Numerical studies of the transition between Néel and valence bond solid phases in two-dimensional quantum antiferromagnets give strong evidence for the remarkable scenario of deconfined criticality, but display strong violations of finite-size scaling that are not yet understood. We show how to realize the universal physics of the Néel-valence-bond-solid (VBS) transition in a three-dimensional classical loop model (this model includes the subtle interference effect that suppresses hedgehog defects in the Néel order parameter). We use the loop model for simulations of unprecedentedly large systems (up to linear size L ¼ 512). Our results are compatible with a continuous transition at which both Néel and VBS order parameters are critical, and we do not see conventional signs of first-order behavior. However, we show that the scaling violations are stronger than previously realized and are incompatible with conventional finitesize scaling, even if allowance is made for a weakly or marginally irrelevant scaling variable. In particular, different approaches to determining the anomalous dimensions η VBS and η Néel yield very different results. The assumption of conventional finite-size scaling leads to estimates that drift to negative values at large sizes, in violation of the unitarity bounds. In contrast, the decay with distance of critical correlators on scales much smaller than system size is consistent with large positive anomalous dimensions. Barring an unexpected reversal in behavior at still larger sizes, this implies that the transition, if continuous, must show unconventional finite-size scaling, for example, from an additional dangerously irrelevant scaling variable. Another possibility is an anomalously weak first-order transition. By analyzing the renormalization group flows for the noncompact CP n−1 field theory (the n-component Abelian Higgs model) between two and four dimensions, we give the simplest scenario by which an anomalously weak first-order transition can arise without fine-tuning of the Hamiltonian.

We show numerically that the "deconfined" quantum critical point between the Néel antiferromagnet and the columnar valence-bond solid, for a square lattice of spin 1=2, has an emergent SO(5) symmetry. This symmetry allows the Néel vector and the valence-bond solid order parameter to be rotated into each other. It is a remarkable (2 þ 1)-dimensional analogue of the SOð4Þ ¼ ½SUð2Þ × SUð2Þ =Z 2 symmetry that appears in the scaling limit for the spin-1=2 Heisenberg chain. The emergent SO(5) symmetry is strong evidence that the phase transition in the (2 þ 1)-dimensional system is truly continuous, despite the violations of finite-size scaling observed previously in this problem. It also implies surprising relations between correlation functions at the transition. The symmetry enhancement is expected to apply generally to the critical two-component Abelian Higgs model (noncompact CP 1 model). The result indicates that in three dimensions there is an SO (5) Many condensed matter systems show higher symmetry in the infrared than they do in the ultraviolet. The liquid-gas critical point is a classical example: although there is no microscopic Z 2 symmetry exchanging liquidlike and gaslike configurations, the fixed point has an emergent Z 2 symmetry and is simply the Ising fixed point. Microscopically, this fixed point is perturbed by operators that break the Z 2 symmetry, but it nevertheless governs the critical behavior because these perturbations are irrelevant under the renormalization group.To reach this critical point two variables, say temperature and pressure, must be tuned. The spin-1=2 Heisenberg chain provides an example of emergent symmetry without such fine-tuning in a quantum setting. The ground state of this model is well known to be critical. Its microscopic symmetries are SU(2) spin rotations, together with spatial symmetries. However the scaling limit of the spin-1=2 chain is the SUð2Þ 1 Wess-Zumino-Witten conformal field theory [1], and this has an SOð4Þ ¼ ½SUð2Þ × SUð2Þ =Z 2 symmetry that is much larger than the global symmetry present microscopically.Physically, this arises as follows [2]. The Néel vectorÑ has three components. There is also a spin-Peierls parameter φ that distinguishes between the two different patterns of dimer (singlet) order and which changes sign under appropriate reflections or translations. We may form the four-component superspinΦ ¼ ðÑ; φÞ, and the emergent SO(4) corresponds to rotations of this vector. Although the dimer and Néel order parameters are utterly inequivalent microscopically, a symmetry between them arises in the infrared. Technically, this again relies on the SO(4)-breaking perturbations of the conformal field theory (CFT) being irrelevant or marginally irrelevant.Naively, one might expect this phenomenon to be special to one spatial dimension, where the enlarged symmetry is related to special properties of 2D conformal invariance (the doubling of conserved currents [1]). We show here however that an analogous symmetry enhancement occurs for the spin-1=2 magnet ...

Recently, it has been suggested that the Many-Body Localized phase can be characterized by local integrals of motion. Here we introduce a Hilbert space preserving renormalization scheme that iteratively finds such integrals of motion exactly. Our method is based on the consecutive action of a similarity transformation using displacement operators. We show, as a proof of principle, localization and the delocalization transition in interacting fermion chains with random onsite potentials. Our scheme of consecutive displacement transformations can be used to study Many Body Localization in any dimension, as well as disorder-free Hamiltonians.PACS numbers: 05.30. Fk, 05.30.Rt, 64.60.ae, 72.15.Rn Since the revival of interest in localization due to disorder [1][2][3][4] it has been suggested that the so-called Many-Body Localized (MBL) phase can be characterized by an extensive set of local integrals of motion (LIOM) or l-bits, τ z i , that commute with each other and the Hamiltonian [3,[6][7][8][9][10]. Consequently, the Hamiltonian can be written in terms of these LIOMs asMany properties of the MBL phase, such as its logarithmic entanglement spread or its insulating behavior, can be derived based on this assumption [10]. The question is, however, what those LIOMs are and how to compute them. Since any sum and product of integrals of motion is itself an integral of motion, the choice of LIOMs is highly arbitrary. Pure mathematically, all projectors onto the (localized) eigenstates are integrals of motion, and out of those one could in principle construct the local integrals of motion. In fact, it is easy to show that all Hamiltonians can be brought into the form dictated by Eqn. (1) [11]. As for the MBL phase, Chandran et al.[3] use the long-time evolved average of an initially local operator as their LIOMs, whereas Ros et al. [9] and Imbrie [7] use perturbative methods to construct local integrals of motion.In this Letter, we construct iteratively a transformation that turns any fermionic Hamiltonian into the classical form of Eqn. (1). This is done by consecutively applying a similarity transformation using a displacement operator exp λ(X † − X). The elegant properties of this transformation allow for a systematic elimination of offdiagonal interaction terms, order by order in the number of fermionic operators involved. Our renormalization scheme can be used to study Hamiltonians in any dimension, with or without disorder.Whether a random interacting system is localized or not, depends on how much the integrals of motion τ z i are spread out. As a proof of principle, we apply our method to diagonalize random interacting chains. In both the localized and the delocalized regime we find agreement with Exact Diagonalization. Throughout the phase diagram we find the effective interactions between the integrals of motion, and we can infer the exponential localization of the integrals of motion in the localized regime.DefinitionsHere we will consider interacting fermions with random onsite potentials[2, 3]as it exte...

No abstract

Presenting an up-to-date report on electronic glasses, this book examines experiments and theories for a variety of disordered materials where electrons exhibit glassy properties. Some interesting mathematical models of idealized systems are also discussed. The authors examine problems in this field, highlighting which issues are currently understood and which require further research. Where appropriate, the authors focus on physical arguments over elaborate derivations. The book provides introductory background material on glassy systems, properties of disordered systems and transport properties so it can be understood by researchers in condensed matter physics who are new to this field.