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Register a new userMagnetic Microphase Inhomogeneity as a Thermodynamic Precursor of Ground State Phase Separation in Weakly Coupled Spin-$frac{3}{2}$ Chains
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$gamma$-CoV$_{2}$O$_{6}$ is a quasi one-dimensional spin-$frac{3}{2}$ magnet that possesses two distinct magnetic orders in the ground state with modulation vectors $k_mathrm{1}$ = ($frac{1}{2}$, 0, 0) and $k_mathrm{2}$ = ($frac{1}{4}$, 0, -$frac{1}{4}$), respectively. Here, we use muon spin relaxation and rotation to reveal the thermodynamics of the magnetic phase separation in this compound. In the paramagnetic (PM) region, short-range correlated spin clusters emerge at $T_mathrm{m}$ $simeq$ 26 K at the $it{partial}$ expense of the PM volume. Upon further cooling, we show that these emergent clusters become spatially coherent at $T_mathrm{{N2}}$ = 7.5 K and eventually form the $k_mathrm{2}$ order at $T^{star}$ = 5.6 K, while the remaining PM spins are driven into the $k_mathrm{1}$ state at $T_mathrm{{N1}}$ = 6.6 K. These results stress magnetic microphase inhomogeneity as a thermodynamic precursor for the ground state phase separation in weakly coupled spin-$frac{3}{2}$ chains.
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We report on the synthesis of a new $gamma$-phase of the spin $S$~=~$frac{3}{2}$ compound SrCo$_2$(PO$_4$)$_2$ together with a detailed structural, magnetic and thermodynamic properties. The $gamma$-phase of SrCo$_2$(PO$_4$)$_2$ crystallizes in a triclinic crystal structure with the space group $Pbar{1}$. Susceptibility and specific heat measurements reveal that SrCo$_2$(PO$_4$)$_2$ orders antiferromagnetically below $T_{rm N}simeq 8.5$,K and the nature of ordering is three dimensional (3D). The magnetic isotherm at temperatures below $T_{rm N}$ shows a field-induced spin-flop transition, related to the magnetocrystalline anisotropy, at an applied field of $sim$~4.5~Tesla. Remarkably, heat capacity shows magnetic-field-induced transitions at $T_{rm N1}$ = 3.6 K and $T_{rm N2}$ = 7.4 K. The magnetic long range ordering (LRO) is also confirmed in both the Knight shift and spin-lattice relaxation rate ($1/T_{1}$) of the $^{31}$P-NMR measurements. However, below the LRO we have not detected any NMR signal due to faster relaxation. We have detected two structurally different phosphorous sites in $gamma$-phase of SrCo$_{2}$(PO$_{4}$)$_{2}$ and they shift differently with temperature.
Neutron scattering has been used to investigate the evolution of the long- and short-range charge-ordered (CO), ferromagnetic (FM), and antiferromagnetic (AF) correlations in single crystals of Pr1-xCaxMnO3. The existence and population of spin clusters as refected by short-range correlations are found to drastically depend on the doping (x) and temperature (T). Concentrated spin clusters coexist with long-range canted AF order in a wide temperature range in x = 0.3 while clusters do not appear in x = 0.4 crystal. In contrast, both CO and AF order parameters in the x = 0.35 crystal show a precipitous decrease below ~ 35 K where spin clusters form. These results provide direct evidence of magnetic phase separation and indicate that there is a critical doping x_c (close to x = 0.35) that divides the phase-separated site-centered from the homogeneous bond-centered or charge-disproportionated CO ground state.
We report a comprehensive investigation of the magnetism of the $S$ = 3/2 triangular-lattice antiferromagnet, $alpha$-CrOOH(D) (delafossites green-grey powder). The nearly Heisenberg antiferromagnetic Hamiltonian ($J_1$ $sim$ 23.5 K) with a weak single-ion anisotropy of $|D|$/$J_1$ $sim$ 4.6% is quantitatively determined by fitting to the electron spin resonance (ESR) linewidth and susceptibility measured at high temperatures. The weak single-ion anisotropy interactions, possibly along with other perturbations, e.g. next-nearest-neighbor interactions, suppress the long-range magnetic order and render the system disordered, as evidenced by both the absence of any clear magnetic reflections in neutron diffraction and the presence of the dominant paramagnetic ESR signal down to 2 K ($sim$ 0.04$J_1$$S^2$), where the magnetic entropy is almost zero. The power-law behavior of specific heat ($C_m$ $sim$ $T^{2.2}$) observed below the freezing temperature of $T_f$ = 25 K in $alpha$-CrOOH or below $T_f$ = 22 K in $alpha$-CrOOD is insensitive to the external magnetic field, and thus is consistent with the theoretical prediction of a gapless U(1) Dirac quantum spin liquid (QSL) ground state. At low temperatures, the spectral weight of the low-energy continuous spin excitations accumulates at the K points of the Brillouin zone, e.g. $|mathbf{Q}|$ = 4$pi$/(3$a$), and the putative Dirac cones are clearly visible. Our work is a first step towards the understanding of the possible Dirac QSL ground state in this triangular-lattice magnet with $S$ = 3/2.
Field-dependent specific heat and neutron scattering measurements were used to explore the antiferromagnetic S=1/2 chain compound CuCl2 * 2((CD3)2SO). At zero field the system acquires magnetic long-range order below TN=0.93K with an ordered moment of 0.44muB. An external field along the b-axis strengthens the zero-field magnetic order, while fields along the a- and c-axes lead to a collapse of the exchange stabilized order at mu0 Hc=6T and mu0 Hc=3.5T, respectively (for T=0.65K) and the formation of an energy gap in the excitation spectrum. We relate the field-induced gap to the presence of a staggered g-tensor and Dzyaloshinskii-Moriya interactions, which lead to effective staggered fields for magnetic fields applied along the a- and c-axes. Competition between anisotropy, inter-chain interactions and staggered fields leads to a succession of three phases as a function of field applied along the c-axis. For fields greater than mu0 Hc, we find a magnetic structure that reflects the symmetry of the staggered fields. The critical exponent, beta, of the temperature driven phase transitions are indistinguishable from those of the three-dimensional Heisenberg magnet, while measurements for transitions driven by quantum fluctuations produce larger values of beta.
We present a model compound with a spin-1/2 frustrated square lattice, in which three ferromagnetic (F) interactions and one antiferromagnetic (AF) compet. Considering the effective spin-1 formed by the dominant F dimer, this square lattice can be mapped to a spin-1 spatially anisotropic triangular lattice. The magnetization curve exhibits gapped behavior indicative of a dominant one-dimensional (1D) AF correlation. In the field-induced gapless phase, the specific heat and magnetic susceptibility show a phase transition to an ordered state with 2D characteristics. These results indicate that the spin-1 Haldane state is extended to the 2D system. We demonstrate that the gapped ground state observed in the present spin-1/2 frustrated square lattice originates from the one-dimensionalization caused by frustration.
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