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      The advent of manganese-substituted sodium vanadium phosphate-based cathodes for sodium-ion batteries and their current progress: a focused review

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          Abstract

          This review summarizes the current status and advancements made in research on manganese-substituted sodium vanadium phosphate-based cathodes, with a focus on their structural evolution, composite formation, morphological tailoring, and fabrication protocols.

          Abstract

          Na 3V 2(PO 4) 3 (NVP) is a member of the sodium superionic conductor (NASICON) family and has been extensively studied as a cathode material for sodium-ion batteries (SIBs) for more than three decades due to its stable voltage platform, high capacity, and stable cycle life. However, the presence of toxic and expensive V elements restricts the utilization of NVP-based SIBs. To overcome this, energy researchers have employed a cation swapping approach, which resulted in new NASICON-type manganese-substituted sodium vanadium phosphate (MSVP) cathodes for SIBs. Na 4MnV(PO 4) 3 (NMVP) is among the new generation of high-energy, risk-free NASICON-type MSVP cathodes, and its use for SIBs was documented in 2016. There has been strong acceptance of MSVP-based cathodes among materials researchers due to their cost and economic advantages. In a short period, considerable work has been done to increase the commercial potential of MSVP-based cathodes for SIBs. This review summarizes the pioneering developments made with MSVP-based cathodes, with a special focus on their structural and electrochemical evolution. This review can serve as a reference for future energy researchers fabricating highly efficient and safer NASICON cathodes not only for SIBs but also for other energy storage applications.

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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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            Na-ion batteries, recent advances and present challenges to become low cost energy storage systems

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              The emerging chemistry of sodium ion batteries for electrochemical energy storage.

              Energy storage technology has received significant attention for portable electronic devices, electric vehicle propulsion, bulk electricity storage at power stations, and load leveling of renewable sources, such as solar energy and wind power. Lithium ion batteries have dominated most of the first two applications. For the last two cases, however, moving beyond lithium batteries to the element that lies below-sodium-is a sensible step that offers sustainability and cost-effectiveness. This requires an evaluation of the science underpinning these devices, including the discovery of new materials, their electrochemistry, and an increased understanding of ion mobility based on computational methods. The Review considers some of the current scientific issues underpinning sodium ion batteries.
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                Author and article information

                Contributors
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                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                January 18 2022
                2022
                : 10
                : 3
                : 1022-1046
                Affiliations
                [1 ]Department of Materials Science and Engineering, Chonnam National University, 300 Yongbong-dong, Bukgu, Gwangju 500-757, South Korea
                [2 ]Graduate School of Science and Technology, Shizuoka University, 3-5-1 Johoku, Naka-Ku, Hamamatsu, Shizuoka 432-8011, Japan
                [3 ]Department of Prosthodontics, Dental Science Research Institute, Chonnam National University, Gwangju 61186, Republic of Korea
                [4 ]Institute for Superconducting & Electronic Materials (ISEM), Australian Institute of Innovative Materials (AIIM), University of Wollongong, North Wollongong, New South Wales 2500, Australia
                [5 ]Institute of Energy Engineering, National Central University, Taoyuan, Taiwan
                [6 ]Department of Materials Science and Engineering, National Yang Ming Chiao Tung University, 1001 University Road, Hsinchu 30010, Taiwan
                Article
                10.1039/D1TA09040B
                8b47fced-bcae-49d9-8d84-4367effbd381
                © 2022

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