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The magnetic and electronic properties of oxyselenides—influence of transition metal ions and lanthanides

McCabe, E.E., Stock, C. (2016) The magnetic and electronic properties of oxyselenides—influence of transition metal ions and lanthanides. Journal of Physics: Condensed Matter, 28 (45). Article Number 453001. ISSN 0953-8984. (doi:10.1088/0953-8984/28/45/453001) (KAR id:58593)

Abstract

Magnetic oxyselenides have been a topic of research for several decades, firstly in the context of photoconductivity and thermoelectricity owing to their intrinsic semiconducting properties and ability to tune the energy gap through metal ion substitution. More recently, interest in the oxyselenides has experienced a resurgence owing to the possible relation to strongly correlated phenomena given the fact that many oxyselenides share a similar structure to unconventional superconducting pnictides and chalcogenides. The two dimensional nature of many oxyselenide systems also draws an analogy to cuprate physics where a strong interplay between unconventional electronic phases and localised magnetism has been studied for several decades. It is therefore timely to review the physics of the oxyselenides in the context of the broader field of strongly correlated magnetism and electronic phenomena. Here we review the current status and progress in this area of research with the focus on the influence of lanthanides and transition metal ions on the intertwined magnetic and electronic properties of oxyselenides. The emphasis of the review is on the magnetic properties and comparisons are made with iron based pnictide and chalcogenide systems.

Item Type: Article
DOI/Identification number: 10.1088/0953-8984/28/45/453001
Uncontrolled keywords: oxyselenides, magnetism, strongly correlated electrons
Subjects: Q Science
Divisions: Divisions > Division of Natural Sciences > Physics and Astronomy
Depositing User: Michael Woods
Date Deposited: 17 Nov 2016 15:34 UTC
Last Modified: 05 Nov 2024 10:49 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/58593 (The current URI for this page, for reference purposes)

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