Published January 15, 2009 | Version v1
Journal article

Electric and ferroelectric properties of PZT/BLT multilayer films prepared by photochemical metal-organic deposition

  • 1. Department of Ceramic Engineering, Yonsei University, 134 Shinchon-Dong, Seodaemun-Ku, Seoul 120-749 (Korea, Republic of)
  • 2. 4D Labs and Department of Chemistry, Simon Fraser University, Burnaby, BC V5A 1S6 (Canada)
  • 3. Research and semiconductor Division, Hynix semiconductor Inc., Icheon-si, Kyoungki-do 467-701 (Korea, Republic of)

Description

The electric and ferroelectric properties of lead zirconate titanate (PZT) and lanthanum-substituted bismuth titanate (BLT) multilayer films prepared using photosensitive precursors were characterized. The electric and ferroelectric properties were investigated by studying the effect of the stacking order of four ferroelectric layers of PZT or BLT in 4-PZT, PZT/2-BLT/PZT, BLT/2-PZT/BLT, and 4-BLT multilayer films. The remnant polarization values of the 4-BLT and BLT/2-PZT/BLT multilayer films were 12 and 17 μC/cm2, respectively. Improved ferroelectric properties of the PZT/BLT multilayer films were obtained by using a PZT intermediate layer. The films which contained a BLT layer on the Pt substrate had improved leakage currents of approximately two orders of magnitude and enhanced fatigue resistances compared to the films with a PZT layer on the Pt substrate. These improvements are due to the reduced number of defects and space charges near the Pt electrodes. The PZT/BLT multilayer films prepared by photochemical metal-organic deposition (PMOD) possessed enhanced electric and ferroelectric properties, and allow direct patterning to fabricate micro-patterned systems without dry etching.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.apsusc.2008.11.011

Additional details

Identifiers

DOI
10.1016/j.apsusc.2008.11.011;
PII
S0169-4332(08)02325-8;

Publishing Information

Journal Title
Applied Surface Science
Journal Volume
255
Journal Issue
7
Journal Page Range
p. 4197-4200
ISSN
0169-4332
CODEN
ASUSEE

Optional Information

Copyright
Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.