arXiv subjects

Petr Doležal

Publications and source records attributed to Petr Doležal.

10 recordsLinked to original sources

arXiv2026

Emergence of a Fluctuating Ground State in Y-kapellasite under Pressure

Y-kapellasite (Y$_3$Cu$_9$(OH)$_{19}$Cl$_8$), which hosts an original anisotropic kagome sublattice, is a promising candidate for studying elusive and complex correlated physics. It exhibits a theoretically predicted in-plane $(1/3, 1/3)$ magnetic order [1] but its magnetic interaction values place it close to a phase boundary to a spin liquid state [2]. Our $μ$SR measurements under hydrostatic pressure demonstrate the complete suppression of static magnetism in favor of a fully dynamical ground state at $2.3$~GPa. Complementary high-pressure x-ray and optical phonon measurements reveal a gradual reduction of the kagome anisotropy, enhancing magnetic frustration without structural transitions. Our results establish Y-kapellasite as a rare clean kagome model in which long-range order is suppressed by pressure-tuned frustration, the first fingerprint for the realization of a quantum spin liquid without strong disorder.

cond-mat.str-el↗

arXiv2025

Phase transformations in metastable $β$ Zr15Nb alloy revealed by in-situ methods

This study examines the phase transitions occurring during linear heating of the Zr15Nb alloy through a comprehensive, multi-technique methodology comprising in-situ high-energy synchrotron X-ray diffraction (HEXRD), electrical resistance measurements, differential scanning calorimetry (DSC), and thermal expansion analysis, supplemented by ex-situ transmission electron microscopy (TEM). The findings reveal a complex sequence of phase transformations and corresponding structural changes over a broad temperature range (from room temperature up to 800 $°$C). Two distinct body-centered cubic (bcc) $β$ phases - $β_{Zr}$ and $β_{Nb}$ - with closely related lattice parameters are identified. At room temperature, the microstructure is characterized by a mixture of the metastable $β_{Zr}$ + $ω_{ath}$ phase. Upon heating, $β_{Zr}$ progressively decomposes, giving rise to the formation of $β_{Nb}$. TEM observation revealed the cuboidal shape of the $ω_{iso}$ particles resulting from the high lattice misfit between $β$ and $ω$ phase. The $ω$ solvus temperature is determined to be approximately 555 $°$C, as evidenced by in situ HEXRD and abrupt changes in the alloy's thermal and electrical properties. The growth of the $α$ phase occurs after the dissolution of the $ω$ phase, resulting in a pronounced increase in thermal expansion.

cond-mat.mtrl-sci↗

arXiv2024

Multiferroic quantum criticality in (Eu,Ba,Sr)TiO$_3$ solid solution

Based on the earlier published theory (\textit{Nature Mat}. \textbf{18}, 223--228 (2019)), a comprehensive experimental investigation of multiferroic quantum critical behavior of (Eu,Ba,Sr)TiO$_3$ polycrystalline and single crystal samples was performed. Presence of the displacive ferroelectric quantum criticality is revealed through non-classical ($T^2$) temperature scaling of inverse dielectric susceptibility up to 60\,K. With increasing hydrostatic pressure, this ferroelectric quantum criticality is gradually suppressed. Inverse magnetic susceptibility follows classical Curie-Weiss law down to 4 K, but quantum fluctuations belonging to an antiferromagnetic phase transition ($T_{\mathrm{N}} < 0.8$ K) change its scaling below 3 K to $T^{(1.7\pm 0.1)}$ and $T^{(2.1\pm 0.2)}$ for samples containing 29\,\% and 25\,\% of Eu$^{2+}$ ions, respectively. Experimental indications of the coexisting ferroelectric and antiferromagnetic, i.e. multiferroic, quantum fluctuations and qualitative explanation why they could be seen only in the immediate proximity of $T_{\mathrm{N}}$ is given.

cond-mat.mtrl-sci↗

arXiv2024

SrCu(OH)$_3$Cl, an ideal isolated equilateral triangle spin $S$ = 1/2 model system

We have investigated the magnetic ground state properties of the quantum spin trimer compound strontium hydroxy copper chloride SrCu(OH)$_3$Cl using bulk magnetization, specific heat measurements, nuclear magnetic resonance (NMR), and electron spin resonance (ESR) spectroscopy. SrCu(OH)$_3$Cl consists of layers with isolated Cu$^{2+}$ triangles and hence provides an opportunity to understand the magnetic ground state of an isolated system of \textit{S} = 1/2 arranged on an equilateral triangle. Although magnetization measurements do not exhibit a phase transition to a long-range ordered state down to \textit{T} = 2 K, they reveal the characteristic behavior of isolated trimers with an exchange of $J = 154$~K. The Curie-Weiss behavior changes around 50--80~K, as is also seen in the NMR spin-lattice relaxation rate. In zero magnetic field, our specific heat data establish a second-order phase transition to an antiferromagnetic ground state below \textit{T}= 1.2 K. We have drawn a magnetic field-temperature ($H$-$T$) phase diagram based on the specific heat measurements. The ESR data show divergence of the linewidth at lower temperatures, which precedes the phase transition to an antiferromagnetic long-range ordered state with unconventional critical exponents. The temperature variation of the $g$-factor further confirms the antiferromagnetic phase transition and reflects the underlying magneto-crystalline anisotropy of the compound.

