纳米材料基催化剂
耐久性
芯(光纤)
催化作用
质子交换膜燃料电池
壳体(结构)
空位缺陷
材料科学
纳米颗粒
氧还原反应
化学
化学工程
纳米技术
复合材料
结晶学
电化学
工程类
物理化学
电极
生物化学
作者
Shangdong Ji,Cong Zhang,Ruiyun Guo,Yongjun Jiang,Tianou He,Qi Zhan,Rui Li,Yangzi Zheng,Yanan Li,Sheng Dai,Xiaolong Yang,Mingshang Jin
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2024-07-24
卷期号:14 (15): 11721-11732
被引量:31
标识
DOI:10.1021/acscatal.4c02045
摘要
Pt-based core–shell nanoparticles have presented a promising generation of high-performance electrocatalysts for proton-exchange membrane fuel cells, with their catalytic performance primarily dependent on the interfacial interaction between the core and Pt shell. Here we systematically investigated the impact of interfacial interaction on electronic structure and electrocatalytic performance by using Pd@Pd–P@Pt core–shell octahedra with precisely controlled shell thicknesses as a well-defined platform. Experimental and theoretical calculation results demonstrate that the Pt–P interfacial interaction would lower the d-band center and increase the vacancy formation energy of Pt sites, thereby substantially enhancing both the activity and durability of the oxygen reduction reaction. Such enhancement effect is highly dependent on the distance between the interface and the Pt sites, which can be tuned via careful manipulation of the shell thickness. Once the shell thickness exceeds 6 atomic layers, the enhancement effect of interfacial interaction on the catalytic performance becomes negligible.
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