Magic compositions in Pd-Au nanoalloys

被引:15
|
作者
Zhu, Beien [1 ,2 ]
Front, Alexis [3 ]
Guesmi, Hazar [4 ]
Creuze, Jerome [5 ]
Legrand, Bernard [6 ]
Mottet, Christine [3 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Appl Phys, Div Interfacial Water, Shanghai 201800, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Appl Phys, Key Lab Interfacial Phys & Technol, Shanghai 201800, Peoples R China
[3] Aix Marseille Univ, CNRS, CINaM UMR7325, Campus Luminy, F-13288 Marseille, France
[4] ICGM MACS, UMR5253, 8 Rue Ecole Normale, F-34296 Montpellier, France
[5] Paris Saclay Univ, Paris Sud Univ, ICMMO SP2M, UMR8182, 15 Rue Georges Clmenceau, F-91405 Orsay, France
[6] Paris Saclay Univ, CEA Saclay, SRMP DMN, F-91191 Gif Sur Yvette, France
关键词
Monte Carlo simulations; Metallic alloy nanoparticles; Surface segregation; Chemical ordering; PALLADIUM-GOLD; CLUSTERS; NANOPARTICLES; NANOCLUSTERS; TRANSITIONS; ATOMS;
D O I
10.1016/j.comptc.2016.12.023
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We identified new magic compositions of Pd-Au nanolloys of simple symmetries according to the icosa-hedral and the cubic truncated octahedral structures. Chemically ordered structures as well as segregated ones are characterized using Monte Carlo simulations in semi-grand canonical ensemble and tight binding semi-empirical potential fitted to ab initio calculations for the Pd-Au system. Ordering and surface (or core) segregation phenomena can be distinguished by their behavior as a function of the temperature: chemical ordering at surface or in the core disappears above a critical temperature (which is lower or equal to the bulk alloy order-disorder temperature), whereas surface/core segregation (core-shell structures) remains at high temperature, although the interfacial profile is less abrupt. (C) 2016 Elsevier B.V. All rights reserved.
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页码:49 / 56
页数:8
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