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B. Lavina

Publications and source records attributed to B. Lavina.

3 recordsLinked to original sources

The observation of bulk superconductivity in Rhombohedral ReO3 under pressure

Understanding how lattice geometry enables superconductivity in oxides remains a central challenge. Here, we report a systematic study of ReO3 up to 80 GPa. Synchrotron X-ray diffraction, Raman spectroscopy, electrical transport, dc magnetic susceptibility, and first-principles calculations establish a sequence of pressure-induced structural transitions, from cubic Pm-3m to Im-3 followed by the emergence of a rhombohedral R-3c phase accompanied by bulk superconductivity with a maximum Tc, onset ~17.5 K. DC magnetic susceptibility and trapped-flux magnetization measurements demonstrate that bulk superconductivity is confined to the pressure range where R-3c phase is dominant. Density functional theory calculations show strong electron-phonon coupling in the hR24-R-3c structure, with substantial contributions from both low-frequency Re vibrations and high-frequency oxygen-related phonon modes, yielding a calculated Tc comparable with the experiment. Upon further compression above ~35-40 GPa, powder X-ray diffraction results indicate a symmetry-lowering structural transition. Whereas the experimental diffraction patterns can be best described by a rhombohedral-derived R32-like average distortion with effective enlargement of the crystallographic unit cell, enthalpy calculations identify a lower-symmetry mP16-P2/c structure driven by phonon instability of the R-3c phase. This reconstructed higher-coordination phase has a reduced density of states at the Fermi level, weaker electron-phonon coupling, and a much lower calculated Tc, providing a microscopic explanation for the loss of bulk superconductivity in the higher-pressure phase. These results show that bulk superconductivity is stabilized within the rhombohedral structure, where pressure-induced lattice reconstruction supports enhanced electron-phonon coupling through cooperative Re-O lattice dynamics.

cond-mat.supr-con↗

Strong enhancement of magnetic ordering temperature and structural/valence transitions in EuPd3S4 under high pressure

We present a comprehensive study of the mixed valent compound, EuPd3S4, by electrical transport, X-ray diffraction, time-domain 151Eu synchrotron Mössbauer spectroscopy, and X-ray absorption spectroscopy measurements under high pressure. The electrical transport measurements show that the antiferromagnetic ordering temperature, TN, increases rapidly from 2.8 K at ambient pressure to 23.5 K at ~19 GPa and plateaus between ~19 and ~29 GPa after which no anomaly associated with TN is detected. A pressure-induced first order structural transition from cubic to tetragonal is observed, with a rather broad coexistence region (~20 GPa to ~32 GPa) that corresponds to the TN plateau. Mössbauer spectroscopy measurements show a clear valence transition from approximately 50:50 Eu2+:Eu3+ to fully Eu3+ at ~28 GPa, consistent with the vanishing of the magnetic order at the same pressure. X-ray absorption data show a transition to a fully trivalent state at a similar pressure. Our results show that pressure first greatly enhances TN, most likely via enhanced hybridization between the Eu 4f states and the conduction band, and then, second, causes a structural phase transition that coincides with the conversion of the europium to a fully trivalent state.

cond-mat.str-el↗

High-pressure structural, elastic, and thermodynamic properties of zircon-type HoPO4 and TmPO4

Zircon-type HoPO4 and TmPO4 have been studied by single-crystal x-ray diffraction and ab initio calculations. We report information on the influence of pressure on the crystal structure, and on the elastic and thermodynamic properties. The equation of state for both compounds is accurately determined. We have also obtained information on the polyhedral compressibility which is used to explain the anisotropic axial compressibility and the bulk compressibility. Both compounds are ductile and more resistive to volume compression than to shear deformation at all pressures. Furthermore, the elastic anisotropy is enhanced upon compression. Finally, the calculations indicate that the possible causes that make unstable the zircon structure are mechanical instabilities and the softening of a silent B1u mode.

cond-mat.mtrl-sci↗