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      Excellent energy storage properties and stability of NaNbO 3–Bi(Mg 0.5Ta 0.5)O 3 ceramics by introducing (Bi 0.5Na 0.5) 0.7Sr 0.3TiO 3

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          Abstract

          NaNbO 3-based (NN) energy storage ceramics exhibit high breakdown electric field strength ( E b) with large recoverable energy storage density ( W rec).

          Abstract

          NaNbO 3-based (NN) energy storage ceramics exhibit high breakdown electric field strength ( E b) with large recoverable energy storage density ( W rec). However, due to their large energy loss density ( W loss) under strong electric fields, maintaining high energy storage efficiency ( η) is a challenge. In this study, to produce a dielectric ceramic with both high W rec and η, a ternary system was designed. By the addition of (Bi 0.5Na 0.5) 0.7Sr 0.3TiO 3 (BNST), the grain size of 0.90NaNbO 3–0.10Bi(Mg 0.5Ta 0.5)O 3 (0.10BMT) was effectively reduced, and the long-range ordered structure was broken, providing an easily turned over dielectric domain to inhibit W loss. The activation energy of the grain boundary increased with the increase in resistivity, indicating that the concentration of free vacancies at the grain boundary was low. The jump barrier of oxygen vacancies in the grain boundary increased, making up for the grain boundary defects, thus increasing E b. When the BNST concentration increased, the E b and W rec of the dielectric ceramics increased. Optimum performance was obtained with the 0.75[0.90NaNbO 3–0.10Bi(Mg 0.5Ta 0.5)O 3]–0.25(Bi 0.5Na 0.5) 0.7Sr 0.3TiO 3 (0.25BNST) ceramic, which exhibited an exceptionally high E b (800 kV cm −1) and W rec (8 J cm −3), while maintaining a relatively high η (90.4%). The ceramics developed in this study showed excellent temperature and frequency stability over 20–200 °C and 1–160 Hz, respectively. In addition, the dielectric properties of the ceramics were maintained after 10 000 hysteresis cycles. The 0.25BNST ceramic showed an exceptionally fast t 0.9 (∼32 ns) and a high C D (614.5A cm −2). This study demonstrates that the energy storage performance and stability of the fabricated 0.25BNST ceramic are superior to those of previously reported dielectric ceramics.

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          Renewable energy resources: Current status, future prospects and their enabling technology

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            • Article: not found

            Perovskite lead-free dielectrics for energy storage applications

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              Potassium–sodium niobate based lead-free ceramics: novel electrical energy storage materials

              A design methodology for developing lead-free bulk ceramics with large recoverable energy storage density was proposed in this study. The development of lead-free bulk ceramics with high recoverable energy density ( W rec ) is of decisive importance for meeting the requirements of advanced pulsed power capacitors toward miniaturization and integration. However, the W rec (<2 J cm −3 ) of lead-free bulk ceramics has long been limited by their low dielectric breakdown strength (DBS < 200 kV cm −1 ) and small saturation polarization ( P s ). In this work, a strategy (compositions control the grain size of lead-free ceramics to submicron scale to increase the DBS, and the hybridization between the Bi 6p and O 2p orbitals enhances the P s ) was proposed to improve the W rec of lead-free ceramics. (K 0.5 Na 0.5 )NbO 3 –Bi(Me 2/3 Nb 1/3 )O 3 solid solutions (where Me 2+ = Mg and Zn) were designed for achieving large P s , and high DBS and W rec . As an example, (1 − x )(K 0.5 Na 0.5 )NbO 3 – x Bi(Mg 2/3 Nb 1/3 )O 3 (KNN–BMN) ceramics were prepared by using a conventional solid-state reaction process in this study. Large P s (41 μC cm −2 ) and high DBS (300 kV cm −1 ) were obtained for 0.90KNN–0.10BMN ceramics, leading to large W rec (4.08 J cm −3 ). The significantly enhanced W rec is more than 2–3 times larger than that of other lead-free bulk ceramics. The findings in this study not only provide a design methodology for developing lead-free bulk ceramics with large W rec but also could bring about the development of a series of KNN-based ceramics with significantly enhanced W rec and DBS in the future. More importantly, this work opens a new research and application field (dielectric energy storage) for (K 0.5 Na 0.5 )NbO 3 -based ceramics.
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                Author and article information

                Contributors
                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                March 2 2021
                2021
                : 9
                : 8
                : 4789-4799
                Affiliations
                [1 ]Collaborative Innovation Center for Exploration of Hidden Nonferrous Metal Deposits and Development of New Materials in Guangxi
                [2 ]Key Laboratory of Nonferrous Materials and New Processing Technology
                [3 ]Ministry of Education
                [4 ]School of Materials Science and Engineering
                [5 ]Guilin University of Technology
                Article
                10.1039/D0TA11022A
                09053857-f55e-4148-8f25-6319f9effa05
                © 2021

                http://rsc.li/journals-terms-of-use

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