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Register a new userAbsence of rejuvenation in a Superspin Glass
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Effects of temperature changes on the nonequilibrium spin-glass dynamics of a strongly interacting ferromagnetic nanoparticle system (superspin glass) are studied. In contrary to atomic spin glasses, strong cooling rate effects are observed, and no evidence for temperature-chaos is found. The flip time of a magnetic moment is much longer than that of an atomic spin and hence much shorter time scales are probed within the experimental time window for a superspin glass than for an atomic spin glass. Within a real space picture the cumulative aging observed for the superspin glass can be explained considering that all investigated length scales are shorter than the temperature-chaos overlap length. The transient relaxation, observed in experiments after temperature changes, can be understood as the adjustment of thermally active droplets, which is mutatis mutandis the Kovacs effect observed in most glassy systems.
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We present the experimental observation of the fluctuation-dissipation theorem (FDT) violation in an assembly of interacting magnetic nanoparticles in the low temperature superspin glass phase. The magnetic noise is measured with a two-dimension electron gas Hall probe and compared to the out of phase ac susceptibility of the same ferrofluid. For intermediate aging times of the order of 1 h, the ratio of the effective temperature $T_{rm eff}$ to the bath temperature T grows from 1 to 6.5 when T is lowered from $T_g$ to 0.3 $T_g$, regardless of the noise frequency. These values are comparable to those measured in an atomic spin glass as well as those calculated for a Heisenberg spin glass.
We report on zero field cooled magnetization relaxation experiments on a concen- trated frozen ferrofluid exhibiting a low temperature superspin glass transition. With a method initially developed for spin glasses, we investigate the field dependence of the relaxations that take place after different aging times. We extract the typical number of correlated spins involved in the aging dynamics. This brings important insights into the dynamical correlation length and its time growth. Our results, consistent with expressions obtained for spin glasses, extend the generality of these behaviours to the class of superspin glasses. Since the typical flipping time is much larger for superspins than for atomic spins, our experiments probe a time regime much closer to that of numerical simulations.
Cryogenic rejuvenation in metallic glasses reported in Ketov et al s experiment (Nature(2015)524,200) has attracted much attention, both in experiments and numerical studies. The atomic mechanism of rejuvenation has been conjectured to be related to the heterogeneity of the glassy state, but the quantitative evidence is still elusive. Here we use molecular dynamics simulations of a model metallic glass to investigate the heterogeneity in the local thermal expansion. We then combine the resulting spatial distribution of thermal expansion with a continuum mechanics calculation to infer the internal stresses caused by a thermal cycle. Comparing the internal stress with the local yield stress, we prove that the heterogeneity in thermomechanical response has the potential to trigger local shear transformations, and therefore to induce rejuvenation during a cryogenic thermal cycling.
We study the effect of shear on the aging dynamics of a colloidal suspension of synthetic clay particles. We find that a shear of amplitude $gamma$ reduces the relaxation time measured just after the cessation of shear by a factor $exp(-gamma/gamma_c)$, with $gamma_c sim 5%$, and is independent of the duration and the frequency of the shear. This simple law for the rejuvenation effect shows that the energy involved in colloidal rearrangements is proportional to the shear amplitude, $gamma$, rather than $gamma^2$, leading to an Eyring-like description of the dynamics of our system.
When a liquid is cooled below its melting temperature it usually crystallizes. However, if the quenching rate is fast enough, it is possible that the system remains in a disordered state, progressively losing its fluidity upon further cooling. When the time needed for the rearrangement of the local atomic structure reaches approximately 100 seconds, the system becomes solid for any practical purpose, and this defines the glass transition temperature $T_g$. Approaching this transition from the liquid side, different systems show qualitatively different temperature dependencies of the viscosity, and, accordingly, they have been classified introducing the concept of fragility. We report experimental observations that relate the microscopic properties of the {it glassy phase} to the fragility. We find that the vibrational properties of the glass {it well below} $T_g$ are correlated with the fragility value. Consequently, we extend the fragility concept to the glassy state and indicate how to determine the fragility uniquely from glass properties well below $T_g$.
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