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    Fragile 3D Order in V1−xMoxO2

    Matthew A. Davenport1, Matthew J. Krogstad2, Logan M. Whitt1, Chaowei Hu3, Tyra C. Douglas1, Ni Ni3, Stephan Rosenkranz2, Raymond Osborn2, and Jared M. Allred1,*

    • 1Department of Chemistry and Biochemistry, The University of Alabama, Tuscaloosa, Alabama 35487, USA
    • 2Materials Science Division, Argonne National Laboratory, Lemont, Illinois 60439, USA
    • 3Department of Physics and Astronomy and California NanoSystems Institute, University of California, Los Angeles, Los Angeles California 90095, USA

    • *jmallred@ua.edu

    Phys. Rev. Lett. 127, 125501 – Published 15 September, 2021

    DOI: https://doi.org/10.1103/PhysRevLett.127.125501

    Abstract

    The metal-to-insulator transition in rutile VO2 has proven uniquely difficult to characterize because of the complex interplay between electron correlations and atomic structure. Here, we report the discovery of the sudden collapse of three-dimensional order in the low-temperature phase of V1−xMoxO2 at x=0.17 and the emergence of a novel frustrated two-dimensional order at x=0.19, with only a slight change in electronic properties. Single crystal diffuse x-ray scattering reveals that this transition from the 3D M1 phase to a 2D variant of the M2 phase results in long-range structural correlations along symmetry-equivalent (11L) planes of the tetragonal rutile structure, yet extremely short-range correlations transverse to these planes. These findings suggest that this two dimensionality results from a novel form of geometric frustration that is essentially structural in origin.

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