Demonstrates improved thermal stability of flexoelectric materials, highlighting a new design strategy for flexible electronics.
Flexoelectricity is an electromechanical coupling phenomenon in which strain gradients induce electric polarization in solids, which have promising applications in flexible electronics, photovoltaic devices, and self-powered sensing systems. However, many flexoelectric materials suffer from poor thermal stability. High-entropy ceramics are materials characterized by multiple elements occupying lattice sites in near-equimolar ratios. The high configurational entropy is believed to stabilize phase structures and enhance the material's overall properties, especially temperature stability. This work employs the compositionally engineered high-entropy perovskite ceramics (Bi0.2X0.2Ba0.2Sr0.2Pb0.2) TiO3 (X = Li, Na, K) to elucidate the mechanisms governing the flexoelectric coefficients and their temperature stability via defect engineering and local strain modulation. Among these compositions, (Bi0.2Na0.2Ba0.2Sr0.2Pb0.2) TiO3 (HEC-Na) exhibits a well-defined perovskite structure and superior mechanical robustness, together with an optimized defect concentration and pinning landscape, as well as a reduced polarization barrier and weakened A–O bond strength. These synergistic factors collectively enhance flexoelectric performance and thermal stability in the HEC-Na system. This study provides a design strategy for next-generation high-sensitivity, thermally stable flexible mechatronic devices based on high-entropy perovskite ceramics.
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Yu et al. (2026) studied this question.
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