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      SnS 2/TiO 2 nanohybrids chemically bonded on nitrogen-doped graphene for lithium–sulfur batteries: synergy of vacancy defects and heterostructures

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          Abstract

          Few-layer, sulfur-deficient SnS 2 sheets and TiO 2 nanocrystals grown on N-doped graphene serve as an efficient polysulfide mediator.

          Abstract

          Despite their high-energy density, low cost and environmental friendliness, the commercial application of lithium–sulfur batteries (LSBs) has been plagued by their severe capacity decay during long-term cycling caused by polysulfide shuttling. Herein, we demonstrate a synergetic vacancy and heterostructure engineering strategy using a nitrogen-doped graphene/SnS 2/TiO 2 (denoted as NG/SnS 2/TiO 2) nanocomposite to enhance the electrochemical performance of LSBs. It is noted that plentiful sulfur vacancy (V s) defects and nanosized heterojunctions are created on the NG/SnS 2/TiO 2 composite as proved using electron paramagnetic resonance, transmission electron microscopy and X-ray photoelectron spectroscopy, which can serve as strong adsorption and activation sites for polar polysulfide intermediates, prevent their dissolution/shuttling, and accelerate their redox reaction. The novel NG/SnS 2/TiO 2–S cathode delivers a high initial capacity of 1064 mA h g −1 at 0.5 C and a high capacity retention rate of 68% after 500 cycles at 0.5 C.

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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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            Rechargeable lithium-sulfur batteries.

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              Designing high-energy lithium-sulfur batteries.

              Due to their high energy density and low material cost, lithium-sulfur batteries represent a promising energy storage system for a multitude of emerging applications, ranging from stationary grid storage to mobile electric vehicles. This review aims to summarize major developments in the field of lithium-sulfur batteries, starting from an overview of their electrochemistry, technical challenges and potential solutions, along with some theoretical calculation results to advance our understanding of the material interactions involved. Next, we examine the most extensively-used design strategy: encapsulation of sulfur cathodes in carbon host materials. Other emerging host materials, such as polymeric and inorganic materials, are discussed as well. This is followed by a survey of novel battery configurations, including the use of lithium sulfide cathodes and lithium polysulfide catholytes, as well as recent burgeoning efforts in the modification of separators and protection of lithium metal anodes. Finally, we conclude with an outlook section to offer some insight on the future directions and prospects of lithium-sulfur batteries.
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                Author and article information

                Contributors
                Journal
                NANOHL
                Nanoscale
                Nanoscale
                Royal Society of Chemistry (RSC)
                2040-3364
                2040-3372
                2018
                2018
                : 10
                : 33
                : 15505-15512
                Affiliations
                [1 ]State Key Laboratory of Advanced Technology for Materials Synthesis and Processing
                [2 ]Wuhan University of Technology
                [3 ]Wuhan
                [4 ]China
                [5 ]Hubei Key Laboratory of Advanced Technology for Automotive Components & Hubei Collaborative Innovation Center for Automotive Components Technology
                [6 ]Wuhan 430070
                [7 ]Department of Materials Science and Engineering
                [8 ]Southern University of Science and Technology of China
                [9 ]Shenzhen
                [10 ]Department of Chemistry and Center Of Super-Diamond and Advanced Films (COSDAF)
                [11 ]City University of Hong Kong
                [12 ]HKSAR
                [13 ]Harbin Institute of Technology
                [14 ]Harbin
                [15 ]Laboratory of Inorganic Materials Chemistry (CMI)
                Article
                10.1039/C8NR04661A
                91c3483f-e93d-4bb9-9540-306d4c49a6f1
                © 2018

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

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