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Jose L. Gonzalez Jimenez

Publications and source records attributed to Jose L. Gonzalez Jimenez.

2 recordsLinked to original sources

Chirality Transfer to the Magnetic Sublattice in the Hybrid Perovskite (R)-/(S)-3-Fluoropyrrolidinium Copper(II) Chloride

Incorporating chiral organic cations into organic-inorganic hybrid materials has been shown to enable the inorganic sublattice to display chiroptical properties. We report a new two-dimensional magnetic ($S=1/2$) chiral metal halide perovskite, (R)- and (S)-$(C_4H_9FN)_2CuCl_4$ (where $(C_4H_9FN)^+$ is 3-fluoropyrrolidinium), which consists of Cu-Cl inorganic layers separated by $(C_4H_9FN)^+$ organic cations. The presence of the chiral $(C_4H_9FN)^+$ organic cation induces formation of chiral magnetic order, even though the inorganic sublattice itself is nearly structurally centrosymmetric. We also report the racemic variant, containing an equal amount of (R)- and (S)- cations, which shows no evidence of chiral magnetic order. When the magnetic susceptibility is measured perpendicular to inorganic Cu-Cl layer propagation direction, an antiferromagnetic phase transition at Néel temperature $T_N = 2.23~K$ is observed in both the chiral and racemic materials, and the existence of the magnetic phase transition is supported by specific heat capacity measurements. Field-induced magnetic chirality is observed through the existence of a second-order magnetoelectric effect in the chiral variant, while no magnetoelectric signal is observed for the racemic material, indicating the absence of magnetic chirality. Our findings demonstrate that materials exhibiting chiral magnetic order can be created through the incorporation of a chiral cation into an organic-inorganic hybrid magnetic material, potentially allowing for the design of tailored materials that combine chiral magnetism with other desirable optical and electronic properties that come from structural chirality.

cond-mat.mtrl-sci↗

Pressure Tuning the Mixture of Eu$^{2+}$ and Eu$^{3+}$ in Eu$_4$Bi$_6$Se$_{13}$

The investigation of crystallographic, electronic, and magnetic characteristics, especially the mixed valences of Eu$^{2+}$ and Eu$^{3+}$ under pressure of a novel europium-based bismuth selenide compound, Eu$_4$Bi$_6$Se$_{13}$, presented. This new compound adopts a monoclinic crystal structure classified under the P$2_1$/m space group (#11). It exhibits distinctive structural features, including substantial Eu-Se coordination numbers, Bi-Se ladders, and linear chains of Eu atoms that propagate along the b-axis. Electronic resistivity assessments indicate that Eu$_{4}$Bi$_{6}$Se$_{13}$ exhibits weak metallic behaviors. Magnetic characterization reveals uniaxial magnetic anisotropy, with a notable spin transition at approximately 1.2 T when the magnetic field is oriented along the b-axis. This behavior, coupled with the specific Eu-Eu interatomic distances and the magnetic saturation observed at low fields, supports the identification of metamagnetic properties attributable to the flipping of europium spins. The Curie-Weiss analysis of the magnetic susceptibility measured both perpendicular and parallel to the b-axis and high-pressure partial fluorescence yield (PFY) results detected by X-ray absorption spectroscopy (XAS) reveal the tendency of the material to enter a mixed valent state where the trivalent state becomes more prominent with the pressure increase or temperature decrease.

cond-mat.mtrl-sci↗