Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/2903
Title: Direct observation of B-site cation displacements in Pb-based complex perovskite relaxor oxides
Authors: Baba-Kishi, KZ
Keywords: Cation displacements
Pb-based relaxor oxides
Perovskites
Issue Date: Feb-2011
Publisher: International Union of Crystallography
Source: Journal of applied crystallography, Feb. 2011, v. 44, no. 1, p. 111-121 How to cite?
Journal: Journal of applied crystallography 
Abstract: Electron diffraction patterns recorded using a scanning transmission electron microscope (STEM) from PbMg[sub ⅓]Nb[sub ⅔]O₃ (PMN) crystallites and PbZn[sub ⅓]Nb[sub ⅔]O₃ (PZN) crystals show weak and systematic continuous diffuse streaking along the <110> directions. Detailed high-angle annular dark-field (HAADF) images recorded via an aberration-corrected STEM show that the B-site cations in PMN and PZN undergo correlated and long-range displacements towards the Pb²⁺ ions on the (110) planes. The planar B-site displacement measured from the centres of the octahedra is about 0.3-0.5 Å in PMN and about 0.20-0.4 Å in PZN. In the HAADF images of the PMN crystallites and PZN crystals studied, there is insufficient evidence for systematic long-range planar displacements of the Pb²⁺ ions. The observed Pb²⁺ ion displacements in PMN and PZN appear randomly distributed, mostly displaced along <110> towards the B-site columns. There is also evidence of possible stress-related distortion in certain unit cells of PMN. In the relaxors studied, two distinct types of displacements were observed: one is the long-range planar B-site spatial displacement on the (110) planes, correlated with the Pb²⁺ ions, possibly resulting in the observed diffuse streaking; the other is short-range Pb²⁺ ion displacement on the (110) planes. The observed displacement status indicates a mutual attraction between the Pb ions and the B-site cations in which the B sites undergo the largest spatial displacements towards the Pb ions along <110>.
URI: http://hdl.handle.net/10397/2903
ISSN: 0021-8898
DOI: 10.1107/S0021889810042214
Rights: © 2011 International Union of Crystallography
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