Critical size and anomalous lattice expansion in nanocrystallineparticles
- 1 August 2000
- journal article
- research article
- Published by American Physical Society (APS) in Physical Review B
- Vol. 62 (5), 3065-3070
- https://doi.org/10.1103/physrevb.62.3065
Abstract
Nanocrystalline barium titanate particles are prepared by the alkoxide method. The lattice constants are obtained from the electron diffraction patterns for various orientations of single particles in the size range of 15–250 nm in diameter. The present result indicates that the structural change from a tetragonal (ferroelectric) phase to a cubic (paraelectric) one occurs around 80 nm in diameter, which is in good agreement with a critical diameter recently reported. Large lattice expansions of more than 2.5% are detected in the particles down to 15 nm in diameter. The origin of the expansion is discussed on the basis of x-ray photoelectron spectroscopic analyses and a computer simulation.Keywords
This publication has 22 references indexed in Scilit:
- Surface relaxation in ferroelectric perovskitesPhysical Review B, 1999
- Structural study on monosize CeO2-x nano-particlesNanostructured Materials, 1999
- Finite size effects in submicron barium titanate particlesFerroelectrics Letters Section, 1998
- Efficient iterative schemes forab initiototal-energy calculations using a plane-wave basis setPhysical Review B, 1996
- Preparation of submicrometer ferroelectric particles by wet-chemical methodsLangmuir, 1994
- BaTiO3 Particle-Size Dependence of Ferroelectricity in BaTiO3/Polymer CompositesJapanese Journal of Applied Physics, 1993
- Effect of Composition and Size of Crystallite on Crystal Phase in Lead Barium TitanateJournal of the American Ceramic Society, 1993
- Lattice dynamics and origin of ferroelectricity in: Linearized-augmented-plane-wave total-energy calculationsPhysical Review B, 1990
- Effective ionic radii in oxides and fluoridesActa Crystallographica Section B: Structural Science, Crystal Engineering and Materials, 1969
- Barium titanate twinning at low temperaturesActa Crystallographica, 1951