Keisuke Ishihama
;
Takao Shimizu
(National Institute for Materials Science)
;
Kazuki Okamoto
;
Akinori Tateyama
;
Wakiko Yamaoka
;
Risako Tsurumaru
;
Shintaro Yoshimura
;
Yusuke Sato
;
Hiroshi Funakubo
Description:
(abstract)Tetragonal (1−x)(Bi,Na)TiO3−xBaTiO3 films exhibit enhanced piezoelectric properties
due to domain switching over a wide composition range. These properties were
observed over a significantly wider composition range than the morphotropic phase
boundary (MPB), which typically has a limited composition range of 1–2%. The
polarization axis was found to be along the in-plane direction for the tetragonal
composition range of x = 0.06–1.0, attributed to the tensile thermal strain from the
substrate during cooling after the film formation. A “two-step increase” in remanent
polarization against an applied maximum electric field was observed at high field region
due to the domain switching, and a very high piezoelectric response (effective d33 value,
denoted as d33,f) over 220 pm/V was achieved for a wide composition range of x = 0.2–
0.5 with high tetragonality, exceeding previously reported values for bulk ceramics.
Moreover, a transverse piezoelectric coefficient, e31,f, of 19 C/m2 measured using a
cantilever structure, was obtained for a composition range of at least 10 at% (for both x
= 0.2 and 0.3). This value is the highest reported for Pb-free piezoelectric thin films and
is comparable to the best data for Pb-based thin films. Reversible domain switching
eliminates the need for conventional MPB compositions, allowing an improvement in
piezoelectric properties over a wider composition range. This strategy could provide a
guideline for the development of environmentally acceptable lead-free piezoelectric
films with composition-insensitive piezoelectric performance to replace Pb-based
materials with the MPB composition, such as PZT.
Rights:
Keyword: Pb-free Piezoelectric film, domain switching, out-of-morphotropic phase boundary composition, tetragonal structure
Date published: 2024-01-10
Publisher: American Chemical Society (ACS)
Journal:
Funding:
Manuscript type: Publisher's version (Version of record)
MDR DOI:
First published URL: https://doi.org/10.1021/acsami.3c13302
Related item:
Other identifier(s):
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Updated at: 2024-12-24 13:58:44 +0900
Published on MDR: 2024-12-24 13:58:44 +0900
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