Extraordinary energy storage performance and thermal stability in sodium niobate-based ceramics modified by the ion disorder and stabilized antiferroelectric orthorhombic R phase

  • Ruirui Kang
  • , Zepeng Wang
  • , Weijie Yang
  • , Xiaopei Zhu
  • , Peng Shi
  • , Yangfei Gao
  • , Pu Mao
  • , Jiantuo Zhao
  • , Lixue Zhang
  • , Xiaojie Lou

Research output: Contribution to journalArticlepeer-review

56 Scopus citations

Abstract

Developing high-performance dielectric capacitors is essential to meet the growing demands of hybrid electric vehicles and high-power applications. The energy storage efficiency and the temperature-variant energy storage properties should be considered besides the energy density. In this work, we prepared (1 −x)(0.8NaNbO3-0.2SrTiO3) −xBi(Zn0.5Sn0.5)O3(abbreviated as (1 −x)(NN-ST) −xBZS) lead-free ceramics, where ion disorder is induced in the A-B sites. The experimental results indicate that the antiferroelectric orthorhombic R phase is stabilized, and the breakdown strength is enhanced due to the decreased grain size after BZS modification, which are conducive to optimizing the energy storage performance. The piezoresponse force microscopy (PFM) observation reveals that the incorporated BZS promotes the reversibility of domains, resulting in enhanced energy storage efficiency. Therefore, an energy density of 5.82 J cm−3and an efficiency of 92.3% are simultaneously obtained in the 0.96(NN-ST) − 0.04BZS composition, and the obtained efficiency in this work reaches a record high in NN-based energy storage ceramics. Especially, the sample displays extraordinary temperature stability, that is, high energy storage density (3.6-4.31 J cm−3) and efficiency (90-95%) are achieved in a wide temperature range from −60 °C to 180 °C. Our work would provide a powerful strategy for designing high-performance energy storage capacitors operating in harsh environments.

Original languageEnglish
Pages (from-to)24387-24396
Number of pages10
JournalJournal of Materials Chemistry A
Volume9
Issue number43
DOIs
StatePublished - 21 Nov 2021

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