Strong enhancement of magnetic ordering temperature and structural/valence transitions in EuPd 3 S 4 under high pressure

Author:

Huyan Shuyuan12ORCID,Ryan Dominic H.3ORCID,Slade Tyler J.12,Lavina Barbara45ORCID,Jose Greeshma6,Wang Haozhe7ORCID,Wilde John M.12ORCID,Ribeiro Raquel A.12ORCID,Zhao Jiyong5,Xie Weiwei7,Bi Wenli6ORCID,Alp Esen E.5ORCID,Bud’ko Sergey L.12ORCID,Canfield Paul C.12ORCID

Affiliation:

1. Ames National Laboratory, US DOE, Iowa State University, Ames, IA 50011

2. Department of Physics and Astronomy, Iowa State University, Ames, IA 50011

3. Physics Department and Centre for the Physics of Materials, McGill University, Montreal, QC H3A 2T8, Canada

4. Center for Advanced Radiation Sources, The University of Chicago, Chicago, IL 60637

5. Advanced Photon Source, Argonne National Laboratory, Argonne, IL 60439

6. Department of Physics, University of Alabama at Birmingham, Birmingham, AL 35294

7. Department of Chemistry, Michigan State University, East Lansing, MI 48824

Abstract

We present a comprehensive study of the inhomogeneous mixed-valence compound, EuPd 3 S 4 , by electrical transport, X-ray diffraction, time-domain 151 Eu synchrotron Mössbauer spectroscopy, and X-ray absorption spectroscopy measurements under high pressure. Electrical transport measurements show that the antiferromagnetic ordering temperature, T N , 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 T N 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 T N plateau. Mössbauer spectroscopy measurements show a clear valence transition from approximately 50:50 Eu 2+ :Eu 3+ to fully Eu 3+ 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 T N , most likely via enhanced hybridization between the Eu 4 f 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.

Funder

U.S. Department of Energy

National Science Foundation

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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