期刊
ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 7, 期 13, 页码 11186-11193出版社
AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.9b00355
关键词
Fuel cell; direct ethanol fuel cell; porous nickel electrode; power density; palladium nanoparticle; electrochemically active surface area
资金
- National Natural Science Foundation of China [51776156, 51806165]
- Natural Science Basic Research Plan in Shaanxi Province of China [2019JM-011]
The low performance and low catalyst utilization of electrodes have been challenging issues for anion-exchange membrane direct liquid fuel cells (AEM DLFCs).. Herein, a high-utilization and high-activity three-dimensional electrode that enables palladium nanoparticles to be directly dispersed on carbon-decorated porous nickel is reported by a facile and well-controlled fabricating method. The as-synthesized Pd@C-Ni electrode possesses an electrochemically active surface area as high as 121.8 m(2) g(-1), 1 order of magnitude higher than conventional Pd/C@CP electrode. The electro-oxidation of ethanol in Pd@C-Ni shows a low onset potential (0.3 V) and a high peak current density (0.16 A cm(-2)) in alkaline environment. When Pd@C-Ni acts as anode in an AEM direct ethanol fuel cell (DEFC), the peak power density up to 202 mW cm(-2) is achieved at 60 degrees C, representing the best performance for oxygen-based AEM DEFCs reported in the open literature under the same operating temperature. Additionally, a stable 16 h discharge at 100 mA cm(-2) demonstrates its good stability. This work presents an effective strategy for high-performance DLFCs.
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