Abstract

In many ferroelectrics, large electromechanical strains are observed near regions of composition- or temperature- driven phase coexistence. Phenomenologically, this is attributed to easy re-orientation of the polarization vector and/or phase transition, although their effects are highly convoluted and difficult to distinguish experimentally. Here, we used synchrotron X-ray scattering and digital image correlation to differentiate between the microscopic mechanisms leading to large electrostrains in an exemplary Pb-free piezoceramic Sn-doped barium calcium zirconate titanate. Large electrostrains of ~0.2% measured at room-temperature are attributed to an unconventional effect, wherein polarization switching is aided by a reversible phase transition near the tetragonal-orthorhombic phase boundary. Additionally, electrostrains of ~0.1% or more could be maintained from room temperature to 140 °C due to a succession of different microscopic mechanisms. In situ X-ray diffraction elucidates that while 90° domain reorientation is pertinent below the Curie temperature (TC), isotropic distortion of polar clusters is the dominant mechanism above TC.

Piezoelectric materials are used for a broad range of industrial and research applications. The authors use synchrotron X-ray scattering and digital imaging correlation to investigate the microscopic mechanisms behind electromechanical strains in a lead-free piezoceramic material, which suggests an unconventional domain switching mechanism and ability to enhance the temperature range of operation by suitable doping strategies.

Details

Title
Large electromechanical strain and unconventional domain switching near phase convergence in a Pb-free ferroelectric
Author
Sarangi, Venkateshwarlu 1 ; Venkataraman, Lalitha K 2   VIAFID ORCID Logo  ; Segouin Valentin 3 ; Marlton, Frederick P 4 ; Hin Ho Chin 1 ; Chernyshov Dmitry 5   VIAFID ORCID Logo  ; Yang, Ren 6   VIAFID ORCID Logo  ; Jørgensen, Mads R, V 7   VIAFID ORCID Logo  ; Nayak Sanjib 1 ; Rödel Jürgen 2   VIAFID ORCID Logo  ; Laurent, Daniel 3   VIAFID ORCID Logo  ; Pramanick Abhijit 1   VIAFID ORCID Logo 

 City University of Hong Kong, Department of Materials Science and Engineering, Hong Kong SAR, China (GRID:grid.35030.35) (ISNI:0000 0004 1792 6846) 
 Technical University of Darmstadt, Department of Materials and Earth Sciences, Darmstadt, Germany (GRID:grid.6546.1) (ISNI:0000 0001 0940 1669) 
 Université Paris-Saclay, CentraleSupélec, CNRS, Laboratorie de Génie Electrique et Electronique de Paris, Gif-sur-Yvette, France (GRID:grid.494567.d) (ISNI:0000 0004 4907 1766); Sorbonne Université, CNRS, Laboratoire de Génie Electrique et Electronique de Paris, Paris, France (GRID:grid.494567.d) 
 Aarhus University, Center for Materials Crystallography, Department of Chemistry and iNANO, Aarhus C, Denmark (GRID:grid.7048.b) (ISNI:0000 0001 1956 2722) 
 SNBL, ESRF, Grenoble, France (GRID:grid.5398.7) (ISNI:0000 0004 0641 6373); Peter the Great St. Petersburg Polytechnic University, St. Petersburg, Russia (GRID:grid.32495.39) (ISNI:0000 0000 9795 6893) 
 Advanced Photon Source, Argonne National Laboratory, Argonne, USA (GRID:grid.187073.a) (ISNI:0000 0001 1939 4845) 
 Aarhus University, Center for Materials Crystallography, Department of Chemistry and iNANO, Aarhus C, Denmark (GRID:grid.7048.b) (ISNI:0000 0001 1956 2722); Lund University, MAX IV Laboratory, Lund, Sweden (GRID:grid.4514.4) (ISNI:0000 0001 0930 2361) 
Publication year
2020
Publication date
2020
Publisher
Nature Publishing Group
e-ISSN
23993650
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2471529410
Copyright
© The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.