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NiCo layered double hydroxide/hydroxide nanosheet heterostructures for highly efficient electro-oxidation of urea
被引:73
|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.
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页码:19206 / 19213
页数:8
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