Please use this identifier to cite or link to this item: https://apo.ansto.gov.au/dspace/handle/10238/10292
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dc.contributor.authorZhang, ZM-
dc.contributor.authorAvdeev, M-
dc.contributor.authorde los Reyes, M-
dc.contributor.authorLumpkin, GR-
dc.contributor.authorKennedy, BJ-
dc.contributor.authorBlanchard, PER-
dc.contributor.authorLiu, S-
dc.contributor.authorTadich, A-
dc.contributor.authorCowie, BCC-
dc.date.accessioned2021-02-03T22:38:03Z-
dc.date.available2021-02-03T22:38:03Z-
dc.date.issued2016-11-01-
dc.identifier.citationZhang, Z., Avdeev, M., de los Reyes, M., Lumpkin, G. R., Kennedy, B. J., Blanchard, P. E. R., Liu, S., Tadich, A., & Cowie, B. C. C. (2016). Probing long- and short-range disorder in Y2Ti2–xHfxO7 by diffraction and spectroscopy techniques. Journal of Physical Chemistry C, 120(46), 26465–26479. doi:10.1021/acs.jpcc.6b07076en_US
dc.identifier.issn1932-7455-
dc.identifier.urihttps://doi.org/10.1021/acs.jpcc.6b07076en_US
dc.identifier.urihttps://apo.ansto.gov.au/dspace/handle/10238/10292-
dc.description.abstractWe studied the long-range average and short-range local structures in Y2Ti2–xHfxO7 (x = 0–2.0) using diffraction and spectroscopy techniques, respectively. Both neutron and synchrotron X-ray powder diffraction data show a clear phase transition of the average structure from ordered pyrochlore to disordered defect-fluorite at x ≈ 1.6; the long-range anion disorder appears to develop gradually throughout the entire pyrochlore region in contrast to the rapid loss of cation ordering from x = 1.4 to 1.6. The commonly observed two-phase region around the pyrochlore/defect-fluorite phase boundary is absent in this system, demonstrating high sample quality. X-ray absorption near-edge structure (XANES) results at the Y L2-, Ti K- and L3,2-, Hf L3-, and O K-edges indicate a gradual local structural evolution across the whole compositional range; the Y coordination number (CN) decreases and the CN around Ti and Hf increases with increasing Hf content (x). The spectroscopic results suggest that the local disorder occurs long before the pyrochlore to defect-fluorite phase boundary as determined by diffraction, and this disorder evolves continuously from short- to medium- and eventually to long-range detectable by diffraction. This study highlights the complex disordering process in pyrochlore oxides and the importance of a multitechnique approach to tackle disorder over different length scales and in the anion and cation sublattices, respectively. The results are important in the context of potential applications of these oxides such as ionic conductors and radiation-resistant nuclear waste forms. © 2016 American Chemical Societyen_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectX-ray spectroscopyen_US
dc.subjectNeutron diffractionen_US
dc.subjectX-ray diffractionen_US
dc.subjectPhase transformationsen_US
dc.subjectPyrochloreen_US
dc.subjectFluoriteen_US
dc.subjectCationsen_US
dc.subjectAnionsen_US
dc.subjectOxidesen_US
dc.subjectCrystal latticesen_US
dc.subjectWaste formsen_US
dc.titleProbing long- and short-range disorder in Y2Ti2–xHfxO7 by diffraction and spectroscopy techniquesen_US
dc.typeJournal Articleen_US
dc.date.statistics2021-01-12-
Appears in Collections:Journal Articles

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