journal article·2022-03-22

Polarization Fatigue Mechanism of High-Power Textured Piezoelectric Ceramics

Haoyang Leng, Yongke Yan, Mark Fanton, Shashank Priya

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Abstract

In conjunction with ultrahigh d33 and Qm, the electrical fatigue behavior of high-power piezoelectric ceramics is highly relevant for practical applications. In this study, a comparative study of fatigue behavior between randomly oriented and ⟨001⟩ textured ceramics is investigated. It is found that ⟨001⟩ textured ceramics exhibit better fatigue resistance behavior in comparison with the random counterpart. The superior fatigue resistance of textured ceramics originates from its smaller domain size with high domain wall density, favorable domain wall switching, and internal stress relaxation during the electric field cycling process. Both mechanical damage and domain wall pinning mechanisms are found to play an important role in influencing the fatigue behavior of high-power textured ceramics. Detailed microstructural analysis along with electrical fatigue measurement under bipolar and unipolar modes is conducted to confirm the mechanisms controlling the degradation as a function of varying fields and temperatures. High-resolution electron microscopy results demonstrate that BaTiO3 (BT) templates present within the textured ceramics do not induce mechanical damage during electric field cycling.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Ferroelectric and Piezoelectric Materials · Acoustic Wave Resonator Technologies · Multiferroics and related materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Materials Science and Engineering, and Materials Research Institute, The Pennsylvania State University, University Park, Pennsylvania 16802, United States

Applied Research Laboratory, The Pennsylvania State University, University Park, Pennsylvania 16801, United States

Funding

Defense Advanced Research Projects Agency · National Science Foundation · Division of Materials Research

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