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Enhanced Energy Storage Properties of (1 − x)PLZST-xBiYO3 Ceramics

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Abstract

In this research, (1 − x)PLZST-xBiYO3 (x = 0–0.05) was prepared by a traditional solid-state process. The space structures of (1 − x)PLZST-xBiYO3 samples changed from hexagonal symmetry for x < 0.01, to monoclinic symmetry for x ≥ 0.01. Dielectric permittivity increased first and then decreased with the increase in BiYO3 content. The relaxor behavior of PLZST was disrupted slightly by BiYO3 doping. Then the local defects were created by BiYO3 doping, which formed weak couplings. The permittivity and maximum polarization were improved with the increase of BiYO3 content. When x = 0.01, Pm achieved the maximum of 9.02 μC/cm2 with an energy efficiency of 86.1%, which also exhibited the highest energy density, 0.679 J/cm3, in (1 − x)PLZST-xBiYO3 ceramics.

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Acknowledgments

This work was supported by the Innovation Foundation of Collaboration Innovation Center of Electronic Materials and Devices (No. ICEM2015-4002) and the China Postdoctoral Science Foundation (No. 2018M633343).

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Authors and Affiliations

  1. State Key Laboratory of Electronic Thin Films and Integrated Devices, Collaboration Innovation Center of Electric Materials and Devices, University of Electronic Science and Technology of China, Chengdu, 610054, Sichuan, People’s Republic of China

    Meng Wei, Hao Yu, Hongwei Chen, Jihua Zhang & Wanli Zhang

  2. China Aerospace Components Engineering Center, China Academy of Space Technology, Beijing, 100094, China

    Zhangdong Tang

  3. Chengdu Micro-Tech Science and Technology Company Ltd, Chengdu, 610054, Sichuan, People’s Republic of China

    Wenjun Wang

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  1. Meng Wei
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  2. Zhangdong Tang
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  3. Wenjun Wang
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  4. Hao Yu
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  5. Hongwei Chen
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  6. Jihua Zhang
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  7. Wanli Zhang
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Correspondence to Jihua Zhang.

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Wei, M., Tang, Z., Wang, W. et al. Enhanced Energy Storage Properties of (1 − x)PLZST-xBiYO3 Ceramics. J. Electron. Mater. 48, 2162–2167 (2019). https://doi.org/10.1007/s11664-019-07004-0

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  • DOI: https://doi.org/10.1007/s11664-019-07004-0

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