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      N,S-Doped hollow carbon nanosheet-encapsulated Co 9S 8 nanoparticles as a highly efficient bifunctional electrocatalyst for rechargeable zinc–air batteries

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          Abstract

          A “MOF on MOF” strategy was proposed for the synthesis of N,S co-doped hollow carbon nanosheets embedded with Co 9S 8 nanoparticles. The resulting material is a highly efficient bifunctional air electrode for Zn–air batteries.

          Abstract

          The development of bifunctional electrocatalysts based on non-noble metals for the oxygen reduction/evolution reactions (ORR/OER) that have rationally designed structures and inexpensive components is of practical significance for the commercialization of rechargeable zinc–air batteries. Here, we report the rational synthesis of Co 9S 8 nanoparticles embedded in N,S co-doped hollow carbon nanosheets (Co 9S 8/NSC) as highly efficient oxygen electrocatalysts. The catalyst is formed when a Co-based zeolitic imidazolate framework (ZIF-67), grown on a Zn-based ZIF (ZIF-8) template, is partially vulcanized following thioacetamide (TAA) and thermal treatment. The resulting catalyst, Co 9S 8/NSC-3, shows satisfactory bifunctional electrocatalytic activity in 0.1 M KOH, in which the half-wave potential ( E 1/2) for the ORR is 0.82 V and the overpotential for the OER at 10 mA cm −2 is just 350 mV. Furthermore, as the air electrode material in a practical demonstration of a rechargeable liquid zinc–air battery, Co 9S 8/NSC-3 exhibits promising battery performance with a high specific capacity of 804 mA h g −1 and a pleasing charge/discharge cyclability of over 140 h at 10 mA cm −2. The satisfactory activity of Co 9S 8/NSC-3 can be attributed to the synergistic effect of the Co 9S 8 nanoparticles with the N,S-doped hollow carbon nanosheet structure, resulting in an effective electrochemically active surface with fully exposed active sites that give fast catalytic kinetics.

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          A two-dimensional zeolitic imidazolate framework with a cushion-shaped cavity for CO2 adsorption

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            Alveolate porous carbon aerogels supported Co9S8 derived from a novel hybrid hydrogel for bifunctional oxygen electrocatalysis

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              Is Open Access

              Nitrogen‐Doped Cobalt Pyrite Yolk–Shell Hollow Spheres for Long‐Life Rechargeable Zn–Air Batteries

              Abstract Limited by the sluggish four‐electron transfer process, designing high‐performance nonprecious electrocatalysts for the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) is urgently desired for efficient rechargeable Zn–air batteries (ZABs). Herein, the successful synthesis of porous nitrogen‐doped cobalt pyrite yolk–shell nanospheres (N‐CoS2 YSSs) is reported. Benefiting from the abundant porosity of the porous yolk–shell structure and unique electronic properties by nitrogen doping, the as‐prepared N‐CoS2 YSSs possess more exposed active surface, thus giving rise to superior activity for reversible oxygen electrocatalysis and outstanding cycling stability (more than 165 h at 10 mA cm−2) in ZABs, exceeding the commercial Pt/C and RuO2 hybrid catalysts. Moreover, the assembled ZABs, delivering a specific capacity of 640 mAh gZn −1, can be used for practical devices. This work provides a novel tactic to engineer sulfides as high efficiency and promising bifunctional oxygen electrocatalysts for advanced metal–air batteries.
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                Author and article information

                Contributors
                Journal
                ICHBD9
                Dalton Transactions
                Dalton Trans.
                Royal Society of Chemistry (RSC)
                1477-9226
                1477-9234
                August 23 2022
                2022
                : 51
                : 33
                : 12630-12640
                Affiliations
                [1 ]Key Laboratory for Green Processing of Chemical Engineering of Xinjiang Bingtuan, School of Chemistry and Chemical Engineering, Shihezi University, Shihezi 832003, China
                [2 ]Bingtuan Industrial Technology Research Institute, Shihezi University, Shihezi 832003, PR China
                Article
                10.1039/D2DT01650H
                28158905-d7ac-423f-8536-fe5ff31da0fd
                © 2022

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

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