No Arabic abstract
We study the two-dimensional kagome-ice model derived from a pyrochlore lattice with second- and third-neighbor interactions. The canted moments align along the local $langle 111 rangle$ axes of the pyrochlore and respond to both in-plane and out-of-plane external fields. We find that the combination of further-neighbor interactions together with the external fields introduces a rich phase diagram with different spin textures. Close to the phase boundaries, metastable $textit{snake}$ domains emerge with extremely long relaxation time. Our kinetic Monte Carlo analysis of the magnetic-field quench process from saturated state shows unusually slow dynamics. Despite that the interior spins are almost frozen in snake domains, the spins on the edge are free to fluctuate locally, leading to frequent creation and annihilation of monopole-anti-monopole bound states. Once the domains are formed, these excitations are localized and can hardly propagate due to the energy barrier of snakes. The emergence of such snake domains may shed light on the experimental observation of dipolar spin ice under tilted fields, and provide a new strategy to manipulate both spin and charge textures in artificial spin ice.
Motivated by recent realizations of Dy$_{2}$Ti$_{2}$O$_{7}$ and Ho$_{2}$Ti$_{2}$O$_{7}$ spin ice thin films, and more generally by the physics of confined gauge fields, we study a model of spin ice thin film with surfaces perpendicular to the $[001]$ cubic axis. The resulting open boundaries make half of the bonds on the interfaces inequivalent. By tuning the strength of these inequivalent orphan bonds, dipolar interactions induce a surface ordering equivalent to a two-dimensional crystallization of magnetic surface charges. This surface ordering can also be expected on the surfaces of bulk crystals. In analogy with partial wetting in soft matter, spins just below the surface are more correlated than in the bulk, but emph{not} ordered. For ultrathin films made of one cubic unit cell, once the surfaces are ordered, a square ice phase is stabilized over a finite temperature window, as confirmed by its entropy and the presence of pinch points in the structure factor. Ultimately, the square ice degeneracy is lifted at lower temperature and the system orders in analogy with the well-known $F$-transition of the $6$-vertex model.
Artificial spin ice systems have seen burgeoning interest due to their intriguing physics and potential applications in reprogrammable memory, logic and magnonics. In-depth comparisons of distinct artificial spin systems are crucial to advancing the field and vital work has been done on characteristic behaviours of artificial spin ices arranged on different geometric lattices. Integration of artificial spin ice with functional magnonics is a relatively recent research direction, with a host of promising early results. As the field progresses, studies examining the effects of lattice geometry on the magnonic response are increasingly significant. While studies have investigated the effects of different lattice tilings such as square and kagome (honeycomb), little comparison exists between systems comprising continuously-connected nanostructures, where spin-waves propagate through the system via exchange interaction, and systems with nanobars disconnected at vertices where spin-waves are transferred via stray dipolar-field. Here, we perform a Brillouin light scattering study of the magnonic response in two kagome artificial spin ices, a continuously-connected system and a disconnected system with vertex gaps. We observe distinctly different high-frequency dynamics and characteristic magnetization reversal regimes between the systems, with key distinctions in system microstate during reversal, internal field profiles and spin-wave mode quantization numbers. These observations are pertinent for the fundamental understanding of artificial spin systems and the design and engineering of such systems for functional magnonic applications.
Finite-temperature spin transport in the quantum Heisenberg spin chain is known to be superdiffusive, and has been conjectured to lie in the Kardar-Parisi-Zhang (KPZ) universality class. Using a kinetic theory of transport, we compute the KPZ coupling strength for the Heisenberg chain as a function of temperature, directly from microscopics; the results agree well with density-matrix renormalization group simulations. We establish a rigorous quantum-classical correspondence between the giant quasiparticles that govern superdiffusion and solitons in the classical continuous Landau-Lifshitz ferromagnet. We conclude that KPZ universality has the same origin in classical and quantum integrable isotropic magnets: a finite-temperature gas of low-energy classical solitons.
We derive exact results for close-packed dimers on the triangular kagome lattice (TKL), formed by inserting triangles into the triangles of the kagome lattice. Because the TKL is a non-bipartite lattice, dimer-dimer correlations are short-ranged, so that the ground state at the Rokhsar-Kivelson (RK) point of the corresponding quantum dimer model on the same lattice is a short-ranged spin liquid. Using the Pfaffian method, we derive an exact form for the free energy, and we find that the entropy is 1/3 ln2 per site, regardless of the weights of the bonds. The occupation probability of every bond is 1/4 in the case of equal weights on every bond. Similar to the case of lattices formed by corner-sharing triangles (such as the kagome and squagome lattices), we find that the dimer-dimer correlation function is identically zero beyond a certain (short) distance. We find in addition that monomers are deconfined on the TKL, indicating that there is a short-ranged spin liquid phase at the RK point. We also find exact results for the ground state energy of the classical Heisenberg model. The ground state can be ferromagnetic, ferrimagnetic, locally coplanar, or locally canted, depending on the couplings. From the dimer model and the classical spin model, we derive upper bounds on the ground state energy of the quantum Heisenberg model on the TKL.
We study the mechanism of decay of a topological (winding-number) excitation due to finite-size effects in a two-dimensional valence-bond solid state, realized in an $S=1/2$ spin model ($J$-$Q$ model) and studied using projector Monte Carlo simulations in the valence bond basis. A topological excitation with winding number $|W|>0$ contains domain walls, which are unstable due to the emergence of long valence bonds in the wave function, unlike in effective descriptions with the quantum dimer model. We find that the life time of the winding number in imaginary time diverges as a power of the system length $L$. The energy can be computed within this time (i.e., it converges toward a quasi-eigenvalue before the winding number decays) and agrees for large $L$ with the domain-wall energy computed in an open lattice with boundary modifications enforcing a domain wall. Constructing a simplified two-state model and using the imaginary-time behavior from the simulations as input, we find that the real-time decay rate out of the initial winding sector is exponentially small in $L$. Thus, the winding number rapidly becomes a well-defined conserved quantum number for large systems, supporting the conclusions reached by computing the energy quasi-eigenvalues. Including Heisenberg exchange interactions which brings the system to a quantum-critical point separating the valence-bond solid from an antiferromagnetic ground state (the putative deconfined quantum-critical point), we can also converge the domain wall energy here and find that it decays as a power-law of the system size. Thus, the winding number is an emergent quantum number also at the critical point, with all winding number sectors becoming degenerate in the thermodynamic limit. This supports the description of the critical point in terms of a U(1) gauge-field theory.