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A Study of the Microchemistry of Nanocrystalline BaTiO3 with Tetragonal and Pseudocubic Room Temperature Symmetries

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dc.contributor.advisor Schulze, Walter Lacey, Robert 2017-02-07T15:24:37Z 2017-02-07T15:24:37Z 2007-09
dc.description Advisory committee members: Robert Condrate, Steven Pilgrim, Scott Misture. Dissertation completed in partial fulfillment of the requirements for the degree of Doctorate of Philosophy in Ceramics at the Kazuo Inamori School of Engineering, New York State College of Ceramics at Alfred University en_US
dc.description.abstract The investigation of possible effects of undesired surface species on barium titanate, one of the most utilized ferroelectric ceramics, constitutes the focus of this work. Six commercial barium titanate powders from three manufacturers representing two different synthesis processes, with average particle sizes from 40 nm to 470 nm, were analyzed in this study. Four of the nanopowders exhibited pseudocubic room temperature symmetry. Diffuse Reflectance Infrared Fourier Transform (DRIFT) spectroscopic analysis of the nanopowders was conducted in ambient atmosphere at room temperature. High temperature DRIFT followed incorporating four avenues of analysis: moisture adsorption studies, deuterium oxide exchange studies, carbon dioxide adsorption studies, and high temperature analysis under dry air and UHP nitrogen atmospheres. At the highest temperature used in this study, 1173K, moisture and the accompanying incorporated protonic impurities were still present. The powders readily readsorbed moisture during rapid cooling, 170K/minute, to room temperature. The smallest powder, as received, formed spherical agglomerates up to 10 μm diameter. These sintered as separate units attaining diameters up to 60 μm during intermediate stage sintering. X-ray photoelectron spectroscopy indicated a surface contamination layer of 10 Å to 18 Å; 50 – 70% of which was barium carbonate, the balance being atmospheric adsorbed species. Samples cooled at 3K/minute after an 1173K calcine retained cubic symmetry as indicated with high temperature X-ray diffraction. However, spectral evidence was obtained indicating that upon the rapid cooling from the 1173K calcine, a reorientation to the room temperature tetragonal symmetry was observed. Further, SEM and TEM supported this finding with visual evidence of interfacial rearrangement including corroborating electron diffraction analysis. This data, therefore, substantiated the hypothesis that the cause of the room temperature pseudocubic structure was strain due to the presence of point defects from protonic impurities in conjunction with the strain between the barium carbonate contamination layer and the barium titanate core. en_US
dc.format.extent 336 pages en_US
dc.language.iso en_US en_US
dc.publisher New York State College of Ceramics at Alfred University. Kazuo Inamori School of Engineering. en_US
dc.relation.ispartof Scholes Library en_US
dc.rights.uri en_US
dc.title A Study of the Microchemistry of Nanocrystalline BaTiO3 with Tetragonal and Pseudocubic Room Temperature Symmetries en_US
dc.type Thesis en_US

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