cond-mat.str-el↗

arXiv2023

Robust intralayer antiferromagnetism and tricriticality in a van der Waals compound: VBr3 case

We studied magnetic states and phase transitions in the van der Waals antiferromagnet VBr3 by specific heat and magnetization measurements of single crystals in high magnetic fields and by ab initio density functional theory calculations focused on exchange interactions. The magnetization behavior resembles Ising antiferromagnets with magnetic moments kept in the out-of-plane direction by strong uniaxial magnetocrystalline anisotropy. The out-of-plane magnetic field induces a spin-flip metamagnetic transition, which is of first-order type at low temperatures while at higher temperatures the transition becomes continuous. The first-order and continuous transition segments in the field-temperature phase diagram meet at a tricritical point at = 12 K. The magnetization response to the in-plane field manifests a continuous spin-flop transition, which at 2 K terminates at a field mu0Hc = 27 T that can serve as an estimate of the anisotropy field in VBr3. The magnetization curves above the metamagnetic transition saturate at the same value of magnetic moment musat = 1.2 muB/f.u., which is much smaller than the spin-only (S = 1) moment of the V3+ ion. The reduced moment can be explained by the existence of a significant orbital magnetic moment antiparallel to the spin. The orbital moment is a key ingredient of a mechanism responsible for the observed large anisotropy. The exact energy evaluation of possible magnetic orders unambiguously shows that the magnetic ground state of VBr3 is the intralayer zigzag antiferromagnetic order that renders the antiferromagnetic ground state significantly more stable against the spin-flip transition than the other options. The calculations also predict that a minimal distortion of the Br ion sublattice causes a radical change of the orbital occupation in the ground state, connected with the formation of the orbital moment and the stability of magnetic order.

cond-mat.mtrl-sci↗

arXiv2023

Formation of Domains within Lower-to-higher Symmetry Structural Transition in CrI$_3$

CrI$_3$ represents one of the most important van der Waals systems on the route to understanding two-dimensional magnetic phenomena. Being arranged in a specific layered structure it also provides a unique opportunity to investigate structural transformations in dimension-confined systems. CrI$_3$ is dimorphic and possesses a higher symmetry low-temperature phase, which is quite uncommon. It contrasts with vanadium trihalides which show a higher symmetry high-temperature. An explanation of this distinct behavior together with a large cycle-dependent transition hysteresis is still an open question. Our low-temperature X-ray diffraction study conducted on CrI$_3$ single crystals complemented by magnetization and specific heat measurements was focused mainly on specific features of the structural transition during cooling. Our results manifest that the structural transition during cooling relates to the formation of structural domains despite the lower symmetry structure transforming to a higher symmetry one. We propose that these domains could control the transition temperature and also the size of thermal hysteresis.

cond-mat.str-el↗

arXiv2022

UI$_3$ -- 5f-electron magnetic van der Waals material

We grew high-quality single crystals of the 5f electron van der Waals compound UI$_3$ and investigated them by measurements of specific heat and magnetization as functions of temperature and magnetic field. UI$_3$ behaves as an antiferromagnet with a first-order magnetic phase transition at the Neél temperature $T_N$ = 2.65 K. It is characterized by a sharp symmetric specific-heat peak which is gradually shifted to lower temperatures by increasing magnetic field applied along either the a- or b-axis. The behavior in magnetic fields reveals orthorhombic magnetocrystalline anisotropy with the hard magnetization direction along the c-axis. The 2-K a- and b-axis magnetization curves exhibit a metamagnetic transition at the critical field $H_c$ = 3 T and 1.8 T, respectively. In higher fields, when the long-range antiferromagnetism is suppressed by a metamagnetic transition, signs of short-range magnetic ordering of antiferromagnetic correlations in the paramagnetic state show up both in specific heat and magnetization. The anomalous S-shape field dependence of a-axis magnetization well above $H_c$ can be understood as the crossover from the correlated paramagnetic regime to the high-field polarized paramagnet. The magnetic phase diagrams for the magnetic field applied along the a- and b-axis, respectively, designed using the mentioned experimental results are presented. We have also found that the UI$_3$ crystals are easily cleavable which predisposes this material for direct investigation of 5f electron magnetism in the 2D limit on exfoliated atomically thin samples.

