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      Symmetric pseudocapacitors based on molybdenum disulfide (MoS 2)-modified carbon nanospheres: correlating physicochemistry and synergistic interaction on energy storage

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          Abstract

          Flower-like MoS 2 modified with carbon nanospheres (CNS) displays energy-storage capability when used as an aqueous symmetric pseudocapacitor.

          Abstract

          Molybdenum disulfide-modified carbon nanospheres (MoS 2/CNS) with two different morphologies (spherical and flower-like) have been synthesized using hydrothermal techniques and investigated as symmetric pseudocapacitors in an aqueous electrolyte. The physicochemical properties of these MoS 2/CNS layered materials have been investigated using surface area analysis (BET), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman, Fourier transform infrared (FTIR) spectroscopy, and advanced electrochemistry, including cyclic voltammetry (CV), galvanostatic cycling with potential limitation (GCPL), long-hour voltage-holding tests, and electrochemical impedance spectroscopy (EIS). The two different MoS 2/CNS layered materials exhibit unique differences in morphology, surface area, and structural parameters, which have been correlated with their electrochemical capacitive properties. The flower-like morphology (f-MoS 2/CNS) shows lattice expansion (XRD), large surface area (BET analysis), and small-sized nanostructures (corroborated by the larger FWHM of the Raman and XRD data). In contrast to the f-MoS 2/CNS, the spherical morphology (s-MoS 2/CNS) shows lattice contraction and small surface area with relatively large-sized nanostructures. The presence of CNS on the MoS 2 structure leads to slight softening of the characteristic Raman bands (E12g and A 1g modes) with larger FWHM. MoS 2 and its CNS-based composites have been tested in symmetric electrochemical capacitors in an aqueous 1 M Na 2SO 4 solution. CNS improves the conductivity of the MoS 2 and synergistically enhances the electrochemical capacitive properties of the materials, especially the f-MoS 2/CNS-based symmetric cells (most notably, in terms of capacitance retention). The f-MoS 2/CNS-based pseudocapacitor shows a maximum capacitance of 231 F g −1, with high energy density 26 W h kg −1 and power density 6443 W kg −1. For the s-MoS 2/CNS-based pseudocapacitor, the equivalent values are 108 F g −1, 7.4 W h kg −1 and 3700 W kg −1. The high-performance of the f-MoS 2/CNS is consistent with its physicochemical properties as determined by the spectroscopy and microscopy data. These findings have opened doors for further exploration of the synergistic effects between MoS 2 graphene-like sheets and CNS for energy storage.

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          Most cited references29

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          A review of electrode materials for electrochemical supercapacitors.

          In this critical review, metal oxides-based materials for electrochemical supercapacitor (ES) electrodes are reviewed in detail together with a brief review of carbon materials and conducting polymers. Their advantages, disadvantages, and performance in ES electrodes are discussed through extensive analysis of the literature, and new trends in material development are also reviewed. Two important future research directions are indicated and summarized, based on results published in the literature: the development of composite and nanostructured ES materials to overcome the major challenge posed by the low energy density of ES (476 references).
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            Anomalous lattice vibrations of single- and few-layer MoS2.

            Molybdenum disulfide (MoS(2)) of single- and few-layer thickness was exfoliated on SiO(2)/Si substrate and characterized by Raman spectroscopy. The number of S-Mo-S layers of the samples was independently determined by contact-mode atomic force microscopy. Two Raman modes, E(1)(2g) and A(1g), exhibited sensitive thickness dependence, with the frequency of the former decreasing and that of the latter increasing with thickness. The results provide a convenient and reliable means for determining layer thickness with atomic-level precision. The opposite direction of the frequency shifts, which cannot be explained solely by van der Waals interlayer coupling, is attributed to Coulombic interactions and possible stacking-induced changes of the intralayer bonding. This work exemplifies the evolution of structural parameters in layered materials in changing from the three-dimensional to the two-dimensional regime.
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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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                Author and article information

                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2016
                2016
                : 4
                : 17
                : 6411-6425
                Affiliations
                [1 ]School of Chemical and Metallurgical Engineering
                [2 ]University of the Witwatersrand
                [3 ]Johannesburg
                [4 ]South Africa
                [5 ]Energy Materials, Materials Science and Manufacturing
                [6 ]Council for Scientific and Industrial Research (CSIR)
                [7 ]Pretoria 0001
                [8 ]Molecular Sciences Institute
                [9 ]School of Chemistry
                Article
                10.1039/C6TA00114A
                c6905d50-4adb-400f-b6f3-c0bdfd7b2264
                © 2016
                History

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