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      Ni 1.5CoSe 5 nanocubes embedded in 3D dual N-doped carbon network as advanced anode material in sodium-ion full cells with superior low-temperature and high-power properties

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          Abstract

          An advanced anode for sodium-ion batteries is prepared by embedding cube-like Ni 1.5CoSe 5 nanoaggregates into 3D dual N-doped carbon network.

          Abstract

          In this study, the double transition metal selenide Ni 1.5CoSe 5 with cube-like nanoaggregate morphology was successfully embedded into a three-dimensional (3D) dual N-doped carbon network, developing an advanced anode material for sodium-ion batteries (SIBs). In the prepared composite, Ni 1.5CoSe 5 nanoparticles were first coated by N-doped carbon (NC), which further aggregated to form nanocubes, and finally embedded into interconnected N-doped reduced graphene oxide (rGO) nanosheets; hence, the material was abbreviated as Ni 1.5CoSe 5@NC@rGO. It delivered a reversible Na-storage capacity of 582.5 mA h g −1 at a low current density of 0.05 A g −1 and exhibited ultra-fast rate properties ( e.g., with the specific capacities of 180.8 and 96.3 mA h g −1 at high current densities of 30 and 50 A g −1, respectively). The much enhanced Na-storage properties were ascribed to the highly conductive 3D network constructed by dual N-doped carbonaceous materials, which acted not only as a highway for ultrafast charge transfer but also as an effective protector for the active Ni 1.5CoSe 5 material and cube-like nanoaggregates with nanometer-sized primary particles. More significantly, the Ni 1.5CoSe 5@NC@rGO electrode also exhibited superior energy storage performance in sodium-ion full cells when coupled with a high-voltage Na 3V 2(PO 4) 2O 2F cathode, making it a promising anode material for practical SIBs.

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          Materials science. Where do batteries end and supercapacitors begin?

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            Pseudocapacitance of MXene nanosheets for high-power sodium-ion hybrid capacitors

            High-power Na-ion batteries have tremendous potential in various large-scale applications. However, conventional charge storage through ion intercalation or double-layer formation cannot satisfy the requirements of such applications owing to the slow kinetics of ion intercalation and the small capacitance of the double layer. The present work demonstrates that the pseudocapacitance of the nanosheet compound MXene Ti2C achieves a higher specific capacity relative to double-layer capacitor electrodes and a higher rate capability relative to ion intercalation electrodes. By utilizing the pseudocapacitance as a negative electrode, the prototype Na-ion full cell consisting of an alluaudite Na2Fe2(SO4)3 positive electrode and an MXene Ti2C negative electrode operates at a relatively high voltage of 2.4 V and delivers 90 and 40 mAh g−1 at 1.0 and 5.0 A g−1 (based on the weight of the negative electrode), respectively, which are not attainable by conventional electrochemical energy storage systems.
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              Advances and Challenges in Metal Sulfides/Selenides for Next-Generation Rechargeable Sodium-Ion Batteries

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                Author and article information

                Contributors
                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                November 20 2018
                2018
                : 6
                : 45
                : 22966-22975
                Affiliations
                [1 ]National & Local United Engineering Laboratory for Power Batteries
                [2 ]Faculty of Chemistry
                [3 ]Northeast Normal University
                [4 ]Changchun
                [5 ]P. R. China
                [6 ]School of Chemistry and Chemical Engineering
                [7 ]Guangzhou University
                [8 ]Guangzhou 510006
                [9 ]China
                [10 ]Collaborative Innovation Center of Advanced Energy Materials
                [11 ]School of Materials and Energy
                [12 ]Guangdong University of Technology
                Article
                10.1039/C8TA09264H
                407aae41-7080-4a61-9e05-f1f03a3c696f
                © 2018

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

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