Venkateshwarlu, Sarangi ; Kodumudi Venkataraman, Lalitha ; Segouin, Valentin ; Marlton, Frederick P. ; Hin, Ho Chin ; Chernyshov, Dmitry ; Ren, Yang ; Jorgensen, Mads R. V. ; Nayak, Sanjib ; Rödel, Jürgen ; Daniel, Laurent ; Pramanick, Abhijit (2020)
Large electromechanical strain and unconventionaldomain switching near phase convergencein a Pb-free ferroelectric.
In: Communications Physics, 3 (193)
doi: 10.1038/s42005-020-00459-2
Artikel, Bibliographie
Kurzbeschreibung (Abstract)
In many ferroelectrics, large electromechanical strains are observed near regions of com-position- or temperature- driven phase coexistence. Phenomenologically, this is attributed toeasy re-orientation of the polarization vector and/or phase transition, although their effectsare highly convoluted and difficult to distinguish experimentally. Here, we used synchrotronX-ray scattering and digital image correlation to differentiate between the microscopicmechanisms leading to large electrostrains in an exemplary Pb-free piezoceramic Sn-dopedbarium calcium zirconate titanate. Large electrostrains of ~0.2% measured at room-temperature are attributed to an unconventional effect, wherein polarization switching isaided by a reversible phase transition near the tetragonal-orthorhombic phase boundary.Additionally, electrostrains of ~0.1% or more could be maintained from room temperature to140 °C due to a succession of different microscopic mechanisms. In situ X-ray diffractionelucidates that while 90° domain reorientation is pertinent below the Curie temperature (TC),isotropic distortion of polar clusters is the dominant mechanism above TC.
Typ des Eintrags: | Artikel |
---|---|
Erschienen: | 2020 |
Autor(en): | Venkateshwarlu, Sarangi ; Kodumudi Venkataraman, Lalitha ; Segouin, Valentin ; Marlton, Frederick P. ; Hin, Ho Chin ; Chernyshov, Dmitry ; Ren, Yang ; Jorgensen, Mads R. V. ; Nayak, Sanjib ; Rödel, Jürgen ; Daniel, Laurent ; Pramanick, Abhijit |
Art des Eintrags: | Bibliographie |
Titel: | Large electromechanical strain and unconventionaldomain switching near phase convergencein a Pb-free ferroelectric |
Sprache: | Englisch |
Publikationsjahr: | 30 Oktober 2020 |
Verlag: | Nature Research |
Titel der Zeitschrift, Zeitung oder Schriftenreihe: | Communications Physics |
Jahrgang/Volume einer Zeitschrift: | 3 |
(Heft-)Nummer: | 193 |
DOI: | 10.1038/s42005-020-00459-2 |
URL / URN: | https://www.nature.com/articles/s42005-020-00459-2 |
Kurzbeschreibung (Abstract): | In many ferroelectrics, large electromechanical strains are observed near regions of com-position- or temperature- driven phase coexistence. Phenomenologically, this is attributed toeasy re-orientation of the polarization vector and/or phase transition, although their effectsare highly convoluted and difficult to distinguish experimentally. Here, we used synchrotronX-ray scattering and digital image correlation to differentiate between the microscopicmechanisms leading to large electrostrains in an exemplary Pb-free piezoceramic Sn-dopedbarium calcium zirconate titanate. Large electrostrains of ~0.2% measured at room-temperature are attributed to an unconventional effect, wherein polarization switching isaided by a reversible phase transition near the tetragonal-orthorhombic phase boundary.Additionally, electrostrains of ~0.1% or more could be maintained from room temperature to140 °C due to a succession of different microscopic mechanisms. In situ X-ray diffractionelucidates that while 90° domain reorientation is pertinent below the Curie temperature (TC),isotropic distortion of polar clusters is the dominant mechanism above TC. |
Fachbereich(e)/-gebiet(e): | 11 Fachbereich Material- und Geowissenschaften 11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft 11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft > Fachgebiet Nichtmetallisch-Anorganische Werkstoffe |
Hinterlegungsdatum: | 03 Feb 2021 10:31 |
Letzte Änderung: | 03 Feb 2021 10:31 |
PPN: | |
Export: | |
Suche nach Titel in: | TUfind oder in Google |
Frage zum Eintrag |
Optionen (nur für Redakteure)
Redaktionelle Details anzeigen |