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Oxygen-vacancy-enriched substrate-less SnOx/La-Sb anode for high-performance electrocatalytic oxidation of antibiotics in wastewater
被引:51
作者:
Yang, Chao
[1
]
Shang, Shanshan
[1
]
Li, Xiao-yan
[1
,2
]
机构:
[1] Univ Hong Kong, Dept Civil Engn, Hong Kong, Peoples R China
[2] Tsinghua Univ, Inst Environm & Ecol, Tsinghua Shenzhen Int Grad Sch, Shenzhen, Peoples R China
基金:
中国国家自然科学基金;
关键词:
SnO(2 )electrode;
Oxygen vacancy;
Moxifloxacin;
La doping;
Electrochemical oxidation;
SYNTHETIC ORGANIC-DYES;
BORON-DOPED DIAMOND;
ELECTROCHEMICAL DEGRADATION;
THIN-FILMS;
TIO2;
ELECTRODES;
DECONTAMINATION;
WASTEWATERS;
TI/SNO2-SB;
DEPOSITION;
D O I:
10.1016/j.jhazmat.2022.129212
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Electrocatalytic oxidation is a promising technology for treating toxic organic pollutants in water and wastewater, but conventional Ti-based anodes often exhibit a short service life and low efficiency in application. Oxygen vacancy (OV)-based defect engineering is an effective activation method for enhancing the electrocatalytic activity of electrodes. Herein, the controllable formation of OV on the surface of a freestanding SnO2-Sb anode was achieved by the quantitative doping of La3+ into the SnO2 crystal structure of the anode for highperformance electrochemical wastewater treatment. The resultant SnOx/La-Sb anode degraded nearly 100% moxifloxacin (MOX, 10 mg L-1) in 30 min, with a low energy consumption of 0.09 kWh m- 3. The SnOx/La-Sb anode with an OV density of 1.09% had the highest degradation rate constant (0.226 min 1), 8 times higher than that of the SnO2-Sb anode and 16 times higher than that of the state-of-the-art boron-doped diamond anode. La3+ doping-induced OV activated the anode surface for electrochemical reactions by boosting the interfacial electron transfer and & BULL;OH generation (103% increase). The novel 3D permeable SnOx/La-Sb anode also exhibited remarkable stability (predicted service life of 59 years) and high-rate performance (> 98%) in a continuous flow through treatment system (< 1 min through the anode).
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