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We present a method to compute the magnetic susceptibility of spin systems at all temperatures in one and two dimensions. It relies on an approximation of the entropy versus energy (microcanonical potential function) on the whole range of energies. The intrinsic constraints on the entropy function and a careful treatment of boundary behaviors allow to extend the standard high temperature series expansions (HTE) towards zero temperature, overcoming the divergence of truncated HTE. This method is benchmarked against two one-dimensional solvable models: the Ising model in longitudinal field and the XY model in a transverse field. With ten terms in the HTE, we find a spin susceptibility within a few % of the exact results in the whole range of temperature. The method is then applied to two two-dimensional models: the supposed-to-be gapped Heisenberg model and the $J_1$-$J_2$-$J_d$ model on the kagome lattice.
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The high temperature expansion (HTE) of the specific heat of a spin system fails at low temperatures, even if it is combined with a Pade approximation. On the other hand we often have information about the low temperature asymptotics (LTA) of the system. Interpolation methods combine both kind of information, HTE and LTA, in order to obtain an approximation of the specific heat that holds for the whole temperature range. Here we revisit the entropy method that has been previously published and propose two variants that better cope with problems of the entropy method for gapped systems. We compare all three methods applied to the antiferromagnetic Haldane spin-one chain and especially apply the second variant, called Log Z method, to the cuboctahedron for different spin quantum numbers. In particular, we demonstrate that the interpolation method is able to detect an extra low-temperature maximum in the specific heat that may appear if a separation of two energy scales is present in the considered system. Finally we illustrate how interpolation also works for classical spin systems.
We present the magnetoresistance (MR) of highly doped monolayer graphene layers grown by chemical vapor deposition on 6H-SiC. The magnetotransport studies are performed on a large temperature range, from $T$ = 1.7 K up to room temperature. The MR exhibits a maximum in the temperature range $120-240$ K. The maximum is observed at intermediate magnetic fields ($B=2-6$ T), in between the weak localization and the Shubnikov-de Haas regimes. It results from the competition of two mechanisms. First, the low field magnetoresistance increases continuously with $T$ and has a purely classical origin. This positive MR is induced by thermal averaging and finds its physical origin in the energy dependence of the mobility around the Fermi energy. Second, the high field negative MR originates from the electron-electron interaction (EEI). The transition from the diffusive to the ballistic regime is observed. The amplitude of the EEI correction points towards the coexistence of both long and short range disorder in these samples.
We present a comprehensive study of single crystals of Na2Co2TeO6, a putative Kitaev honeycomb magnet, focusing on its low-temperature phase behaviors. A new thermal phase transition is identified at 31.0 K, below which the system develops a two-dimensional (2D) long-range magnetic order. This order precedes the well-known 3D order below 26.7 K, and is likely driven by strongly anisotropic interactions. Surprisingly, excitations from the 3D order do not support the orders commonly accepted zigzag nature, and are instead consistent with a triple-q description. The 3D order exerts a fundamental feedback on high-energy excitations that likely involve orbital degrees of freedom, and it remains highly frustrated until a much lower temperature is reached. These findings render Na2Co2TeO6 a spin-orbit entangled frustrated magnet that hosts very rich physics.
Exact diagonalization of finite spin-1/2 chains with periodic boundary conditions is applied to the ground state (gs) of chains with ferromagnetic (F) exchange $J_1 < 0$between first neighbors, antiferromagnetic (AF) exchange $J_2 = alpha J_1 > 0$between second neighbors, and axial anisotropy $0 le Delta le 1$. In zero field, the gs is in the $S_z = 0$ sector for the relevant parameters and is doubly degenerate at multiple points $gamma_m = (alpha_m, Delta_m)$ in the $alpha$, $Delta$ plane. Degeneracy under inversion at sites or spin parity or both leads, respectively, to a bond order wave (BOW), to staggered magnetization or to vector chiral (VC) order. Exact results up to $N = 28$ spins directly yield order parameters and spin correlation functions whose weak N dependencies allow inferences about infinite chains. The high-spin gs at $J_2 = 0$ changes discontinuously at $gamma_1 = (-1/4, 1)$ to a singlet in the isotropic ($Delta = 1$) chain. The transition from high to low spin $S(alpha, Delta)$ is continuous for $ Delta < Delta_B = 0.95 pm 0.01$ on the degeneracy line $alpha_1(Delta)$. The gs has staggered magnetization between $Delta_A = 0.72$ and $Delta_B$, and a BOW for $Delta < Delta_A$. When both inversion and spin parity are reversed at $gamma_m$, the correlation functions $C(p)$ for spins separated by $p$ sites are identical. $C(p)$ minima are shifted by $pi/2$ from the minima of VC order parameters at separation $p$, consistent with right and left-handed helices along the z axis and spins in the xy plane. Degenerate gs of finite chains are related to quantum phase diagrams of extended $alpha$, $Delta$ chains, with good agreement for order parameters along the line $alpha_1(Delta)$.
The spin ice materials, including Ho2Ti2O7 and Dy2Ti2O7, are rare earth pyrochlore magnets which, at low temperatures, enter a constrained paramagnetic state with an emergent gauge freedom. Remarkably, the spin ices provide one of very few experimentally realised examples of fractionalization because their elementary excitations can be regarded as magnetic monopoles and, over some temperature range, the spin ice materials are best described as liquids of these emergent charges. In the presence of quantum fluctuations, one can obtain, in principle, a quantum spin liquid descended from the classical spin ice state characterised by emergent photon-like excitations. Whereas in classical spin ices the excitations are akin to electrostatic charges, in the quantum spin liquid these charges interact through a dynamic and emergent electromagnetic field. In this review, we describe the latest developments in the study of such a quantum spin ice, focussing on the spin liquid phenomenology and the kinds of materials where such a phase might be found.
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