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Microscopic theory of the insulating electronic ground states of the actinide dioxides AnO(2) (An= U, Np, Pu, Am, and Cm)
Uppsala University, Disciplinary Domain of Science and Technology, Physics, Department of Physics and Astronomy.
Uppsala University, Disciplinary Domain of Science and Technology, Physics, Department of Physics and Astronomy, Materials Theory.
2013 (English)In: Physical Review B. Condensed Matter and Materials Physics, ISSN 1098-0121, E-ISSN 1550-235X, Vol. 88, no 19, 195146- p.Article in journal (Refereed) Published
Abstract [en]

The electronic states of the actinide dioxides AnO(2) (with An= U, Np, Pu, Am, and Cm) are investigated employing first-principles calculations within the framework of the local density approximation + U(LDA + U) approach, implemented in a full-potential linearized augmented plane-wave scheme. A systematic analysis of the An-5f states is performed which provides intuitive connections between the electronic structures and the local crystalline fields of the f states in the AnO(2) series. Particularly the mechanisms leading to the experimentally observed insulating ground states are investigated. These are found to be caused by the strong spin-orbit and Coulomb interactions of the 5f orbitals; however, as a result of the different configurations, thismechanismworks in distinctly different ways for each of the AnO(2) compounds. In agreement with experimental observations, the nonmagnetic states of plutonium and curium dioxide are computed to be insulating, whereas those of uranium, neptunium, and americium dioxides require additional symmetry breaking to reproduce the insulator ground states, a condition which is met with magnetic phase transitions. We show that the occupancy of the An-f orbitals is closely connected to each of the appearing insulating mechanisms. We furthermore investigate the detailed constitution of the noncollinear multipolar moments for transverse 3q magnetic ordered states in UO2 and longitudinal 3q high-rank multipolar ordered states in NpO2 and AmO2.

Place, publisher, year, edition, pages
2013. Vol. 88, no 19, 195146- p.
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Natural Sciences
Identifiers
URN: urn:nbn:se:uu:diva-212849DOI: 10.1103/PhysRevB.88.195146ISI: 000327315000002OAI: oai:DiVA.org:uu-212849DiVA: diva2:680330
Available from: 2013-12-17 Created: 2013-12-16 Last updated: 2017-12-06Bibliographically approved

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Oppeneer, Peter M.

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