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dc.contributor.author Pearce C.I.
dc.contributor.author Pattrick R.A.D.
dc.contributor.author Vaughan D.J.
dc.contributor.author Henderson C.M.B.
dc.contributor.author Laan G.V.D.
dc.date.accessioned 2024-10-14T08:52:07Z
dc.date.available 2024-10-14T08:52:07Z
dc.date.issued 2006
dc.identifier https://www.elibrary.ru/item.asp?id=14693767
dc.identifier.citation Geochimica et Cosmochimica Acta, 2006, 70, 18, 4635-4642
dc.identifier.issn 0016-7037
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/45848
dc.description.abstract The determination of the oxidation states of copper and iron in sulfides, and chalcopyrite (CuFeS2) in particular, using 2p X-ray photoemission spectroscopy (XPS) and L2,3-edge X-ray absorption spectroscopy (XAS) is revisited. Reassessment of the published spectra derived by these methods produces consistent results and reveals the 'd count' in the copper compounds to be intermediate between d9 and d10. Nevertheless, these covalent copper compounds can be divided into those nominally monovalent and those nominally divalent. The Fe L2,3-edge XAS of chalcopyrite, along with Mössbauer data, confirm the presence of high-spin Fe3+. Chalcopyrite, despite recent published reports to the contrary, clearly belongs to the monovalent copper class. © 2006 Elsevier Inc. All rights reserved.
dc.title COPPER OXIDATION STATE IN CHALCOPYRITE: MIXED CU D9 AND D10 CHARACTERISTICS
dc.type Статья
dc.identifier.doi 10.1016/j.gca.2006.05.017


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