On the Atomic Scale Diffusion in Au-Ag Nanoparticles

被引:2
|
作者
Olshin, Pavel K. [1 ]
Sheardy, Alex T. [1 ]
Zhukovskyi, Maksym A. [2 ]
Mukasyan, Alexander S. [1 ,2 ]
机构
[1] Univ Notre Dame, Dept Chem & Biomol Engn, Notre Dame, IN 46556 USA
[2] Univ Notre Dame, Notre Dame Integrated Imaging Facil, Notre Dame, IN 46556 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2024年 / 128卷 / 09期
关键词
SELF-DIFFUSION; GOLD; CLUSTERS;
D O I
10.1021/acs.jpcc.3c08368
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 reported in situ scanning electron microscopy studies of the diffusion process in individual core-shell Au-Ag particles in the temperature range of 548-723 K. The diameter of the Au core was similar to 6 nm, and the thickness of the Ag shell was 6.5 nm. We studied diffusion across defect-free boundaries between the metals with a spatial resolution of 0.11 nm. The activation energy and frequency factor for defect-free particles are E-a = 167 +/- 6 kJ/mol and D-0 = (1.8 +/- 0.6) <middle dot> 10(-3) cm(2)/s, respectively. These values are similar to those for bulk materials. The diffusion coefficient for the particles with boundary defects was shown to be several orders of magnitude higher than that for the defect-free particles. Obtained results allow us to rationally explain all reported results on solid-state diffusion in the Au-Ag systems, mainly that the self-alloying is primarily the result of the defects rather than the size of the particles.
引用
收藏
页码:4079 / 4085
页数:7
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