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V. N. Glazkov

Publications and source records attributed to V. N. Glazkov.

At least 19 recordsLinked to original sources

Experimental observation of decoupled spin subsystems in decorated square kagomé lattice magnets of the nabokoite family

The square kagomé lattice (SKL) offers a model platform for investigating geometric frustration in 2D systems. Nabokoite-family compounds \nabok{A}{X} (A=Na, K, Cs, Rb and X=Cl, Br) extend this physics to a 3D network, where 2D SKL layers are decorated by interlayer spins. Using electron paramagnetic resonance (EPR), we demonstrate a dramatic splitting of this complex exchange network into two virtually decoupled spin subsystems: absolute calibration of the electron paramagnetic resonance (EPR) absorption reveals that only a fraction of all copper spins in nabokoites is EPR-active and this fraction of the spins orders at the Néel point. Comparison of the EPR absorption and static susceptibility indicates that contribution of the EPR-silent spin subsystem to total magnetic susceptibility decreases on cooling. This direct observation of coexisting magnetic order and possible spin-liquid dynamics within a single compound challenges conventional models of unified exchange networks in decorated frustrated lattices.

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Collinear and noncollinear antiferromagnetic ordering in a highly frustrated decorated square kagomé lattice antiferromagnets of the nabokoite family

Nabokoite family compounds ACu$_7$(TeO$_4$)(SO4)$_5$X (A=Na, K, Rb, Cs; X=Cl, Br) host frustrated 2D square kagom'{e} lattice layers decorated by additional inter-layer magnetic ions. We study magnetic order in nabokoites with multi-frequency electron spin resonance spectroscopy and thermodynamic measurement (specific heat, magnetization and dielectric permittivity). Our study reveals that the choice of the low-temperature ground state is qualitatively different in light-alkali-ion (K, Na) and heavy-alkali-ion (Rb, Cs) compounds. Heavy-alkali-ion nabokoites order in conventional collinear antiferromagnetic pattern with easy-axis anisotropy. The parameters of the ordered antiferromagnetic state are very close for all heavy-alkali-ion subfamily. Light-alkali-ion members of nabokoite family demonstrate much more complicated route to the ordered state: firstly, a ferroelectric transition at 25-90K lifts the frustration and thus pre-cooks the low-temperature ordering; secondly, an unusual noncollinear magnetic order develops via two-step phase transition with first transition temperature $T_{c1}\simeq 5-6$K and the second transition at $T_{c2}\simeq 3-4$K. Noncollinear order is evidenced by observation of characteristic non-Larmor antiferromagnetic resonance mode. Spin dynamics of light-alkali-ion nabokoites is characterized by three zero-field magnon gaps and two spin-reorientation fields, the values of magnon gaps and critical fields are quite different for different compounds. The finite-size cluster modeling of pyramidal structural block of nabokoite structure combined suggests that the critical closeness of the nabokoite exchange coupling parameters to the border-line between the different quantum ground state of pyramidal building block of nabokoite structure could be the clue to the choice of qualitatively different ordered state in light- and heavy-alkali-ion nabokoites.

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Stabilization of the collinear plateau phase by thermal fluctuations in the disordered triangular lattice antiferromagnet Rb$_{(1-x)}$K$_{x}$Fe(MoO$_4$)$_2$

The triangular lattice antiferromagnet RbFe(MoO$_4$)$_2$ orders antiferromagnetically in a planar 120$^\circ$-structure below $T_\textrm{N}\approx 4$ K. A striking feature of RbFe(MoO$_4$)$_2$ magnetic phase diagram is the presence of collinear ``1/3-plateau'' magnetic phase, which is stabilized by thermal and quantum fluctuations at magnetization $M\approx \frac{1}{3} M_\textrm{sat}$. Static disorder caused by impurities is predicted to act against the effect of fluctuations and to suppress collinear plateau phase (Maryasin and Zhitomirsky, PRL 111, 247201 (2013)). Balance between ``dynamic'' thermal and quantum fluctuations and ``static'' impurity-induced disorder is temperature-sensitive, which allows thermal fluctuations to take over the effect of static disorder and leads to the revival of the fluctuation-stabilized ``1/3-plateau'' phase on heating. Here we present experimental results directly confirming this prediction and demonstrating re-establishment of the plateau-like phase in the diluted Rb$_{(1-x)}$K$_{x}$Fe(MoO$_4$)$_2$ sample at moderate dilution level $x=15$\% on heating as the effect of thermal fluctuations increases.

