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      Electroceramics for High-Energy Density Capacitors: Current Status and Future Perspectives

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          Abstract

          Materials exhibiting high energy/power density are currently needed to meet the growing demand of portable electronics, electric vehicles and large-scale energy storage devices. The highest energy densities are achieved for fuel cells, batteries, and supercapacitors, but conventional dielectric capacitors are receiving increased attention for pulsed power applications due to their high power density and their fast charge–discharge speed. The key to high energy density in dielectric capacitors is a large maximum but small remanent (zero in the case of linear dielectrics) polarization and a high electric breakdown strength. Polymer dielectric capacitors offer high power/energy density for applications at room temperature, but above 100 °C they are unreliable and suffer from dielectric breakdown. For high-temperature applications, therefore, dielectric ceramics are the only feasible alternative. Lead-based ceramics such as La-doped lead zirconate titanate exhibit good energy storage properties, but their toxicity raises concern over their use in consumer applications, where capacitors are exclusively lead free. Lead-free compositions with superior power density are thus required. In this paper, we introduce the fundamental principles of energy storage in dielectrics. We discuss key factors to improve energy storage properties such as the control of local structure, phase assemblage, dielectric layer thickness, microstructure, conductivity, and electrical homogeneity through the choice of base systems, dopants, and alloying additions, followed by a comprehensive review of the state-of-the-art. Finally, we comment on the future requirements for new materials in high power/energy density capacitor applications.

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          Advanced materials for energy storage.

          Popularization of portable electronics and electric vehicles worldwide stimulates the development of energy storage devices, such as batteries and supercapacitors, toward higher power density and energy density, which significantly depends upon the advancement of new materials used in these devices. Moreover, energy storage materials play a key role in efficient, clean, and versatile use of energy, and are crucial for the exploitation of renewable energy. Therefore, energy storage materials cover a wide range of materials and have been receiving intensive attention from research and development to industrialization. In this Review, firstly a general introduction is given to several typical energy storage systems, including thermal, mechanical, electromagnetic, hydrogen, and electrochemical energy storage. Then the current status of high-performance hydrogen storage materials for on-board applications and electrochemical energy storage materials for lithium-ion batteries and supercapacitors is introduced in detail. The strategies for developing these advanced energy storage materials, including nanostructuring, nano-/microcombination, hybridization, pore-structure control, configuration design, surface modification, and composition optimization, are discussed. Finally, the future trends and prospects in the development of advanced energy storage materials are highlighted.
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            Carbon-based supercapacitors produced by activation of graphene.

            Supercapacitors, also called ultracapacitors or electrochemical capacitors, store electrical charge on high-surface-area conducting materials. Their widespread use is limited by their low energy storage density and relatively high effective series resistance. Using chemical activation of exfoliated graphite oxide, we synthesized a porous carbon with a Brunauer-Emmett-Teller surface area of up to 3100 square meters per gram, a high electrical conductivity, and a low oxygen and hydrogen content. This sp(2)-bonded carbon has a continuous three-dimensional network of highly curved, atom-thick walls that form primarily 0.6- to 5-nanometer-width pores. Two-electrode supercapacitor cells constructed with this carbon yielded high values of gravimetric capacitance and energy density with organic and ionic liquid electrolytes. The processes used to make this carbon are readily scalable to industrial levels.
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              Perspective on the Development of Lead-free Piezoceramics

                Author and article information

                Journal
                Chem Rev
                Chem Rev
                cr
                chreay
                Chemical Reviews
                American Chemical Society
                0009-2665
                1520-6890
                28 April 2021
                26 May 2021
                : 121
                : 10
                : 6124-6172
                Affiliations
                []Department of Materials Science and Engineering, University of Sheffield , Sheffield S1 3JD, U.K.
                [& ]The Henry Royce Institute , Sir Robert Hadfield Building, Sheffield S1 3JD, U.K.
                [§ ]Inner Mongolia Key Laboratory of Ferroelectric-related New Energy Materials and Devices, School of Materials and Metallurgy, Inner Mongolia University of Science and Technology , Baotou 014010, China
                []Laboratory of Thin Film Techniques and Optical Test, Xi’an Technological University , Xi’an 710032, China
                []Christian Doppler Laboratory for Advanced Ferroic Oxides, Sheffield Hallam University , Sheffield S1 1WB, U.K.
                [# ]Electronic Materials Research Lab, Key Lab of Education Ministry/International Center for Dielectric Research, School of Electronic and Information Engineering, Xi’an Jiaotong University , Xi’an 710049, China
                []Shenzhen Institute of Advanced Electronic Materials, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences , Shenzhen 518055, China
                [@ ]Institute for Superconducting and Electronic Materials, Australian Institute for Innovative Materials, University of Wollongong , Wollongong, NSW 2500, Australia
                Author notes
                Author information
                http://orcid.org/0000-0003-1842-8067
                http://orcid.org/0000-0001-7411-4658
                http://orcid.org/0000-0001-6957-2494
                http://orcid.org/0000-0001-6139-6887
                http://orcid.org/0000-0003-3893-6544
                Article
                10.1021/acs.chemrev.0c01264
                8277101
                33909415
                9fa567f1-2c1a-43b6-9ef8-c8c97a2ef3f3
                © 2021 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 30 November 2020
                Funding
                Funded by: Engineering and Physical Sciences Research Council, doi 10.13039/501100000266;
                Award ID: EP/L017563/1
                Funded by: National Natural Science Foundation of China, doi 10.13039/501100001809;
                Award ID: 51602060
                Funded by: National Natural Science Foundation of China, doi 10.13039/501100001809;
                Award ID: 51402005
                Funded by: Engineering and Physical Sciences Research Council, doi 10.13039/501100000266;
                Award ID: EP/S019367/1
                Funded by: Engineering and Physical Sciences Research Council, doi 10.13039/501100000266;
                Award ID: EP/R00661X/1
                Funded by: Engineering and Physical Sciences Research Council, doi 10.13039/501100000266;
                Award ID: EP/P025285/1
                Funded by: Engineering and Physical Sciences Research Council, doi 10.13039/501100000266;
                Award ID: EP/P02470X/1
                Funded by: Engineering and Physical Sciences Research Council, doi 10.13039/501100000266;
                Award ID: EP/N010493/1
                Categories
                Review
                Custom metadata
                cr0c01264
                cr0c01264

                Chemistry
                Chemistry

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