Understanding the valency of rare earths from first-principles theory

Strange, Paul, Svane, Axel, Temmerman, Walter, Szotek, Zdzislawa, Winter, Herman (1999) Understanding the valency of rare earths from first-principles theory. Nature, 399 . pp. 756-758. ISSN 0028-0836. E-ISSN 1476-4687. (doi:10.1038/21595) (Access to this publication is currently restricted. You may be able to access a copy if URLs are provided)

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Abstract

The rare-earth metals have high magnetic moments and a diverse range of magnetic structures. Their magnetic properties are determined by the occupancy of the strongly localized 4f electronic shells, while the outer s-d electrons determine the bonding and other electronic properties. Most of the rare-earth atoms are divalent, but generally become trivalent in the metallic state. In some materials, the energy difference between these valence states is small and, by changing some external parameter (such as pressure), a transition from one to the other occurs. But the mechanism underlying this transition and the reason for the differing valence states are not well understood. Here we report first-principles electronic-structure calculations that enable us to determine both the valency and the lattice size as a function of atomic number, and hence understand the valence transitions. We find that there are two types of f electrons: localized core-like f electrons that determine the valency, and delocalized band-like f electrons that are formed through hybridization with the s-d bands and which participate in bonding. The latter are found only in the trivalent systems; if their number exceeds a certain threshold, it becomes energetically favourable for these electrons to localize, causing a transition to a divalent ground state.

Item Type: Article
DOI/Identification number: 10.1038/21595
Subjects: Q Science > QC Physics > QC176 Solid state physics
Divisions: Faculties > Sciences > School of Physical Sciences
Depositing User: Paul Strange
Date Deposited: 02 Sep 2015 11:44 UTC
Last Modified: 29 May 2019 15:58 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/50359 (The current URI for this page, for reference purposes)
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