Unraveling the Role of F in Electrochemical Ozone Generation on the F-Doped PbO2 Electrode

被引:6
作者
Yu, Qiuyang [1 ]
Jiang, Ziyi [1 ]
Yin, Jinlong [1 ]
Chen, Shengli [1 ]
Hu, Xiaohong [1 ]
机构
[1] Wuhan Univ, Hubei Key Lab Electrochem Power Source, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
关键词
RAY PHOTOELECTRON-SPECTRA; OXYGEN EVOLUTION; LEAD DIOXIDE; ANODIC EVOLUTION; WATER ELECTROLYSIS; ELECTROCATALYSIS; ADSORPTION; KINETICS; SURFACE; OXIDE;
D O I
10.1021/acs.jpcc.2c05174
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
Because of its metal-like conductivity, excellent catalytic activity, and acid resistance, lead dioxide (PbO2) is the most used electrocatalyst for the practical electrochemical ozone electrodes or electrolytes can significantly improve EOP activity. However, there is still lack of valid evidence on understanding the role of doping F in the PbO2 electrode. In this work, we report a comprehensive study on the effect of F on EOP activity on electrochemically prepared PbO2 electrodes. F doping suppresses the side reaction of dioxygen (O-2) evolution by inhibiting the formation of an alpha phase impurity of PbO2 electrodes. The more hydrophobic surfaces by doping F promote O-2 adsorption as evidenced by low-temperature O-2-temperature-programmed desorption experiments and thus are more favorable for ozone (O-3) generation. The in situ isotope labeling oxygen (O-18(2)) experiment proves that at room temperature, O-2 can adsorb and dissociate on the operando PbO2 electrode surface and participate in the formation of O-3 molecules. This work provides a comprehensive understanding of doping F for enhanced EOP.
引用
收藏
页码:19397 / 19408
页数:12
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