Intercalation Route to Complex Perovskites AM(0.2)Ta(0.8)O(2.8)N(0.2) (A = Sr, Bo; M = Li, Na): Neutron Diffraction and Nuclear Magnetic Resonance Study

Title
Intercalation Route to Complex Perovskites AM(0.2)Ta(0.8)O(2.8)N(0.2) (A = Sr, Bo; M = Li, Na): Neutron Diffraction and Nuclear Magnetic Resonance Study
Author(s)
김영일백윤기[백윤기]Maxim Avdeev[Maxim Avdeev]
Keywords
PHOTOCATALYTIC HYDROGEN-PRODUCTION; HIGH-DIELECTRIC-CONSTANT; OXYNITRIDE PEROVSKITES; CHEMICAL-SHIFTS; CRYSTAL-GROWTH; SOLAR-CELLS; MAS NMR; NA-23; LITHIUM; ORDER
Issue Date
201501
Publisher
AMER CHEMICAL SOC
Citation
CRYSTAL GROWTH & DESIGN, v.15, no.1, pp.53 - 61
Abstract
Oxynitride-type complex perovskites, AM(0.2)Ta(0.8)O(2.8)N(0.2) (A = Sr, Ba; M = Li, Na), were synthesized by the ammonolytic heating of a layered perovskite, A(5)Ta(4)O(15), with 0.5M(2)CO(3). A Rietveld refinement of the synchrotron X-ray and neutron powder diffraction patterns confirmed the complete structural transformation from a hexagonal layered-perovskite to a three-dimensional perovskite type, as well as the stabilization of alkali cations on the octahedral sites rather than on the dodecahedral sites in the latter. In all four compounds, M+ and Ta5+ were disordered completely despite a charge difference as much as 4. The crystal symmetry of the average structure depended on the size of the dodecahedral cation: simple cubic for BaM0.2Ta0.8O2.8N0.2 and body-centered tetragonal for SrM0.2Ta0.8O2.8N0.2. This trend coincides with the symmetry transition from BaTaO2N (Pm (3) over barm) to SrTaO2N (I4/mcm). In both SrM0.2Ta0.8O2.8N0.2, nitrogen atoms preferentially occupied the c-axial 4a site of the tetragonal cell. Solid state magic angle spinning nuclear magnetic resonance spectroscopy showed that SrNa0.2Ta0.8O2.8N0.2 and BaNa0.2Ta0.8O2.8N0.2 exhibited marked downfield shifts of 23Na, manifesting an octahedral coordination. On the other hand, the Li-7 NMR of SrLi0.2Ta0.8O2.8N0.2 and BaLi0.2Ta0.8O2.8N0.2 indicated a highly symmetrical coordination environment of Li.
URI
http://hdl.handle.net/YU.REPOSITORY/33658http://dx.doi.org/10.1021/cg500739s
ISSN
1528-7483
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