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      Zinc-salt assisted synthesis of three-dimensional oxygen and nitrogen co-doped hierarchical micro-meso porous carbon foam for supercapacitors

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          Abstract

          Nitrogen and oxygen co-doped hierarchical micro-mesoporous carbon foams has been synthesized by pyrolyzation treatment of a preliminary foam containing melamine and formaldehyde as nitrogen, carbon and oxygen precursors and Zn(NO 3) 2. 6H 2O and pluronic F127 as micro-meso pores generators. Several characterizations including thermal gravimetric analysis (TGA), X-ray diffraction (XRD) and Raman spectroscopy, FTIR and X-ray photoelectron spectroscopy, N 2 adsorption–desorption, field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM) were performed on the prepared foams. X-ray diffraction patterns, Raman spectra and N 2 adsorption–desorption results confirmed that ZnO has pronounced effect on the graphitization of the prepared carbon foam. From X-ray diffraction, thermal gravimetric and N 2 adsorption–desorption analysis results it was confirmed that the carbothermal reaction and the elimination of ZnO and also the elimination of pluronic F127 are the main factors for the induction of porosities in the foam structure. The presence of Zn(NO 3) 2. 6H 2O and pluronic F127 in the initial composition of the preliminary foam results in the specific surface area as high as 1176 m 2.g −1 and pore volume of 0.68 cm 3.g −1. X-ray photoelectron and FTIR spectroscopy analyses results approved the presence of nitrogen (about 1.9 at %) in the form of pyridinic, graphitic and nitrogen oxide and oxygen (about 7.5 at. %) functional groups on the surface of the synthesized carbon foam. Electrochemistry analysis results including cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) and also electrochemical impedance spectroscopy (EIS) analysis illustrated the formation of an electric double layer supercapacitor with the capacitance as high as 137 Fg −1.

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          Carbons and electrolytes for advanced supercapacitors.

          Electrical energy storage (EES) is one of the most critical areas of technological research around the world. Storing and efficiently using electricity generated by intermittent sources and the transition of our transportation fleet to electric drive depend fundamentally on the development of EES systems with high energy and power densities. Supercapacitors are promising devices for highly efficient energy storage and power management, yet they still suffer from moderate energy densities compared to batteries. To establish a detailed understanding of the science and technology of carbon/carbon supercapacitors, this review discusses the basic principles of the electrical double-layer (EDL), especially regarding the correlation between ion size/ion solvation and the pore size of porous carbon electrodes. We summarize the key aspects of various carbon materials synthesized for use in supercapacitors. With the objective of improving the energy density, the last two sections are dedicated to strategies to increase the capacitance by either introducing pseudocapacitive materials or by using novel electrolytes that allow to increasing the cell voltage. In particular, advances in ionic liquids, but also in the field of organic electrolytes, are discussed and electrode mass balancing is expanded because of its importance to create higher performance asymmetric electrochemical capacitors. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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            Nitrogen-doped mesoporous carbon of extraordinary capacitance for electrochemical energy storage.

            Carbon-based supercapacitors can provide high electrical power, but they do not have sufficient energy density to directly compete with batteries. We found that a nitrogen-doped ordered mesoporous few-layer carbon has a capacitance of 855 farads per gram in aqueous electrolytes and can be bipolarly charged or discharged at a fast, carbon-like speed. The improvement mostly stems from robust redox reactions at nitrogen-associated defects that transform inert graphene-like layered carbon into an electrochemically active substance without affecting its electric conductivity. These bipolar aqueous-electrolyte electrochemical cells offer power densities and lifetimes similar to those of carbon-based supercapacitors and can store a specific energy of 41 watt-hours per kilogram (19.5 watt-hours per liter).
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              Physical Interpretations of Nyquist Plots for EDLC Electrodes and Devices

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                Author and article information

                Contributors
                Motejadded@iust.ac.ir
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                8 November 2021
                8 November 2021
                2021
                : 11
                : 21798
                Affiliations
                GRID grid.411748.f, ISNI 0000 0001 0387 0587, Nanotechnology Department, School of Advanced Technologies, , Iran University of Science and Technology, ; 16846 Narmak, Tehran Iran
                Article
                1151
                10.1038/s41598-021-01151-3
                8576033
                34750418
                48c29a26-652f-49fe-8d61-075b17a89b1c
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 26 April 2021
                : 25 October 2021
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                © The Author(s) 2021

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                chemistry,energy science and technology,materials science,nanoscience and technology

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