{"title":"Effect of Interfacial Interaction on Electrocatalytic Activity and Durability of Pt-Based Core–Shell Nanocatalysts","authors":"Shangdong Ji, Cong Zhang, Ruiyun Guo, Yongjun Jiang, Tianou He, Qi Zhan, Rui Li, Yangzi Zheng, Yanan Li, Sheng Dai, Xiaolong Yang, Mingshang Jin","doi":"10.1021/acscatal.4c02045","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":"5 1","pages":""},"PeriodicalIF":11.3000,"publicationDate":"2024-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acscatal.4c02045","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
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.
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.