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      Ultrafine nickel–cobalt alloy nanoparticles incorporated into three-dimensional porous graphitic carbon as an electrode material for supercapacitors

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          Abstract

          A facile method was developed to synthesize ultrafine Ni–Co alloy nanoparticles embedded into 3D porous graphitic carbon, an excellent electrode material for supercapacitors.

          Abstract

          Metal oxides are a class of promising electrode materials for supercapacitors because of their high theoretical energy density; however, the low electrical conductivity and instability of metal oxides limit their large-scale practical applications. Here we report a facile and scalable method to synthesize ultrafine nickel–cobalt alloy nanoparticles (5–10 nm) embedded into three-dimensional porous graphitic carbon (3D Ni–Co@PGC) using NaCl as the template to create a porous structure and glucose as the carbon source by pyrolysis treatment at 800 °C under N 2 atmosphere. As an electrode material for supercapacitors, the ultrafine Ni–Co alloy nanoparticles of 3D Ni–Co@PGC not only serve as current collectors, but also their surfaces convert to corresponding metal oxides when exposed to an alkaline electrolyte, responsible for redox reactions in pseudocapacitors, exhibiting high supercapacitor performance. The results demonstrate that the supercapacitor assembled with 3D Ni–Co@PGC electrodes shows high energy density (1091, 1064 and 1041 F g −1 at 1, 2 and 4 A g −1, respectively), long cycling life and excellent rate capability at a high charge/discharge current. Furthermore, an asymmetric supercapacitor assembled by using 3D Ni–Co@PGC as the positive electrode and active carbon as the negative electrode shows a high energy density of 33.7 W h kg −1 and remarkable cycling stability (98% capacitance retention over 4000 cycles). The superior performance of the 3D Ni–Co@PGC constructed supercapacitor can be ascribed to its high surface area (265 m 2 g −1), porous structure and excellent electrical conductivity, favourable for the exposure of reaction active sites, redox-related mass transport and electron transfer, respectively.

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          Pseudocapacitive oxide materials for high-rate electrochemical energy storage

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            Nanoporous metal/oxide hybrid electrodes for electrochemical supercapacitors.

            Electrochemical supercapacitors can deliver high levels of electrical power and offer long operating lifetimes, but their energy storage density is too low for many important applications. Pseudocapacitive transition-metal oxides such as MnO(2) could be used to make electrodes in such supercapacitors, because they are predicted to have a high capacitance for storing electrical charge while also being inexpensive and not harmful to the environment. However, the poor conductivity of MnO(2) (10(-5)-10(-6) S cm(-1)) limits the charge/discharge rate for high-power applications. Here, we show that hybrid structures made of nanoporous gold and nanocrystalline MnO(2) have enhanced conductivity, resulting in a specific capacitance of the constituent MnO(2) (~1,145 F g(-1)) that is close to the theoretical value. The nanoporous gold allows electron transport through the MnO(2), and facilitates fast ion diffusion between the MnO(2) and the electrolytes while also acting as a double-layer capacitor. The high specific capacitances and charge/discharge rates offered by such hybrid structures make them promising candidates as electrodes in supercapacitors, combining high-energy storage densities with high levels of power delivery.
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              Graphene oxide--MnO2 nanocomposites for supercapacitors.

              A composite of graphene oxide supported by needle-like MnO(2) nanocrystals (GO-MnO(2) nanocomposites) has been fabricated through a simple soft chemical route in a water-isopropyl alcohol system. The formation mechanism of these intriguing nanocomposites investigated by transmission electron microscopy and Raman and ultraviolet-visible absorption spectroscopy is proposed as intercalation and adsorption of manganese ions onto the GO sheets, followed by the nucleation and growth of the crystal species in a double solvent system via dissolution-crystallization and oriented attachment mechanisms, which in turn results in the exfoliation of GO sheets. Interestingly, it was found that the electrochemical performance of as-prepared nanocomposites could be enhanced by the chemical interaction between GO and MnO(2). This method provides a facile and straightforward approach to deposit MnO(2) nanoparticles onto the graphene oxide sheets (single layer of graphite oxide) and may be readily extended to the preparation of other classes of hybrids based on GO sheets for technological applications.
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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
                : 43
                : 17080-17086
                Article
                10.1039/C6TA06022F
                fab1a154-a849-4790-85f6-e8ad2b5bd1ae
                © 2016
                History

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