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High-frequency dielectric anomalies in a highly frustrated square kagome lattice nabokoite family compounds ACu$_7$(TeO$_4$)(SO$_4$)$_5$Cl (A=Na, K, Rb, Cs)

Nabokoite family compounds ACu$_7$(TeO$_4$)(SO$_4$)$_5$Cl (A=Na, K, Cs, Rb) are candidates for the experimental realization of highly-frustrated 2D square kagome lattice (SKL). Their magnetic subsystem includes SKL layers decorated by additional copper ions. All members of this family are characterized by quite high Curie-Weiss temperatures ($\sim 80-200$ K), but magnetic ordering was reported only for Na and K compounds at a much lower temperatures below 4 K. We report here results of the study of high-frequency ($\sim 10$ GHz) dielectric properties of this family of compounds. Our study revealed presence of the strong dielectric anomaly both in the real and imaginary parts of high-frequency dielectric permittivity for Na and K compounds approx. 100 and 26 K, correspondingly, presumably related to antiferroelectric ordering. Additionally, much weaker anomalies were observed at approximately 5K indicating possible interplay of magnetic and lattice degrees of freedom. We discuss possible relation between the structure rearrangements accompanying dielectric anomalies and a delayed magnetic ordering in the nabokoite family compounds.

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Static and resonant properties of decorated square kagome lattice compound KCu$_7$(TeO$_4$)(SO$_4$)$_5$Cl

The magnetic subsystem of nabokoite, KCu$_7$(TeO$_4$)(SO$_4$)$_5$Cl, is constituted by copper ions forming a buckled square kagomé lattice decorated by quasi-isolated ions. This combination determines peculiar physical properties of this compound evidenced in electron spin resonance (ESR) spectroscopy, dielectric permittivity $\varepsilon$, magnetization $M$ and specific heat $C_p$ measurements. At lowering temperature, the magnetic susceptibility $χ= M/H$ passes through a broad hump inherent for low-dimensional magnetic systems at about 150 K and a sharp peak at antiferromagnetic phase transition at $T_N = 3.2 $K. The $C_p(T,H)$ curves demonstrate additional peak-like anomaly at $T_{peak}= 5.7$K robust to magnetic field. The latter can be ascribed to low-lying singlet excitations filling the singlet-triplet gap in magnetic excitation spectrum of the square kagomé lattice [J.Richter, O.Derzhko and J.Schnack, Phys. Rev. B \textbf{105} (2022) 144427]. ESR spectroscopy provides indications that antiferromagnetic structure below $T_N$ is non-collinear. Separate issue is the observation of antiferroelectric-type behavior in $\varepsilon$ at low temperatures, which tentatively reduces the symmetry and partially lifts frustration of magnetic interactions of decorating copper ions with buckled square kagomé lattice. These complex thermodynamic and resonant properties signal the presence of two weakly coupled magnetic subsystems in nabokoite, namely a spin-liquid in square kagomé lattice layers and an antiferromagnet represented by decorating ions.

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Strongly anisotropic magnetocaloric effect in a dipolar magnet LiGdF$_4$

We report the detailed study of the magnetocaloric effect (MCE) in a dipolar-Heisenberg magnet LiGdF$_4$ using magnetization measurements performed on a single crystal sample. Entropy variation on isothermal demagnetization from the magnetic field up to 3 T is determined in the temperature range 2-10 K for two principal directions of the applied field (parallel and perpendicular to the tetragonal $c$-axis of the crystal). The MCE is found to be highly anisotropic, with the cooling efficiency being up to twice higher at $H\parallel c$. The results are nicely interpreted in the frame of a conventional molecular field approach taking into account considerable anisotropy of the paramagnetic Curie-Weiss temperature. These results are compared to earlier studies of MCE in powder samples of LiGdF$_4$ [T. Numazawa et al., AIP Conf. Proc. 850, 1579 (2006)] as well as with analogous data for other well known magnetocaloric materials. Our findings may open new possibilities to enhance the efficiency of magnetic refrigeration in the liquid helium-4 temperature range.

