Metallization without Charge Transfer in CuReO<sub>4</sub> Perrhenate under Pressure

Using high-pressure synchrotron X-ray diffraction combined with Raman spectroscopy and density-functional calculations, we determined the sequence of the pressure-induced transformations in CuReO<sub>4</sub>. At 1.5 GPa, the lattice symmetry changes from <i>I</i>4<sub>1</sub><i>cd</i> to <i>I</i>4<sub>1</sub>/<i>a</i> with the transformation of isolated ReO<sub>4</sub>-tetrahedra into infinite chains of ReO<sub>6</sub>-octahedra. The second, isosymmetric transition at 7 GPa leads to the formation of a NbO<sub>2</sub>-type structure with the octahedral oxygen coordination for both Cu<sup>1+</sup> and Re<sup>7+</sup> cations. Both transitions are of the first order and accompanied by discontinuities in the unit-cell volume of 7 and 14%, respectively. Density-functional calculations predict the metallic state of the high-pressure NbO<sub>2</sub>-type phase of CuReO<sub>4</sub>, and this prediction is in-line with the disappearance of the Raman signal above 7 GPa and visual observations (darkness/reflection of the sample). This metallization is caused by the increased bandwidth of both Cu 3d and Re 5d bands without any significant charge transfer between Cu and Re. At ambient pressure, the crystal structure of CuReO<sub>4</sub> is retained between 4 and 700 K (melting point), showing a negative thermal expansion along the <i>c</i>-axis and a positive expansion along the <i>a</i>-axis within the entire temperature range.

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Journal
Inorganic Chemistry
Published
2025-03-20
DOI
https://doi.org/10.1021/acs.inorgchem.4c05051
Primary Topic
Advanced Condensed Matter Physics
Type
article
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article

Metallization without Charge Transfer in CuReO4 Perrhenate under Pressure

Helmut Ehrenberg, Maxim Avdeev, Alexander A. Tsirlin, Anatoliy Senyshyn et al.
Inorganic Chemistry
Advanced Condensed Matter Physics
article

Metallization without Charge Transfer in CuReO4 Perrhenate under Pressure

Helmut Ehrenberg, Maxim Avdeev, Alexander A. Tsirlin, Anatoliy Senyshyn, Daria Mikhailova, Stanislav M. Avdoshenko, Michael Hanfland, Jens Engel, Yurii Prots, Angelina Sarapulova, Konstantin V. Glazyrin, Ulrich Schwarz, Leonid Dubrovinsky
article en

Abstract

Using high-pressure synchrotron X-ray diffraction combined with Raman spectroscopy and density-functional calculations, we determined the sequence of the pressure-induced transformations in CuReO<sub>4</sub>. At 1.5 GPa, the lattice symmetry changes from <i>I</i>4<sub>1</sub><i>cd</i> to <i>I</i>4<sub>1</sub>/<i>a</i> with the transformation of isolated ReO<sub>4</sub>-tetrahedra into infinite chains of ReO<sub>6</sub>-octahedra. The second, isosymmetric transition at 7 GPa leads to the formation of a NbO<sub>2</sub>-type structure with the octahedral oxygen coordination for both Cu<sup>1+</sup> and Re<sup>7+</sup> cations. Both transitions are of the first order and accompanied by discontinuities in the unit-cell volume of 7 and 14%, respectively. Density-functional calculations predict the metallic state of the high-pressure NbO<sub>2</sub>-type phase of CuReO<sub>4</sub>, and this prediction is in-line with the disappearance of the Raman signal above 7 GPa and visual observations (darkness/reflection of the sample). This metallization is caused by the increased bandwidth of both Cu 3d and Re 5d bands without any significant charge transfer between Cu and Re. At ambient pressure, the crystal structure of CuReO<sub>4</sub> is retained between 4 and 700 K (melting point), showing a negative thermal expansion along the <i>c</i>-axis and a positive expansion along the <i>a</i>-axis within the entire temperature range.

Inorganic ChemistryVol. 64(12)
Karlsruhe Institute of Technology (DE), The University of Sydney (AU), Australian Nuclear Science and Technology Organisation (AU), University of Augsburg (DE), Deutsches Elektronen-Synchrotron DESY (DE), European Synchrotron Radiation Facility (FR), Leibniz Institute for Solid State and Materials Research (DE), Heinz Maier-Leibnitz Zentrum (DE), Max Planck Institute for Chemical Physics of Solids (DE), Fraunhofer Institute for Solar Energy Systems (DE), Centre Marc Bloch (DE), University of Bayreuth (DE), Technical University of Munich (DE), Technische Universität Dresden (DE), Leipzig University (DE)
Openalex Percentile: Top 97%
Advanced Condensed Matter Physics
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