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Picosecond anisotropic phase separation governing photoinduced phase stability in submicron Ti3O5 crystals

  • Ritwika Mandal
  • , Maciej Lorenc
  • , Marco Cammarata
  • , Matteo Levantino
  • , Serhane Zerdane
  • , Étienne Janod
  • , Laurent Cario
  • , Hiroko Tokoro
  • , Shin Ichi Ohkoshi
  • , Elzbieta Trzop
  • , Marina Servol
  • , Guénolé Huitric
  • , Hervé Cailleau
  • , Vinh Ta Phuoc
  • , Florian Banhart
  • , Cristian Enachescu
  • , Laurentiu Stoleriu
  • , Céline Mariette
  • IPR (Institut de Physique de Rennes) - UMR 6251
  • Institut des Matériaux de Nantes
  • Centre national de la recherche scientifique
  • European Synchrotron Radiation Facility
  • Paul Scherrer Institut
  • University of Tokyo
  • University of Tsukuba
  • Université de Picardie Jules Verne
  • Université de Tours
  • UMR 7504 CNRS-ULP
  • Alexandru Ioan Cuza University

Research output: Contribution to journalArticlepeer-review

Abstract

Recently developed ceramic material Ti3O5 exhibits fascinating application properties, from ultrafast switching between metallic and insulating phases to light-to-heat conversion and storage. While the states conferring such properties are not spatially homogeneous, the origin of phase separation and the link between the phase coexistence and dynamics, key for stability of such states, is still little known. In this work, we use time-resolved X-ray diffraction and numerical simulations to establish rules by which the dynamics of heat-driven transition in laser excited Ti3O5 crystallites occur in space and time. The studies are conducted on submicron Ti3O5 crystallites and span a broad timescale allowing separation of phase change regimes. Our results reveal the influence of nanoscopic morphology on the mechanism of macroscopic transformation triggered by laser excitation.

Original languageEnglish
Article number209
JournalCommunications Materials
Volume6
Issue number1
DOIs
Publication statusPublished - 1 Dec 2025

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