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Magnetic resonance in the quasi-2D square lattice easy-plane antiferromagnet Ba$_2$MnGe$_2$O$_7$

We report results of a multi-frequency (0.8-60 GHz) electron spin resonance study of the spin dynamics in the quasi-2D square lattice antiferromagnet Ba$_2$MnGe$_2$O$_7$ both in antiferromagnetically ordered and paramagnetic phases. We directly observe two zero-field gaps in the excitation spectrum of the ordered phase, the larger one being due to easy-plane anisotropy, and the smaller one indicates the presence of fourth-order in-plane anisotropy probably related to the multiferroic properties of this compound. We observe effects of hyperfine interaction on the electron spin resonance spectra in the antiferromagnetically ordered state, which turns out to be comparable with in-plane anisotropy. The hyperfine field strength is found from the observed low-temperature electron spin resonance data. The spin dynamics of the paramagnetic phase is characterized by strong broadening of the ESR absorption line, which can be ascribed to the vortex dynamics of a 2D magnet.

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Microscopic spin Hamiltonian for a dipolar-Heisenberg magnet LiGdF4 from EPR measurements

Low-temperature electron paramagnetic resonance measurements are performed on single crystals of LiY_{1-x}Gd_xF_4 with weak x=0.005 and moderate x=0.05 concentration of Gd ions. Modeling of the experimental spectra allows us to precisely determine microscopic parameters of the spin Hamiltonian of the parent LiGdF4 material, including the nearest-neighbor exchange constant. The obtained parameters are further tested by comparing a strongly anisotropic Curie-Weiss temperature obtained for LiGdF4 in our static magnetization measurements with theoretically computed values. We find a fine balance between principal magnetic interactions in LiGdF4, which results in a hidden magnetic frustration presumably leading to a delayed magnetic ordering and an enhanced magnetocaloric effect at low temperatures.

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Antiferromagnetic resonance in a spin-gap magnet with strong single-ion anisotropy

Quasi-one-dimensional magnet NiCl$_2\cdot$4SC(NH$_2$)$_2$, usually abbreviated as DTN, does not order at zero field down to $T=0$: due to the strong single-ion anisotropy of the "easy plane" type acting on $S=1$ Ni$^{2+}$ ions, the $S_z=0$ ground state is separated from $S_z=\pm 1$ excitations by an energy gap. Once the magnetic field is applied along the main anisotropy axis, the gap closes at $B_{c1}=2.18$ T and the field-induced antiferromagnetic order arises. The low-energy excitations spectrum of this field-induced ordered state includes two branches of excitations, one of them have to be a gapless Goldstone mode. Recent studies of excitations spectrum in a field-induced ordered state of DTN (T.Soldatov et.al, Phys.Rev.B 101, 104410 (2020)) have revealed that Goldstone mode became gapped as magnetic field deviates from the main symmetry axis. This paper proposes simple description of antiferromagnetic resonance modes of quasi-one-dimensional quantum $S=1$ magnet with strong single-ion anisotropy. The approach used is based on a combination of the strong coupling model for the anisotropic spin chain with the conventional mean-field model of antiferromagnetic resonance. The resulting model fits to the known experimental results without additional tuning parameters.

