Bifunctional integrated electrode for high-efficient hydrogen production coupled with 5-hydroxymethylfurfural oxidation

被引:135
作者
Song, Yuke [1 ]
Xie, Wenfu [1 ]
Song, Yingjie [1 ]
Li, Hao [2 ]
Li, Shijin [1 ]
Jiang, Shan [1 ]
Lee, Jin Yong [2 ]
Shao, Mingfei [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Sungkyunkwan Univ, Dept Chem, Suwon 16419, South Korea
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2022年 / 312卷
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Hydrogen evolution; Integrated electrode; Biomass oxidation; Transition-metal phosphides; Coupled oxidation; ELECTROCHEMICAL OXIDATION; WATER; PERFORMANCE; NANOSHEETS; COBALT; ACID; NI;
D O I
10.1016/j.apcatb.2022.121400
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 sluggish oxygen evolution reaction (OER) limits the efficiency of overall water splitting, which thereby hinders hydrogen evolution reaction (HER). Here, we demonstrate a bifunctional CoNiP nanosheet integrated electrode (CoNiP-NIE) to boost HER and replace OER by 5-hydroxymethylfurfural oxidation reaction (HMFOR) to obtain high-valued 2,5-furandicarboxylic acid (FDCA). The as-developed CoNiP-NIE exhibits a constant high Faradaic efficiency more than 82% for HMFOR in a wide potential from 1.40 V to 1.70 V vs. RHE, which stand at the top level among the reported electrocatalysts. Moreover, the low overpotential for HER further indicates its high efficiency in the H2 generation. Based on the bifunctional activity of CoNiP, an electrochemical hydrogen evolution coupled with biomass oxidation device is constructed, which delivers lower voltage (1.46 V) for anode oxidation and higher evolution rate of H-2 (41.2 L h(-1) m(-2)) than water splitting (1.76 V, 16.1 L h(-1) m(-2)).
引用
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页数:9
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