Nanoscale core-shell structure and recrystallization of swift heavy ion tracks in SrTiO3

Ashish Kumar Gupta, Eva Zarkadoula, Maxim Ziatdinov, Sergei V. Kalinin, Vikas Reddy Paduri, Jordan A. Hachtel, Yanwen Zhang, Christina Trautmann, William J. Weber, Ritesh Sachan

Research output: Contribution to journalArticlepeer-review

Abstract

It is widely accepted that the interaction of swift heavy ions with many complex oxides is predominantly governed by the electronic energy loss that gives rise to nanoscale amorphous ion tracks along the penetration direction. The question of how electronic excitation and electron-phonon coupling affect the atomic system through defect production, recrystallization, and strain effects has not yet been fully clarified. To advance the knowledge of the atomic structure of ion tracks, we irradiated single crystalline SrTiO3 with 629 MeV Xe ions and performed comprehensive electron microscopy investigations complemented by molecular dynamics simulations. This study shows discontinuous ion-track formation along the ion penetration path, comprising an amorphous core and a surrounding few monolayer thick shell of strained/defective crystalline SrTiO3. Using machine-learning-aided analysis of atomic-scale images, we demonstrate the presence of 4-8% strain in the disordered region interfacing with the amorphous core in the initially formed ion tracks. Under constant exposure of the electron beam during imaging, the amorphous part of the ion tracks readily recrystallizes radially inwards from the crystalline-amorphous interface under the constant electron-beam irradiation during the imaging. Cation strain in the amorphous region is observed to be significantly recovered, while the oxygen sublattice remains strained even under the electron irradiation due to the present oxygen vacancies. The molecular dynamics simulations support this observation and suggest that local transient heating and annealing facilitate recrystallization process of the amorphous phase and drive Sr and Ti sublattices to rearrange. In contrast, the annealing of O atoms is difficult, thus leaving a remnant of oxygen vacancies and strain even after recrystallization. This work provides insights for creating and transforming novel interfaces and nanostructures for future functional applications.

Original languageEnglish
Pages (from-to)14366-14377
Number of pages12
JournalNanoscale
Volume16
Issue number30
DOIs
StatePublished - Jul 1 2024

Funding

RS acknowledges the support of faculty start-up funding at Oklahoma State University. The electron microscopic data acquisition in this research was conducted at the Center for Nanophase Materials Sciences at ORNL, which is a DOE Office of Science User Facility. EZ (theory and simulation work) was supported by the Center for Nanophase Materials Sciences, (CNMS), which is a US Department of Energy, Office of Science User Facility at Oak Ridge National Laboratory. The results presented here are based on a UMAT experiment that was carried out on the UNILAC accelerator at the GSI Helmholtz Center for Heavy Ion Research, Darmstadt (Germany) in the frame of FAIR Phase-0. The contribution of WJW was supported by the National Science Foundation under Grant No. DMR-2104228. YZ was supported as part of the Laboratory Directed Research and Development Program at Idaho National Laboratory under the Department of Energy (DOE) Idaho Operations Office (an agency of the U.S. Government) Contract DE-AC07-05ID145142. SVK was supported by the US Department of Energy, Office of Science, Office of Basic Energy Sciences, as part of the Energy Frontier Research Centers program: CSSAS \u2013 The Center for the Science of Synthesis Across Scales \u2013 under Award Number DE-SC0019288.

FundersFunder number
Basic Energy Sciences
Oklahoma State University
Oak Ridge National Laboratory
Center for Nanophase Materials Sciences
U.S. Department of Energy
Idaho National Laboratory
Laboratory Directed Research and Development
Office of Science
National Science FoundationDMR-2104228
Idaho Operations Office, U.S. Department of EnergyDE-AC07-05ID145142
CSSASDE-SC0019288

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