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

Abstract

We present a comprehensive study of the inhomogeneous mixed-valence compound, EuPd₃S₄, by electrical transport, X-ray diffraction, time-domain ¹⁵¹Eu synchrotron Mössbauer spectroscopy, and X-ray absorption spectroscopy measurements under high pressure. Electrical transport measurements show that the antiferromagnetic ordering temperature, <i>T_N</i>, 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 <i>T_N</i> is detected. A pressure-induced first-order structural transition from cubic to tetragonal is observed, with a rather broad coexistence region (~20 GPa to ~30 GPa) that corresponds to the <i>T_N</i> 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 <i>T_N</i>, most likely via enhanced hybridization between the Eu 4<i>f</i> 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.