Flipping the switch on magnetism in strontium titanate
- Nancy Ambrosiano
- Communications Office
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Semiconductor material can be magnetized with light, suggesting new technology opportunities
LOS ALAMOS, N.M., March 27, 2014—Interest in oxide-based semiconductor electronics has exploded in recent years, fueled largely by the ability to grow atomically precise layers of various oxide materials. One of the most important materials in this burgeoning field is strontium titanate (SrTiO3), a nominally nonmagnetic wide-bandgap semiconductor, and researchers at Los Alamos National Laboratory have found a way to magnetize this material using light, an effect that persists for hours at a time.
“One doesn’t normally think of this material as being able to support magnetism. It’s supposed to be useful – but magnetically uninteresting – stuff. So when we started shining light on it and saw what appeared to be extremely long-lived magnetic signals – that persisted for hours even after we turned the light off – it came as quite a surprise,” said Scott Crooker, lead scientist on the project at Los Alamos.
Studies of strontium titanate’s electrical and optical properties abound, it’s not a new material – in fact it was marketed in the 1950s and ‘60s as a “faux diamond” product before cubic zirconium gained popularity. Though often used in industry for its robust dielectric properties, its potential magnetic properties were less well understood. A renewed interest in SrTiO3 was recently sparked by observations of an unexpected and emergent magnetization in strontium titanate-based structures.
“There’ve been tantalizing hints in recent years that there might be more to SrTiO3 than originally thought. When layered with other ‘nominally non-magnetic’ oxides, a handful of recent experiments around the world have shown not only superconductivity but also an unexpected magnetism. So that piqued our interest in this material,” Crooker said.
"This is really something completely new in oxide materials like these - the ability to write permanent magnetic patterns into an otherwise non-magnetic material. The challenge will be to properly understand how and why this works, and to increase the temperature at which it can be done. The exciting possibility is to potentially use this to store data in some way,” said collaborator Chris Leighton of the University of Minnesota.
In a paper published this week in Nature Materials, Crooker and collaborators illustrated a new aspect to the nature of magnetism in strontium titanate, reporting the observation of an optically induced and persistent magnetization in crystals of SrTiO3 when they are slightly oxygen-deficient.
Using samples prepared by collaborators in Leighton’s group, Crooker and Los Alamos colleagues William Rice and Joe Thompson used magnetic circular dichroism spectroscopy and also SQUID magnetometry to show that circularly polarized light can induce an extremely long-lived magnetic moment in SrTiO3 at zero applied magnetic field.
These signals appear below 18 Kelvin, persist for hours below 10 K, and can be controlled in both magnitude and sign via the circular polarization and wavelength of blue/green light in the range spanning 400-500 nm. As such, magnetic patterns can be “written” into SrTiO3, and subsequently read out, using light alone. These effects occur only in crystals containing oxygen vacancies, revealing a detailed interplay between magnetism, lattice defects and light in an archetypal complex oxide material.
This work was funded by Laboratory Directed Research and Development Exploratory Research at Los Alamos National Laboratory under the auspices of the US DOE Office of Science.
The work at the University of Minnesota was funded by the National Science Foundation.
- "Persistent Optically Induced Magnetism in Oxygen-Deficient Strontium Titanate” W.D. Rice, P. Ambwani, M. Bombeck, J. D. Thompson, G. Haugstad, C. Leighton, and S. A. Crooker, accepted and in press, Nature Materials (2014).
Caption for image below: A demonstration that magnetic information can be optically written into SrTiO3, stored, and then optically read out. Here, the circular polarization and the magnetization direction were reversed at each subsequent letter. Image credit, Nature Materials.
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