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      Template-synthesis of a poly(ionic liquid)-derived Fe 1− x S/nitrogen-doped porous carbon membrane and its electrode application in lithium–sulfur batteries†

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      Materials Advances
      RSC

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          Abstract

          This study deals with the facile synthesis of Fe 1− x S nanoparticle-containing nitrogen-doped porous carbon membranes (denoted as Fe 1− x S/N-PCMs) via vacuum carbonization of hybrid porous poly(ionic liquid) (PIL) membranes, and their successful use as a sulfur host material to mitigate the shuttle effect in lithium–sulfur (Li–S) batteries. The hybrid porous PIL membranes as the sacrificial template were prepared via ionic crosslinking of a cationic PIL with base-neutralized 1,1′-ferrocenedicarboxylic acid, so that the iron source was molecularly incorporated into the template. The carbonization process was investigated in detail at different temperatures, and the chemical and porous structures of the carbon products were comprehensively analyzed. The Fe 1− x S/N-PCMs prepared at 900 °C have a multimodal pore size distribution with a satisfactorily high surface area and well-dispersed iron sulfide nanoparticles to physically and chemically confine the LiPSs. The sulfur/Fe 1− x S/N-PCM composites were then tested as electrodes in Li–S batteries, showing much improved capacity, rate performance and cycle stability, in comparison to iron sulfide-free, nitrogen-doped porous carbon membranes.

          Abstract

          We designed a novel Fe 1− x S/N-doped porous carbon membrane and applied it as a sulfur host material to moderate the shuttle effect in lithium–sulfur batteries.

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          In situ click chemistry generation of cyclooxygenase-2 inhibitors

          Cyclooxygenase-2 isozyme is a promising anti-inflammatory drug target, and overexpression of this enzyme is also associated with several cancers and neurodegenerative diseases. The amino-acid sequence and structural similarity between inducible cyclooxygenase-2 and housekeeping cyclooxygenase-1 isoforms present a significant challenge to design selective cyclooxygenase-2 inhibitors. Herein, we describe the use of the cyclooxygenase-2 active site as a reaction vessel for the in situ generation of its own highly specific inhibitors. Multi-component competitive-binding studies confirmed that the cyclooxygenase-2 isozyme can judiciously select most appropriate chemical building blocks from a pool of chemicals to build its own highly potent inhibitor. Herein, with the use of kinetic target-guided synthesis, also termed as in situ click chemistry, we describe the discovery of two highly potent and selective cyclooxygenase-2 isozyme inhibitors. The in vivo anti-inflammatory activity of these two novel small molecules is significantly higher than that of widely used selective cyclooxygenase-2 inhibitors.
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            More Reliable Lithium-Sulfur Batteries: Status, Solutions and Prospects

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              Highly nitrogen doped carbon nanofibers with superior rate capability and cyclability for potassium ion batteries

              Potassium-ion batteries are a promising alternative to lithium-ion batteries. However, it is challenging to achieve fast charging/discharging and long cycle life with the current electrode materials because of the sluggish potassiation kinetics. Here we report a soft carbon anode, namely highly nitrogen-doped carbon nanofibers, with superior rate capability and cyclability. The anode delivers reversible capacities of 248 mAh g–1 at 25 mA g–1 and 101 mAh g–1 at 20 A g–1, and retains 146 mAh g–1 at 2 A g–1 after 4000 cycles. Surface-dominated K-storage is verified by quantitative kinetics analysis and theoretical investigation. A full cell coupling the anode and Prussian blue cathode delivers a reversible capacity of 195 mAh g–1 at 0.2 A g–1. Considering the cost-effectiveness and material sustainability, our work may shed some light on searching for K-storage materials with high performance.
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                Author and article information

                Journal
                Mater Adv
                Mater Adv
                MA
                MAADC9
                Materials Advances
                RSC
                2633-5409
                25 June 2021
                2 August 2021
                25 June 2021
                : 2
                : 15
                : 5203-5212
                Affiliations
                [a] Department of Materials and Environmental Chemistry, Stockholm University Stockholm 10691 Sweden jiayin.yuan@ 123456mmk.su.se
                [b] Department for Electrochemical Energy Storage, Helmholtz-Zentrum Berlin für Materialien und Energie Hahn-Meitner Platz 1 Berlin 14109 Germany yan.lu@ 123456helmholtz-berlin.de
                [c] Institute of Chemistry, University of Potsdam 14476 Potsdam Germany
                Author information
                https://orcid.org/0000-0003-3055-0073
                https://orcid.org/0000-0003-1016-5135
                Article
                d1ma00441g
                10.1039/d1ma00441g
                8328078
                34382003
                a1b3d034-bdc6-4161-8273-18332703b9c4
                This journal is © The Royal Society of Chemistry
                History
                : 17 May 2021
                : 18 June 2021
                Page count
                Pages: 10
                Funding
                Funded by: European Research Council, doi 10.13039/501100000781;
                Award ID: NAPOLI-639720
                Funded by: Svenska Forskningsrådet Formas, doi 10.13039/501100001862;
                Award ID: 2018-05351
                Funded by: Knut och Alice Wallenbergs Stiftelse, doi 10.13039/501100004063;
                Award ID: KAW 2017.0166
                Categories
                Chemistry
                Custom metadata
                Paginated Article

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