Wang, D., Fan, Z., Zhou, D. et al. (6 more authors) (2018) Bismuth ferrite-based lead-free ceramics and multilayers with high recoverable energy density. Journal of Materials Chemistry A, 6 (9). pp. 4133-4144. ISSN 2050-7488
Abstract
Lead-free ceramics with high recoverable energy density (W rec ) and energy storage efficiency (η) are attractive for advanced pulsed power capacitors to enable greater miniaturization and integration. In this work, dense bismuth ferrite (BF)-based, lead-free 0.75(Bi 1-x Nd x )FeO 3 -0.25BaTiO 3 (BNxF-BT) ceramics and multilayers were fabricated. A transition from a mixed pseudocubic and R3c to a purely pseudocubic structure was observed as x increased with the optimum properties obtained for mixed compositions. The highest energy densities, W ∼ 4.1 J cm -3 and W rec ∼ 1.82 J cm -3 , were achieved for BN15F-BT, due to the enhanced breakdown field strength (BDS ∼ 180 kV cm -1 ) and large maximum polarization (P max ∼ 40 μC cm -2 ). The multilayers of this composition possessed both a high W rec of 6.74 J cm -3 and η of 77% and were stable up to 125 °C. Nd doped BF-based ceramics with enhanced BDS and large W rec are therefore considered promising candidates for lead-free energy storage applications.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2018 Royal Society of Chemistry. This is an author produced version of a paper subsequently published in Journal of Materials Chemistry A. Uploaded in accordance with the publisher's self-archiving policy. |
Dates: |
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Institution: | The University of Sheffield |
Academic Units: | The University of Sheffield > Faculty of Engineering (Sheffield) > Department of Materials Science and Engineering (Sheffield) |
Depositing User: | Symplectic Sheffield |
Date Deposited: | 16 Mar 2018 13:26 |
Last Modified: | 24 Aug 2020 07:47 |
Published Version: | https://doi.org/10.1039/c7ta09857j |
Status: | Published |
Publisher: | Royal Society of Chemistry |
Refereed: | Yes |
Identification Number: | 10.1039/c7ta09857j |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:128628 |