What is it about?

With the growing demand for sensing and monitoring technologies in extreme environments such as aerospace systems and deep-well drilling, the development of high-temperature piezoelectric ceramics with high Curie temperature (TC) and strong piezoelectric activity (d33) has become an urgent challenge in the field of functional materials. Conventional lead-based piezoelectric ceramics are difficult to meet the requirements of high-temperature operation due to their relatively low Curie temperatures and environmental concerns. To address this issue, Prof. Chen Yu’s team from the School of Mechanical Engineering at Chengdu University achieved a synergistic enhancement in d33, TC, and kp through Li/Mn co-doping. The optimized composition, KBT–LM55, exhibited a d33 of 30 pC/N, an increased TC of 590 °C, and a kp of 6.4%, while retaining approximately 80% of its initial d33 after annealing at 500 °C for 4 h. Furthermore, high-temperature ultrasonic transducer verification was successfully conducted, demonstrating promising application potential.

Featured Image

Why is it important?

(1) A Li/Mn co-doping strategy was proposed to synergistically optimize the crystal structure and electrical properties of KBT. After the co-substitution of Li/Mn for K/Bi sites, the KBT main phase was not only stabilized, but the content of the secondary phase Bi₁.₇₄Ti₂O₆.₆₂₄ was also effectively reduced. Meanwhile, the lattice anisotropy, TiO₆ octahedral distortion, and interlayer coupling were regulated, thereby providing a structural foundation for performance enhancement. (2) A balanced regulation between leakage suppression and polarization response was achieved while maintaining domain-wall mobility. Li/Mn doping transformed the dielectric behavior of KBT from a sharp λ-type phase transition to a diffuse or relaxor-like response, while effectively suppressing high-temperature leakage conduction and improving insulating properties. This regulation did not simply sacrifice polarization capability; rather, it enabled a balance between conductive loss suppression and domain-wall motion through defect-chemistry modulation. (3) The optimized composition KBT–LM55 was obtained and further validated in a high-temperature ultrasonic transducer. KBT–LM55 exhibited the best overall performance, with a d₃₃ of 30 pC/N, kp of 6.4%, TC of 590 °C, and a room-temperature tanδ as low as 0.23%. After annealing at 500 °C for 4 h, approximately 80% of the initial d₃₃ was retained, and resonance measurements showed that kp remained stable up to 325 °C. Furthermore, a pulse–echo ultrasonic transducer fabricated based on this material maintained stable signals at 250 °C, with a center frequency of 2.24 MHz, a −6 dB bandwidth of 33.95%, and a peak-to-peak voltage (Vp-p) of 1.94 V.

Perspectives

In my view, the core significance of this work lies not merely in achieving enhanced piezoelectric performance, but in establishing an effective connection among structural regulation, defect modulation, and device-level application in high-temperature piezoelectric ceramics. KBT possesses an intrinsically high Curie temperature and the structural advantages of bismuth-layered ferroelectrics; however, it has long been limited by insufficient piezoelectric activity, secondary-phase formation, and high-temperature leakage conduction. Through Li/Mn co-doping, we stabilized the main phase, regulated TiO₆ octahedral distortion, and optimized defect chemistry, thereby achieving a balance between conductive loss suppression and domain-wall motion. As a result, the material simultaneously exhibited high d₃₃, TC, and kₚ values. More importantly, the optimized KBT–LM55 ceramic was further validated in a high-temperature ultrasonic transducer, demonstrating that this material is not limited to property-level evaluation but holds promising potential for high-temperature acoustic device applications.

骏楠 王

Read the Original

This page is a summary of: Li/Mn co-doped K 0.5 Bi 4.5 Ti 4 O 15 high-tempe..., Journal of Advanced Ceramics, April 2026, Tsinghua University Press,
DOI: 10.26599/jac.2026.9221277.
You can read the full text:

Read

Resources

Contributors

The following have contributed to this page