NiCo layered double hydroxide/hydroxide nanosheet heterostructures for highly efficient electro-oxidation of urea

被引:64
|
作者
Yan, Xiaodong [1 ]
Hu, Qing-Tao [1 ]
Wang, Guihua [1 ]
Zhang, Wen-Da [1 ]
Liu, Jiangyong [3 ]
Li, Tao [1 ]
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
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
Urea electro-oxidation; Catalyst; Nickel cobalt binary metal; hydroxide; Nanosheet; Heterostructure; ELECTROCATALYTIC OXIDATION; NANOWIRE ARRAYS; NICKEL; OXIDE; HYDROXIDE; CO2; CATALYSTS; GRAPHENE; COBALT; ARCHITECTURE;
D O I
10.1016/j.ijhydene.2020.05.052
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
Urea oxidation is an important reaction for direct urea fuel cells as well as hydrogen production and/or water remediation via electrolysis using urea-rich wastewater. The key to efficient urea oxidation is to explore a well-designed high-performing catalyst. Herein, NiCo layered double hydroxide/hydroxide (NiCo LDH/NiCo(OH)(2)) microspheres composed of ultrasmall nanosheets have been grown on Ni foam by a solution method at room temperature. The NiCo LDH/NiCo(OH)(2) heterostructures have been confirmed by TEM and XRD analysis. The high activity with a small onset potential of 0.29 V vs. Hg/HgO is mainly attributed to the rich NiCo LDH-NiCo(OH)(2) interfaces and the bimetallic nature of the catalysts. The NiCo LDH/NiCo(OH)(2) heterostructures can be promising catalysts for urea oxidation and offer new insights into the design of high-performance nickel-based catalysts. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:19206 / 19213
页数:8
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