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      Progress of 2D MXene as an Electrode Architecture for Advanced Supercapacitors: A Comprehensive Review

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          Abstract

          Supercapacitors, designed to store more energy and be proficient in accumulating more energy than conventional batteries with numerous charge–discharge cycles, have been developed in response to the growing demand for energy. Transition metal carbides/nitrides called MXenes have been the focus of researchers’ cutting-edge research in energy storage. The 2D-layered MXenes are a hopeful contender for the electrode material due to their unique properties, such as high conductivity, hydrophilicity, tunable surface functional groups, better mechanical properties, and outstanding electrochemical performance. This newly developed pseudocapacitive substance benefits electrochemical energy storage because it is rich in interlayer ion diffusion pathways and ion storage sites. Making MXene involves etching the MAX phase precursor with suitable etchants, but different etching methods have distinct effects on the morphology and electrochemical properties. It is an overview of the recent progress of MXene and its structure, synthesis, and unique properties. There is a strong emphasis on the effects of shape, size, electrode design, electrolyte behavior, and other variables on the charge storage mechanism and electrochemical performance of MXene-based supercapacitors. The electrochemical application of MXene and the remarkable research achievements in MXene-based composites are an intense focus. Finally, in light of further research and potential applications, the challenges and future perspectives that MXenes face and the prospects that MXenes present have been highlighted.

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          Most cited references190

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          2D metal carbides and nitrides (MXenes) for energy storage

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            Conductive two-dimensional titanium carbide 'clay' with high volumetric capacitance.

            Safe and powerful energy storage devices are becoming increasingly important. Charging times of seconds to minutes, with power densities exceeding those of batteries, can in principle be provided by electrochemical capacitors--in particular, pseudocapacitors. Recent research has focused mainly on improving the gravimetric performance of the electrodes of such systems, but for portable electronics and vehicles volume is at a premium. The best volumetric capacitances of carbon-based electrodes are around 300 farads per cubic centimetre; hydrated ruthenium oxide can reach capacitances of 1,000 to 1,500 farads per cubic centimetre with great cyclability, but only in thin films. Recently, electrodes made of two-dimensional titanium carbide (Ti3C2, a member of the 'MXene' family), produced by etching aluminium from titanium aluminium carbide (Ti3AlC2, a 'MAX' phase) in concentrated hydrofluoric acid, have been shown to have volumetric capacitances of over 300 farads per cubic centimetre. Here we report a method of producing this material using a solution of lithium fluoride and hydrochloric acid. The resulting hydrophilic material swells in volume when hydrated, and can be shaped like clay and dried into a highly conductive solid or rolled into films tens of micrometres thick. Additive-free films of this titanium carbide 'clay' have volumetric capacitances of up to 900 farads per cubic centimetre, with excellent cyclability and rate performances. This capacitance is almost twice that of our previous report, and our synthetic method also offers a much faster route to film production as well as the avoidance of handling hazardous concentrated hydrofluoric acid.
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              Two-dimensional transition metal carbides.

              Herein we report on the synthesis of two-dimensional transition metal carbides and carbonitrides by immersing select MAX phase powders in hydrofluoric acid, HF. The MAX phases represent a large (>60 members) family of ternary, layered, machinable transition metal carbides, nitrides, and carbonitrides. Herein we present evidence for the exfoliation of the following MAX phases: Ti(2)AlC, Ta(4)AlC(3), (Ti(0.5),Nb(0.5))(2)AlC, (V(0.5),Cr(0.5))(3)AlC(2), and Ti(3)AlCN by the simple immersion of their powders, at room temperature, in HF of varying concentrations for times varying between 10 and 72 h followed by sonication. The removal of the "A" group layer from the MAX phases results in 2-D layers that we are labeling MXenes to denote the loss of the A element and emphasize their structural similarities with graphene. The sheet resistances of the MXenes were found to be comparable to multilayer graphene. Contact angle measurements with water on pressed MXene surfaces showed hydrophilic behavior.
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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                14 November 2023
                28 November 2023
                : 8
                : 47
                : 44375-44394
                Affiliations
                []Centre for Advanced Materials Research, Department of Physics, Government College for Women, University of Kerala , Thiruvananthapuram, Kerala 695014, India
                []St Thomas College (Autonomous) , Thrissur, Kerala 68001, India
                Author notes
                Article
                10.1021/acsomega.3c02002
                10688139
                38046319
                4b1dc297-e754-4207-8a85-99fb53400ecb
                © 2023 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
                : 02 April 2023
                : 26 October 2023
                : 16 October 2023
                Funding
                Funded by: Department of Science and Technology, Ministry of Science and Technology, India, doi 10.13039/501100001409;
                Award ID: NA
                Categories
                Review
                Custom metadata
                ao3c02002
                ao3c02002

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