Exsolved Co3O4 with tunable oxygen vacancies for electrocatalytic H2O2 production

被引:43
作者
Yan, Lina [1 ]
Cheng, Xing [1 ]
Wang, Yueshuai [2 ]
Wang, Zhaozhao [3 ]
Zheng, Lirong [4 ]
Yan, Yong [1 ]
Lu, Yue [2 ]
Sun, Shaorui [1 ]
Qiu, Wenge [1 ]
Chen, Ge [1 ]
机构
[1] Beijing Univ Technol, Fac Environm & Life, Beijing Key Lab Green Catalysis & Separat, Beijing 100124, Peoples R China
[2] Beijing Univ Technol, Fac Mat & Mfg, Beijing Key Lab Microstruct & Properties Solids, Beijing 100124, Peoples R China
[3] Hebei Univ Engn, Hebei Technol Innovat Ctr Water Pollut Control &, Sch Energy & Environm Engn, Handan 056038, Peoples R China
[4] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Exsolution; Cobaltosic oxide; Oxygen vacancy; ORR; Hydrogen peroxide production; HYDROGEN-PEROXIDE; ELECTROCHEMICAL SYNTHESIS; PERFORMANCE; SELECTIVITY; REDUCTION; 1ST-PRINCIPLES; CARBON;
D O I
10.1016/j.mtener.2021.100931
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
The electrochemical production of hydrogen peroxide via the two-electron (2e(-)) oxygen reduction reaction (ORR) is an environmentally friendly method and is expected to be an alternative means to the industrial anthraquinone process. It is particularly suitable for on-site and small-scale H2O2 requirements. The development of earth-abundant catalysts with high activity and selectivity toward H2O2 is highly desirable and challenging. Here, we have prepared Co3O4 with tunable oxygen vacancies (OVs) and strongly coupled it to nitrogen-doped carbon nanotubes through an exsolution strategy. The Co3O4 with a higher OV concentration exhibits a higher 2e(-) ORR activity, higher H2O2 selectivity, and lower H2O2 reduction reaction (H2O2RR) activity so that effectively improving the production rate of H2O2 (1.6 mol peroxide/gcatalyst/h at 0.0 VRHE) in acidic media. The catalyst is also used as a cathode for the electro-Fenton process and degrades up to 80% of 40 mg/L of rhodamine B solution within 25 min. Density functional theory calculation shows that the *OOH binding energy (Delta G(*OOH)) could decrease on increasing the numbers of OVs, which subsequently benefits the protonation of *OOH to generate H2O2. (c) 2021 Elsevier Ltd. All rights reserved.
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页数:8
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