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Magnetic resonance of collective paramagnets with gapped excitations spectrum

Some magnets due to particular geometry of the exchange bonds do not undergo transition to the conventional magnetically ordered state despite of the presence of significant exchange couplings. Instead, a collective paramagnetic state is formed. The later state can remain stable down to $T=0$ if the ground state of this magnet turns out to be nonmagnetic singlet separated from the excited triplet states by an energy gap. Low-temperature spin dynamics of the collective paramagnets with gapped excitations spectrum (or spin-gap magnets) can be described in terms of a dilute gas of the triplet excitations. Applied magnetic field can suppress the energy gap, resulting in the formation of the gapless spin-liquid state or even leading to the unusual phenomenon of field-induced antiferromagnetic order. Introduction of defects in the crystallographic structure of the spin-gap magnet can result either in the formation of multi-spin paramagnetic center or in the formation of randomly distributed modified exchange bonds in the crystal. This review includes results of electron spin resonance (ESR) spectroscopy study of several representative quantum paramagnets with gapped excitations spectrum: quasy-two-dimensional magnet \phcc{}, quasy-one-dimensional magnets of "spin-tube" type \sul{} and "spin-ladder" type \dimpy{}. We will demonstrate that ESR absorption spectra reveal common features of these systems: ESR spectroscopy allows to observe and characterize fine structure if the triplet energy levels, to identify many-particles relaxation processes in the gas of triplet excitations and to observe collective spin-wave oscillations in the field induced antiferromagnetically ordered state, as well as to observe some individual features of the studied systems.

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Anisotropy-induced soliton excitation in magnetized strong-rung spin ladders

We report low temperature electron spin resonance experimental and theoretical studies of an archetype $S=1/2$ strong-rung spin ladder material (C$_{5}$H$_{12}$N)$_{2}$CuBr$_{4}$. Unexpected dynamics is detected deep in the Tomonaga-Luttinger spin liquid regime. Close to the point where the system is half-magnetized (and believed to be equivalent to a gapless easy plane chain in zero field) we observed orientation-dependent spin gap and anomalous $g$-factor values. Field theoretical analysis demonstrates that the observed low-energy excitation modes in magnetized (C$_{5}$H$_{12}$N)$_{2}$CuBr$_{4}$ are solitonic excitations caused by Dzyaloshinskii-Moriya interaction presence.

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Splitting of antiferromagnetic resonance modes in the quasi-two-dimensional collinear antiferromagnet Cu(en)(H$_2$O)$_2$SO$_4$

Low-temperature magnetic resonance study of the quasi-two-dimensional antiferromagnet Cu(en)(H$_2$O)$_2$SO$_4$ (en = C$_2$H$_8$N$_2$) was performed down to 0.45~K. This compound orders antiferromagnetically at 0.9K. The analysis of the resonance data within the hydrodynamic approach allowed to identify anisotropy axes and to estimate the anisotropy parameters for the antiferromagnetic phase. Dipolar spin-spin coupling turns out to be the main contribution to the anisotropy of the antiferromagnetic phase. The splitting of the resonance modes and its non-monotonous dependency on the applied frequency was observed below 0.6K in all three field orientations. Several models were discussed to explain the origin of the nontrivial splitting and the existence of inequivalent magnetic subsystems in Cu(en)(H$_2$O)$_2$SO$_4$ was chosen as the most probable source.

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Electron spin resonance study of spin relaxation in the strong-leg spin ladder with nonmagnetic dilution

We have studied electron spin resonance (ESR) absorption spectra for the nonmagnetically diluted strong-leg spin ladder magnet ({C}$_{7}$H$_{10}$N)$_{2}$Cu$_{(1-x)}$Zn$_{x}$Br$_{4}$ (abbreviated as DIMPY) down to 450 mK. Formation of the clusters with non-zero net magnetization is confirmed; the cluster-cluster interaction is evidenced by the concentration dependence of ESR absorption. High-temperature spin-relaxation time was found to increase with non-magnetic dilution. The ESR linewidth analysis proves that the Dzyaloshinskii-Moriya (DM) interaction remains the dominant spin-relaxation channel in diluted DIMPY. Experimental data indicate that the dilution results in the weakening of the effective DM interaction, which can be interpreted as total suppression of DM interaction in the close vicinity of impurity atom.

