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Pd Monolayer on the 3D-Hollow-Porous Au Microsphere as an Advanced Electrocatalyst for the Ethanol Oxidation Reaction
被引:14
作者:
Chen, De Ping
[1
,2
]
Yuan, Lei
[1
]
Li, Meng Jue
[2
]
Han, Wen Jing
[1
]
Liu, Xu Dong
[1
]
Liu, Xi Chuan
[1
]
Wang, Chao Yang
[1
]
机构:
[1] China Acad Engn Phys, Res Ctr Laser Fus, Mianyang 621900, Sichuan, Peoples R China
[2] Chengdu Technol Univ, Sch Mat & Environm Engn, Chengdu 611730, Peoples R China
关键词:
hollow-porous structure;
ethanol oxidation;
electrocatalyst;
Pd monolayer;
Au microsphere;
PLATINUM-MONOLAYER;
BIMETALLIC NANOCRYSTALS;
ALCOHOL OXIDATION;
FACILE SYNTHESIS;
PALLADIUM;
SHELL;
NANOPARTICLES;
CATALYSTS;
ELECTROOXIDATION;
STABILITY;
D O I:
10.1021/acsaem.2c00369
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:
Pd is a highly active non-Pt anode in direct ethanol fuel cells, and its morphology and structural composition heavily influence its electrocatalytic efficiency. In this study, three-dimensional (3D)-hollow Au microspheres (HNPs-Au) as a support for the Pd monolayer (HNPs-Au@Pd) were synthesized using a simple template method and galvanic replacement reaction. The experimental results and theoretical calculations show that the presence of HNPs-Au enhances the catalytic activity of ethanol oxidation in alkaline media, improving the electroactivity of metallic Pd. Benefiting from the 3D-hollow-porous structure and the significant synergistic impact between Au and Pd (balancing the adsorption energy of the intermediate and reactant molecules), HNPs-Au@Pd achieves a 10.8-fold mass activity and a 3.3-fold enhancement of the specific activity for the ethanol oxidation reaction when compared to commercial Pd/C. The present work not only enriches the preparation strategy of porous metal materials but also opens up a sector for the construction of anodic electrocatalysts with a wide range of applications.
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页码:5087 / 5098
页数:12
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