{"title":"界面相互作用对铂基核壳纳米催化剂电催化活性和耐久性的影响","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":13.1000,"publicationDate":"2024-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"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\":13.1000,\"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}","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
摘要
铂基核壳纳米粒子是质子交换膜燃料电池中很有前途的一代高性能电催化剂,其催化性能主要取决于核壳与铂壳之间的界面相互作用。在此,我们以精确控制壳厚度的 Pd@Pd-P@Pt 核壳八面体为定义明确的平台,系统地研究了界面相互作用对电子结构和电催化性能的影响。实验和理论计算结果表明,铂-钯界面相互作用会降低铂位点的 d 带中心,增加铂位点的空位形成能,从而大幅提高氧还原反应的活性和持久性。这种增强效应在很大程度上取决于界面与铂位点之间的距离,而这可以通过仔细调节外壳厚度来调整。一旦外壳厚度超过 6 个原子层,界面相互作用对催化性能的增强效果就可以忽略不计了。
Effect of Interfacial Interaction on Electrocatalytic Activity and Durability of Pt-Based Core–Shell Nanocatalysts
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.