Metal-organic framework-derived Ni@C and NiO@C as anode catalysts for urea fuel cells

被引:48
|
作者
Thao Quynh Ngan Tran [1 ]
Park, Bang Ju [2 ]
Yun, Woo Hyun [3 ]
Tien Nhac Duong [3 ]
Yoon, Hyon Hee [3 ]
机构
[1] Ind Univ Ho Chi Minh City, Dept Machine & Equipment, Nguyen Van Bao, Hcmc, Vietnam
[2] Gachon Univ, Dept Elect Engn, 1342 Seongnam Daero, Seongnam 13120, Gyeonggi Do, South Korea
[3] Gachon Univ, Dept Chem & Bio Engn, 1342 Seongnam Daero, Seongnam 13120, Gyeonggi Do, South Korea
基金
新加坡国家研究基金会;
关键词
ELECTROCATALYTIC OXIDATION; DIRECT METHANOL; NICKEL; ELECTROOXIDATION; PERFORMANCE; GRAPHENE; GLUCOSE; NANOSHEETS; ELECTRODE;
D O I
10.1038/s41598-019-57139-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Highly porous self-assembled nanostructured Ni@C and NiO@C were synthesized via calcination of a Ni-based metal-organic framework. The morphology, structure, and composition of as synthesized Ni@C and NiO@C were characterized by SEM, FIB-SEM, TEM, and XRD. The electro-catalytic activity of the Ni@C and NiO@C catalysts towards urea oxidation was investigated using cyclic voltammetry. It was found that the Ni@C had a higher residual carbon content and a higher specific surface area than NiO@C, thus exhibiting an enhanced electrochemical performance for urea oxidation. A direct urea fuel cell with Ni@C as an anode catalyst featured an excellent maximum power density of 13.8 mW cm(-2) with 0.33 M urea solution in 1 M KOH as fuel and humidified air as oxidant at 50 degrees C, additionally showing excellent stability during continuous 20-h operation. Thus, this work showed that the highly porous carbon-supported Ni catalysts derived from Ni-based metal-organic framework can be used for urea oxidation and as an efficient anode material for urea fuel cells.
引用
收藏
页数:10
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