The qualitative difference in low-energy properties of spin S quantum antiferromagnetic chains with integer S and half-odd-integer S discovered by Haldane [F. D. M. Haldane, arXiv:1612.00076 (1981); Phys. Lett. A 93, 464–468 (1983); Phys. Rev. Lett. 50, 1153–1156 (1983)] and Tasaki [Tasaki, Graduate Texts in Physics (Springer, 2020)] can be intuitively understood in terms of the valence-bond picture proposed by Affleck et al. [I. Affleck, Phys. Rev. Lett. 59, 799 (1987); Commun. Math. Phys. 115, 477–528 (1988)]. Here, we develop a similarly intuitive diagrammatic explanation of the qualitative difference between chains with odd S and even S, which is at the heart of the theory of symmetry-protected topological (SPT) phases. (There is a 24 min video in which the essence of the present work is discussed: https://youtu.be/URsf9e_PLlc.) More precisely, we define one-parameter families of states, which we call the asymmetric valence-bond solid (VBS) states, that continuously interpolate between the Affleck–Kennedy–Lieb–Tasaki (AKLT) state and the trivial zero state in quantum spin chains with S = 1 and 2. The asymmetric VBS state is obtained by systematically modifying the AKLT state. It always has exponentially decaying truncated correlation functions and is a unique gapped ground state of a short-ranged Hamiltonian. We also observe that the asymmetric VBS state possesses the time-reversal, the Z2×Z2, and the bond-centered inversion symmetries for S = 2 but not for S = 1. This is consistent with the known fact that the AKLT model belongs to the trivial SPT phase if S = 2 and to a nontrivial SPT phase if S = 1. Although such interpolating families of disordered states were already known, our construction is unified and is based on a simple physical picture. It also extends to spin chains with general integer S and provides us with an intuitive explanation of the essential difference between models with odd and even spins.
The local enhancement of antiferromagnetic correlations near vacancies observed in a variety of spin systems is analyzed in a single framework. Variational calculations suggest that the resonating-valence-bond character of the spin correlations at short distances is responsible for the enhancement. Numerical results for uniform spin chains, with and without frustration, dimerized chains, ladders, and two dimensional clusters are in agreement with our conjecture. This short distance phenomenon occurs independently of the long distance behavior of the spin correlations in the undoped system. Experimental predictions for a variety of compounds are briefly discussed.
Abstract. We study the structure of quantum ground states of simplex solid models, which are generalizations of the valence bond construction for quantum antiferromagnets originally proposed by Affleck, Kennedy, Lieb, and Tasaki (AKLT) (1987 Phys. Rev. Lett . 59 799). Whereas the AKLT states are created by application of bond singlet operators for spins, the simplex solid construction is based on N -simplex singlet operators for spins. In both cases, a discrete one-parameter family of translationally-invariant models with exactly solvable ground states is defined on any regular lattice, and the equal time ground state correlations are given by the finite temperature correlations of an associated classical model on the same lattice, owing to the product form of the wave functions when expressed in a coherent state representation. We study these classical companion models via a mix of Monte Carlo simulations, mean-field arguments, and low-temperature effective field theories. Our analysis reveals that the ground states of edge- and face-sharing cubic lattice simplex solid models are long range ordered for sufficiently large values of the discrete parameter, whereas the ground states of the models on the kagome (2D) and hyperkagome (3D) lattices are always quantum disordered. The kagome simplex solid exhibits strong local order absent in its three-dimensional hyperkagome counterpart, a contrast that we rationalize with arguments similar to those leading to ‘order by disorder’.
We propose that a valence-bond-solid (VBS) order can be stabilized in certain two-dimensional antiferromagnets due to spin-lattice coupling. In contrast to the VBS state of the Affleck-Kennedy-Lieb-Tasaki (AKLT) type, the spin-lattice coupling-induced VBS state can occur when
2S is not an integer multiple of the coordination number
z.
S=2 spins on the triangular lattice with
z=6 is discussed as an example. Within the Schwinger boson mean-field theory the ground state is derived as the direct product of states, one of which represents the conventional long-range ordered spins, and the other given by the $\sqrt{3}\ifmmode\times\else\texttimes\fi{}\sqrt{3}$ modulation of the valence bond amplitudes. Excitation spectrum for the modulated valence bond state is worked out within the single-mode approximation. The spectrum offers a new collective mode, distinct from the spin wave excitations of the magnetically ordered ground state, and observable in neutron scattering.
Spin models that have been proposed to describe dimerized chains, ladders, two-dimensional antiferromagnets, and other compounds are studied here when some spins are replaced by spinless vacancies, such as it occurs by Zn doping. A small percentage of vacancies rapidly destroys the spin gap, and their presence induces enhanced antiferromagnetic correlations near those vacancies. The study is performed with computational techniques which includes Lanczos, world-line Monte Carlo, and the density-matrix renormalization-group methods. Since the phenomenon of enhanced antiferromagnetism is found to occur in several models and cluster geometries, a common simple explanation for its presence may exist. It is argued that the resonating-valence-bond character of the spin correlations at short distances of a large variety of models is responsible for the presence of robust staggered spin correlations near vacancies and lattice edges. The phenomenon takes place regardless of the long distance properties of the ground state, and it is caused by a ``pruning'' of the available spin singlets in the vicinity of the vacancies. The effect produces a broadening of the low-temperature NMR signal for the compounds analyzed here. This broadening should be experimentally observable in the structurally dimerized chain systems $\mathrm{Cu}({\mathrm{NO}}_{3}{)}_{2}\ensuremath{\cdot}2.5{\mathrm{H}}_{2}\mathrm{O}$,
CuWO4,
(VO)2P2O7, and
Sr14Cu24O41, in ladder materials such as
SrCu2O3, in the spin-Peierls systems
CuGeO3 and
NaV2O5, and in several others since it is a universal effect common to a wide variety of models and compounds. In addition, it is argued that the N\'eel order observed in
SrCu2O3 upon Zn doping is induced by the local antiferromagnetic order discussed in this paper, enhanced by a favorable ratio between the actual Heisenberg couplings along chains and rungs, as reported in recent experimental literature. Based on this reasoning it is predicted here that other ladder materials such as Zn-doped
Cu2(C5H12N2)2Cl4 will not present N\'eel order at small Zn concentrations.