Steering benzyl alcohol electrooxidation coupled with hydrogen evolution via hetero-interface construction

被引:3
|
作者
Du, Xin [1 ]
Xie, Wenfu [2 ]
Wang, Yanfei [3 ]
Li, Hao [4 ]
Li, Jinze [1 ]
Li, Yang [1 ]
Song, Yuke [1 ]
Li, Zhenhua [1 ]
Lee, Jin Yong [4 ]
Shao, Mingfei [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Beijing Forestry Univ, Coll Environm Sci & Engn, Engn Res Ctr Water Pollut Source Control & Ecoreme, Beijing Key Lab Source Control Technol Water Pollu, Beijing 100083, Peoples R China
[3] Petrochina Petrochem Res Inst, Beijing, Peoples R China
[4] Sungkyunkwan Univ, Dept Chem, Suwon 16419, South Korea
基金
中国国家自然科学基金; 新加坡国家研究基金会;
关键词
benzyl alcohol oxidation; coupling system; electrocatalysis; hetero-interface; hydrogen production; ELECTROCATALYTIC 5-HYDROXYMETHYLFURFURAL OXIDATION; LIQUID-PHASE OXIDATION; OXYGEN EVOLUTION; CUO NANOWIRES; INTERFACE; ELECTRODE; BEHAVIOR; ALLOY;
D O I
10.1002/aic.18469
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
It is still a challenge to develop electrocatalyst for the efficient adsorption and conversion of organic molecule in aqueous media. Herein, a hetero-interface structure based on CuO@Ni(OH)2 is rationally designed to enhance the performance of benzyl alcohol oxidation to benzoic acid. A high Faradaic efficiency of 99% and the yield of 3.09 mmol cm-2 h-1 are achieved at 1.70 V versus reversible hydrogen electrode, outperforming the previously reported electrocatalysts. Furthermore, a membrane-free flow electrolyzer was assembled based on CuO@Ni(OH)2 hetero-interface, exhibiting a much high yielding of benzoic acid (6.73 mmol cm-2 h-1) and hydrogen (0.35 L cm-2 h-1) with excellent stability. Both experimental data and density functional theory calculations verify that the electron is tend to accumulate at the hetero-interface, thus accelerating the adsorption of reactant and intermediate and reducing the energy barrier of the conversion of benzyl alcohol to benzoic acid.
引用
收藏
页数:12
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