Abstract

Bismuth titanate (Bi4Ti3O12, BIT) piezoelectric materials have attracted increasing attention due to their high-temperature applications. However, it is quite challenging to simultaneously achieve outstanding piezoelectric properties and high Curie temperature in BIT-based systems. In this study, oxygen vacancy defects tailoring strategy was utilized to solve this problem, excellent piezoelectric coefficient (32.1 pC/N), and ultrahigh Curie temperature (659 °C) are gotten in Bi4Ti3-x(Mn1/3Nb2/3)xO12 (BTMN) ceramics, which are among the top values in the BIT-based ceramics. More importantly, the (Mn1/3Nb2/3)(4+δ)+ complex-ion modified Bi4Ti3O12-based ceramics are characterized with excellent piezoelectric stability up to 500 °C (d33 > 30.0 pC/N at 500 °C)) and significantly reduced conductivity (only ∼ 10−7 Ω−1 cm−1 at 500 °C). Moreover, enhanced ferroelectricity and good dielectric stability were also obtained. The better comprehensive properties can be ascribed to two aspects. First, the concentration of oxygen vacancy defects is obviously reduced, and their distribution is effectively controlled in BITMN ceramics. Second, the introduction of (Mn1/3Nb2/3)(4+δ)+ complex-ion gives rise to the antiphase boundaries and massive ferroelectric domain walls. This works not only reveal the high potential of BITMN ceramics for high-temperature piezoelectric applications but also deepen the understanding of the structure-properties relationship in BIT-based materials.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.