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An environmentally-benign NaNbO3 based perovskite antiferroelectric alternative to traditional lead-based counterparts

  • Aiwen Xie
  • , He Qi
  • , Ruzhong Zuo*
  • , Ao Tian
  • , Jun Chen
  • , Shujun Zhang*
  • *Corresponding author for this work

Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review

Abstract

Perovskite-structured antiferroelectric (AFE) materials, which are dominated by PbZrO3 based solid solutions, are of particular importance owing to their excellent electromechanical properties. The driving force for new development of AFE materials is the result of environmental regulations which require the exclusion of lead components. However, currently reported lead-free AFE materials either show inferior stability or need extremely high driving fields (EA-F) for AFE-FE phase transition. Here we report a new NaNbO3-based solid solution with a room-temperature stable AFE phase and completely reversible field induced AFE-FE phase transition, possessing a relatively low EA-F of ∼8 kV mm-1, a large repeatable strain of ∼0.29%, and a large polarization difference (Pmax ∼ 24 μC cm-2, Pr ∼ 0 μC cm-2). The local and average structures were studied by transmission electron microscopy, in situ Raman spectrum and synchrotron X-ray diffraction, revealing that the solid solution with ≥16 mol% SrTiO3 belongs to the Pnma space group and exhibits nanoscale stripe domains of ∼55 nm, and reversibly responds to large external electric fields. This makes it a competitive lead-free AFE candidate for future applications of high-power energy-storage capacitors and large-displacement actuators. This journal is © The Royal Society of Chemistry.
Original languageEnglish
Pages (from-to)15153-15161
Number of pages9
JournalJournal of Materials Chemistry C
Volume7
Issue number48
Online published21 Nov 2019
DOIs
Publication statusPublished - 28 Dec 2019
Externally publishedYes

Funding

This work was financially supported by the National Natural Science Foundation of China (Grant No. 51472069 and U1432113). S. Z. thanks ARC (FT140100698) for the support.

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