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Extensive experimental and numerical studies of the non-equilibrium dynamics of spin glasses subjected to temperature or bond perturbations have been performed to investigate chaos and memory effects in selected spin glass systems. Temperature shift and cycling experiments were performed on the strongly anisotropic Ising-like system {ising} and the weakly anisotropic Heisenberg-like system {AgMn}, while bond shift and cycling simulations were carried out on a 4 dimensional Ising Edwards-Anderson spin glass. These spin glass systems display qualitatively the same characteristic features and the observed memory phenomena are found to be consistent with predictions from the ghost domain scenario of the droplet scaling model.
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A range of ferroic glasses, magnetic, polar, relaxor and strain glasses, are considered together from the perspective of spin glasses. Simple mathematical modelling is shown to provide a possible conceptual unification to back similarities of experimental observations, without considering all possible complexities and alternatives.
It is argued that the main characteristic features of displacive relaxor ferrolectrics of the form ${rm{A(B,B)}rm{O}}_3$ with isovalent ${rm{B,B}}$ can be explained and understood in terms of a soft-pseudospin analogue of conventional spin glasses as extended to itinerant magnet systems. The emphasis is on conceptual comprehension and on stimulating new perspectives with respect to previous and future studies. Some suggestions are made for further studies both on actual real systems and on test model systems to probe further. The case of heterovalent systems is also considered briefly.
As well as several different kinds of periodically ordered ferroic phases, there are now recognized several different examples of ferroic glassiness, although not always described as such and in material fields of study that have mostly been developed separately. In this chapter an attempt is made to indicate common conceptual origins and features, observed or anticipated. Throughout, this aim is pursued through the use of simple models, in an attempt to determine probable fundamental origins within a larger picture of greater complication, and analogies between systems in different areas, both experimental and theoretical, in the light of significant progress in spin glass understanding.
Spin-charge conversion via inverse spin Hall effect (ISHE) is essential for enabling various applications of spintronics. The spin Hall response usually follows a universal scaling relation with longitudinal electric resistivity and has mild temperature dependence because elementary excitations play only a minor role in resistivity and hence ISHE. Here we report that the ISHE of metallic glasses shows nearly two orders of magnitude enhancements with temperature increase from a threshold of 80-100 K to glass transition points. As electric resistivity changes only marginally in the temperature range, the anomalous temperature dependence is in defiance of the prevailing scaling law. Such a giant temperature enhancement can be well described by a two-level thermal excitation model of glasses and disappears after crystallization, suggesting a new mechanism which involves unique thermal excitations of glasses. This finding may pave new ways to achieve high spin-charge conversion efficiency at room and higher temperatures for spintronic devices and to detect structure and dynamics of glasses using spin currents.
Due to high viscosity, glassy systems evolve slowly to the ordered state. Results of molecular dynamics simulation reveal that the structural ordering in glasses becomes observable over experimental (finite) time-scale for the range of phase diagram with high values of pressure. We show that the structural ordering in glasses at such conditions is initiated through the nucleation mechanism, and the mechanism spreads to the states at extremely deep levels of supercooling. We find that the scaled values of the nucleation time, $tau_1$ (average waiting time of the first nucleus with the critical size), in glassy systems as a function of the reduced temperature, $widetilde{T}$, are collapsed onto a single line reproducible by the power-law dependence. This scaling is supported by the simulation results for the model glassy systems for a wide range of temperatures as well as by the experimental data for the stoichiometric glasses at the temperatures near the glass transition.
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