期刊
APPLIED CATALYSIS B-ENVIRONMENTAL
卷 281, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.apcatb.2020.119535
关键词
Co3O4 oxygen vacancies; Fluorine substitution; Electrocatalysts; Oxygen evolution reaction
资金
- National Nature Science Foundation of China [21805209]
- Fundamental Research Funds for the Central Universities at Tongji University
- Fundamental Research Funds for the Central Universities at Jilin University
By introducing oxygen vacancies and fluorine anions, the catalytic activity for oxygen evolution reaction (OER) was enhanced. Theoretical calculations were consistent with experimental results, providing a pathway for designing new defective fluorinated oxides.
Mesoporous Co3O3.87 square(0.13) (square represents oxygen vacancies) and Co3O3.87F0.13 electrocatalysts, integrating ad-vantages of oxygen vacancies and fluorine anion, were deployed. Co3O3.87 square(0.13) and Co3O3.87F0.13 showed enhanced oxygen evolution reaction (OER) with overpotentials of 440 mV and 430 mV at 10 mA cm(-2), Tafel slopes of 56 mV dec(-1) and 56 mV dec(-1), turnover frequency (TOF eta= 400 mV) of 0.023 s(-1) and 0.042 s(-1) respectively, as compared to Co3O4 (520 mV, 64 mV dec(-1), 0.0005 s(-1)) in the alkaline medium. Physicochemical characterizations showed that oxygen vacancies and the substituted fluorine modified the electronic structure, leading to the enhanced activity for OER process, consistent with the theoretical calculation. This approach provides ideas for rational design of new defective fluorinated oxide, with the feasible extension of such an approach to a wide variety of transition metal oxides.
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