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      Recent Progress in Liquid Electrolyte-Based Li–S Batteries: Shuttle Problem and Solutions

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          Li-O2 and Li-S batteries with high energy storage.

          Li-ion batteries have transformed portable electronics and will play a key role in the electrification of transport. However, the highest energy storage possible for Li-ion batteries is insufficient for the long-term needs of society, for example, extended-range electric vehicles. To go beyond the horizon of Li-ion batteries is a formidable challenge; there are few options. Here we consider two: Li-air (O(2)) and Li-S. The energy that can be stored in Li-air (based on aqueous or non-aqueous electrolytes) and Li-S cells is compared with Li-ion; the operation of the cells is discussed, as are the significant hurdles that will have to be overcome if such batteries are to succeed. Fundamental scientific advances in understanding the reactions occurring in the cells as well as new materials are key to overcoming these obstacles. The potential benefits of Li-air and Li-S justify the continued research effort that will be needed.
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            Lithium metal anodes for rechargeable batteries

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              A highly ordered nanostructured carbon-sulphur cathode for lithium-sulphur batteries.

              The Li-S battery has been under intense scrutiny for over two decades, as it offers the possibility of high gravimetric capacities and theoretical energy densities ranging up to a factor of five beyond conventional Li-ion systems. Herein, we report the feasibility to approach such capacities by creating highly ordered interwoven composites. The conductive mesoporous carbon framework precisely constrains sulphur nanofiller growth within its channels and generates essential electrical contact to the insulating sulphur. The structure provides access to Li+ ingress/egress for reactivity with the sulphur, and we speculate that the kinetic inhibition to diffusion within the framework and the sorption properties of the carbon aid in trapping the polysulphides formed during redox. Polymer modification of the carbon surface further provides a chemical gradient that retards diffusion of these large anions out of the electrode, thus facilitating more complete reaction. Reversible capacities up to 1,320 mA h g(-1) are attained. The assembly process is simple and broadly applicable, conceptually providing new opportunities for materials scientists for tailored design that can be extended to many different electrode materials.
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                Author and article information

                Journal
                Electrochemical Energy Reviews
                Electrochem. Energ. Rev.
                Springer Science and Business Media LLC
                2520-8489
                2520-8136
                December 2018
                November 7 2018
                December 2018
                : 1
                : 4
                : 599-624
                Article
                10.1007/s41918-018-0021-0
                b93c53d5-e500-4fb9-b50e-8a87b578b3d5
                © 2018

                http://www.springer.com/tdm

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