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      Aliovalent A-site engineered AgNbO 3 lead-free antiferroelectric ceramics toward superior energy storage density

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          Abstract

          Aliovalent A-site engineering enables superior energy storage density in AgNbO 3 lead-free antiferroelectric ceramics.

          Abstract

          Lead-free dielectric capacitors with high energy storage density and temperature-insensitive performance are pivotal to pulsed power systems. In this work, a pronounced recoverable energy storage density ( W rec) was achieved in AgNbO 3-based lead-free antiferroelectric ceramics, by aliovalent A-site Sm mediation. The Sm modification was found to alter the crystal structure and enhance the interaction among the ions by affecting the electronic structure, leading to improved antiferroelectricity. The Sm 0.03Ag 0.91NbO 3 solid solution exhibited a superior W rec of 5.2 J cm −3 with a high energy storage efficiency ( η) of 68.5% at an applied electric field of 290 kV cm −1. Excellent temperature stability of W rec with a minimal variation of less than 4% from room temperature up to 140 °C was also observed. Meanwhile, the Sm 0.03Ag 0.91NbO 3 ceramic also exhibited an ultrafast discharge speed (∼20 μs) and high discharge energy density (4.2 J cm −3). Ginzburg–Landau–Devonshire (GLD) phenomenology revealed that the significantly stabilized antiferroelectricity and the cation disorder were responsible for the ultrahigh W rec and η. The extraordinary energy storage performance indicates the Sm xAg 1−3xNbO 3 system a promising candidate for advanced pulsed power capacitors. More importantly, the results show that aliovalent A-site engineering is an effective way to achieve high energy storage density.

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          Revised effective ionic radii and systematic studies of interatomic distances in halides and chalcogenides

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            Flexible high-temperature dielectric materials from polymer nanocomposites.

            Dielectric materials, which store energy electrostatically, are ubiquitous in advanced electronics and electric power systems. Compared to their ceramic counterparts, polymer dielectrics have higher breakdown strengths and greater reliability, are scalable, lightweight and can be shaped into intricate configurations, and are therefore an ideal choice for many power electronics, power conditioning, and pulsed power applications. However, polymer dielectrics are limited to relatively low working temperatures, and thus fail to meet the rising demand for electricity under the extreme conditions present in applications such as hybrid and electric vehicles, aerospace power electronics, and underground oil and gas exploration. Here we describe crosslinked polymer nanocomposites that contain boron nitride nanosheets, the dielectric properties of which are stable over a broad temperature and frequency range. The nanocomposites have outstanding high-voltage capacitive energy storage capabilities at record temperatures (a Weibull breakdown strength of 403 megavolts per metre and a discharged energy density of 1.8 joules per cubic centimetre at 250 degrees Celsius). Their electrical conduction is several orders of magnitude lower than that of existing polymers and their high operating temperatures are attributed to greatly improved thermal conductivity, owing to the presence of the boron nitride nanosheets, which improve heat dissipation compared to pristine polymers (which are inherently susceptible to thermal runaway). Moreover, the polymer nanocomposites are lightweight, photopatternable and mechanically flexible, and have been demonstrated to preserve excellent dielectric and capacitive performance after intensive bending cycles. These findings enable broader applications of organic materials in high-temperature electronics and energy storage devices.
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              Homogeneous/Inhomogeneous-Structured Dielectrics and their Energy-Storage Performances.

              The demand for dielectric capacitors with higher energy-storage capability is increasing for power electronic devices due to the rapid development of electronic industry. Existing dielectrics for high-energy-storage capacitors and potential new capacitor technologies are reviewed toward realizing these goals. Various dielectric materials with desirable permittivity and dielectric breakdown strength potentially meeting the device requirements are discussed. However, some significant limitations for current dielectrics can be ascribed to their low permittivity, low breakdown strength, and high hysteresis loss, which will decrease their energy density and efficiency. Thus, the implementation of dielectric materials for high-energy-density applications requires the comprehensive understanding of both the materials design and processing. The optimization of high-energy-storage dielectrics will have far-reaching impacts on the sustainable energy and will be an important research topic in the near future.
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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
                June 11 2019
                2019
                : 7
                : 23
                : 14118-14128
                Affiliations
                [1 ]Guangxi Key Laboratory of Processing for Non-ferrous Metallic and Featured Materials
                [2 ]School of Resources, Environment and Materials
                [3 ]Guangxi University
                [4 ]Nanning 530004
                [5 ]China
                [6 ]Department of Chemistry
                [7 ]Tsinghua University
                [8 ]Beijing 100084
                [9 ]Department of Applied Physics
                [10 ]The Hong Kong Polytechnic University
                [11 ]Kowloon
                [12 ]Hong Kong SAR
                [13 ]School of Optical and Electronic Information
                [14 ]Huazhong University of Science and Technology
                [15 ]Wuhan 430074
                [16 ]College of Materials Science and Engineering
                [17 ]Guilin University of Technology
                [18 ]Guilin 541004
                Article
                10.1039/C9TA02053E
                ff2fe2a7-4d0e-4830-8976-0897cf990fea
                © 2019

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

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