No Arabic abstract
We study the response of a thermal state of the Hubbard-like system to either global or local non-Hermitian perturbation, which coalesces the degenerate ground state within the $U(1)$ symmetry breaking phase. We show that the dynamical response of the system is strongly sensitive to the underlying quantum phase transition (QPT) from a Mott insulator to a superfluid state. The Uhlmann fidelity in the superfluid phase decays to a steady value determined by the order of the exceptional point (EP) within the subspace spanned by the degenerate ground states but remains almost unchanged in the Mott insulating phase. It demonstrates that the phase diagram at zero temperature is preserved even though a local probing field is applied. Specifically, two celebrated models including the Bose-Hubbard model and the Jaynes-Cummings-Hubbard model are employed to demonstrate this property in the finite-size system, wherein fluctuations of the boson and polariton number are observed based on EP dynamics. This work presents an alternative approach to probe the superfluid-insulator QPT at non-zero temperature.
Quantum gases of light, as photons or polariton condensates in optical microcavities, are collective quantum systems enabling a tailoring of dissipation from e.g. cavity loss. This makes them a tool to study dissipative phases, an emerging subject in quantum manybody physics. Here we experimentally demonstrate a non-Hermitian phase transition of a photon Bose-Einstein condensate to a new dissipative phase, characterized by a biexponential decay of the condensates second-order coherence. The phase transition occurs due to the emergence of an exceptional point in the quantum gas. While Bose-Einstein condensation is usually connected to ordinary lasing by a smooth crossover, the observed phase transition separates the novel, biexponential phase from both lasing and an intermediate, oscillatory condensate regime. Our findings pave the way for studies of a wide class of dissipative quantum phases, for instance in topological or lattice systems.
We present a muon spin relaxation study of the Mott transition in BaCoS_2 using two independent control parameters: (i) pressure p to tune the electronic bandwidth and (ii) Ni-substitution x on the Co site to tune the band filling. For both tuning parameters, the antiferromagnetic insulating state first transitions to an antiferromagnetic metal and finally to a paramagnetic metal without undergoing any structural phase transition. BaCoS_2 under pressure displays minimal change in the ordered magnetic moment S_ord until it collapses abruptly upon entering the antiferromagnetic metallic state at p_cr ~ 1.3 GPa. In contrast, S_ord in the Ni-doped system Ba(Co_{1-x}Ni_{x})S_{2} steadily decreases with increasing x until the antiferromagnetic metallic region is reached at x_cr ~ 0.22. In both cases, significant phase separation between magnetic and nonmagnetic regions develops when approaching p_cr or x_cr, and the antiferromagnetic metallic state is characterized by weak, random, static magnetism in a small volume fraction. No dynamical critical behavior is observed near the transition for either tuning parameter. These results demonstrate that the quantum evolution of both the bandwidth- and filling-controlled metal-insulator transition at zero temperature proceeds as a first-order transition. This behavior is common to magnetic Mott transitions in RENiO_3 and V_2O_3, which are accompanied by structural transitions without the formation of an antiferromagnetic metal phase.
We study a non-Hermitian and non-unitary version of the two-dimensional Chalker-Coddington network model with balanced gain and loss. This model belongs to the class D^dagger with particle-hole symmetry^dagger and hosts both the non-Hermitian skin effect as well as exceptional points. By calculating its two-terminal transmission, we find a novel contact effect induced by the skin effect, which results in a non-quantized transmission for chiral edge states. In addition, the model exhibits an insulator to supermetal transition, across which the transmission changes from exponentially decaying with system size to exponentially growing with system size. In the clean system, the critical point separating insulator from supermetal is characterized by a non-Hermitian Dirac point that produces a quantized critical transmission of 4, instead of the value of 1 expected in Hermitian systems. This change in critical transmission is a consequence of the balanced gain and loss. When adding disorder to the system, we find a critical exponent for the divergence of the localization length u approx 1, which is the same as that characterizing the universality class of two-dimensional Hermitian systems in class D. Our work provides a novel way of exploring the localization behavior of non-Hermitian systems, by using network models, which in the past proved versatile tools to describe Hermitian physics.
The discovery of novel phases of matter is at the core of modern physics. In quantum materials, subtle variations in atomic-scale interactions can induce dramatic changes in macroscopic properties and drive phase transitions. Despite their importance, the mesoscale processes underpinning phase transitions often remain elusive because of the vast differences in timescales between atomic and electronic changes and thermodynamic transformations. Here, we photoinduce and directly observe with x-ray scattering an ultrafast enhancement of the structural long-range order in the archetypal Mott system V2O3. Despite the ultrafast change in crystal symmetry, the change of unit cell volume occurs an order of magnitude slower and coincides with the insulator-to-metal transition. The decoupling between the two structural responses in the time domain highlights the existence of a transient photoinduced precursor phase, which is distinct from the two structural phases present in equilibrium. X-ray nanoscopy reveals that acoustic phonons trapped in nanoscale blocks govern the dynamics of the ultrafast transition into the precursor phase, while nucleation and growth of metallic domains dictate the duration of the slower transition into the metallic phase. The enhancement of the long-range order before completion of the electronic transition demonstrates the critical role the non-equilibrium structural phases play during electronic phase transitions in correlated electrons systems.
We report a global effect induced by the local complex field, associated with the spin-exchange interaction. High-order exceptional point up to ($N+1$)-level coalescence is created at the critical local complex field applied to the $N$-size quantum spin chain. The ($N+1$)-order coalescent level is a saturated ferromagnetic ground state in the isotropic spin system. Remarkably, the final state always approaches the ground state for an arbitrary initial state with any number of spin flips; even if the initial state is orthogonal to the ground state. Furthermore, the switch of macroscopic magnetization is solely driven by the time and forms a hysteresis loop in the time domain. The retentivity and coercivity of the hysteresis loop mainly rely on the non-Hermiticity. Our findings highlight the cooperation of non-Hermiticity and the interaction in quantum spin system, suggest a dynamical framework to realize magnetization, and thus pave the way for the non-Hermitian quantum spin system.