Understanding Chemical Ordering in Bimetallic Nanoparticles from Atomic-Scale Simulations: The Competition between Bulk, Surface, and Strain
Journal article, 2018

Bimetallic nanoparticles are highly relevant for applications in, e.g., catalysis, sensing, and energy harvesting. Their properties are determined by their shape, size, and, most notably, their chemical configuration, i.e., the elemental distribution throughout the particle. To fully exploit their potential, a comprehensive understanding of the coupling among size, shape, and chemical ordering is crucial. Here, we employ hybrid molecular dynamics-Monte Carlo simulations to reveal the energetics of two prototypical nanoalloys, Ag-Cu and Au-Pd, by comprehensive sampling across the full composition range, while considering both size and shape as parameters. Our simulations expose the interplay among bulk thermodynamics, surface energetics, and strain. Relative to the bulk, the behavior of Au-Pd nanoalloys is dominated by surface segregation, and is thus largely independent of particle size and shape. By contrast, strain plays a key role in the Ag-Cu system, in which size and, even more so, shape have a strong impact on the overall energetics and accordingly the elemental distribution. This effect is reflected by the sign of the mixing energy curve, which in the case of the Ag-Cu system changes from positive to negative when going from the bulk to the nanoscale. Although this suggests miscibility, it is rather a manifestation of segregation to different sites.

Author

Magnus Rahm

Chalmers, Physics, Materials and Surface Theory

Paul Erhart

Chalmers, Physics, Materials and Surface Theory

Journal of Physical Chemistry C

1932-7447 (ISSN) 1932-7455 (eISSN)

Vol. 122 49 28439-28445

Nanolegeringar för plasmoniska tillämpningar

Swedish Research Council (VR), 2016-01-01 -- 2019-12-31.

Subject Categories

Physical Chemistry

Other Chemistry Topics

Theoretical Chemistry

DOI

10.1021/acs.jpcc.8b10874

More information

Latest update

1/2/2019 2