Systematics of vibrational properties of Au nanoparticles: a molecular dynamics approach

Abstract

This paper reports the results of a Molecular Dynamics (MD) study of the vibrational properties of spherical Au nanoparticles with a number of atoms (N) varying in the range 1985 ≤ N ≤ 53 117. The LAMMPS code is adopted to calculate the vibrational density of states (VDOS), represented by D(ω) versus ω function. Two interatomic potentials, an EAM and a MEAM are used. The first part of the work is devoted to the D(ω) versus ω relation of macroscopic Au, which is obtained by MD simulations as well as by a density-functional-theory calculation using the Vienna Ab Initio Simulation Package and the PHONOPY code. Additional experimental and theoretical results on the VDOS of Au are used to compare with the present results. Next, the effect of changing N and the interatomic potential upon the VDOS of the nanoparticles is established. In particular, the effect of the surface vibrational modes upon the results is discussed. Various moment frequency parameters ω_D(j) expressing averages of the D(ω) versus ω function are evaluated, and expressed as Debye temperatures θ_D(j), using standard relations. Attending to the relevance of these quantities in the description of the thermodynamic properties of macroscopic solids, values of θ_D(j) corresponding to j = −3, 0, 1, 2 and 4 are reported. On this basis, a picture of the systematic effects of changing N upon the θ_D(j) values is established both for the EAM and the MEAM potential. In addition, various interrelations between the θ_D(j) values for nanoparticles are presented. In particular, remarkably simple correlations are reported between the average quantities θ_D(0), θ_D(1), θ_D(2) and θ_D(4) and θ_D(−3) i.e., the Debye temperature which accounts for the low-frequency part of the spectrum. Finally, a discussion is reported of the relation between θ_D(−3) and other properties that are usually adopted as a measure of cohesion in macroscopic solids. To this aim, new correlations involving the nanoscopic counterpart of the temperature of fusion of macroscopic elements as well as the cohesive energy for Au nanoparticles are presented.