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First 14-Layer Twinned Hexagonal Perovskite Ba14Mn1.75Ta10.5O42: Atomic-Scale Imaging of Cation Ordering
Author(s) -
Fengqiong Tao,
Cécile Genevois,
Fengqi Lu,
Xiaojun Kuang,
Florence Porcher,
Liangju Li,
Tao Yang,
Wenbo Li,
Di Zhou,
Mathieu Allix
Publication year - 2016
Publication title -
chemistry of materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.741
H-Index - 375
eISSN - 1520-5002
pISSN - 0897-4756
DOI - 10.1021/acs.chemmater.6b01566
Subject(s) - crystallography , stacking , scanning transmission electron microscopy , materials science , perovskite (structure) , vacancy defect , octahedron , atomic units , electron energy loss spectroscopy , transmission electron microscopy , chemistry , crystal structure , nanotechnology , physics , organic chemistry , quantum mechanics
Formation of hexagonal perovskite with mixed cubic and hexagonal stacking of AO3 layers becomes more and more difficult when the number of layers in the stacking repeating unit increases. So far, the highest number of layers reported for twinned hexagonal perovskite is 12, with alternative 5 consecutive cubic layers and one hexagonal layer in the (h)2 sequence. Here, we present the unexpected formation of a 14-layer twinned hexagonal perovskite with a stacking sequence (h)2 for the BaO3 layers on the Ba14Mn1.75Ta10.5O42 (Ba8MnTa6O24) composition, the first example of twinned hexagonal perovskite with a periodicity exceeding 12-layers. The B-cation and vacancy distributions are characterized by multiple efficient and complementary techniques including neutron and synchrotron powder diffraction, scanning transmission electron microscopy-high angle annular dark field (STEM-HAADF) imaging, and electron energy loss spectroscopy (EELS) and X-ray energy dispersive spectroscopy (EDS) elemental mapping....

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