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Indication of single-crystal PuO2 oxidation from O 1s x-ray absorption spectra
Uppsala University, Disciplinary Domain of Science and Technology, Physics, Department of Physics and Astronomy, Soft X-Ray Physics.
Uppsala University, Disciplinary Domain of Science and Technology, Physics, Department of Physics and Astronomy, Soft X-Ray Physics.
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2011 (English)In: Physical Review B. Condensed Matter and Materials Physics, ISSN 1098-0121, E-ISSN 1550-235X, Vol. 83, no 7, 075113- p.Article in journal (Refereed) Published
Abstract [en]

The electronic structure of single-crystal PuO2 is studied using O 1s x-ray absorption (XA) and x-ray emission. Interpretation of the experimental data is supported by extensive first-principles calculations on the basis of the density functional theory + U approach. The measured XA spectra show a significant difference in intensity for the first two peaks between different spots or areas on the single crystal. Our theoretical simulations show that the first peak, at similar to 531 eV, can be attributed to O 2p-Pu 5f hybridization, while the second peak, at similar to 533.4 eV, is due to hybridization of O 2p with Pu d states. The reasons for the observed differences in the O 1s XA spectra are explored by calculating a number of defect structures PuO2+x as well as by simulating the existence of Pu(V) sites. Our results indicate the presence of oxidation states higher than Pu(IV) in some areas of the single crystal. The findings also suggest that plutonium oxide with a Pu fraction in an oxidation state higher than Pu(IV) consists of inequivalent Pu sites with (PuO2)-O-(IV) and (PuO2)-O-(V) rather than representing a system where the Pu oxidation state is constantly fluctuating between Pu(IV) and Pu(V).

Place, publisher, year, edition, pages
2011. Vol. 83, no 7, 075113- p.
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Physical Sciences
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URN: urn:nbn:se:uu:diva-148485DOI: 10.1103/PhysRevB.83.075113ISI: 000287484500002OAI: oai:DiVA.org:uu-148485DiVA: diva2:402249
Available from: 2011-03-07 Created: 2011-03-07 Last updated: 2017-12-11Bibliographically approved

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Oppeneer, Peter

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