CeO2 as an "electron pump" to boost the performance of Co4N in electrocatalytic hydrogen evolution, oxygen evolution and biomass oxidation valorization

被引:123
作者
Zhou, Peiyun [1 ]
Hai, Guangtong [2 ]
Zhao, Gongchi [1 ]
Li, Rushuo [1 ]
Huang, Xiubing [1 ]
Lu, Yunfeng [3 ]
Wang, Ge [1 ,4 ]
机构
[1] Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing Adv Innovat Ctr Mat Genome Engn, Beijing Key Lab Funct Mat Mol & Struct Construct, Beijing 100083, Peoples R China
[2] Tsinghua Univ, Dept Chem Engn, Beijing 100084, Peoples R China
[3] Univ Calif Los Angeles, Dept Chem & Biomol Engn, Los Angeles, CA 90095 USA
[4] Univ Sci & Technol Beijing, Shunde Grad Sch, Shunde 528399, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2023年 / 325卷
基金
中国国家自然科学基金;
关键词
Heterointerfaces; HER; OER; HMFOR; Alkaline electrolysis; POROUS NANOWIRES; CARBONATE; ALKALINE;
D O I
10.1016/j.apcatb.2023.122364
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
Developing multifunctional electrocatalysts with excellent hydrogen evolution reaction (HER), oxygen evolution reaction (OER) and 5-hydroxymethylfurfural oxidation reaction (HMFOR) activities will contribute to "carbon neutrality". Here, CeO2 is introduced into the Co4N system as an "electron pump" to attract electrons to transfer from Co4N to CeO2. The interface electronic structure optimization enables Co4N@CeO2 to exhibit excellent HER, OER, and HMFOR performance. Specifically, to deliver 10 mA cm(-2) current density, (1) it only requires low overpotentials of 49 and 263 mV for HER and OER in 1.0 M KOH, respectively; (2) it merely needs an ultra-low potential of 1.22 V-RHE for HMFOR in 1.0 M KOH + 300 mM HMF, which is 273 mV lower than the required potential in 1.0 M KOH. Theoretical calculation results show that the introduction of CeO2 effectively reduces the barriers for potential-determining steps of HER and OER, and optimizes OH- adsorption to promote the HMFOR process.
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页数:14
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