Searcharxiv⌕ Search

arXiv subjects

M. Tovar

Publications and source records attributed to M. Tovar.

9 recordsLinked to original sources
arXiv2026

Competing Ordering Modes in the Distorted Quantum Kagome Material Clinoatacamite Cu$_2$Cl(OH)$_3$

We have studied the magnetic properties of clinoatacamite Cu$_2$Cl(OH)$_3$, the parent compound of the quantum spin liquid candidate herbertsmithite and a longstanding puzzle among frustrated quantum magnets. As we reveal using density-functional theory, clinoatacamite belongs to the class of distorted kagome antiferromagnets with the kagome plane being embedded into a low-symmetry crystal structure. By means of thermodynamic measurements, muon spin rotation/relaxation as well as neutron diffraction on single crystals, we find in zero magnetic field complex behavior below $T_\mathrm{I}$ = 18.1 K which unfolds in three temperature regions I-III. We propose this complexity in multicritical clinoatacamite to arise from the competition of antiferromagnetic ordering modes from the underconstrained manifold of modes, which can lead to a metamagnetic texture in zero field.

cond-mat.str-el↗
arXiv2013

Evolution of Magnetism in Single-Crystal Honeycomb Iridates

We report the successful synthesis of single-crystals of the layered iridate, (Na$_{1-x}$Li$_{x}$)$_2$IrO$_3$, $0\leq x \leq 0.9$, and a thorough study of its structural, magnetic, thermal and transport properties. The new compound allows a controlled interpolation between Na$_2$IrO$_3$ and Li$_2$IrO$_3$, while maintaing the novel quantum magnetism of the honeycomb Ir$^{4+}$ planes. The measured phase diagram demonstrates a dramatic suppression of the Néel temperature, $T_N$, at intermediate $x$ suggesting that the magnetic order in Na$_2$IrO$_3$ and Li$_2$IrO$_3$ are distinct, and that at $x\approx 0.7$, the compound is close to a magnetically disordered phase that has been sought after in Na$_2$IrO$_3$ and Li$_2$IrO$_3$. By analyzing our magnetic data with a simple theoretical model we also show that the trigonal splitting, on the Ir$^{4+}$ ions changes sign from Na$_2$IrO$_3$ and Li$_2$IrO$_3$, and the honeycomb iridates are in the strong spin-orbit coupling regime, controlled by $\jeff=1/2$ moments.

cond-mat.str-el↗
arXiv2013

R-M interactions in R2BaMO5 (R=Y or Gd and M=Cu or Zn)

R2BaMO5 (R = Gd, Y and M = Cu, Zn) oxides have been studied by specific heat, dc magnetic susceptibility, and electron paramagnetic resonance (EPR). For one member of the series without magnetic moment at M, namely Gd2BaZnO5, measurements reveal long range antiferromagnetic order at TN(Gd2BaZnO5) = 2.3(0.1)K, much lower than the Curie Weiss temperature of Θ=15.9(0.3)K. This indicates the existence of competing interactions that introduce a large degree of magnetic frustration in the system. For Y2BaCuO5 the Cu Cu interactions are responsible for the broad maximum in the magnetic contribution to the specific heat centered at 18.5(0.01)K that stretches beyond the instrumental limit of 25K. The strong Cu Cu interactions also present in Gd2BaCuO5, combined with the Gd-Cu interaction, polarize the Gd sublattice giving measurable contributions to the specific heat in the same temperature range. In addition, they broaden the Gd EPR line and saturate its integrated intensity. The ordering temperature of Gd ions is raised to TN(Gd2BaCuO5)=12.0(0.1)K.

cond-mat.mtrl-sci↗
arXiv2007

Sr2CrOsO6: Endpoint of a spin polarized metal-insulator transition by 5d band filling

In the search for new spintronic materials with high spin-polarization at room-temperature, we have synthesized an osmium based double perovskite with a Curie-temperature of 725 K. Our combined experimental results confirm the existence of a sizable induced magnetic moment at the Os site, supported by band-structure calculations in agreement with a proposed kinetic energy driven mechanism of ferrimagnetism in these compounds. The intriguing property of Sr2CrOsO6 is that it is at the endpoint of a metal-insulator transition due to 5d band filling, and at the same time ferrimagnetism and high-spin polarization is preserved.

