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

Author:

Chaturvedi VipulORCID,Ghosh SupriyaORCID,Gautreau Dominique,Postiglione William M.ORCID,Dewey John E.ORCID,Quarterman Patrick,Balakrishnan Purnima P.ORCID,Kirby Brian J.ORCID,Zhou HuaORCID,Cheng Huikai,Huon AmandaORCID,Charlton TimothyORCID,Fitzsimmons Michael R.ORCID,Korostynski Caroline,Jacobson Andrew,Figari Lucca,Barriocanal Javier Garcia,Birol TuranORCID,Mkhoyan K. AndreORCID,Leighton ChrisORCID

Abstract

AbstractCobalt 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 Pr1-xCaxCoO3). Here, we show that in thin films of the complex perovskite (Pr1-yYy)1-xCaxCoO3-δ, 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.

Funder

DOE | SC | Basic Energy Sciences

National Science Foundation

U.S. Department of Energy

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary

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