文献类型：期刊文献

英文题名：Gold Segregation Improves Electrocatalytic Activity of Icosahedron Au@Pt Nanocluster: Insights from Machine Learning?

作者：Chen, Dingming;Lai, Zhuangzhuang;Zhang, Jiawei;Chen, Jianfu;Hu, Peijun;Wang, Haifeng[1]

机构：[1]East China Univ Sci & Technol, Sch Chem & Mol Engn, Ctr Computat Chem, Key Lab Adv Mat, Shanghai 200237, Peoples R China; East China Univ Sci & Technol, Sch Chem & Mol Engn, Res Inst Ind Catalysis, Shanghai 200237, Peoples R China

年份：2021

卷号：39

期号：11

起止页码：3029

外文期刊名：CHINESE JOURNAL OF CHEMISTRY

收录：;WOS:【SCI-EXPANDED(收录号:WOS:000692937900001)】；

基金：This project was supported by the National Natural Science Foundation of China (Nos. 21873028, 91945302), the National Ten Thousand Talent Program for Young Top-notch Talents in China, Shanghai ShuGuang Project (No. 17SG30), and the Fundamental Research Funds for the Central Universities.

语种：英文

外文关键词：Machine learning; Density functional calculations; Genetic algorithm; Nanostructures; O-O activation

摘要：Main observation and conclusion As a common electrocatalytic system, Au-Pt alloy particles are often prepared as Au-core-Pt-shell (Au@Pt) to make full use of platinum. However, Au has a strong tendency to segregate to the outer surface, leading to the redistribution of the active sites. Unfortunately, the mechanism of such reconstruction and its effect on the electrocatalytic activity have not been thoroughly discussed, largely owing to the complexity of in-situ characterization and computational modeling. Herein, by taking the 55-atom Au13Pt42 core-shell nanocluster as an example, we utilized the neural network potential at density functional theory (DFT) level and the genetic algorithm to search the complex global configurational space. It turns out that it is thermodynamically favorable when all gold atoms are segregated to the surface and the shape of the cluster tends to change from icosahedron to a distorted amorphous structure (at a reduced core, DRC) with a unique gold distribution. Towards understanding the dynamic activity variation of oxygen reduction reaction (ORR) on this bimetallic Au@Pt system, oxygen adsorption energy calculations show that this reconstruction could not only increase the number of adsorption sites but also dramatically improve the ORR catalytic activity of each site, thus enhance the overall ORR reactivity.