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Theories of photoinduced phase transitions have developed along with the progress in experimental studies, especially concerning their nonlinear characters and transition dynamics. At an early stage, paths from photoinduced local structural distortions to global ones are explained in classical statistical models. Their dynamics are governed by transition probabilities and inevitably stochastic, but they were sufficient to describe coarse-grained time evolutions. Recently, however, a variety of dynamics including ultrafast ones are observed in different electronic states. They are explained in relevant electronic models. In particular, a coherent lattice oscillation and coherent motion of a macroscopic domain boundary need appropriate interactions among electrons and lattice displacements. Furthermore, some transitions proceed almost in one direction, which can be explained by considering relevant electronic processes. We describe the history of theories of photoinduced phase transitions and discuss a future perspective.
We present an analytical strong-disorder renormalization group theory of the quantum phase transition in the dissipative random transverse-field Ising chain. For Ohmic dissipation, we solve the renormalization flow equations analytically, yielding as
Utrafast control of material physical properties represents a rapid developing field in condensed matter physics. Yet, accessing to the long-lived photoinduced electronic states is still in its early stage, especially with respect to an insulator to
Topological magnon insulators are the bosonic analogs of electronic topological insulators. They are manifested in magnetic materials with topologically nontrivial magnon bands as realized experimentally in a quasi-two-dimensional (quasi-2D) kagome f
The classification of phase transitions is a central and challenging task in condensed matter physics. Typically, it relies on the identification of order parameters and the analysis of singularities in the free energy and its derivatives. Here, we p
We find that the first-order quantum phase transitions~(QPTs) are characterized by intrinsic jumps of relevant operators while the continuous ones are not. Based on such an observation, we propose a bond reversal method where a quantity $mathcal{D}$,