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Register a new userSpin Correlations in the Dipolar Pyrochlore Antiferromagnet Gd2Sn2O7
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We investigate spin correlations in the dipolar Heisenberg antiferromagnet Gd2Sn2O7 using polarised neutron-scattering measurements in the correlated paramagnetic regime. Using Monte Carlo methods, we show that our data are sensitive to weak further-neighbour exchange interactions of magnitude ~0.5% of the nearest-neighbour interaction, and are compatible with either antiferromagnetic next-nearest neighbour interactions, or ferromagnetic third-neighbour interactions that connect spins across hexagonal loops. Calculations of the magnetic scattering intensity reveal rods of diffuse scattering along [111] reciprocal-space directions, which we explain in terms of strong antiferromagnetic correlations parallel to the set of <110> directions that connect a given spin with its nearest neighbours. Finally, we demonstrate that the spin correlations in Gd2Sn2O7 are highly anisotropic, and correlations parallel to third-neighbour separations are particularly sensitive to critical fluctuations associated with incipient long-range order.
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The study of randomness in low-dimensional quantum antiferromagnets is at the forefront of research in the field of strongly correlated electron systems, yet there have been relatively few experimental model systems. Complementary neutron scattering and numerical experiments demonstrate that the spin-diluted Heisenberg antiferromagnet La2Cu(1-z)(Zn,Mg)zO4 is an excellent model material for square-lattice site percolation in the extreme quantum limit of spin one-half. Measurements of the ordered moment and spin correlations provide important quantitative information for tests of theories for this complex quantum-impurity problem.
The spin-liquid phase of two highly frustrated pyrochlore magnets Gd2Ti2O7 and Gd2Sn2O7 is probed using electron spin resonance in the temperature range 1.3 - 30 K. The deviation of the absorption line from the paramagnetic position u =gamma H observed in both compounds below the Curie-Weiss temperature Theta_CW ~ 10 K, suggests an opening up of a gap in the excitation spectra. On cooling to 1.3 K (which is above the ordering transition T_N ~ 1.0 K) the resonance spectrum is transformed into a wide band of excitations with the gap amounting to Delta ~ 26 GHz (1.2 K) in Gd2Ti2O7 and 18 GHz (0.8 K) in Gd2Sn2O7. The gaps increase linearly with the external magnetic field. For Gd2Ti2O7 this branch co-exists with an additional nearly paramagnetic line absent in Gd2Sn2O7. These low lying excitations with gaps, which are preformed in the spin-liquid state, may be interpreted as collective spin modes split by the single-ion anisotropy.
We use numerical linked cluster (NLC) expansions to compute the specific heat, C(T), and entropy, S(T), of a quantum spin ice model of Yb2Ti2O7 using anisotropic exchange interactions recently determined from inelastic neutron scattering measurements and find good agreement with experimental calorimetric data. In the perturbative weak quantum regime, this model has a ferrimagnetic ordered ground state, with two peaks in C(T): a Schottky anomaly signalling the paramagnetic to spin ice crossover followed at lower temperature by a sharp peak accompanying a first order phase transition to the ferrimagnetic state. We suggest that the two C(T) features observed in Yb2Ti2O7 are associated with the same physics. Spin excitations in this regime consist of weakly confined spinon-antispinon pairs. We suggest that conventional ground state with exotic quantum dynamics will prove a prevalent characteristic of many real quantum spin ice materials.
ersn, is considered, together with erti, as a realization of the XY antiferromagnet on the pyrochlore lattice. We present magnetization measurements confirming that ersn, does not order down to 100 mK but exhibits a freezing below 200 mK. Our neutron scattering experiments evidence the strong XY character of the er moment and point out the existence of short range correlations in which the magnetic moments are in peculiar configurations, the Palmer-Chalker states, predicted theoretically for an XY pyrochlore antiferromagnet with dipolar interactions. Our estimation of the ersn, parameters confirm the role of the latter interactions on top of relatively weak and isotropic exchange couplings.
In $A_{3}$Cr$_{2}$O$_{8}$, where $A$ = Sr or Ba, the Cr$^{5+}$ ions surrounded by oxygen ions in a tetrahedral coordination are Jahn-Teller active. The Jahn-Teller distortion leads to a structural transition and a related emergence of three twinned monoclinic domains below the structural phase transition. This transition is highly dynamic over an extended temperature range for $A$ = Sr. We have investigated mixed compounds Ba$_{3-x}$Sr$_{x}$Cr$_{2}$O$_{8}$ with $x=2.9$ and $x=2.8$ by means of X-ray and neutron diffraction, Raman scattering and calorimetry. Based on the obtained evolution of the phonon frequencies, we find a distinct suppression of the orbital-lattice fluctuation regime with increasing Ba content. This stands in contrast to the linear behaviour exhibited by unit cell volumes, atomic positions and intradimer spin-spin exchange interactions.
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