ترغب بنشر مسار تعليمي؟ اضغط هنا

Tracking the connection between disorder and energy landscape in glasses using geologically hyperaged amber

107   0   0.0 ( 0 )
 نشر من قبل Carino Ferrante
 تاريخ النشر 2019
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

Fossil amber offers the unique opportunity of investigating an amorphous material which has been exploring its energy landscape for more than 110 Myears of natural aging. By applying different x-ray scattering methods to amber before and after annealing the sample to erase its thermal history, we identify a link between the potential energy landscape and the structural and vibrational properties of glasses. We find that hyperaging induces a depletion of the vibrational density of states in the THz region, also ruling the sound dispersion and attenuation properties of the corresponding acoustic waves. Critically, this is accompanied by a densification with structural implications different in nature from that caused by hydrostatic compression. Our results, rationalized within the framework of fluctuating elasticity theory, reveal how upon approaching the bottom of the potential energy landscape (9% decrease in the fictive temperature $T_f$) the elastic matrix becomes increasingly less disordered (6%) and longer-range correlated (22%).



قيم البحث

اقرأ أيضاً

We present results of numerical simulations on a one-dimensional Ising spin glass with long-range interactions. Parameters of the model are chosen such that it is a proxy for a short-range spin glass above the upper critical dimension (i.e. in the me an-field regime). The system is quenched to a temperature well below the transition temperature $T_c$ and the growth of correlations is observed. The spatial decay of the correlations at distances less than the dynamic correlation length $xi(t)$ agrees quantitatively with the predictions of a static theory, the metastate, evaluated according to the replica symmetry breaking (RSB) theory. We also compute the dynamic exponent $z(T)$ defined by $xi(t) propto t^{1/z(T)}$ and find that it is compatible with the mean-field value of the critical dynamical exponent for short range spin glasses.
We study the problem of glassy relaxations in the presence of an external field in the highly controlled context of a spin-glass simulation. We consider a small spin glass in three dimensions (specifically, a lattice of size L=8, small enough to be e quilibrated through a Parallel Tempering simulations at low temperatures, deep in the spin glass phase). After equilibrating the sample, an external field is switched on, and the subsequent dynamics is studied. The field turns out to reduce the relaxation time, but huge statistical fluctuations are found when different samples are compared. After taking care of these fluctuations we find that the expected linear regime is very narrow. Nevertheless, when regarded as a purely numerical method, we find that the external field is extremely effective in reducing the relaxation times.
Recent numerical studies on glassy systems provide evidences for a population of non-Goldstone modes (NGMs) in the low-frequency spectrum of the vibrational density of states $D(omega)$. Similarly to Goldstone modes (GMs), i. e., phonons in solids, N GMs are soft low-energy excitations. However, differently from GMs, NGMs are localized excitations. Here we first show that the parental temperature $T^*$ modifies the GM/NGM ratio in $D(omega)$. In particular, the phonon attenuation is reflected in a parental temperature dependency of the exponent $s(T^*)$ in the low-frequency power law $D(omega) sim omega^{s(T^*)}$, with $2 leq s(T^*) leq 4 $. Secondly, by comparing $s(T^*)$ with $s(p)$, i. e., the same quantity obtained by pinning mttp{a} $p$ particle fraction, we suggest that $s(T^*)$ reflects the presence of dynamical heterogeneous regions of size $xi^3 propto p$. Finally, we provide an estimate of $xi$ as a function of $T^*$, finding a mild power law divergence, $xi sim (T^* - T_d)^{-alpha/3}$, with $T_d$ the dynamical crossover temperature and $alpha$ falling in the range $alpha in [0.8,1.0]$.
Landaus theory of phase transitions is adapted to treat independently relaxing regions in complex systems using nanothermodynamics. The order parameter we use governs the thermal fluctuations, not a specific static structure. We find that the entropy term dominates the thermal behavior, as is reasonable for disordered systems. Consequently, the thermal equilibrium occurs at the internal-energy maximum, so that the minima in a potential-energy landscape have negligible influence on the dynamics. Instead the dynamics involves normal thermal fluctuations about the free-energy minimum, with a time scale that is governed by the internal-energy maximum. The temperature dependence of the fluctuations yields VTF-like relaxation rates and approximate time-temperature superposition, consistent with the WLF procedure for analyzing the dynamics of complex fluids; while the size dependence of the fluctuations provides an explanation for the distribution of relaxation times and heterogeneity that are found in glass-forming liquids, thus providing a unified picture for several features in the dynamics of disordered materials.
We present a numerical investigation of the density fluctuations in a model glass under cyclic shear deformation. At low amplitude of shear, below yielding, the system reaches a steady absorbing state in which density fluctuations are suppressed reve aling a clear fingerprint of hyperuniformity up to a finite length scale. The opposite scenario is observed above yielding, where the density fluctuations are strongly enhanced. We demonstrate that the transition to this state is accompanied by a spatial phase separation into two distinct hyperuniform regions, as a consequence of shear band formation above the yield amplitude.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا