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      Microscopic Simulations of Electrochemical Double-Layer Capacitors

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          Abstract

          Electrochemical double-layer capacitors (EDLCs) are devices allowing the storage or production of electricity. They function through the adsorption of ions from an electrolyte on high-surface-area electrodes and are characterized by short charging/discharging times and long cycle-life compared to batteries. Microscopic simulations are now widely used to characterize the structural, dynamical, and adsorption properties of these devices, complementing electrochemical experiments and in situ spectroscopic analyses. In this review, we discuss the main families of simulation methods that have been developed and their application to the main family of EDLCs, which include nanoporous carbon electrodes. We focus on the adsorption of organic ions for electricity storage applications as well as aqueous systems in the context of blue energy harvesting and desalination. We finally provide perspectives for further improvement of the predictive power of simulations, in particular for future devices with complex electrode compositions.

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          Physisorption of gases, with special reference to the evaluation of surface area and pore size distribution (IUPAC Technical Report)

          Gas adsorption is an important tool for the characterisation of porous solids and fine powders. Major advances in recent years have made it necessary to update the 1985 IUPAC manual on Reporting Physisorption Data for Gas/Solid Systems. The aims of the present document are to clarify and standardise the presentation, nomenclature and methodology associated with the application of physisorption for surface area assessment and pore size analysis and to draw attention to remaining problems in the interpretation of physisorption data.
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            Origin of the Overpotential for Oxygen Reduction at a Fuel-Cell Cathode

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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

                Journal
                Chem Rev
                Chem Rev
                cr
                chreay
                Chemical Reviews
                American Chemical Society
                0009-2665
                1520-6890
                07 April 2022
                22 June 2022
                : 122
                : 12 , Computational Electrochemistry
                : 10860-10898
                Affiliations
                []Sorbonne Université, CNRS , Physico-chimie des Électrolytes et Nanosystèmes Interfaciaux, PHENIX, F-75005 Paris, France
                []Réseau sur le Stockage Electrochimique de l’Energie (RS2E), FR CNRS 3459 , 80039 Amiens, France
                []Sorbonne Université, CNRS , Physico-chimie des Electrolytes et Nanosystèmes Interfaciaux, PHENIX, F-75005 Paris, France
                [§ ]Réseau sur le Stockage Électrochimique de l’Énergie (RS2E), FR CNRS 3459 , 80039 Amiens, France
                []Institut Universitaire de France (IUF) , 75231 Paris Cedex 05, France
                Author notes
                Author information
                https://orcid.org/0000-0003-3560-9273
                https://orcid.org/0000-0001-5198-4650
                https://orcid.org/0000-0002-1753-491X
                Article
                10.1021/acs.chemrev.1c00925
                9227719
                35389636
                a2370ee0-5faa-4c37-81cf-e0de909cab56
                © 2022 The Authors. Published by American Chemical Society

                Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works ( https://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 03 November 2021
                Funding
                Funded by: H2020 European Research Council, doi 10.13039/100010663;
                Award ID: 771294
                Funded by: Agence Nationale de la Recherche, doi 10.13039/501100001665;
                Award ID: ANR-10-LABX-0076
                Funded by: H2020 European Research Council, doi 10.13039/100010663;
                Award ID: 863473
                Categories
                Review
                Custom metadata
                cr1c00925
                cr1c00925

                Chemistry
                Chemistry

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