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Reminiscence of a magnetization plateau in a magnetization processes of toy-model triangular and tetrahedral clusters

We discuss magnetization curves of a toy-model trigonal and tetrahedral clusters. Nonlinearity of magnetization with local minimum of differential susceptibility resembling known magnetization plateaus of triangular-lattice and pyrochlore lattice antiferromagnets is observed at intermediate temperature range $ J\lesssim T\lesssimΘ$ (here $J$ is the exchange coupling constant and $Θ$ is a Curie-Weiss temperature). This behavior is due to increased statistical weight of the states with intermediate total spin of the cluster, which is related to the `order-by-disorder' mechanism of plateau stabilization of a macroscopic frustrated magnet.

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Experimental study of antiferromagnetic resonance in noncollinear antiferromagnet Mn$_{3}$Al$_{2}$Ge$_{3}$O$_{12}$

We have measured antiferromagnetic resonance (AFMR) frequency-field dependences for aluminum-manganese garnet Mn$_{3}$Al$_{2}$Ge$_{3}$O$_{12}$ at frequencies from 1 to 125 GHz and at the fields up to 60 kOe. Three AFMR modes were observed for all orientations, their zero field gaps are about 40 and 70 GHz. Andreev-Marchenko hydrodynamic theory [Sov. Phys. Usp. 130, 39 (1980)] well describes experimental frequency-field dependences. We have observed hysteresis of resonance absorption as well as history dependence of resonance absorption near gap frequencies below 10 kOe in all three measured field orientations, which are supposedly due to the sample domain structure. Observation of the AFMR signal at the frequencies from 1 to 5 GHz allows to estimate repulsion of nuclear and electron modes of spin precession in the vicinity of spin-reorientation transition at H||[100].

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Formation of the S=1 paramagnetic centers in the bond-diluted spin-gap magnet

Electron spin resonance experiment reveals that non-magnetic bond doping of the spin-gap magnet (C$_4$H$_{12}$N$_2$)Cu$_2$Cl$_6$ (abbreviated PHCC) results in the formation of $S=1$ paramagnetic centers that dominate low-temperature ESR response. We have followed evolution of this signal with doping impurity content and have found that these centers concentration is quadratic over the impurity content. We also observe coexistence of the ESR responses from these local centers and from delocalized triplet excitations over certain temperature range.

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ESR study of the spin ladder with uniform Dzyaloshinskii-Moria interaction

Evolution of the ESR absorption in a strong-leg spin ladder magnet (C$_7$H$_{10}$N$_2$)$_2$CuBr$_4$ (abbreviated as DIMPY) is studied from 300K to 400mK. Temperature dependence of the ESR relaxation follows a staircase of crossovers between different relaxation regimes. We ague that the main mechanism of ESR line broadening in DIMPY is uniform Dzyaloshinskii-Moria interaction ($|\vec{D}|=0.20$K) with an effective longitudinal component along an exchange bond of Cu ions within the legs resulting from the low crystal symmetry of DIMPY and nontrivial orbital ordering. The same Dzyaloshinskii-Moriya interaction results in the lifting of the triplet excitation degeneracy, revealed through the weak splitting of the ESR absorption at low temperatures.

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Formation of gapless triplets in the bond-doped spin-gap antiferromagnet (C$_4$H$_{12}$N$_2$)(Cu$_2$Cl$_6$)

We report results of an electron spin resonance (ESR) study of a spin-gap antiferromagnet (C$_4$H$_{12}$N$_2$)(Cu$_2$Cl$_6$) (nicknamed PHCC) with chlorine ions partially substituted by bromine. We found that up to 10% of nominal doping the contribution of the random defects to the absorption spectra remains at about 0.1% per copper ion, almost the same as in the pure system. Instead, a particular kind of ESR absorption corresponding to gapless S=1 triplets is observed at low temperatures in samples with high nominal bromine content x>5%. Increase of bromine concentration also leads to the systematic broadening of ESR absorption line indicating reduction of the quasi-particles lifetime.

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