Cation Disordering by Rapid Crystal Growth in Olivine-Phosphate Nanocrystals

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On the basis of Pauling's first rule for ionic bonding, the coordination number of cations with oxygen anions can be determined by comparison of their relative ionic size ratio. In contrast to simple oxides, various site occupancies by multicomponent cations with similar sizes usually occur in complex oxides, resulting in distinct physical properties. Through an unprecedented combination of in situ high-temperature high-resolution electron microscopy, crystallographic image processing, geometric phase analysis, and neutron powder diffraction, we directly demonstrate that while the initial crystallites after nucleation during crystallization have a very high degree of ordering, significant local cation disordering is induced by rapid crystal growth in Li-intercalation metal-phosphate nanocrystals. The findings in this study show that control of subsequent crystal growth during coarsening is of great importance to attain a high degree of cation atomic-level visualization in real time.
Publisher
AMER CHEMICAL SOC
Issue Date
2012-06
Language
English
Article Type
Article
Citation

NANO LETTERS, v.12, no.6, pp.3068 - 3073

ISSN
1530-6984
DOI
10.1021/nl300909h
URI
http://hdl.handle.net/10203/103100
Appears in Collection
EEW-Journal Papers(저널논문)MS-Journal Papers(저널논문)
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