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      Fabricating multifunctional nanoparticle membranes by a fast layer-by-layer Langmuir–Blodgett process: application in lithium–sulfur batteries

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          Abstract

          This article reports two new Langmuir–Blodgett techniques designed to create ordered, multifunctional nanoparticle films.

          Abstract

          The Langmuir–Blodgett technique is a powerful and widely used method for preparing coatings of amphiphilic molecules at air/water interfaces with thickness control down to a single molecule. Here, we report two new LB techniques designed to create ordered, multifunctional nanoparticle films. The methods utilize Marangoni stresses produced by surfactants at a fluid/solid/gas interface and self-assembly of nanoparticles to facilitate rapid creation of ultrathin films of carbon, metal-oxide nanoparticles, polymers, and combinations of these materials on any non-reactive support in a layer-by-layer configuration. Using polyolefin separators in lithium sulfur electrochemical cells as an example, we illustrate how the method can be used to create structured membranes for regulating mass and charge transport. We further show that a layered MWCNT/SiO 2/MWCNT nanomaterial created in a clip-like configuration, with gravimetric areal coverage of ∼130 μg cm −2 and a thickness of ∼3 μm, efficiently intercept and reutilize dissolved lithium polysulfides for improving electrochemical performances of lithium sulfur batteries.

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          Most cited references49

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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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              Graphene-wrapped sulfur particles as a rechargeable lithium-sulfur battery cathode material with high capacity and cycling stability.

              We report the synthesis of a graphene-sulfur composite material by wrapping poly(ethylene glycol) (PEG) coated submicrometer sulfur particles with mildly oxidized graphene oxide sheets decorated by carbon black nanoparticles. The PEG and graphene coating layers are important to accommodating volume expansion of the coated sulfur particles during discharge, trapping soluble polysulfide intermediates, and rendering the sulfur particles electrically conducting. The resulting graphene-sulfur composite showed high and stable specific capacities up to ∼600 mAh/g over more than 100 cycles, representing a promising cathode material for rechargeable lithium batteries with high energy density.
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                Author and article information

                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2016
                2016
                : 4
                : 38
                : 14709-14719
                Affiliations
                [1 ]Department of Chemical and Biomoleular Engineering
                [2 ]Cornell University
                [3 ]Ithaca
                [4 ]USA
                [5 ]Center for Energy Convergence
                [6 ]Department of Materials Science & Engineering
                [7 ]NOHMs Technologies
                [8 ]Rochester
                Article
                10.1039/C6TA06018H
                be0dfc05-f91c-4667-a09b-ee1b3db49745
                © 2016
                History

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