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Structural investigation of californium under pressure
KTH, School of Industrial Engineering and Management (ITM), Materials Science and Engineering, Applied Material Physics. Department of Physics and Materials Science, Uppsala University.
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2013 (English)In: Physical Review B. Condensed Matter and Materials Physics, ISSN 1098-0121, E-ISSN 1550-235X, Vol. 87, no 21, 214111- p.Article in journal (Refereed) Published
Abstract [en]

The high-pressure structural behavior of californium has been studied experimentally and theoretically up to 100 GPa. A valence change from divalent to trivalent forms was observed under modest pressure revealing californium to be the only actinide to exhibit more than one metallic valence at near to ambient conditions as is the case for cerium in the lanthanide series. Three metallic valencies and four different crystallographic phases were observed in californium as a function of pressure. High-pressure techniques, synchrotron radiation, and ab initio electronic structure calculations of total energies were used to investigate the material and to determine the role which californium's 5f electrons play in influencing these transitions. The crystallographic structures observed are similar to those found in the preceding actinide elements, curium and americium, with the initially localized 5f states becoming completely delocalized under the influence of high pressure.

Place, publisher, year, edition, pages
American Physical Society , 2013. Vol. 87, no 21, 214111- p.
Keyword [en]
5f Electrons, Cerium Metal, Crystal-Structures, Delocalization, Transition, Americium, Valence, Phase, State, Diffraction
National Category
Physical Sciences
Identifiers
URN: urn:nbn:se:kth:diva-124720DOI: 10.1103/PhysRevB.87.214111ISI: 000321060500001Scopus ID: 2-s2.0-84879733877OAI: oai:DiVA.org:kth-124720DiVA: diva2:638284
Funder
EU, European Research CouncilSwedish Research CouncilSwedish Foundation for Strategic Research
Note

QC 20130729

Available from: 2013-07-29 Created: 2013-07-29 Last updated: 2017-12-06Bibliographically approved

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CiteExportLink to record
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