【摘 要】
：
As a common electrocatalytic system,Au-Pt alloy particles are often prepared as Au-core-Pt-shell (Au@Pt) to make full use of plati-num.However,Au has a strong tendency to segregate to the outer surface,leading to the redistribution of the active sites.Unf
【机 构】
：
Key Laboratory for Advanced Materials,Centre for Computational Chemistry and Research Institute of I
论文部分内容阅读
As a common electrocatalytic system,Au-Pt alloy particles are often prepared as Au-core-Pt-shell (Au@Pt) to make full use of plati-num.However,Au has a strong tendency to segregate to the outer surface,leading to the redistribution of the active sites.Unfortu-nately,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 reac-tion (ORR) on this bimetallic Au@Pt system,oxygen adsorption energy calculations show that this reconstruction could not only in-crease the number of adsorption sites but also dramatically improve the ORR catalytic activity of each site,thus enhance the overall ORR reactivity.
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