Selenate-based heterojunction with cobalt–nickel paired site for electrocatalytic oxidation of 5-hydroxymethylfurfural coupling water splitting to produce hydrogen

被引:0
|
作者
Yang, Zhengru [1 ]
Hui, Jia [2 ]
Fan, Wangxi [1 ]
Liu, Pengcheng [1 ]
Zhang, Chunyong [1 ]
Dong, Shuang [3 ]
Yang, Zhou [1 ]
机构
[1] Department of Chemistry and Chemical Engineering, & Jiangsu Key Laboratory of Clean Energy Storage and Conversion, Jiangsu University of Technology, Jiangsu, Changzhou,213001, China
[2] Engineering Technology and Materials Research Center, China Academy of Transportation Sciences, Beijing,100029, China
[3] School of Chemical Engineering and Materials, Changzhou Institute of Technology, Jiangsu, Changzhou,213032, China
基金
中国国家自然科学基金;
关键词
Bioremediation - Hydrogen evolution reaction - Nickel;
D O I
10.1016/j.jechem.2024.09.045
中图分类号
学科分类号
摘要
It is very appealing that 5-hydroxymethylfurfural (HMF) is electrocatalytical oxidized as 2,5-furandicarboxylic acid (FDCA) linking to non-classical cathodic hydrogen (H2) production. However, the electrocatalysts for electrocatalytic HMF oxidative reaction (e-HMFOR) have been facing low Faradaic efficiency (FE) and high water splitting voltage. Herein, we propose a strategy of the NiSeO3@(CoSeO3)4 heterojunction by constructing a Co-Ni paired site, where the Co site is in charge of adsorbing for HMF while the electrons are transferred to the Ni site, thus giving the NiSeO3@(CoSeO3)4 heterojunction superior electrocatalytic performances for e-HMFOR and water splitting. By optimizing conditions, the NiSeO3@(CoSeO3)4 heterojunction has high conversion of 99.7%, high selectivity of 99.9%, and high FE of 98.4% at 1.3 V, as well as low cell voltage of 1.31 V at 10 mA cm−2 in 1 M KOH + 0.1 M HMF. This study offers a potential insight for e-HMFOR to high value-added FDCA coupling water splitting to produce H2 in an economical manner. © 2024 Science Press
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页码:156 / 162
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