Polarization comparison of Pb(Zr,Ti)O3 and Bi4Ti3O12-based ferroelectrics
Creators
- 1. Department of Innovative and Engineered Materials, Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, G1-32, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8502 (Japan) and PRESTO, Japan Science and Technology Corporation (JST), Kawaguchi, 332-0012 (Japan)
- 2. Department of Innovative and Engineered Materials, Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, G1-32, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8502 (Japan)
- 3. Department of Chemistry, Sophia University, 7-1 Kioi-cho, Chiyoda-ku, Tokyo 102-8554 (Japan)
- 4. Application Laboratory, Bruker AXS, 3-9-A-6 Moriya-cho, Kanazawa-ku, Yokohama 221-0022 (Japan)
Description
The spontaneous polarization (P s) values of Pb(Zr,Ti)O3 (PZT) and Bi4Ti3O12-based ferroelectrics were compared based on data obtained from epitaxially-grown films. These two materials are the most promising candidates for use in ferroelectric random access memory (FeRAM). The P s of tetragonal Pb(Zr0.35Ti0.65)O3 films was estimated to be about 90 μC/cm2 based on data from perfectly (0 0 1)-oriented, polar-axis-oriented films. On the other hand, the P s value of (Bi3.5Nd0.5)Ti3O12 was estimated to be 56-58 μC/cm2 based on data from (1 0 0)/(0 1 0)- (1 1 0)-, and (1 0 4)/(0 1 4)-oriented epitaxial films. This value is the largest yet reported for bismuth layer-structured ferroelectrics. For both systems, the P s value generally increased with increasing Curie temperature (T c). However, it decreased when the T c became very high and approached the values for PbTiO3 and Bi4Ti3O12. This decrease is attributed to pinning of the domain motion in the bulk. On the other hand, the obtained one-axis film, which is essential to diminish the cell-to-cell property distribution, had a (1 0 0)/(0 0 1) and (1 1 1) orientations for Pb(Zr0.35Ti0.65)O3 films, or a (0 0 1) orientation for (Bi3.5Nb0.5)Ti3O12 films. Based on our findings, we expect the maximum remanent polarization (P r) values to be almost the same for both materials
Additional details
Identifiers
- DOI
- 10.1016/j.mseb.2004.12.087;
- PII
- S0921-5107(04)00636-1;
Publishing Information
- Journal Title
- Materials Science and Engineering. B, Solid-State Materials for Advanced Technology
- Journal Volume
- 118
- Journal Issue
- 1-3
- Journal Page Range
- p. 23-27
- ISSN
- 0921-5107
- CODEN
- MSBTEK
Conference
- Title
- Symposium D: Functional oxides for advanced semiconductor technologies
- Acronym
- EMRS spring meeting 2004
- Dates
- 24-28 May 2004
- Place
- Strasbourg (France)
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 37114488
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- BISMUTH; BISMUTH COMPOUNDS; COMPARATIVE EVALUATIONS; CURIE POINT; DISTRIBUTION; EPITAXY; FERROELECTRIC MATERIALS; FILMS; LAYERS; ORIENTATION; PIEZOELECTRICITY; POLARIZATION; PZT; RANDOMNESS; TETRAGONAL LATTICES
- Descriptors DEC
- CRYSTAL GROWTH METHODS; CRYSTAL LATTICES; CRYSTAL STRUCTURE; DIELECTRIC MATERIALS; ELECTRICITY; ELEMENTS; EVALUATION; LEAD COMPOUNDS; MATERIALS; METALS; OXYGEN COMPOUNDS; PHYSICAL PROPERTIES; THERMODYNAMIC PROPERTIES; TITANATES; TITANIUM COMPOUNDS; TRANSITION ELEMENT COMPOUNDS; TRANSITION TEMPERATURE; ZIRCONATES; ZIRCONIUM COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2005 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.