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Andrej Kancko

Publications and source records attributed to Andrej Kancko.

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Spin-orbit-entangled $J_{\rm eff}=\frac{1}{2}$ magnetism and unconventional spin freezing in the bond-disordered pyrochlore antiferromagnet NaCdCo$_2$F$_7$

Bond disorder in frustrated pyrochlore antiferromagnets can give rise to fundamentally different quantum ground states depending on the nature of the local magnetic moments. Here, we show that the bond-disordered $J_{\rm eff}=\frac{1}{2}$ pyrochlore antiferromagnet NaCdCo$_2$F$_7$ realizes an unconventional spin-glass-like state with continued dynamics, in stark contrast to its isostructural $S=\frac{1}{2}$ NaCdCu$_2$F$_7$ counterpart. High-field magnetization and Co $L_{2,3}$-edge XAS/XMCD establish spin-orbit-entangled $J_{\rm eff}=\frac{1}{2}$ Co$^{2+}$ moments with a substantial unquenched orbital contribution, consistent with local $XY$ anisotropy seen in the isostructural Na$A''$Co$_2$F$_7$ ($A''$ = Ca, Sr) analogues. $\mu$SR and $^{23}$Na NMR measurements reveal progressive slowing of spin fluctuations below $\sim10$ K, culminating in a partially frozen state with persistent low-temperature dynamics that deviates from a canonical spin glass. Comparison with the isostructural bond-disordered pyrochlore NaCdCu$_2$F$_7$, which realizes a random-singlet state, reveals a fundamentally different response of spin-orbit-entangled Co$^{2+}$ moments to bond disorder. These results identify spin-orbit coupling as a key ingredient governing the fate of bond-disordered frustrated pyrochlore magnets.

cond-mat.str-el

Strongly Quenched Kramers Doublet Magnetism in SmMgAl11O19

We report magnetic susceptibility, isothermal magnetization, and specific-heat measurements on the rare-earth hexaaluminate SmMgAl$_{11}$O$_{19}$, where Sm$^{3+}$ realizes a strongly quenched Kramers doublet on a triangular lattice with an exceptionally weak net exchange scale. The Curie--Weiss analysis yields strongly reduced ground-doublet $g$ factors, $g_{ab}\simeq 0.65$ and $g_{c}\simeq 0.70$. This indicates that the low-temperature response is governed primarily by single-ion physics, with crystal-field splitting and $J$-multiplet mixing jointly renormalizing the Sm$^{3+}$ moment, rather than collective exchange. For $H \parallel c$, the specific heat shows no $\lambda$-type anomaly down to 0.35~K but evolves into a well-defined two-level Schottky peak whose gap grows linearly with field, yielding $g_c\simeq0.62$ and recovering nearly all of $R\ln2$ at high fields, thereby confirming an effective $S_{\mathrm{eff}}=\tfrac12$ Kramers doublet description for $T\lesssim10$~K. Together, these results establish SmMgAl$_{11}$O$_{19}$ as a weak-exchange, nearly single-ion triangular Kramers magnet in which frustration produce an anisotropic low-field correlated regime without inducing long-range order.

cond-mat.str-el

Random singlet physics in the $S = \frac{1}{2}$ pyrochlore antiferromagnet NaCdCu$_2$F$_7$

We report a random singlet ground state in the $S=\frac{1}{2}$ Heisenberg pyrochlore antiferromagnet NaCdCu$_2$F$_7$. Cationic Na$^+$/Cd$^{2+}$ disorder on the pyrochlore $A$ site generates a broad distribution of Cu$^{2+}$--F$^-$--Cu$^{2+}$ exchange couplings, introducing intrinsic magnetic bond disorder. Despite strong antiferromagnetic interactions ($\theta_{\mathrm{CW}}=-72$~K), no magnetic order or global spin freezing is observed in DC and AC susceptibility, specific heat or $^{23}$Na nuclear magnetic resonance to 120 mK, with muon spin relaxation experiments confirming persistent spin dynamics to 58 mK. $T$-linear specific heat, a Curie-like susceptibility tail, and power-law scaling with data collapse in $\chi(T)$, $M(H)$, $C_{\mathrm{mag}}/T$, $^{23}$Na $(1/T_1T)$ and the muon spin polarization $P(t)$ reveal a disorder-driven network of random singlets and orphan spins. Scaling across multiple bulk and local probes is consistent with a broad distribution of exchange energies, $P[\mathcal{J}] \sim \mathcal{J}^{-\alpha}$. This behavior contrasts with previously-studied Na$A''B_2$F$_7$ pyrochlore fluorides, where magnetic bond disorder precipitates spin-glass freezing, underscoring the crucial role of strong $S=\frac{1}{2}$ quantum fluctuations in NaCdCu$_2$F$_7$.

cond-mat.str-el

Absence of Long-Range Order and Magnetic Anisotropy in the Triangular Magnet NdMgAl$_{11}$O$_{19}$

