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      The mechanism of ultrafast supercapacitors

      1 , 2 , 3 , 4 , 5
      Journal of Materials Chemistry A
      Royal Society of Chemistry (RSC)

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          Abstract

          Batteries and supercapacitors can be explained by the same impedance model involving diffusion, but neither is controlled by ‘semi-infinite’ diffusion.

          Abstract

          While microporous carbon is considered as a prime candidate for the energy storage application of supercapacitors, graphene is usually used for AC line-filtering capacitors. Surprisingly, the rate capability of the latter is a few orders of magnitude higher than that of the former. The interesting point is that such ultrafast performance can be achieved when the graphene sheets are vertically aligned, as the rate capability of ordinary graphene electrodes is similar to that of microporous supercapacitors. Understanding the actual role of the graphene alignment can shed light on the underlying mechanism to design faster supercapacitors for the energy storage purpose too. It is discussed that the classic double layer models cannot explain the critical importance of the graphene orientation. By reviewing the experimental evidence reported in the literature, the possibility of a different mechanism is justified. Furthermore, the impedance model of supercapacitors, which can be a guiding star in this direction, is explained from a practical perspective.

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          Flexible MXene/Graphene Films for Ultrafast Supercapacitors with Outstanding Volumetric Capacitance

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            Is Open Access

            Advanced Energy Storage Devices: Basic Principles, Analytical Methods, and Rational Materials Design

            Abstract Tremendous efforts have been dedicated into the development of high‐performance energy storage devices with nanoscale design and hybrid approaches. The boundary between the electrochemical capacitors and batteries becomes less distinctive. The same material may display capacitive or battery‐like behavior depending on the electrode design and the charge storage guest ions. Therefore, the underlying mechanisms and the electrochemical processes occurring upon charge storage may be confusing for researchers who are new to the field as well as some of the chemists and material scientists already in the field. This review provides fundamentals of the similarities and differences between electrochemical capacitors and batteries from kinetic and material point of view. Basic techniques and analysis methods to distinguish the capacitive and battery‐like behavior are discussed. Furthermore, guidelines for material selection, the state‐of‐the‐art materials, and the electrode design rules to advanced electrode are proposed.
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              Interconnected carbon nanosheets derived from hemp for ultrafast supercapacitors with high energy.

              We created unique interconnected partially graphitic carbon nanosheets (10-30 nm in thickness) with high specific surface area (up to 2287 m(2) g(-1)), significant volume fraction of mesoporosity (up to 58%), and good electrical conductivity (211-226 S m(-1)) from hemp bast fiber. The nanosheets are ideally suited for low (down to 0 °C) through high (100 °C) temperature ionic-liquid-based supercapacitor applications: At 0 °C and a current density of 10 A g(-1), the electrode maintains a remarkable capacitance of 106 F g(-1). At 20, 60, and 100 °C and an extreme current density of 100 A g(-1), there is excellent capacitance retention (72-92%) with the specific capacitances being 113, 144, and 142 F g(-1), respectively. These characteristics favorably place the materials on a Ragone chart providing among the best power-energy characteristics (on an active mass normalized basis) ever reported for an electrochemical capacitor: At a very high power density of 20 kW kg(-1) and 20, 60, and 100 °C, the energy densities are 19, 34, and 40 Wh kg(-1), respectively. Moreover the assembled supercapacitor device yields a maximum energy density of 12 Wh kg(-1), which is higher than that of commercially available supercapacitors. By taking advantage of the complex multilayered structure of a hemp bast fiber precursor, such exquisite carbons were able to be achieved by simple hydrothermal carbonization combined with activation. This novel precursor-synthesis route presents a great potential for facile large-scale production of high-performance carbons for a variety of diverse applications including energy storage.
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                Author and article information

                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2018
                2018
                : 6
                : 7
                : 2866-2876
                Affiliations
                [1 ]The Engineering Research Institute
                [2 ]Ulster University
                [3 ]Newtownabbey BT37 OQB
                [4 ]UK
                [5 ]School of Chemistry and Chemical Engineering
                Article
                10.1039/C7TA10013B
                99fac8c8-17e9-4970-ad80-9b23f36444df
                © 2018

                http://rsc.li/journals-terms-of-use

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