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Register a new userEntropy Signatures of Topological Phase Transitions
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We review the behavior of the entropy per particle in various two-dimensional electronic systems. The entropy per particle is an important characteristic of any many body system that tells how the entropy of the ensemble of electrons changes if one adds one more electron. Recently, it has been demonstrated how the entropy per particle of a two-dimensional electron gas can be extracted from the recharging current dynamics in a planar capacitor geometry. These experiments pave the way to the systematic studies of entropy in various crystal systems including novel two-dimensional crystals such as gapped graphene, germanene and silicene. Theoretically, the entropy per particle is linked to the temperature derivative of the chemical potential of the electron gas by the Maxwell relation. Using this relation, we calculate the entropy per particle in the vicinity of topological transitions in various two-dimensional electronic systems. We show that the entropy experiences quantized steps at the points of Lifshitz transitions in a two-dimensional electronic gas with a parabolic energy spectrum. In contrast, in doubled-gapped Dirac materials, the entropy per particles demonstrates characteristic spikes once the chemical potential passes through the band edges. The transition from a topological to trivial insulator phase in germanene is manifested by the disappearance of a strong zero-energy resonance in the entropy per particle dependence on the chemical potential. We conclude that studies of the entropy per particle shed light on multiple otherwise hidden peculiarities of the electronic band structure of novel two-dimensional crystals.
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We propose a characterization tool for studies of the band structure of new materials promising for the observation of topological phase transitions. We show that a specific resonant feature in the entropy per electron dependence on the chemical potential may be considered as a fingerprint of the transition between topological and trivial insulator phases. The entropy per electron in a honeycomb two-dimensional crystal of germanene subjected to the external electric field is obtained from the first principle calculation of the density of electronic states and the Maxwell relation. We demonstrate that, in agreement to the recent prediction of the analytical model, strong spikes in the entropy per particle dependence on the chemical potential appear at low temperatures. They are observed at the values of the applied bias both below and above the critical value that corresponds to the transition between the topological insulator and trivial insulator phases, while the giant resonant feature in the vicinity of zero chemical potential is strongly suppressed at the topological transition point, in the low temperature limit. In a wide energy range, the van Hove singularities in the electronic density of states manifest themselves as zeros in the entropy per particle dependence on the chemical potential.
The traditional concept of phase transitions has, in recent years, been widened in a number of interesting ways. The concept of a topological phase transition separating phases with a different ground state topology, rather than phases of different symmetries, has become a large widely studied field in its own right. Additionally an analogy between phase transitions, described by non-analyticities in the derivatives of the free energy, and non-analyticities which occur in dynamically evolving correlation functions has been drawn. These are called dynamical phase transitions and one is often now far from the equilibrium situation. In these short lecture notes we will give a brief overview of the history of these concepts, focusing in particular on the way in which dynamical phase transitions themselves can be used to shed light on topological phase transitions and topological phases. We will go on to focus, first, on the effect which the topologically protected edge states, which are one of the interesting consequences of topological phases, have on dynamical phase transitions. Second we will consider what happens in the experimentally relevant situations where the system begins either in a thermal state rather than the ground state, or exchanges particles with an external environment.
The discovery of 2-dimensional (2D) materials, such as CrI3, that retain magnetic ordering at monolayer thickness has resulted in a surge of research in 2D magnetism from both pure and applied perspectives. Here, we report a magneto-Raman spectroscopy study on multilayered CrI3, focusing on two new features in the spectra which appear at temperatures below the magnetic ordering temperature and were previously assigned to high frequency magnons. We observe a striking evolution of the Raman spectra with increasing magnetic field in which clear, sudden changes in intensities of the modes are attributed to the interlayer ordering changing from antiferromagnetic to ferromagnetic at a critical magnetic field. Our work highlights the sensitivity of the Raman modes to weak interlayer spin ordering in CrI3. In addition, we theoretically examine potential origins for the new modes, which we deduce are unlikely single magnons.
We investigate the Loschmidt amplitude and dynamical quantum phase transitions in multiband one dimensional topological insulators. For this purpose we introduce a new solvable multiband model based on the Su-Schrieffer-Heeger model, generalized to unit cells containing many atoms but with the same symmetry properties. Such models have a richer structure of dynamical quantum phase transitions than the simple two-band topological insulator models typically considered previously, with both quasiperiodic and aperiodic dynamical quantum phase transitions present. Moreover the aperiodic transitions can still occur for quenches within a single topological phase. We also investigate the boundary contributions from the presence of the topologically protected edge states of this model. Plateaus in the boundary return rate are related to the topology of the time evolving Hamiltonian, and hence to a dynamical bulk-boundary correspondence. We go on to consider the dynamics of the entanglement entropy generated after a quench, and its potential relation to the critical times of the dynamical quantum phase transitions. Finally, we investigate the fidelity susceptibility as an indicator of the topological phase transitions, and find a simple scaling law as a function of the number of bands of our multiband model which is found to be the same for both bulk and boundary fidelity susceptibilities.
We study the effect of electrostatic disorder on the conductivity of a three-dimensional antiferromagnetic insulator (a stack of quantum anomalous Hall layers with staggered magnetization). The phase diagram contains regions where the increase of disorder first causes the appearance of surface conduction (via a topological phase transition), followed by the appearance of bulk conduction (via a metal-insulator transition). The conducting surface states are stabilized by an effective time-reversal symmetry that is broken locally by the disorder but restored on long length scales. A simple self-consistent Born approximation reliably locates the boundaries of this socalled statistical topological phase.
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