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Room-temperature valence transition in a strain-tuned perovskite oxide.

Authors :
Chaturvedi V
Ghosh S
Gautreau D
Postiglione WM
Dewey JE
Quarterman P
Balakrishnan PP
Kirby BJ
Zhou H
Cheng H
Huon A
Charlton T
Fitzsimmons MR
Korostynski C
Jacobson A
Figari L
Barriocanal JG
Birol T
Mkhoyan KA
Leighton C
Source :
Nature communications [Nat Commun] 2022 Dec 15; Vol. 13 (1), pp. 7774. Date of Electronic Publication: 2022 Dec 15.
Publication Year :
2022

Abstract

Cobalt oxides have long been understood to display intriguing phenomena known as spin-state crossovers, where the cobalt ion spin changes vs. temperature, pressure, etc. A very different situation was recently uncovered in praseodymium-containing cobalt oxides, where a first-order coupled spin-state/structural/metal-insulator transition occurs, driven by a remarkable praseodymium valence transition. Such valence transitions, particularly when triggering spin-state and metal-insulator transitions, offer highly appealing functionality, but have thus far been confined to cryogenic temperatures in bulk materials (e.g., 90 K in Pr <subscript>1-x</subscript> Ca <subscript>x</subscript> CoO <subscript>3</subscript> ). Here, we show that in thin films of the complex perovskite (Pr <subscript>1-y</subscript> Y <subscript>y</subscript> ) <subscript>1-x</subscript> Ca <subscript>x</subscript> CoO <subscript>3-δ</subscript> , heteroepitaxial strain tuning enables stabilization of valence-driven spin-state/structural/metal-insulator transitions to at least 291 K, i.e., around room temperature. The technological implications of this result are accompanied by fundamental prospects, as complete strain control of the electronic ground state is demonstrated, from ferromagnetic metal under tension to nonmagnetic insulator under compression, thereby exposing a potential novel quantum critical point.<br /> (© 2022. The Author(s).)

Details

Language :
English
ISSN :
2041-1723
Volume :
13
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
36522321
Full Text :
https://doi.org/10.1038/s41467-022-35024-8