Chen, Jun ; Wang, Xiaowei ; Jo, Wook ; Rödel, Jürgen (2010)
Microstructure and Electrical Properties of (1−x)Bi(Li1/3Zr2/3)O3-xPbTiO3Piezoelectric Ceramics.
In: Journal of the American Ceramic Society, 93 (6)
doi: 10.1111/j.1551-2916.2010.03625.x
Artikel, Bibliographie
Kurzbeschreibung (Abstract)
A new type of BiMeO3–PbTiO3 was prepared by using Li1+ as part of the Me site cations. Several (1−x)Bi(Li,Me″)O3–xPbTiO3 compositions were prepared with Me″ cations of a higher valence (Me″=Ti4+, Zr4+, Mn4+, Sn4+, Nb5+, and Ta5+). (1−x)Bi(Li,Me″)O3–xPbTiO3 exhibits a low solubility of Bi(Li,Me″)O3 in PbTiO3. Although there are many possible compositions of (1−x)Bi(Li,Me″)O3–xPbTiO3, no morphotropic phase boundary was found. After the initial screening, (1−x)Bi(Li1/3Zr2/3)O3–xPbTiO3 was identified as the most promising material for actuator applications due to its relatively large solubility limit (x=0.7) and low lattice distortion (c/a=1.036). It was then chosen for systematical study with respect to structure, ferroelectric, and piezoelectric properties. In addition, La was further added to improve the piezoelectric properties of (1−x)Bi(Li1/3Zr2/3)O3–xPbTiO3. The temperature dependence of 0.3Bi(Li1/3Zr2/3)O3−0.7PbTiO3 and 0.3(Bi0.9La0.1)(Li1/3Zr2/3)O3−0.7PbTiO3 was assessed by investigating the dielectric constantinline imageand large-signal d33. 0.3Bi(Li1/3Zr2/3)O3−0.7PbTiO3 exhibits a dielectric constantinline imagewith a low loss (0.025), ferroelectric properties (EC=5.9 kV/mm, Pr=20.8 μC/cm2, and Psat=25.9 μC/cm2), piezoelectric coefficients (small-signal d33=78 pC/N and large-signal d33=106 pm/V), and Curie temperature (TC=290°C). La (10 mol%) substitution for Bi acts as a soft role with an enhanced d33 (98 pC/N) and reduced TC (215°C).
| Typ des Eintrags: | Artikel |
|---|---|
| Erschienen: | 2010 |
| Autor(en): | Chen, Jun ; Wang, Xiaowei ; Jo, Wook ; Rödel, Jürgen |
| Art des Eintrags: | Bibliographie |
| Titel: | Microstructure and Electrical Properties of (1−x)Bi(Li1/3Zr2/3)O3-xPbTiO3Piezoelectric Ceramics |
| Sprache: | Englisch |
| Publikationsjahr: | Juni 2010 |
| Titel der Zeitschrift, Zeitung oder Schriftenreihe: | Journal of the American Ceramic Society |
| Jahrgang/Volume einer Zeitschrift: | 93 |
| (Heft-)Nummer: | 6 |
| DOI: | 10.1111/j.1551-2916.2010.03625.x |
| Kurzbeschreibung (Abstract): | A new type of BiMeO3–PbTiO3 was prepared by using Li1+ as part of the Me site cations. Several (1−x)Bi(Li,Me″)O3–xPbTiO3 compositions were prepared with Me″ cations of a higher valence (Me″=Ti4+, Zr4+, Mn4+, Sn4+, Nb5+, and Ta5+). (1−x)Bi(Li,Me″)O3–xPbTiO3 exhibits a low solubility of Bi(Li,Me″)O3 in PbTiO3. Although there are many possible compositions of (1−x)Bi(Li,Me″)O3–xPbTiO3, no morphotropic phase boundary was found. After the initial screening, (1−x)Bi(Li1/3Zr2/3)O3–xPbTiO3 was identified as the most promising material for actuator applications due to its relatively large solubility limit (x=0.7) and low lattice distortion (c/a=1.036). It was then chosen for systematical study with respect to structure, ferroelectric, and piezoelectric properties. In addition, La was further added to improve the piezoelectric properties of (1−x)Bi(Li1/3Zr2/3)O3–xPbTiO3. The temperature dependence of 0.3Bi(Li1/3Zr2/3)O3−0.7PbTiO3 and 0.3(Bi0.9La0.1)(Li1/3Zr2/3)O3−0.7PbTiO3 was assessed by investigating the dielectric constantinline imageand large-signal d33. 0.3Bi(Li1/3Zr2/3)O3−0.7PbTiO3 exhibits a dielectric constantinline imagewith a low loss (0.025), ferroelectric properties (EC=5.9 kV/mm, Pr=20.8 μC/cm2, and Psat=25.9 μC/cm2), piezoelectric coefficients (small-signal d33=78 pC/N and large-signal d33=106 pm/V), and Curie temperature (TC=290°C). La (10 mol%) substitution for Bi acts as a soft role with an enhanced d33 (98 pC/N) and reduced TC (215°C). |
| Fachbereich(e)/-gebiet(e): | 11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft > Fachgebiet Nichtmetallisch-Anorganische Werkstoffe 11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft 11 Fachbereich Material- und Geowissenschaften |
| Hinterlegungsdatum: | 20 Jun 2011 08:51 |
| Letzte Änderung: | 05 Mär 2013 09:48 |
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