The exotic magnetic properties of the pyrochlore Pr$_2$Zr$_2$O$_7$ are determined by the coupling of spin, orbital, and lattice degrees of freedom. Magnetism in this material originates from the non-Kramers Pr$^{3+}$ ion, and the exotic behavior has been discussed both in the framework of dipole-quadrupole properties of magnetic moments and disorder splitting the non-Kramers doublet. We use magneto-Raman spectroscopy to probe the crystal electric field (CEF) excitations of Pr$^{3+}$ in magnetic fields up to 14 T applied along the [100] and [111] crystallographic directions at 2 K. For $\mathrm{B}\parallel[100]$, the field evolution of the Raman active crystal field modes is quantitatively described by conventional Zeeman splitting of the Pr$^{3+}$ ground state doublet, including the thermally populated upper Zeeman branch at elevated temperature. For $\mathrm{}{B}\parallel[111]$, the spectra separate into responses from the triangular and kagome sublattices, and the CEF excitations of Pr$^{3+}$ on the triangular lattice exhibit the expected Zeeman shift consistent with full moments polarization. In contrast, the CEF excitations of Pr$^{3+}$ on the kagome lattice do not split as expected and instead broaden strongly with increasing field. This behavior is inconsistent with a static polarized configuration and is captured phenomenologically by a motional-narrowing description in which the kagome plane moments fluctuate between Zeeman-split levels on a meV timescale. This result offers a natural explanation for the reduced magnetization observed in $\mathrm{}{B}\parallel[111]$ and provides further evidence of the dipole-quadrupole properties of magnetic moments. It highlights Raman scattering as a sensitive probe of exotic spin-orbital dynamics in frustrated magnets.
Kagome lattices host rich magnetic, topological, and transport phenomena owing to their geometric frustration and strong spin correlations. Here we present a systematic neutron scattering study of the kagome metal Y$_{0.5}$Fe$_3$Sn$_3$, which orders into a collinear $c$-axis antiferromagnetic (AF) state below $T_N =$ 5...
Jin-Zhi Ding, Yang Liu, F. Pan et al.· Physical review B· 0 citations
Geometrically frustrated triangular-lattice antiferromagnets exhibit a delicate competition between magnetic order and quantum spin liquid (QSL) behavior, with the Yb-based delafossite family $A$Yb$X_2$ providing a structurally clean platform for exploring this physics. Here, we report a comprehensive study of single-c...
B. Belbase, A. Unnikrishnan, Piyush Chhallare et al.· 1 citation
The relevance of spin, lattice and orbital degrees of freedom in the quasi-2D Ising-like magnet Li$_2$FeSiO$_4$ is demonstrated by thermal expansion and specific heat measurements supported by numerical studies. By means of thermodynamic and Gr\"uneisen analysis, we separate the orbital signatures and quantify the ener...
W. Hergett, K. Ackermann, S. Spachmann et al.· 0 citations
Ce$_2$Te$_5$ is a layered $f$-electron van der Waals magnet in which reduced dimensionality and inequivalent Ce sites give rise to competing magnetic interactions. We investigate its magnetic ground state using muon spin relaxation ($\mu$SR), neutron powder diffraction (NPD), and inelastic neutron scattering (INS). Zer...
R. Tripathi, D. Adroja, C. Ritter et al.· 0 citations
We report an electron paramagnetic resonance (EPR) study of Dy${^3+}$ in CaWO$_4$ single crystals spanning dopant concentrations from 80~ppb to 247~ppm. The $g$ factors of the ground Kramers doublet at the $S_4$ point-group site, $g_\parallel = 7.22 \pm 0.01$ and $g_\perp = 5.45 \pm 0.01$, and the hyperfine constants o...
Achutha Kumar, Larissa Aboudem-Joumessi, R. Dassonneville et al.· 0 citations
The magnetic ground states of rare-earth frustrated magnets can be governed by competing energy scales arising from crystal-field anisotropy, exchange interactions, and long-range dipolar interactions. Here we investigate this interplay in the triangular-lattice antiferromagnet NaBaEr(BO$_3$)$_2$ by combining magnetiza...
Cheng Su, Yong-Lin Wang, Zi-Hang Gao et al.· 0 citations
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