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Solution Chemistry, Substrate, and Processing Effects on Chemical Homogeneity in Lead Zirconate Titanate Thin Films.

Authors :
Ihlefeld, Jon F.
Kotula, Paul G.
Gauntt, Bryan D.
Gough, Dara V.
Brennecka, Geoff L.
Lu, Ping
Spoerke, Erik D.
Alford, N.
Source :
Journal of the American Ceramic Society. Jul2015, Vol. 98 Issue 7, p2028-2038. 11p. 2 Black and White Photographs, 8 Graphs.
Publication Year :
2015

Abstract

The effects of chemistry, substrate, and processing conditions on through-thickness cation distributions are explored in solution-derived morphotropic composition lead zirconate titanate (PZT) films. Films prepared from chelate-based and conventional sol-gel chemistries were spin cast onto Pt/ZnO/SiO2/Si and Pt/Ti/SiO2/Si substrates and pyrolyzed at 300°C, 350°C, and 400°C prior to crystallization at 700°C either in a preheated furnace or via rapid thermal processing. For films crystallized within a conventional furnace on Pt/ZnO/SiO2/Si substrates no chemical gradients were observed. All films prepared on Pt/Ti/SiO2/Si substrates had increased titanium concentrations near the PZT/Pt interfaces, and the source is shown to be titanium diffusing from the substrate metallization stack. The effect of heating method and rate was explored in films prepared on Pt/ZnO/SiO2/Si substrates with 15°C, 50°C, and 100°C/s heating rates within a rapid thermal annealer. Only one solution chemistry-heating rate combination resulted in the formation of a chemical gradient: a conventional sol-gel chemistry and a 50°C/s heating rate. Infrared spectroscopy of pyrolyzed gel films showed absorption spectra differences in the bonding structure between the two chemistries with the conventional sol-gel-derived films exhibiting a signature more similar to that of a PbTiO3 gel, suggestive of a gel-structure source of gradient formation during crystallization. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00027820
Volume :
98
Issue :
7
Database :
Academic Search Index
Journal :
Journal of the American Ceramic Society
Publication Type :
Academic Journal
Accession number :
108336802
Full Text :
https://doi.org/10.1111/jace.13576