arXiv subjects

A. L. Barra

Publications and source records attributed to A. L. Barra.

6 recordsLinked to original sources

arXiv2026

Magnetic-field-induced magnon portfolio in a van der Waals magnet

Magnonic excitations are investigated in chromium oxychloride (CrOCl), a van der Waal (vdW) antiferromagnet prone to a multitude of magnetic phase transitions, with absorption experiments in a broad continuous energy range. At low magnetic fields, the magnon spectra show a strong bi-axial anisotropy and inform on the relative weights of the effective exchange coupling and the system anisotropies. As the magnetic field increases, magnons characteristic of a canted phase are first observed, with peculiarities attributed to in-plane anisotropies and magnon-magnon coupling. Subsequently, a hysteretic magnon spectrum appears as the system transitions to a ferrimagnetic state, with two new magnon branches partly coexisting with the lower energy canted phase branch, indicating the formation of spatially separated magnetic phases. Further changes in the magnon spectrum in higher magnetic fields accompany transitions to the different canted magnetic phases previously reported. Our experiments show that competing exchange interactions and ground states broaden the options to generate different kinds of magnonic excitations in the same vdW material upon the variation of external parameters.

cond-mat.mtrl-sci↗

arXiv2022

Microscopic parameters of the van der Waals CrSBr antiferromagnet from microwave absorption experiments

Microwave absorption experiments employing a phase-sensitive external resistive detection are performed for a topical van der Waals antiferromagnet CrSBr. The field dependence of two resonance modes is measured in an applied field parallel to the three principal crystallographic directions, revealing anisotropies and magnetic transitions in this material. To account for the observed results, we formulate a microscopic spin model with a bi-axial single-ion anisotropy and inter-plane exchange. Theoretical calculations give an excellent description of full magnon spectra enabling us to precisely determine microscopic interaction parameters for CrSBr.

cond-mat.mes-hall↗

arXiv2001

Electron Spin Resonance of Ni-doped CuGeO$_3$ in the paramagnetic, spin-Peierls and antiferromagnetic states: Comparison with non-magnetic impurities

We have performed Electron Spin Resonance measurements on single crystals of the doped spin-Peierls compounds CuGe$_{1-y}$Si$_y$O$_3$ and Cu$_{1-x}$M$_x$GeO$_3$ with M = Zn, Mg, Ni ($x, y\leq 0.1$). The first part of our experiments was performed in the paramagnetic and spin-Peierls phases at 9.5, 95 and 190 GHz. All non-magnetic impurities (Si, Zn and Mg) were found to hardly affect the position and linewidth of the single line resonance, in spite of the moment formation due to the broken chains. In contrast to Si, Zn and Mg-doping, the presence of Ni (S = 1) at low concentration induces a spectacular shift towards high fields of the ESR line (up to 40% for x=0.002), together with a large broadening. This shift is strictly proportional to the ratio of Ni to Cu susceptibilities: Hence it is strongly enhanced below the spin-Peierls transition. We interpret this shift and the broadening as due to the exchange field induced by the Ni ions onto the strongly exchange coupled Cu spins. Second, the antiferromagnetic resonance was investigated in Ni-doped samples. The frequency vs magnetic field relation of the resonance is well explained by the classical theory with orthorhombic anisotropy, with $g$ values remarkably reduced, in accordance with the study of the spin-Peierls and paramagnetic phases. The easy, second-easy, and hard axes are found to be $a$, $c$, and $b$ axes, respectively. These results, which are dominated by the single ion anisotropy of Ni$^{2+}$, are discussed in comparison with those in the Zn- and Si-doped CuGeO$_3$.

cond-mat.str-el↗

arXiv2001

The origin of second-order transverse magnetic anisotropy in Mn12-acetate

The problem of the role of transverse fields in Mn12-acetate, a molecular nanomagnet, is still open. We present structural evidences that the disorder of the acetic acid of crystallization indices sizeable distortion of the Mn(III) sites, giving rise to six different isomers, four of them with symmetry lower than tetragonal. Using a ligand field approach the effect of the structure modifications on the second order transverse magnetic anisotropy, forbidden in tetragonal symmetry, has been evaluated. The order of magnitude of the quadratic transverse anisotropies well agree with the values derived by the analysis of the field sweep dependence of the hysteresis loops performed by Mertes et al. (Phys. Rev. Lett 87, 227205 (2001)) and allows to better simulate the EPR spectra.

cond-mat.mes-hall↗

arXiv2001

Tuning of the magnetic properties of the high spin molecular cluster Fe8

The synthesis, crystal structure and magnetic characterization of a high spin cluster comprising eight iron ions, are presented in this contribution. The cluster has formula [(tacn)6Fe8O2(OH)12Br4.3(ClO4)3.7]6H2O, (Fe8PCL) where tacn is the organic ligand 1,4,7-triazacyclononane. It can be considered a derivative of Fe8Br8, a cluster whose low temperature dynamics of the magnetization has been deeply investigated, where four of the bromide ions have been replaced by perchlorate anions. The structure of the central core of the two molecules, [Fe8O(OH)12(tacn)6]8+, is essentially the same, but Fe8PCL has a higher symmetry (Fe8Br8 crystallizes in the acentric P1 space group, while Fe8PCL crystallizes in the P21/c space group, monoclinic). The magnetic properties of Fe8PCL suggest it is very similar to Fe8Br having a S=10 ground state as well. The zero field splitting parameters were accurately determined by HF-EPR measurements. The two clusters have similar axial anisotropy but Fe8PCL has a larger transverse anisotropy. Ac susceptibility measurements revealed the cluster behaves like a superparamagnetic particle. However, due to the occurrence of large terms in the transverse anisotropy, the temperature dependence of the relaxation time can not be reproduced by a simple Arrhenius law. As observed in Fe8Br8, below 350 mK the relaxation time becomes temperature independent, indicating that a pure tunneling regime is attained. The comparison of the tunneling rate in the two clusters shows that in the perchlorate derivative the relaxation process is 35 times faster. The observed ratio of the tunneling rates is in reasonable agreement with that calculated from the tunneling splitting, i.e. the energy difference between the two almost degenerate lowest levels Ms = +/-10, in the two clusters.

cond-mat.mes-hall↗

arXiv1997

High frequency EPR spectra of a molecular nanomagnet provide a key to understand Quantum Tunneling of the Magnetization

EPR spectra have been recorded in very high field, up to 25T, and at high frequency, up to 525 GHz, on a polycristalline sample of Mn12ac (see paper for detailed formula), the first example of molecular cluster behaving like a nanomagnet. The simulation of the spectra has provided an accurate determination of the parameters of the spin hamiltonian (see paper for formula and values of the various parameters). The presence of the fourth order term in the total spin justifies the irregularities in the spacing of the jumps, recently observed in the hysteresis loop of Mn12ac and attributed to acceleration of the relaxation of the magnetization due to Quantum Tunneling between degenerate M states of the ground S=10 multiplet of the cluster. The term in (S_+^4 + S_-^4) is responsible of the transverse magnetic anisotropy and plays a crucial role in the mechanism of Quantum Tunneling. The HF-EPR spectra have for the first time evidenced its presence and quantified it.

cond-mat.mtrl-sci↗