cond-mat.str-el↗

arXiv2021

Macroscopic time reversal symmetry breaking by staggered spin-momentum interaction

Time-reversal (T) symmetry breaking is a fundamental physics concept underpinning a broad science and technology area, including topological magnets, axion physics, dissipationless Hall currents, or spintronic memories. A best known conventional model of macroscopic T-symmetry breaking is a ferromagnetic order of itinerant Bloch electrons with an isotropic spin interaction in momentum space. Anisotropic electron interactions, on the other hand, have been a domain of correlated quantum phases, such as the T-invariant nematics or unconventional superconductors. Here we report discovery of a broken-T phase of itinerant Bloch electrons with an unconventional anisotropic spin-momentum interaction, whose staggered nature leads to the formation of two ferromagnetic-like valleys in the momentum space with opposite spin splittings. We describe qualitatively the effect by deriving a non-relativistic single-particle Hamiltonian model. Next, we identify the unconventional staggered spin-momentum interaction by first-principles electronic structure calculations in a four-sublattice antiferromagnet Mn5Si3 with a collinear checkerboard magnetic order. We show that the staggered spin-momentum interaction is set by nonrelativistic spin-symmetries which were previously omitted in relativistic physics classifications of spin interactions and topological quasiparticles. Our measurements of a spontaneous Hall effect in epilayers of antiferromagnetic Mn5Si3 with vanishing magnetization are consistent with our theory predictions. Bloch electrons with the unconventional staggered spin interaction, compatible with abundant low atomic-number materials, strong spin-coherence, and collinear antiferromagnetic order open unparalleled possibilities for realizing T-symmetry broken spin and topological quantum phases.

cond-mat.mes-hall↗

arXiv2019

Crystal Structures and Phase Transitions of the van-der-Waals Ferromagnet VI3

The results of a single-crystal X-ray-diffraction study of the evolution of crystal structures of VI3 with temperature with emphasis on phase transitions are presented. Some related specific-heat and magnetization data are included. The existence of the room-temperature trigonal crystal structure R-3 (148) has been confirmed. Upon cooling, VI3 undergoes a structural phase transition to a monoclinic phase at Ts ~ 79 K. Ts is reduced in magnetic fields applied along the trigonal c-axis. When VI3 becomes ferromagnetic at TFM1 ~ 50 K, magnetostriction-induced changes of the monoclinic-structure parameters are observed. Upon further cooling, the monoclinic structure transforms into a triclinic variant at 32 K which is most likely occurring in conjunction with the previously reported transformation of the ferromagnetic structure. The observed phenomena are preliminarily attributed to strong magnetoelastic interactions.

cond-mat.str-el↗

arXiv2017

Effect of lattice distortion on U magnetic moments in $\mathrm{U_{4}Ru_{7}Ge_{6}}$ studied by polarized neutron diffraction

Small spontaneous lattice distortion of a cubic ferromagnet at temperatures below $T_{\mathrm{C}}$ is expected, but usually a neglected phenomenon. This study is focused on such effect on the example of $\mathrm{U_{4}Ru_{7}Ge_{6}}$. We propose the lattice distortion from the cubic space group to a lower symmetry as a result of our DFT calculations. The strong spin-orbit coupling on the U site plays the most essential role, that should lower the symmetry of the system and give rise to the two different U sites (U1 and U2). We bring convincing experimental evidence for this splitting resulting from our polarized neutron diffraction experiment. Proper treatment of the flipping ratios collected in the ordered state and in the paramagnetic state reveals dramatically different magnetic moments on the U1 and U2 sites. We have reached good agreement of the results from the MAXENT method and from direct fitting of the data. The ratio of the orbital and spin component on the U2 site is lower than for the free $\mathrm{U^{3+}}$ or $\mathrm{U^{4+}}$ ion and points to a strong hybridization between the U $5f$ and Ru $4d$ wave functions. The same ratio on the U1 site is unexpectedly low. This would mean that its orbital component is almost quenched. We have observed the absence of a magnetic moment on the Ru1 site, but a rather large induced moment on the Ru2 site. Very similar results were obtained also in the paramagnetic state in the regime induced by the magnetic field. It points to the intimate coupling of the magnetic ordering and structural distortion as it is possible to split the U site in to two different polarizing paramagnetic U moments above $T_{\mathrm{C}}$ by a strong magnetic field. We propose that the difference between the magnetic moment on the U sites is caused by the change of local point symmetry of the sites that is tightly bound to the role of the strong spin-orbit interaction.

cond-mat.str-el↗