Please use this identifier to cite or link to this item: https://apo.ansto.gov.au/dspace/handle/10238/10908
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dc.contributor.authorJiang, P-
dc.contributor.authorHuang, Q-
dc.contributor.authorAvdeev, M-
dc.contributor.authorTao, F-
dc.contributor.authorZhou, L-
dc.contributor.authorGao, W-
dc.contributor.authorCong, R-
dc.contributor.authorYang, T-
dc.date.accessioned2021-06-28T00:55:00Z-
dc.date.available2021-06-28T00:55:00Z-
dc.date.issued2018-06-08-
dc.identifier.citationJiang, P., Huang, Q., Avdeev, M., Tao, F., Zhou, L., Gao, W., Cong, R., & Yang, T. (2018). Substitution-induced structure evolution and Zn2+/Ga3+ ordering in “114” oxides MAZn2Ga2O7 (M = Ca2+, Sr2+; A = Sr2+, Ba2+). Inorganic chemistry, 57(13), 7770-7779. doi:10.1021/acs.inorgchem.8b00845en_US
dc.identifier.issn1520-510X-
dc.identifier.urihttps://doi.org/10.1021/acs.inorgchem.8b00845en_US
dc.identifier.urihttps://apo.ansto.gov.au/dspace/handle/10238/10908-
dc.description.abstractThe “114” oxides LnBa(Co/Fe)4O7+δ represent a new family of materials that exhibits intriguing physical properties, including geometrically frustrated magnetism, oxygen storage, and magnetoelectric couplings. Various chemical substitutions have been conducted to modify their crystal and magnetic structures as well as physical properties. However, the principles beneath the substitution-induced structural evolution and charge/cationic ordering have not yet been understood. Thus, in this contribution, two complete solid solutions of MAZn2Ga2O7 (M = Ca2+, Sr2+; A = Sr2+, Ba2+) were designed, synthesized, and characterized by Rietveld refinements based on high-resolution X-ray diffraction (XRD) and neutron diffraction (ND) data. The structure symmetry of MAZn2Ga2O7 is determined by the cationic size mismatch between M and A cations that can be defined by the tolerance factor t, i.e., symmetry transitions from P63mc (t > 0.87) to P31c (0.87 > t > 0.75) and to Pna21 (t < 0.75) were observed for MAZn2Ga2O7, associated with the rotation of T1O4 tetrahedra in the triangular layers. The Zn2+/Ga3+ ordering at T sites is also a consequence of the increase or decrease of the average sizes of M and A cations. A small concentration of interstitial oxygen ions can be obtained in Sr2Zn2–xGa2+xO7+x/2 (x = 0.1, 0.2); however, no oxygen ionic conduction was observed at high temperatures, indicating the migration ability of the interstitial oxygen was very limited. © 2018 American Chemical Societyen_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectMultigroup theoryen_US
dc.subjectOxygenen_US
dc.subjectCationsen_US
dc.subjectMagnetic propertiesen_US
dc.subjectPhysical propertiesen_US
dc.subjectChemical propertiesen_US
dc.subjectNeutron diffractionen_US
dc.subjectX-ray diffractionen_US
dc.titleSubstitution-induced structure evolution and Zn2+/Ga3+ ordering in “114” oxides MAZn2Ga2O7 (M = Ca2+, Sr2+; A = Sr2+, Ba2+)en_US
dc.typeJournal Articleen_US
dc.date.statistics2021-06-16-
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