cond-mat.str-el↗
arXiv2002

Charge disproportionation in YNiO$_{3}$ : ESR and susceptibility study

We present a study of the magnetic properties of YNiO$_{3}$ in the paramagnetic range, above and below the metal-insulator (MI) transition. The dc susceptibility, $χ_{dc}$ (measured up to 1000 K) is a decreasing function of T for $T >$150 K (the Néel temperature) and we observe two different Curie-Weiss regimes corresponding to the metallic and insulator phases. In the metallic phase, this behaviour seems to be associated with the small ionic radius of Y% $^{3+}$. The value of the Curie constant for T$<$ T$_{MI}$ allows us to discard the possibility of Ni$^{3+}$ localization. An electron spin resonance (ESR) spectrum is visible in the insulator phase and only a fraction of the Ni ions contributes to this resonance. We explain the ESR and $χ_{dc}$ behaviour for T $<$ T$_{MI}$ in terms of charge disproportionation of the type 2Ni$% ^{3+}\to $ Ni$^{2+}$+Ni$^{4+},$ that is compatible with the previously observed structural transition across T$_{MI}$.

cond-mat.str-el↗
arXiv2002

High temperature susceptibility in electron doped Ca1-xYxMnO3: Double Exchange vs Superexchange

We present a study of the magnetic properties of the electron doped manganites Ca1-xYxMnO3 (for 0<=x<=0.25) in the paramagnetic regime. For the less doped samples (x<=0.1) the magnetic susceptibility, c(T), follows a Curie-Weiss (CW) law only for T > 450 K and, below this temperature, c^-1(T) shows a ferrimagnetic-like curvature. We approached the discussion of these results in terms of a simple mean-field model where double exchange, approximated by a ferromagnetic Heisenberg-like interaction between Mn3+ and Mn4+ ions, competes with classical superexchange. For higher levels of doping (x>=0.15), the CW behaviour is observed down to the magnetic ordering temperature (Tmo) and a better description of c(T) was obtained by assuming full delocalization of the eg electrons. In order to explore the degree of delocalization as a function of T and x, we analyzed the problem through Montecarlo simulations. Within this picture we found that at high T the electrons doped are completely delocalized but, when Tmo is approached, they form magnetic polarons of large spin that cause the observed curvature in c^-1(T) for x<=0.1.

cond-mat.str-el↗
arXiv2002

Evidence of strong antiferromagnetic coupling between localized and itinerant electrons in ferromagnetic Sr2FeMoO6

Magnetic dc susceptibility ($χ$) and electron spin resonance (ESR) measurements in the paramagnetic regime, are presented. We found a Curie-Weiss (CW) behavior for $χ$(T) with a ferromagnetic $Θ= 446(5)$ K and $μ_{eff} = 4.72(9) μ_{B}/f.u.$, this being lower than that expected for either $Fe^{3+}(5.9μ_{B})$ or $Fe^{2+}(4.9μ_{B})$ ions. The ESR g-factor $g = 2.01(2)$, is associated with $Fe^{3+}$. We obtained an excellent description of the experiments in terms of two interacting sublattices: the localized $Fe^{3+}$ ($3d^{5}$) cores and the delocalized electrons. The coupled equations were solved in a mean-field approximation, assuming for the itinerant electrons a bare susceptibility independent on $T$. We obtained $χ_{e}^{0} = 3.7$ $10^{-4}$ emu/mol. We show that the reduction of $μ_{eff}$ for $Fe^{3+}$ arises from the strong antiferromagnetic (AFM) interaction between the two sublattices. At variance with classical ferrimagnets, we found that $Θ$ is ferromagnetic. Within the same model, we show that the ESR spectrum can be described by Bloch-Hasegawa type equations. Bottleneck is evidenced by the absence of a $g$-shift. Surprisingly, as observed in CMR manganites, no narrowing effects of the ESR linewidth is detected in spite of the presence of the strong magnetic coupling. These results provide evidence that the magnetic order in $Sr_{2}FeMoO_{6}$ does not originates in superexchange interactions, but from a novel mechanism recently proposed for double perovskites.

cond-mat.mtrl-sci↗
arXiv2001

Magnetic polarons in Ca_(1-x)Y_xMnO_3

Experimental evidence show that in the magnetoresistive manganite Ca_(1-x) Y_xMnO_3, ferromagnetic (FM) polarons arises in an antiferromagnetic (AF) background, as a result of the doping with Yttrium. This hypothesis is supported in this work by classical Monte Carlo (MC) calculations performed on a model where FM Double Exchange (DE) and AF Superexhange (SE) compite.

cond-mat↗