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      The Many Deaths of Supercapacitors: Degradation, Aging, and Performance Fading

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          Abstract

          High‐performance electrochemical applications have expedited the research in high‐power devices. As such, supercapacitors, including electrical double‐layer capacitors (EDLCs) and pseudocapacitors, have gained significant attention due to their high power density, long cycle life, and fast charging capabilities. Yet, no device lasts forever. It is essential to understand the mechanisms behind performance degradation and aging so that these bottlenecks can be addressed and tailored solutions can be developed. Herein, the factors contributing to the aging and degradation of supercapacitors, including electrode materials, electrolytes, and other aspects of the system, such as pore blocking, electrode compositions, functional groups, and corrosion of current collectors are examined. The monitoring and characterizing of the performance degradation of supercapacitors, including electrochemical methods, in situ, and ex situ techniques are explored. In addition, the degradation mechanisms of different types of electrolytes and electrode materials and the effects of aging from an industrial application standpoint are analyzed. Next, how electrode degradations and electrolyte decompositions can lead to failure, and pore blocking, electrode composition, and other factors that affect the device's lifespan are examined. Finally, the future directions and challenges for reducing supercapacitors' performance degradation, including developing new materials and methods for characterizing and monitoring the devices are summarized.

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          We describe monocrystalline graphitic films, which are a few atoms thick but are nonetheless stable under ambient conditions, metallic, and of remarkably high quality. The films are found to be a two-dimensional semimetal with a tiny overlap between valence and conductance bands, and they exhibit a strong ambipolar electric field effect such that electrons and holes in concentrations up to 10 13 per square centimeter and with room-temperature mobilities of ∼10,000 square centimeters per volt-second can be induced by applying gate voltage.
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              Materials for electrochemical capacitors.

              Electrochemical capacitors, also called supercapacitors, store energy using either ion adsorption (electrochemical double layer capacitors) or fast surface redox reactions (pseudo-capacitors). They can complement or replace batteries in electrical energy storage and harvesting applications, when high power delivery or uptake is needed. A notable improvement in performance has been achieved through recent advances in understanding charge storage mechanisms and the development of advanced nanostructured materials. The discovery that ion desolvation occurs in pores smaller than the solvated ions has led to higher capacitance for electrochemical double layer capacitors using carbon electrodes with subnanometre pores, and opened the door to designing high-energy density devices using a variety of electrolytes. Combination of pseudo-capacitive nanomaterials, including oxides, nitrides and polymers, with the latest generation of nanostructured lithium electrodes has brought the energy density of electrochemical capacitors closer to that of batteries. The use of carbon nanotubes has further advanced micro-electrochemical capacitors, enabling flexible and adaptable devices to be made. Mathematical modelling and simulation will be the key to success in designing tomorrow's high-energy and high-power devices.
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                Author and article information

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                Journal
                Advanced Energy Materials
                Advanced Energy Materials
                Wiley
                1614-6832
                1614-6840
                August 2023
                June 16 2023
                August 2023
                : 13
                : 29
                Affiliations
                [1 ]INM – Leibniz Institute for New Materials Campus D2 2 66123 Saarbrücken Germany
                [2 ]Institute of Technical Chemistry and Environmental Chemistry and Center for Energy and Environmental Chemistry Jena (CEEC Jena) Friedrich‐Schiller‐University Jena Philosophenweg 7a 07743 Jena Germany
                [3 ]Skeleton Technologies GmbH Schücostraße 8 01900 Großröhrsdorf Germany
                [4 ]Helmholtz Institute Ulm (HIU) Helmholtzstrasse 11 89081 Ulm Germany
                [5 ]Karlsruhe Institute of Technology (KIT) P.O. Box 3640 76021 Karlsruhe Germany
                [6 ]Nantes Université CNRS Institut des Matériaux de Nantes Jean Rouxel IMN Nantes 44000 France
                [7 ]Réseau Sur Le Stockage Electrochimique de L'Energie (RS2E) CNRS FR 3459 33 rue Saint Leu Amiens Cedex 80039 France
                [8 ]Saarland University Campus D2 2 66123 Saarbrücken Germany
                [9 ]Saarene – Saarland Center for Energy Materials and Sustainability Campus C4 2 66123 Saarbrücken Germany
                Article
                10.1002/aenm.202301008
                07e7fdc5-8a79-433e-be73-d1ac11261c43
                © 2023

                http://creativecommons.org/licenses/by/4.0/

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