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      Atomic-layer-deposited ultrathin Co9S8 on carbon nanotubes: an efficient bifunctional electrocatalyst for oxygen evolution/reduction reactions and rechargeable Zn–air batteries

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          Abstract

          ALD-synthesized Co 9S 8/CNT shows superior bifunctional electrocatalytic performance toward OER and ORR, and therefore it is an excellent oxygen electrocatalyst for rechargeable Zn–air batteries.

          Abstract

          The oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) are the key processes in many renewable energy conversion systems, and the development of high-performance non-precious bifunctional OER/ORR electrocatalysts is of crucial importance for various energy conversion devices, such as rechargeable metal–air batteries and regenerative fuel cells. Herein, we report a novel efficient bifunctional OER/ORR catalyst of Co 9S 8/CNT, which is synthesized using an advanced technique of atomic layer deposition (ALD) for conformally coating a uniform thin layer of Co 9S 8 on a high-surface-area carbon-nanotube (CNT) network scaffold. The ALD-synthesized Co 9S 8/CNT catalyst displays remarkable electrocatalytic performance with excellent catalytic activity and stability toward both the OER and ORR, and is further demonstrated to be a superior bifunctional oxygen catalyst for high-performance rechargeable Zn–air batteries. The fabricated aqueous rechargeable Zn–air batteries are able to deliver a remarkably high power density with superior long-term cycling stability, and the fabricated solid-state rechargeable Zn–air batteries are able to display very good flexibility and stability upon bending. Therefore, we believe that the ALD-synthesized bifunctional Co 9S 8/CNT electrocatalyst will have broad and promising applications for renewable energy conversion devices.

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          Most cited references42

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          What Are Batteries, Fuel Cells, and Supercapacitors?

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            Atomic layer deposition: an overview.

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              Water photolysis at 12.3% efficiency via perovskite photovoltaics and Earth-abundant catalysts.

              Although sunlight-driven water splitting is a promising route to sustainable hydrogen fuel production, widespread implementation is hampered by the expense of the necessary photovoltaic and photoelectrochemical apparatus. Here, we describe a highly efficient and low-cost water-splitting cell combining a state-of-the-art solution-processed perovskite tandem solar cell and a bifunctional Earth-abundant catalyst. The catalyst electrode, a NiFe layered double hydroxide, exhibits high activity toward both the oxygen and hydrogen evolution reactions in alkaline electrolyte. The combination of the two yields a water-splitting photocurrent density of around 10 milliamperes per square centimeter, corresponding to a solar-to-hydrogen efficiency of 12.3%. Currently, the perovskite instability limits the cell lifetime.
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                Author and article information

                Journal
                JMCAET
                J. Mater. Chem. A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2017
                2017
                : 5
                : 40
                : 21353-21361
                Affiliations
                [1 ]School of Advanced Materials
                [2 ]Shenzhen Graduate School
                [3 ]Peking University
                [4 ]Shenzhen 518055
                [5 ]China
                Article
                10.1039/C7TA06243E
                ee098e3f-727f-48e9-b419-83fb530c6bed
                © 2017
                History

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