Defects-rich nickel nanoparticles grown on nickel foam as integrated electrodes for electrocatalytic oxidation of urea

被引:35
|
作者
Yan, Xiaodong [1 ]
Zhang, Wen-Da [1 ]
Hu, Qing-Tao [1 ]
Liu, Jiangyong [3 ]
Li, Tao [1 ]
Liu, Yuan [4 ]
Gu, Zhi-Guo [1 ,2 ]
机构
[1] Jiangnan Univ, Sch Chem & Mat Engn, Key Lab Synthet & Biol Colloids, Minist Educ, Wuxi 214122, Jiangsu, Peoples R China
[2] Jiangnan Univ, Int Joint Res Ctr Photorespons Mol & Mat, Sch Chem & Mat Engn, Wuxi 214122, Jiangsu, Peoples R China
[3] Yangzhou Univ, Sch Chem & Chem Engn, Yangzhou 225002, Jiangsu, Peoples R China
[4] Tsinghua Univ, Sch Mat Sci & Engn, State Key Lab New Ceram & Fine Proc, Beijing 100084, Peoples R China
基金
中国国家自然科学基金; 中央高校基本科研业务费专项资金资助;
关键词
Electro-oxidation; Catalysts; Urea; Nickle nanoparticles; Defects; OXIDE NANOPARTICLES; OXYGEN EVOLUTION; ELECTROOXIDATION; HYDROXIDE; CATALYST; NANOSHEETS; NI(OH)(2); MECHANISM; COBALT;
D O I
10.1016/j.ijhydene.2019.09.004
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
Designing highly efficient, low cost and long-term stable electro-catalysts is the key step for the commercial applications of fuel cells. Electro-oxidation of urea, a hydrogen-rich fuel, is the anodic reaction of direct urea fuel cells. Herein, defects-rich nickel nanoparticles grown on nickel foam as integrated electrodes have been designed and easily fabricated by incomplete reduction of Ni(OH)(2). The Ni2+ defects coupled with oxygen vacancies are proposed to be mainly present in the form of amorphous NiOx. which is the island phase in the metallic nickel nanoparticles and confirmed by transmission electron microscopy and X-ray photoelectron spectroscopy. The synergistic effect between metallic metal with high conductivity and numerous defects with good affinity to O contributes to the high catalytic activity towards oxidation of urea with an onset potential of 0.35 V vs Hg/ HgO in 2 M KOH +0.33 M urea. Additionally, the defects-rich nickel nanoparticles present good long-term stability. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:27664 / 27670
页数:7
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