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Magnetotransport and superconducting properties are investigated for uniformly La-doped SrTiO3 films and GdTiO3/SrTiO3 heterostructures, respectively. GdTiO3/SrTiO3 interfaces exhibit a high-density 2D electron gas on the SrTiO3 side of the interface, while, for the SrTiO3 films, carriers are provided by the dopant atoms. Both types of samples exhibit ferromagnetism at low temperatures, as evidenced by a hysteresis in the magnetoresistance. For the uniformly doped SrTiO3 films, the Curie temperature is found to increase with doping and to coexist with superconductivity for carrier concentrations on the high-density side of the superconducting dome. The Curie temperature of the GdTiO3/SrTiO3 heterostructures scales with the thickness of the SrTiO3 quantum well. The results are used to construct a stability diagram for the ferromagnetic and superconducting phases of SrTiO3 .
Plain Language Summary
Letting two insulating oxides, such as LaAlO3 and SrTiO3 , meet at an interface, what do you see? The emergence of a two-dimensional electron liquid at the interface with many fundamentally exciting new collective electronic properties, as discovered by Ohtomo and Hwang in 2004, and investigated by many others since then. One of the most interesting and consuming puzzles is the coexistence of ferromagnetism and superconductivity in this electron gas, as the two properties are generally considered to be incompatible: The former arises from net spin alignment in a particular direction, whereas the latter involves the pairing of a spin-up and a spin-down electron, implying no net spin. By what mechanisms does the coexistence come about then, and what is the origin of the ferromagnetism in the electron gas since neither of the two bulk oxides involved is ferromagnetic? In this experimental paper, we present new crucial evidence, by studying the magnetotransport properties of a set of carefully designed samples, that the ferromagnetism arises from intrinsic properties of the SrTiO3 , taking a significant step forward toward ultimate answers to these questions.
The samples we have investigated are, by design, of two types: high-density electron liquids at GdTiO3/SrTiO3 interfaces and uniformly La-doped SrTiO3 films with thickness in the range from nanometers to tens of nanometers. The charge-carrier electrons are introduced in two fundamentally different ways: through the interface in the first type, and through the dopant atoms in the second. By identifying a hysteretic dependence of each sample’s magnetoresistance on the applied magnetic field and analyzing the temperature dependence of the magnetoresistance, we are able to draw a number of conclusions: (1) The charge-carrier density and temperature are the parameters crucial to determining whether or not the ferromagnetism-superconductivity coexistence appears. (2) Superconductivity occurs in a low-carrier-density, low-temperature domelike region of the two-parameter space whereas ferromagnetism appears on the high-density side of the superconductivity dome; for a range of intermediate carrier densities, which correspond to those achieved in the doped SrTiO3 films, both properties coexist. (3) The ferromagnetism emerges as a general result of collective electronic interaction intrinsic to doped SrTiO3 .
This study should stimulate further discussions and research. The GdTiO3/SrTiO3 interface is intrinsically interesting both in its own right, with GdTiO3 being a ferrimagnetic Mott insulator, and as a system of comparison for LaAlO3 and SrTiO3 . The origin of the ferromagnetism also suggests that magnetic properties of these systems may be manipulated, a possibility that would make these structures of interest for spintronic applications.
Title
Carrier-Controlled Ferromagnetism in SrTiO3
Author
Moetakef, Pouya; Williams, James R; Ouellette, Daniel G; Kajdos, Adam P; Goldhaber-Gordon, David; Allen, S James; Stemmer, Susanne
Publication date
Apr-Jun 2012
American Physical Society
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2550543467
Copyright
© 2012. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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