No Arabic abstract
We study the effects of bond and site disorder in the classical $J_{1}$-$J_{2}$ Heisenberg model on a square lattice in the order-by-disorder frustrated regime $2J_{2}>left|J_{1}right|$. Combining symmetry arguments, numerical energy minimization and large scale Monte Carlo simulations, we establish that the finite temperature Ising-like transition of the clean system is destroyed in the presence of any finite concentration of impurities. We explain this finding via a random-field mechanism which generically emerges in systems where disorder locally breaks the same real-space symmetry spontaneously globally broken by the associated order parameter. We also determine that the phase replacing the clean one is a paramagnet polarized in the nematic glass order with non-trivial magnetic response. This is because disorder also induces non-collinear spin-vortex-crystal order and produces a conjugated transverse dipolar random field. As a result of these many competing effects, the associated magnetic susceptibilities are non-monotonic functions of the temperature. As a further application of our methods, we show the generation of random axes in other frustrated magnets with broken SU(2) symmetry. We also discuss the generality of our findings and their relevance to experiments.
We consider magnon excitations in the spin-glass phase of geometrically frustrated antiferromagnets with weak exchange disorder, focussing on the nearest-neighbour pyrochlore-lattice Heisenberg model at large spin. The low-energy degrees of freedom in this system are represented by three copies of a U(1) emergent gauge field, related by global spin-rotation symmetry. We show that the Goldstone modes associated with spin-glass order are excitations of these gauge fields, and that the standard theory of Goldstone modes in Heisenberg spin glasses (due to Halperin and Saslow) must be modified in this setting.
Symmetries play a central role in single-particle localization. Recent research focused on many-body localized (MBL) systems, characterized by new kind of integrability, and by the area-law entanglement of eigenstates. We investigate the effect of a non-Abelian $SU(2)$ symmetry on the dynamical properties of a disordered Heisenberg chain. While $SU(2)$ symmetry is inconsistent with the conventional MBL, a new non-ergodic regime is possible. In this regime, the eigenstates exhibit faster than area-law, but still a strongly sub-thermal scaling of entanglement entropy. Using exact diagonalization, we establish that this non-ergodic regime is indeed realized in the strongly disordered Heisenberg chains. We use real-space renormalization group (RSRG) to construct approximate excited eigenstates, and show their accuracy for systems of size up to $L=26$. As disorder strength is decreased, a crossover to the thermalizing phase occurs. To establish the ultimate fate of the non-ergodic regime in the thermodynamic limit, we develop a novel approach for describing many-body processes that are usually neglected by RSRG, accessing systems of size $L>2000$. We characterize the resonances that arise due to such processes, finding that they involve an ever growing number of spins as the system size is increased. The probability of finding resonances grows with the system size. Even at strong disorder, we can identify a large lengthscale beyond which resonances proliferate. Presumably, this eventually would drive the system to a thermalizing phase. However, the extremely long thermalization time scales indicate that a broad non-ergodic regime will be observable experimentally. Our study demonstrates that symmetries control dynamical properties of disordered, many-body systems. The approach introduced here provides a versatile tool for describing a broad range of disordered many-body systems.
We study the ferromagnetic phase transition in a randomly layered Heisenberg model. A recent strong-disorder renormalization group approach [Phys. Rev. B 81, 144407 (2010)] predicted that the critical point in this system is of exotic infinite-randomness type and is accompanied by strong power-law Griffiths singularities. Here, we report results of Monte-Carlo simulations that provide numerical evidence in support of these predictions. Specifically, we investigate the finite-size scaling behavior of the magnetic susceptibility which is characterized by a non-universal power-law divergence in the Griffiths phase. In addition, we calculate the time autocorrelation function of the spins. It features a very slow decay in the Griffiths phase, following a non-universal power law in time.
We study a quenched disordered d=3 tJ Hamiltonian with static vacancies as a model of nonmagnetic impurities in high-Tc materials. Using a position-space renormalization-group approach, we calculate the evolution of the finite-temperature phase diagram with impurity concentration p, and find several features with close experimental parallels: away from half-filling we see the rapid destruction of a spin-singlet phase (analogous to the superconducting phase in cuprates) which is eliminated for p > 0.05; in the same region for these dilute impurity concentrations we observe an enhancement of antiferromagnetism. The antiferromagnetic phase near half-filling is robust against impurity addition, and disappears only for p > 0.40.
The interplay between geometric frustration (GF) and bond disorder is studied in the Ising kagome lattice within a cluster approach. The model considers antiferromagnetic (AF) short-range couplings and long-range intercluster disordered interactions. The replica formalism is used to obtain an effective single cluster model from where the thermodynamics is analyzed by exact diagonalization. We found that the presence of GF can introduce cluster freezing at very low levels of disorder. The system exhibits an entropy plateau followed by a large entropy drop close to the freezing temperature. In this scenario, a spin-liquid (SL) behavior prevents conventional long-range order, but an infinitesimal disorder picks out uncompensated cluster states from the multi degenerate SL regime, potentializing the intercluster disordered coupling and bringing the cluster spin-glass state. To summarize, our results suggest that the SL state combined with low levels of disorder can activate small clusters, providing hypersensitivity to the freezing process in geometrically frustrated materials and playing a key role in the glassy stabilization. We propose that this physical mechanism could be present in several geometrically frustrated materials. In particular, we discuss our results in connection to the recent experimental investigations of the Ising kagome compound Co$_3$Mg(OH)$_6$Cl$_2$.