive photothermal environmental governing materials. (c) 2023 Elsevier B.V. All rights reserved.
引用
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页数:12
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