Editors: | F. Kongoli, E. Aifantis, T. Vougiouklis, A. Bountis, P. Mandell, R. Santilli, A. Konstantinidis, G. Efremidis. |
Publisher: | Flogen Star OUTREACH |
Publication Year: | 2022 |
Pages: | 235 pages |
ISBN: | 978-1-989820-64-3(CD) |
ISSN: | 2291-1227 (Metals and Materials Processing in a Clean Environment Series) |
We studied the uniaxial compression behavior of micro- and nanoparticles of several elemental metals (Au [1], Ni [2], Ag [3], Mo [4]) and alloys (Ni-Fe, Ni-Co [5], Au-Ag). The particles were obtained by solid state dewetting of thin metal films and multilayers deposited on sapphire substrates. The high homological temperatures employed in the dewetting process ensure the low concentration of dislocations and their sources in the particles. The particles compressed with a flat diamond punch exhibit purely elastic behavior up to very high values of strain approaching 10%, followed by a catastrophic plastic collapse. The uniaxial yield strength of the particles defined as an engineering stress at the point of catastrophic collapse reached the astonishing values of 34 GPa and 46 GPa for the smallest faceted particles of Ni and Mo, respectively. The atomistic molecular dynamic simulations of the particle compression demonstrated that the catastrophic plastic yielding of the particles is associated with the multiple nucleation of dislocations at the facet corners or inside the particles. The latter, homogeneous nucleation mode resulted in higher particle strength. The size effect in compression was observed both in the experiments and in atomistic simulations, with smaller particles exhibiting higher compressive strength. In contrast with the solute hardening observed in bulk alloys, alloying the pure metal nanoparticles with a second component resulted in significant decrease of their strength. Finally, we produced Au-Ag core-shell nanoparticles by coating the single crystalline Ag nanoparticles with a polycrystalline Au shell. The core-shell nanoparticles exhibited much lower strength than their single crystalline pure Ag counterparts. We related this decrease in strength with the activity of grain boundaries in the polycrystalline Au shell.