Published July 19, 2019 | Version Supplemental Material + Published
Journal Article Open

Evidence for the weakly coupled electron mechanism in an Anderson-Blount polar metal

  • 1. ROR icon California Institute of Technology
  • 2. ROR icon Northwestern University
  • 3. ROR icon National Institute for Materials Science
  • 4. ROR icon Institute of Physics

Abstract

Over 50 years ago, Anderson and Blount proposed that ferroelectric-like structural phase transitions may occur in metals, despite the expected screening of the Coulomb interactions that often drive polar transitions. Recently, theoretical treatments have suggested that such transitions require the itinerant electrons be decoupled from the soft transverse optical phonons responsible for polar order. However, this decoupled electron mechanism (DEM) has yet to be experimentally observed. Here we utilize ultrafast spectroscopy to uncover evidence of the DEM in LiOsO_3, the first known band metal to undergo a thermally driven polar phase transition (T_c ≈ 140 K). We demonstrate that intra-band photo-carriers relax by selectively coupling to only a subset of the phonon spectrum, leaving as much as 60% of the lattice heat capacity decoupled. This decoupled heat capacity is shown to be consistent with a previously undetected and partially displacive TO polar mode, indicating the DEM in LiOsO_3.

Additional Information

© 2019 The Author(s). This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. Received 08 February 2019; Accepted 14 June 2019; Published 19 July 2019. Data availability: The datasets generated are/or analyzed during the current study are available from the corresponding author on reasonable request. This work was supported by the U.S. Department of Energy under Grant no. DE SC0010533. D.H. also acknowledges funding from the David and Lucile Packard Foundation and support for instrumentation from the Institute for Quantum Information and Matter, an NSF Physics Frontiers Center (PHY-1733907). N.J.L. acknowledges support from the Institute for Quantum Information and Matter Postdoctoral Fellowship. N.Z.K. was supported by U.S. DOE-BES Grant no. DE-SC0012375. D.P. and J.M.R. were supported by ARO (Award no. W911NF-15-1-0017). Y.G.S. was supported by the National Key Research and Development Program of China (Nos. 2017YFA0302901 and 2016YFA0300604). We thank Rohit Prasankumar for helpful conversations, Qingming Zhang for sharing unpublished Raman data, and Stefano Lupi for sharing unpublished reflectivity results.

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Published - s41467-019-11172-2.pdf

Supplemental Material - 41467_2019_11172_MOESM1_ESM.pdf

Supplemental Material - 41467_2019_11172_MOESM2_ESM.pdf

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Additional details

Identifiers

PMCID
PMC6642157
Eprint ID
97292
Resolver ID
CaltechAUTHORS:20190719-102955020

Funding

Department of Energy (DOE)
DE-SC0010533
David and Lucile Packard Foundation
Institute for Quantum Information and Matter (IQIM)
NSF
PHY-1733907
Department of Energy (DOE)
DE-SC0012375
Army Research Office (ARO)
W911NF-15-1-0017
National Key Research and Development Program of China
2017YFA0302901
National Key Research and Development Program of China
2016YFA0300604

Dates

Created
2019-07-19
Created from EPrint's datestamp field
Updated
2022-02-25
Created from EPrint's last_modified field

Caltech Custom Metadata