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Register a new userStrong frustration due to competing ferromagnetic and antiferromagnetic interactions: magnetic properties of M(VO)2(PO4)2 (M = Ca and Sr)
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We present a detailed investigation of the magnetic properties of complex vanadium phosphates M(VO)2(PO4)2 (M = Ca, Sr) by means of magnetization, specific heat, 31P NMR measurements, and band structure calculations. Experimental data evidence the presence of ferro- and antiferromagnetic interactions in M(VO)2(PO4)2 resulting in a nearly vanishing Curie-Weiss temperature theta_{CW} < 1 K that contrasts with the maximum of magnetic susceptibility at 3 K. Specific heat and NMR measurements also reveal weak exchange couplings with the thermodynamic energy scale J_c = 10-15 K. Additionally, the reduced maximum of the magnetic specific heat indicates strong frustration of the spin system. Band structure calculations show that the spin systems of the M(VO)2(PO4)2 compounds are essentially three-dimensional with the frustration caused by competing ferro- and antiferromagnetic interactions. Both calcium and strontium compounds undergo antiferromagnetic long-range ordering at T_N = 1.5 K and 1.9 K, respectively. The spin model reveals an unusual example of controllable frustration in three-dimensional magnetic systems.
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Whereas magnetic frustration is typically associated with local-moment magnets in special geometric arrangements, here we show that SrCo$_{2}$As$_{2}$ is a candidate for frustrated itinerant magnetism. Using inelastic neutron scattering (INS), we find that antiferromagnetic (AF) spin fluctuations develop in the square Co layers of SrCo$_{2}$As$_{2}$ below $Tapprox100$ K centered at the stripe-type AF propagation vector of $(frac{1}{2},~frac{1}{2})$, and that their development is concomitant with a suppression of the uniform magnetic susceptibility determined via magnetization measurements. We interpret this switch in spectral weight as signaling a temperature-induced crossover from an instability towards FM ordering to an instability towards stripe-type AF ordering on cooling, and show results from Monte-Carlo simulations for a $J_{1}$-$J_{2}$ Heisenberg model that illustrate how the crossover develops as a function of the frustration ratio $-J_1/(2J_2)$. By putting our INS data on an absolute scale, we quantitatively compare them and our magnetization data to exact-diagonalization calculations for the $J_{1}$-$J_{2}$ model [N. Shannon et al., Eur. Phys. J. B 38, 599 (2004)], and show that the calculations predict a lower level of magnetic frustration than indicated by experiment. We trace this discrepancy to the large energy scale of the fluctuations ($J_{text{avg}}gtrsim75$ meV), which, in addition to the steep dispersion, is more characteristic of itinerant magnetism.
We have studied polycrystalline Yb4LiGe4, a ternary variant of the R5T4 family of layered compounds characterized by a very strong coupling between the magnetic and crystallographic degrees of freedom. The system is mixed valent, with non-magnetic Yb2+ and magnetic Yb3+ present, and is characterized by coexisting ferromagnetic and antiferromagnetic correlations. We present measurements of resistivity, AC-susceptibility, specific heat, and muon spin relaxation (muSR), below 1 K. The low temperature measurements suggest a transition to a mesoscopically inhomogeneous magnetically ordered state below 2 K characterized by fluctuations well below the ordering temperature. This unusual state is believed to result from the enhanced two-dimensionality produced by Li substitution and frustration effects inherent in the Yb sub-lattice geometry.
The local structure of correlated spin-orbit insulator Sr$_{2-x}$M$_x$IrO$_4$ (M = K, La) has been investigated by Ir L$_3$-edge extended x-ray absorption fine structure measurements. The measurements were performed as a function of temperature for different dopings induced by substitution of Sr with La or K. It is found that Ir-O bonds have strong covalency and they hardly show any change across the Neel temperature. In the studied doping range, neither Ir-O bonds nor their dynamics, measured by their mean square relative displacements, show any appreciable change upon carrier doping, indicating possibility of a nanoscale phase separation in the doped system. On the other hand, there is a large increase of the static disorder in Ir-Sr correlation, larger for K doping than La doping. Similarities and differences with respect to the local lattice displacements in cuprates are briefly discussed.
We report observation of strong magnetic proximity coupling in a heterostructured superconductor Sr$_2$VO$_3$FeAs, determined by the upper critical fields $H_{c2}(T)$ measurements up to 65 T. Using the resistivity and the radio-frequency measurements for both $H parallel ab$ and $H parallel c$, we found a strong upward curvature of $H_{c2}^c(T)$, together with a steep increase of $H_{c2}^{ab}(T)$ near $T_c$, yielding the anisotropic factor $gamma_H=H_{c2}^{ab}/H_{c2}^c$ up to $sim$ 20, the largest value among iron-based superconductors. These are attributed to the Jaccarino-Peter effect, rather than to the multiband effect, due to strong exchange interaction between itinerant Fe spins of the FeAs layers and localized V spins of Mott-insulating SrVO$_3$ layers. These findings provide evidence for strong antiferromagnetic proximity coupling, comparable with the intralayer superexchange interaction of SrVO$_3$ layer and sufficient to induce magnetic frustration in Sr$_2$VO$_3$FeAs.
In search of a quantum phase transition between the two-dimensional ($2$D) ferromagnetism of CaCo$_{2-y}$As$_{2}$ and stripe-type antiferromagnetism in SrCo$_{2}$As$_{2}$, we rather find evidence for $1$D magnetic frustration between magnetic square Co layers. We present neutron diffraction data for Ca$_{1-x}$Sr$_{x}$Co$_{2-y}$As$_{2}$ that reveal a sequence of $x$-dependent magnetic transitions which involve different stacking of $2$D ferromagnetically-aligned layers with different magnetic anisotropy. We explain the $x$-dependent changes to the magnetic order by utilizing classical analytical calculations of a $1$D Heisenberg model where single-ion magnetic anisotropy and frustration of antiferromagnetic nearest- and next-nearest-layer exchange are all composition dependent.
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