Abstract
Relaxation dynamics are the central topic in glassy physics. Recently, there is an emerging view that mechanical strain plays a similar role as temperature in altering the relaxation dynamics. Here, we report that mechanical strain in a model metallic glass modulates the relaxation dynamics in unexpected ways. We find that a large strain amplitude makes a fragile liquid become stronger, reduces dynamical heterogeneity at the glass transition and broadens the loss spectra asymmetrically, in addition to speeding up the relaxation dynamics. These findings demonstrate the distinctive roles of strain compared with temperature on the relaxation dynamics and indicate that dynamical heterogeneity inherently relates to the fragility of glass-forming materials.
Highlights
Relaxation dynamics are the central topic in glassy physics
The basic question whether temperature and stress have similar or different role in relaxation dynamics of metallic glasses (MGs) is still not clear. We address this issue by studying the relaxation spectra of a model MG in the parameter space of temperature, frequency and strain amplitude, via a recently proposed molecular dynamics simulation of dynamical mechanical spectroscopy (MD-DMS)[27] together with structural analysis
We find that mechanical strain accelerates the relaxation dynamics as previously assumed and alters it in unexpected ways: a fragile MG gradually becomes a strong one under increasing strain, together with a phenomenon of broadening the peak of a relaxation on the loss spectra only for the lowtemperature side
Summary
Relaxation dynamics are the central topic in glassy physics. Recently, there is an emerging view that mechanical strain plays a similar role as temperature in altering the relaxation dynamics. We find that mechanical strain accelerates the relaxation dynamics as previously assumed and alters it in unexpected ways: a fragile MG gradually becomes a strong one under increasing strain, together with a phenomenon of broadening the peak of a relaxation on the loss spectra only for the lowtemperature side (while the high-temperature side remains almost unchanged). These processes are accompanied by a suppression of dynamical heterogeneity at the glass transition, demonstrating the key role of dynamical heterogeneity in controlling the fragility of glass-forming materials
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