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.
引用
收藏
页码:5087 / 5098
页数:12
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