It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
The coupling of ordered electronic phases with lattice, spin, and orbital degrees of freedom are of central interest in strongly correlated systems. Their interplay has been intensively studied from femtosecond to picosecond time scales, while their dynamics beyond nanoseconds are usually assumed to follow lattice cooling. Here, we report an unusual slowing down of the recovery of an electronic phase across a first-order phase transition. Following optical excitation, the recovery time of both transient optical reflectivity and X-ray diffraction intensity from the charge-ordered superstructure in a La1/3Sr2/3FeO3 thin film increases by orders of magnitude as the sample temperature approaches the phase transition temperature. In this regime, the recovery time becomes much longer than the lattice cooling time. The combined experimental and theoretical investigation shows that the slowing down of electronic recovery corresponds to the pseudo-critical dynamics that originates from magnetic interactions close to a weakly first-order phase transition.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details


1 Advanced Photon Source, Argonne National Laboratory, Argonne, IL, USA
2 Materials Science Division, Argonne National Laboratory, Argonne, IL, USA
3 Center for Nanoscale Materials, Argonne National Laboratory, Argonne, IL, USA; Department of Chemistry, Northwestern University, Evanston, IL, USA
4 Materials Science Division, Argonne National Laboratory, Argonne, IL, USA; Department of Physics, University of Illinois at Chicago, Chicago, IL, USA
5 Advanced Photon Source, Argonne National Laboratory, Argonne, IL, USA; School of Physical Sciences, Dublin City University, Dublin, Ireland
6 Materials Science Division, Argonne National Laboratory, Argonne, IL, USA; Center for Nanoscale Materials, Argonne National Laboratory, Argonne, IL, USA