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      Facile synthesis of hybrid CNTs/NiCo 2S 4 composite for high performance supercapacitors

      research-article
      1 , 2 , 1 , 2 , a , 1 , 2 , 3
      Scientific Reports
      Nature Publishing Group

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          Abstract

          In this work, a novel carbon nanotubes (CNTs)/NiCo 2S 4 composite for high performance supercapacitors was prepared via a simple chemical bath deposition combined with a post-anion exchange reaction. The morphologies and phase structures of the composites were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), Raman spectroscopy (Raman), X-ray photoelectron spectroscopy (XPS) and low-temperature sorption of nitrogen (BET). The electro-chemical tests revealed that the CNT/NiCo 2S 4 composite exhibited high electrochemical performance, because the CNTs were used as a conductive network for the NiCo 2S 4 hexagonal nanoplates. Compared with pure NiCo 2S 4 and the mechanically mixed CNTs/NiCo 2S 4 composite, the CNTs/NiCo 2S 4 composite electrode material exhibited excellent supercapacitive performance, such as a high specific capacitance up to 1537 F/g (discharge current density of 1 A/g) and an outstanding rate capability of 78.1% retention as the discharge current density increased to 100 A/g. It is therefore expected to be a promising alternative material in the area of energy storage.

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          Oxygen bridges between NiO nanosheets and graphene for improvement of lithium storage.

          Graphene has been widely used to dramatically improve the capacity, rate capability, and cycling performance of nearly any electrode material for batteries. However, the binding between graphene and these electrode materials has not been clearly elucidated. Here we report oxygen bridges between graphene with oxygen functional groups and NiO from analysis by X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, and Raman spectroscopy and confirm the conformation of oxygen bridges by the first-principles calculations. We found that NiO nanosheets (NiO NSs) are bonded strongly to graphene through oxygen bridges. The oxygen bridges mainly originate from the pinning of hydroxyl/epoxy groups from graphene on the Ni atoms of NiO NSs. The calculated adsorption energies (1.37 and 1.84 eV for graphene with hydroxyl and epoxy) of a Ni adatom on oxygenated graphene by binding with oxygen are comparable with that on graphene (1.26 eV). However, the calculated diffusion barriers of the Ni adatom on the oxygenated graphene surface (2.23 and 1.69 eV for graphene with hydroxyl and epoxy) are much larger than that on the graphene (0.19 eV). Therefore, the NiO NS is anchored strongly on the graphene through a C-O-Ni bridge, which allows a high reversible capacity and excellent rate performance. The easy binding/difficult dissociating characteristic of Ni adatoms on the oxygenated graphene facilitates fast electron hopping from graphene to NiO and thus the reversible lithiation and delithiation of NiO. We believe that the understanding of this oxygen bridge between graphene and NiO will lead to the development of other high-performance electrode materials.
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            Carbon Nanotubes for Supercapacitor

            As an electrical energy storage device, supercapacitor finds attractive applications in consumer electronic products and alternative power source due to its higher energy density, fast discharge/charge time, low level of heating, safety, long-term operation stability, and no disposable parts. This work reviews the recent development of supercapacitor based on carbon nanotubes (CNTs) and their composites. The purpose is to give a comprehensive understanding of the advantages and disadvantages of carbon nanotubes-related supercapacitor materials and to find ways for the improvement in the performance of supercapacitor. We first discussed the effects of physical and chemical properties of pure carbon nanotubes, including size, purity, defect, shape, functionalization, and annealing, on the supercapacitance. The composites, including CNTs/oxide and CNTs/polymer, were further discussed to enhance the supercapacitance and keep the stability of the supercapacitor by optimally engineering the composition, particle size, and coverage.
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              MWCNT/V2O5 core/shell sponge for high areal capacity and power density Li-ion cathodes.

              A multiwall carbon nanotube (MWCNT) sponge network, coated by ALD V(2)O(5), presents the key characteristics needed to serve as a high-performance cathode in Li-ion batteries, exploiting (1) the highly electron-conductive nature of MWCNT, (2) unprecedented uniformity of ALD thin film coatings, and (3) high surface area and porosity of the MWCNT sponge material for ion transport. The core/shell MWCNT/V(2)O(5) sponge delivers a stable high areal capacity of 816 μAh/cm(2) for 2 Li/V(2)O(5) (voltage range 4.0-2.1 V) at 1C rate (1.1 mA/cm(2)), 450 times that of a planar V(2)O(5) thin film cathode. At much higher current (50×), the areal capacity of 155 μAh/cm(2) provides a high power density of 21.7 mW/cm(2). The compressed sponge nanoarchitecture thus demonstrates exceptional robustness and energy-power characteristics for thin film cathode structures for electrochemical energy storage.
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                Author and article information

                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group
                2045-2322
                11 July 2016
                2016
                : 6
                : 29788
                Affiliations
                [1 ]Shenzhen Research Institute, Wuhan University , Shenzhen 518057, China
                [2 ]School of Physics and Technology, and MOE Key Laboratory of Artificial Micro- and Nano-structures, Wuhan University , Wuhan 430072, China
                [3 ]Center for Electron Microscopy, Wuhan University , Wuhan 430072, China
                Author notes
                Article
                srep29788
                10.1038/srep29788
                4942691
                27406239
                05773108-be14-42f0-9015-c9974b9fbb54
                Copyright © 2016, Macmillan Publishers Limited

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 14 January 2016
                : 21 June 2016
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