| Literature DB >> 25798917 |
Anna L Smith1,2, Philippe E Raison1, Laura Martel1, Damien Prieur1, Thibault Charpentier3, Gilles Wallez4,5, Emmanuelle Suard6, Andreas C Scheinost7, Christoph Hennig7, Philippe Martin8, Kristina O Kvashnina9, Anthony K Cheetham2, Rudy J M Konings1.
Abstract
The crystal structure of trisodium uranate, which forms following the interaction between sodium and hyperstoichiometric urania, has been solved for the first time using powder X-ray and neutron diffraction, X-ray absorption near-edge structure spectroscopy, and solid-state (23)Na multiquantum magic angle spinning nuclear magnetic resonance. The compound, isostructural with Na3BiO4, has monoclinic symmetry, in space group P2/c. Moreover, it has been shown that this structure can accommodate some cationic disorder, with up to 16(2)% sodium on the uranium site, corresponding to the composition α-Na3(U1-x,Nax)O4 (0 < x < 0.18). The α phase adopts a mixed valence state with the presence of U(V) and U(VI). The two polymorphs of this compound described in the literature, m- and β-Na3(U1-x,Nax)O4, have also been investigated, and their relationship to the α phase has been established. The completely disordered low-temperature cubic phase corresponds to a metastable phase. The semiordered high-temperature β phase is cubic, in space group Fd3̅m.Entities:
Year: 2015 PMID: 25798917 DOI: 10.1021/acs.inorgchem.5b00136
Source DB: PubMed Journal: Inorg Chem ISSN: 0020-1669 Impact factor: 5.165