Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userQuenching of the Haldane gap in LiVSi2O6 and related compounds
207
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
We report results of susceptibility chi and 7Li NMR measurements on LiVSi2O6. The temperature dependence of the magnetic susceptibility chi(T) exhibits a broad maximum, typical for low-dimensional magnetic systems. Quantitatively it is in agreement with the expectation for an S=1 spin chain, represented by the structural arrangement of V ions. The NMR results indicate antiferromagnetic ordering below T_N=24 K. The intra- and interchain coupling J and J_p for LiVSi2O6, and also for its sister compounds LiVGe2O6, NaVSi2O6 and NaVGe2O6, are obtained via a modified random phase approximation which takes into account results of quantum Monte Carlo calculations. While J_p is almost constant across the series, J varies by a factor of 5, decreasing with increasing lattice constant along the chain direction. The comparison between experimental and theoretical susceptibility data suggests the presence of an easy-axis magnetic anisotropy, which explains the formation of an energy gap in the magnetic excitation spectrum below T_N, indicated by the variation of the NMR spin-lattice relaxation rate at T << T_N.
rate research
Read More
We use extensive DMRG calculations to show that a classification of SU(n) spin chains with regard to the existence of spinon confinement and hence a Haldane gap obtained previously for valence bond solid models applies to SU(n) Heisenberg chains as well. In particular, we observe spinon confinement due to a next-nearest neighbor interaction in the SU(4) representation 10 spin chain.
Ordered double perovskite oxides of the general formula, A2BBO6, have been known for several decades to have interesting electronic and magnetic properties. However, a recent report of a spectacular negative magnetoresistance effect in a specific member of this family, namely Sr2FeMoO6, has brought this class of compounds under intense scrutiny. It is now believed that the origin of magnetism in this class of compounds is based on a novel kinetically-driven mechanism. This new mechanism is also likely to be responsible for the unusually high temperature ferromagnetism in several other systems, such as dilute magnetic semiconductors, as well as in various half-metallic ferromagnetic systems, such as Heussler alloys.
We report experimental and theoretical evidence that Rb$_2$Cu$_2$Mo$_3$O$_{12}$ has a nonmagnetic tetramer ground state of a two-leg ladder comprising antiferromagnetically coupled frustrated spin-$1/2$ chains and exhibits a Haldane spin gap of emergent spin-1 pairs. Three spin excitations split from the spin-1 triplet by a Dzyaloshinskii-Moriya interaction are identified in inelastic neutron-scattering and electron spin resonance spectra. A tiny magnetic field generates ferroelectricity without closing the spin gap, indicating a novel class of ferroelectricity induced by a vector spin chirality order.
Several spin systems with low dimensionality develop a spin-dimer phase within a molecular orbital below TS, competing with long-range antiferromagnetic order. Very often, preferential orbital occupancy and ordering are the actual driving force for dimerization, as in the so-called orbitally-driven spin-Peierls compounds (MgTi2O4, CuIr2S4, La4Ru2O10, NaTiSi2O6, etc.). Through a microscopic analysis of the thermal conductivity k (T) in La4Ru2O10, we show that the orbital occupancy fluctuates rapidly above TS, resulting in an orbital-liquid state. The strong orbital-lattice coupling introduces dynamic bond-length fluctuations that scatter the phonons to produce a k (T) proportional to T (i.e. glass-like) above TS. This phonon-glass to phonon-crystal transition is shown to occur in other spin-dimer systems, like NaTiSi2O6, pointing to a general phenomenon.
We have determined the magnetic phase diagram of the quasi-one-dimensional $S=$ 1 Heisenberg antiferromagnet $Ni (C_5 H_{14} N_2)_2 N_3 (PF_6)$ by specific heat measurements to 150 mK in temperature and 32 T in magnetic field. When field is applied along the spin-chain direction, a new phase appears at $H_{c2}approx 14$ T. For the previously known phases of field-induced order, accurate determination is made of the power-law exponents of the ordering temperature near the zero-temperature critical field $H_c$, owing to the four-fold improvement of the minimum temperature over the previous work. The results are compared with the predictions based on the Bose-Einstein condensation of triplet excitations. Substituting deuterium for hydrogen is found to slightly reduce the interchain exchange.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
