Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userUnravelling competing microscopic interactions at a phase boundary: a single crystal study of the metastable antiferromagnetic pyrochlore Yb$_{2}$Ge$_{2}$O$_{7}$
154
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
We report inelastic neutron scattering measurements from our newly synthesized single crystals of the structurally metastable antiferromagnetic pyrochlore Yb$_{2}$Ge$_{2}$O$_{7}$. We determine the four symmetry-allowed nearest-neighbor anisotropic exchange parameters via fits to linear spin wave theory supplemented by fits of the high-temperature specific heat. The exchange parameters so-determined are strongly correlated to the values determined for the $g$-tensor components, as previously observed for the related Yb pyrochlore Yb$_{2}$Ti$_{2}$O$_{7}$. To address this issue, we directly determined the $g$-tensor from electron paramagnetic resonance of 1% Yb-doped Lu$_{2}$Ge$_{2}$O$_{7}$, thus enabling an unambiguous determination of the exchange parameters. Our results show that Yb$_{2}$Ge$_{2}$O$_{7}$ resides extremely close to the classical phase boundary between an antiferromagnetic $Gamma_5$ phase and a splayed ferromagnet phase. By juxtaposing our results with recent ones on Yb$_{2}$Ti$_{2}$O$_{7}$, our work illustrates that the Yb pyrochlore oxides represent ideal systems for studying quantum magnets in close proximity to classical phase boundaries.
rate research
Read More
Elastic neutron scattering, ac susceptibility, and specific heat experiments on the pyrochlores Er$_{2}$Ge$_{2}$O$_{7}$ and Yb$_{2}$Ge$_{2}$O$_{7}$ show that both systems are antiferromagnetically ordered in the $Gamma_5$ manifold. The ground state is a $psi_{3}$ phase for the Er sample and a $psi_{2}$ or $psi_{3}$ phase for the Yb sample, which suggests Order by Disorder(ObD) physics. Furthermore, we unify the various magnetic ground states of all known R$_{2}$B$_{2}$O$_{7}$ (R = Er, Yb, B = Sn, Ti, Ge) compounds through the enlarged XY type exchange interaction $J_{pm}$ under chemical pressure. The mechanism for this evolution is discussed in terms of the phase diagram proposed in the theoretical study [Wong et al., Phys. Rev. B 88, 144402, (2013)].
Cubic Y$_{2}$Ti$_{2}$O$_{7}$ single crystals doped with Er$^{3+}$ and Yb$^{3+}$ ions have been studied by the methods of electron spin resonance (ESR) and selective laser spectroscopy. ESR spectra exhibit signals from rare-earth ions that substitute for yttrium ions in sites with local trigonal symmetry. The $g$ tensor components are determined. The results of optical investigations indicate that impurity centers of several types are formed; the sublevel energies of the ground and excited multiplets of these centers are found. Among the great variety of detected optical centers, the centers that dominate in the formation of ESR spectra are discriminated. An analysis of the experimental data using the exchange-charge model have made it possible to determine the sets of parameters of the crystal field for Er$^{3+}$ and Yb$^{3+}$ ions substituting Y$^{3+}$ ions in regular crystallographic sites in pyrochlore Y$_{2}$Ti$_{2}$O$_{7}$.
CaFe$_{2}$O$_{4}$ is an $S=5/2$ antiferromagnet exhibiting two magnetic orders which shows regions of coexistence at some temperatures. Using a Greens function formalism, we model neutron scattering data of the spin wave excitations in this material, ellucidating the microscopic spin Hamiltonian. In doing so, we suggest that the low temperature A phase order $(uparrowuparrowdownarrowdownarrow)$ finds its origins in the freezing of antiphase boundaries created by thermal fluctuations in a parent B phase order $(uparrowdownarrowuparrowdownarrow)$. The low temperature magnetic order observed in CaFe$_{2}$O$_{4}$ is thus the result of a competition between the exchange coupling along $c$, which favors the B phase, and the single-ion anisotropy which stabilizes thermally-generated antiphase boundaries, leading to static metastable A phase order at low temperatures.
We report Resonant Inelastic X-ray Scattering (RIXS) study of the magnetic excitation spectrum in a highly insulating Eu$_{2}$Ir$_{2}$O$_{7}$ single crystal that exhibits a metal-insulator transition at $T_{MI}$ = 111(7) K. A propagating magnon mode with 20 meV bandwidth and 28 meV magnon gap is found in the excitation spectrum at 7 K, which is expected in the all-in-all-out (AIAO) magnetically ordered state. This magnetic excitation exhibits substantial softening as temperature is raised towards $T_{MI}$, and turns into highly damped excitation in the paramagnetic phase. Remarkably, the softening occurs throughout the whole Brillouin zone including the zone boundary. This observation is inconsistent with magnon renormalization expected in a local moment system, and indicates that the strength of electron correlation in Eu$_{2}$Ir$_{2}$O$_{7}$ is only moderate, so that electron itinerancy should be taken into account in describing its magnetism.
We explore the spin states in the quantum spin chain compound SrCo$_{2}$V$_{2}$O$_{8}$ up to 14.9 T and down to 50 mK, using single-crystal neutron diffraction. Upon cooling in zero-field, antiferromagnetic (AFM) order of Neel type develops at $T_mathrm{{N}}$ $simeq$ 5.0 K. Applying an external magnetic field ($H$ $parallel$ $c$-axis) destabilizes the Neel order, leading to an order-disorder transition when applying a field between $T_mathrm{{N}}$ and $sim$ 1.5 K. Below 1.5 K, we observe a Neel to longitudinal spin density wave (LSDW) order transition at 3.9 T, and a LSDW to emergent AFM order transition at 7.0 T. Our results also reveal several unique signatures for the states of the spins that are not present in the isostructural counterpart BaCo$_{2}$V$_{2}$O$_{8}$.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