We investigated the rare-earth triangular-lattice antiferromagnet NdMgAl$_{11}$O$_{19}$ using single-crystal magnetization (1.8~K $\leq T \leq$ 300~K, $\mu_0 H \leq 7$~T) and specific-heat measurements down to 45~mK. The dc susceptibility confirms a well-isolated Kramers doublet ground state with pronounced Ising-type anisotropy, with $g_c \approx 3.7$ and $g_{ab} \approx 1.45$. Curie--Weiss fits yield weak, anisotropic antiferromagnetic exchange, with $\theta_c = -0.54$~K and $\theta_{ab} = -0.87$~K. Heat-capacity measurements show no long-range magnetic order down to 40~mK, corresponding to a frustration index $f \gtrsim 20$. Instead, $C_m/T$ exhibits a broad maximum near 0.081~K whose magnitude and field evolution are consistent with short-range correlations in an anisotropic triangular lattice. Applied magnetic fields open a Zeeman gap where the specific-heat anomaly follows $\Delta = g \mu_B \mu_0 H$, and $M(H,T)$ is well described by a Brillouin function for an effective $J = 1/2$ moment. The field tuning of the low-temperature entropy manifold allows self-cooling from 1.8~K to 53~mK by adiabatic demagnetisation from a 9~T field. These results identify NdMgAl$_{11}$O$_{19}$ as a nearly ideal weak-exchange triangular magnet with a field-tunable correlated ground state, where two-dimensional crossover effects may emerge from frustrated XXZ interactions.

cond-mat.str-el

Glassy disordered ground states in the frustrated pyrochlore and fluorite antiferromagnets NaCd$M_2$F$_7$ ($M$ = Ni$^{2+}$, Mn$^{2+}$)

We report the crystal structures, magnetic and thermodynamic properties of two magnetically frustrated $A$'$A$"$M_2$F$_7$-type antiferromagnets, NaCdNi$_2$F$_7$ and NaCdMn$_2$F$_7$. While NaCdNi$_2$F$_7$ forms a stable pyrochlore structure (SG: $Fd \overline{3} m$, #227) with magnetic $S$ = 1 Ni$^{2+}$ ions on the frustrated pyrochlore 16$c$ site and fully disordered non-magnetic Na$^+$/Cd$^{2+}$ ions on the pyrochlore 16$d$ site, NaCdMn$_2$F$_7$ favors the defect-fluorite structure (SG: $Fm \overline{3} m$, #225) with magnetic $S$ = 5/2 Mn$^{2+}$ and non-magnetic Na$^+$ and Cd$^{2+}$ ions fully disordered on the fluorite 4$a$ site. This is a result of the Mn$^{2+}$ ionic radius being too close to the average Na$^+$/Cd$^{2+}$ ionic radius, hindering the cationic site ordering towards the stable pyrochlore structure. In both cases, dominant antiferromagnetic interactions $\theta_{CW,Ni}$ = -91.2(5) K and $\theta_{CW,Mn}$ = -42.4(4) K are noted, with no magnetic transition until $T_{f,Ni}$ = 3.2 K and $T_{f,Mn}$ = 2.0 K, implying substantial frustration, with frustration indices $f_{Ni}$ = 28.5 and $f_{Mn}$ = 21. AC susceptibility measurements and bifurcation of ZFC/FC low-field magnetization indicate a glassy ground-state, precipitated by the magnetic-bond-disorder stemming from the inherent structural disorder.

cond-mat.str-el

Robustness of the pyrochlore structure in rare-earth A2Ir2O7 iridates and pressure-induced structural transformation in IrO2

A comprehensive study of the structural properties of the heavily investigated rare-earth A2Ir2O7 series under extreme conditions is presented. The series is covered by studying iridates with A = Pr, Sm, Dy-Lu. Temperature- and pressure-dependent synchrotron X-ray powder diffraction experiments reveal robustness of the pyrochlore structure throughout the rare-earth series, down to 4 K and up to 20 GPa. The thermal expansivity and pressure compressibility are determined, including Debye temperature, bulk modulus and Grüneisen parameter. Temperature and pressure evolution of the fractional coordinate of oxygen at 48f Wyckoff position, the sole free atomic position parameter, is investigated and discussed regarding the antiferromagnetic ordering of the Ir magnetic moments. In addition, the pressure evolution of the crystal structure of an IrO2 minority phase is followed. The tetragonal rutile-type structure is orthorhombically distorted at 15 GPa, and the orthorhombic structure is not fully stabilised up to 20 GPa.

cond-mat.mtrl-sci

Structural and spin-glass properties of single crystal $J_{eff}$ = 1/2 pyrochlore antiferromagnet NaCdCo$_2$F$_7$ : correlating $T_f$ with magnetic-bond-disorder

Weak bond disorder disrupts the expected spin-liquid ground-state of the ideal $S$ = 1/2 Heisenberg pyrochlore antiferromagnet. Here we introduce a single crystal study of the structural and magnetic properties of the bond-disordered pyrochlore NaCdCo$_2$F$_7$. The magnetic susceptibility appears isotropic, with a large negative Curie-Weiss temperature ($θ_{CW}$ = -108(1) K), however no magnetic order is observed on cooling until a spin-glass transition at $T_f$ = 4.0 K. AC-susceptibility measurements show a frequency-dependent shift of the associated cusp in $χ$ at $T_f$, that can be fitted well by the empirical Vogel-Fulcher law. The magnetic moment of $μ_{eff}$ = 5.4(1) $μ_{B}$/Co$^{2+}$ indicates a significant orbital contribution and heat capacity measurements show that down to 1.8 K, well below $T_f$, only $S_{mag}$ ~2/3 Rln(2) of the magnetic entropy is recovered, suggestive of residual continued dynamics. Structural and magnetism comparisons are made with the other known members of the Na$A$Co$_2$F$_7$ family ($A$ = Ca$^{2+}$, Sr$^{2+}$), confirming the expected relationship between spin-glass freezing temperature, and extent of magnetic bond disorder brought about by the size mismatch between A-site ions.

cond-mat.str-el