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Title: Giant thermally-enhanced electrostriction and polar surface phase in L a 2 M o 2 O 9 oxygen ion conductors

Journal Article · · Physical Review Materials
 [1];  [2];  [3];  [4];  [4];  [5];  [5];  [3];  [5];  [6];  [4];  [2]
  1. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Center for Nanophase Materials Science (CNMS); Argonne National Lab. (ANL), Argonne, IL (United States). X-ray Science Division
  2. Australian National Univ., Canberra, ACT (Australia). Research School of Chemistry
  3. Univ. of Cambridge (United Kingdom). Dept. of Earth Sciences
  4. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Center for Nanophase Materials Science (CNMS)
  5. Argonne National Lab. (ANL), Argonne, IL (United States). X-ray Science Division
  6. Univ. of Washington, Seattle, WA (United States). Dept. of Mechanical Engineering

Ferroelectrics possess spontaneous electric polarization at macroscopic scales which nonetheless imposes strict limitations on the material classes. Recent discoveries of untraditional symmetry-breaking phenomena in reduced material dimensions have indicated feasibilities to extend polar properties to broader types of materials, potentially opening up the freedom for designing materials with hybrid functionalities. Here in this paper, we report the unusual electromechanical properties of La2Mo2O9 (LAMOX) oxygen ion conductors, systematically investigated at both bulk and surface length levels. We first observed giant electrostriction effects in La2Mo2O9 bulk ceramics that are thermally enhanced in concert with their low-energy oxygen-vacancy hopping dynamics. Moreover, while no clear bulk polarization was detected, the surface phases of LAMOX were found to be manifestly polar, likely originating from the coupling between the intrinsic structural flexibilities with strain gradients (i.e., flexoelectricity) and/or chemical heterogeneities present in the materials. These findings identify La2Mo2O9 as a promising electromechanical material system and suggest that the flexible structural and chemical configurations in ionically active materials could enable fundamentally different venues to accommodate electric polarization.

Research Organization:
Argonne National Laboratory (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
AC02-06CH11357; AC05-00OR22725
OSTI ID:
1465143
Alternate ID(s):
OSTI ID: 1434987
Journal Information:
Physical Review Materials, Vol. 2, Issue 4; ISSN 2475-9953
Publisher:
American Physical Society (APS)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 12 works
Citation information provided by
Web of Science

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