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      A super high performance asymmetric supercapacitor based on Co3S4/NiS nanoplates electrodes

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          Abstract

          In this paper, we successfully designed and synthesized Co 3S 4/NiS nanoplates by both ion-exchange action and Ostwald ripening reactions during the sulfurization process.

          Abstract

          In this paper, we successfully designed and synthesized Co 3S 4/NiS nanoplates by both ion-exchange action and Ostwald ripening reactions during the sulfurization process. As asymmetric supercapacitor electrode material, Co 3S 4/NiS exhibited an ultra-high specific capacitance of 1810 mF cm −2 at a current density of 4 mA cm −2, 12 times larger than the pristine Co 3O 4 electrode, as well as good rate capability and excellent cycling stability. The asymmetric supercapacitor based on Co 3S 4/NiS can work steadily at a voltage of 1.6 V and deliver a high energy density of 6.44 W h m −2 at a high power density of 32 W m −2. Moreover, we applied this device to successfully light light-emitting-diodes in a simulated solar illumination system. The perfect integration of two types of capacitor materials into Co 3S 4/NiS satisfies the requirements of high energy density supercapacitor. Co 3S 4/NiS nanoplates may have practical applications in the field of energy storage.

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          Synthesis of nitrogen-doped porous carbon nanofibers as an efficient electrode material for supercapacitors.

          Supercapacitors (also known as ultracapacitors) are considered to be the most promising approach to meet the pressing requirements of energy storage. Supercapacitive electrode materials, which are closely related to the high-efficiency storage of energy, have provoked more interest. Herein, we present a high-capacity supercapacitor material based on the nitrogen-doped porous carbon nanofibers synthesized by carbonization of macroscopic-scale carbonaceous nanofibers (CNFs) coated with polypyrrole (CNFs@polypyrrole) at an appropriate temperature. The composite nanofibers exhibit a reversible specific capacitance of 202.0 F g(-1) at the current density of 1.0 A g(-1) in 6.0 mol L(-1) aqueous KOH electrolyte, meanwhile maintaining a high-class capacitance retention capability and a maximum power density of 89.57 kW kg(-1). This kind of nitrogen-doped carbon nanofiber represents an alternative promising candidate for an efficient electrode material for supercapacitors.
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            Boosted Charge Transfer in SnS/SnO2 Heterostructures: Toward High Rate Capability for Sodium-Ion Batteries

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              Edge-oriented MoS2 nanoporous films as flexible electrodes for hydrogen evolution reactions and supercapacitor devices.

              A simple method to fabricate edge-oriented MoS2 films with sponge-like morphologies is demonstrated. They are directly fabricated through the reaction of sulfur vapor with anodically formed Mo oxide sponge-like films on flexible Mo substrates. The edge-oriented MoS2 film delivers excellent hydrogen evolution reaction (HER) activity with enhanced kinetics and long-term cycling stability. The material also has superior energy-storage performance when working as a flexible, all-solid-state supercapacitor device.
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                Author and article information

                Journal
                RSCACL
                RSC Advances
                RSC Adv.
                Royal Society of Chemistry (RSC)
                2046-2069
                2016
                2016
                : 6
                : 100
                : 97482-97490
                Affiliations
                [1 ]Anhui Key Laboratory of Molecule-Based Materials
                [2 ]The Key Laboratory of Functional Molecular Solids
                [3 ]Ministry of Education
                [4 ]College of Chemistry and Materials Science
                [5 ]Anhui Normal University
                [6 ]Shandong Provincial Cancer Hospital and Institute
                [7 ]Jinan 250117
                [8 ]China
                Article
                10.1039/C6RA18624F
                e0e679f2-e6a0-483e-b736-39448e88d651
                © 2016
                History

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