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      Dual-defect surface engineering of bimetallic sulfide nanotubes towards flexible asymmetric solid-state supercapacitors

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          Abstract

          Nickel cobalt sulfide (NiCo 2S 4) is a promising battery-type material for electrochemical energy storage.

          Abstract

          Nickel cobalt sulfide (NiCo 2S 4) is a promising battery-type material for electrochemical energy storage. However, the slow charge transfer kinetics and ion diffusion as well as the deficiency of electrochemically active sites hinder the practical application of NiCo 2S 4. Defect engineering at the atomic level is adopted to improve charge storage kinetics, through the incorporation of P dopants and S vacancies onto the surface of a NiCo 2S 4 nanotube (P-NiCo 2S 4−x). Experimental results reveal that the introduction of these defects effectively increases the electrical conductivity and induces the formation of low oxidation state Ni and Co species, accelerating the charge transfer kinetics and enabling rich faradaic redox chemistry. Moreover, the partial substitution of S sites with P improves the covalent nature of P-NiCo 2S 4−x, facilitating surface electroactivity. The as-prepared P-NiCo 2S 4−x shows a high specific capacity of 1806.4 C g −1 at 1 A g −1 and a 95.5% capacity retention after 5000 cycles at a high current density of 30 A g −1. Flexible solid-state asymmetric supercapacitors with P-NiCo 2S 4−x and activated carbon as the positive and negative electrodes, respectively, deliver a high energy density of 68.2 W h kg −1 at 800 W kg −1 and excellent cycling stability. Moreover, the device exhibits good mechanical flexibility with negligible capacitance decay under different bending states.

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          Filling the oxygen vacancies in Co3O4 with phosphorus: an ultra-efficient electrocatalyst for overall water splitting

          It is of essential importance to design an electrocatalyst with excellent performance for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in water splitting. It is of essential importance to design an electrocatalyst with excellent performance for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in water splitting. Co 3 O 4 has been developed as a highly efficient OER electrocatalyst, but it has almost no activity for HER. In a previous study, it has been demonstrated that the formation of oxygen vacancies (V O ) in Co 3 O 4 can significantly enhance the OER activity. However, the stability of V O needs to be considered, especially under the highly oxidizing conditions of the OER process. It is a big challenge to stabilize the V O in Co 3 O 4 while reserving the excellent activity. Filling the oxygen vacancies with heteroatoms in the V O -rich Co 3 O 4 may be a smart strategy to stabilize the V O by compensating the coordination numbers and obtain an even surprising activity due to the modification of electronic properties by heteroatoms. Herein, we successfully transformed V O -rich Co 3 O 4 into an HER-OER electrocatalyst by filling the in situ formed V O in Co 3 O 4 with phosphorus (P-Co 3 O 4 ) by treating Co 3 O 4 with Ar plasma in the presence of a P precursor. The relatively lower coordination numbers in V O -Co 3 O 4 than those in pristine Co 3 O 4 were evidenced by X-ray adsorption spectroscopy, indicating that the oxygen vacancies were created after Ar plasma etching. On the other hand, the relatively higher coordination numbers in P-Co 3 O 4 than those in V O -Co 3 O 4 and nearly same coordination number as that in pristine Co 3 O 4 strongly suggest the efficient filling of P in the vacancies by treatment with Ar plasma in the presence of a P precursor. The Co–O bonds in Co 3 O 4 consist of octahedral Co 3+ (O h )–O and tetrahedral Co 2+ (T d )–O (Oh, octahedral coordination by six oxygen atoms and T d , tetrahedral coordination by four oxygen atoms). More Co 3+ (O h )–O are broken when oxygen vacancies are formed in V O -Co 3 O 4 , and more electrons enter the octahedral Co 3d orbital than those entering the tetrahedral Co 3d orbital. Then, with the filling of P in the vacancy site, electrons are transferred out of the Co 3d states, and more Co 2+ (T d ) than Co 3+ (O h ) are left in P-Co 3 O 4 . These results suggest that the favored catalytic ability of P-Co 3 O 4 is dominated by the Co 2+ (T d ) site. P-Co 3 O 4 shows superior electrocatalytic activities for HER and OER (among the best non-precious metal catalysts). Owing to its superior efficiency, P-Co 3 O 4 can directly catalyze overall water splitting with excellent performance. The theoretical calculations illustrated that the improved electrical conductivity and intermediate binding by P-filling contributed significantly to the enhanced HER and OER activity of Co 3 O 4 .
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            Formation of nickel cobalt sulfide ball-in-ball hollow spheres with enhanced electrochemical pseudocapacitive properties.

            While the synthesis of hollow structures of transition metal oxides is well established, it is extremely challenging to fabricate complex hollow structures for mixed transition metal sulfides. Here we report an anion exchange method to synthesize a complex ternary metal sulfides hollow structure, namely nickel cobalt sulfide ball-in-ball hollow spheres. Uniform nickel cobalt glycerate solid spheres are first synthesized as the precursor and subsequently chemically transformed into nickel cobalt sulfide ball-in-ball hollow spheres. When used as electrode materials for electrochemical capacitors, these nickel cobalt sulfide hollow spheres deliver a specific capacitance of 1,036 F g(-1) at a current density of 1.0 A g(-1). An asymmetric supercapacitor based on these ball-in-ball structures shows long-term cycling performance with a high energy density of 42.3 Wh kg(-1) at a power density of 476 W kg(-1), suggesting their potential application in high-performance electrochemical capacitors.
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              Defect Engineering of Oxygen‐Deficient Manganese Oxide to Achieve High‐Performing Aqueous Zinc Ion Battery

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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 24 2020
                2020
                : 8
                : 45
                : 24053-24064
                Affiliations
                [1 ]Shanghai Key Laboratory of Multidimensional Information Processing
                [2 ]East China Normal University
                [3 ]200241 Shanghai
                [4 ]China
                [5 ]Shanghai Institute of Intelligent Electronics Systems
                [6 ]School of Mechanical Engineering
                [7 ]Yonsei University
                [8 ]Seoul 120-749
                [9 ]South Korea
                [10 ]Fudan University
                [11 ]Shanghai 200433
                [12 ]School of Physics and Electronic Science
                Article
                10.1039/D0TA08979F
                c24793cf-c61b-4232-844c-181d4c591ed8
                © 2020

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

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