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Tribological properties of materials play an important role in engineering applications. Up to now, a number of experimental studies have identified correlations between tribological parameters and the mechanical response. Using molecular dynamics simulations, we study abrasive wear behavior via nanoscratching of a Cu$_{64.5}$Zr$_{35.5}$ metallic glass. The evolution of the normal and transverse forces and hardness values follows the behavior well known for crystalline substrates. In particular, the generation of the frontal pileup weakens the response of the material to the scratching tip and leads to a decrease of the transverse hardness as compared to the normal hardness. However, metallic glasses soften with increasing temperature, particularly above the glass transition temperature thus showing a higher tendency to structurally relax an applied stress. This plastic response is analyzed focusing on local regions of atoms which underwent strong von-Mises strains, since these are the basis of shear-transformation zones and shear bands. The volume occupied by these atoms increases with temperature, but large increases are only observed above the glass transition temperature. We quantify the generation of plasticity by the concept of plastic efficiency, which relates the generation of plastic volume inside the sample with the formation of external damage, viz. the scratch groove. In comparison to nanoindentation, the generation rate of the plastic volume during nanoscratching is significantly temperature dependent making the glass inside more damage-tolerant at lower temperature but more damage-susceptible at elevated temperatures.
Using molecular dynamics simulation, we study the plastic zone created during nanoindentation of a large CuZr glass system. The plastic zone consists of a core region, in which virtually every atom undergoes plastic rearrangement, and a tail, where t
The atomic theory of elasticity of amorphous solids, based on the nonaffine response formalism, is extended into the nonlinear stress-strain regime by coupling with the underlying irreversible many-body dynamics. The latter is implemented in compact
We numerically study the evolution of the vibrational density of states $D(omega)$ of zero-temperature glasses when their kinetic stability is varied over an extremely broad range, ranging from poorly annealed glasses obtained by instantaneous quench
We image local structural rearrangements in soft colloidal glasses under small periodic perturbations induced by thermal cycling. Local structural entropy $S_{2}$ positively correlates with observed rearrangements in colloidal glasses. The high $S_{2
Dynamics of protein self-assembly on the inorganic surface and the resultant geometric patterns are visualized using high-speed atomic force microscopy. The time dynamics of the classical macroscopic descriptors such as 2D Fast Fourier Transforms (FF