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      Achieving long cycle life for all-solid-state rechargeable Li-I 2 battery by a confined dissolution strategy

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          Abstract

          Rechargeable Li-I 2 battery has attracted considerable attentions due to its high theoretical capacity, low cost and environment-friendliness. Dissolution of polyiodides are required to facilitate the electrochemical redox reaction of the I 2 cathode, which would lead to a harmful shuttle effect. All-solid-state Li-I 2 battery totally avoids the polyiodides shuttle in a liquid system. However, the insoluble discharge product at the conventional solid interface results in a sluggish electrochemical reaction and poor rechargeability. In this work, by adopting a well-designed hybrid electrolyte composed of a dispersion layer and a blocking layer, we successfully promote a new polyiodides chemistry and localize the polyiodides dissolution within a limited space near the cathode. Owing to this confined dissolution strategy, a rechargeable and highly reversible all-solid-state Li-I 2 battery is demonstrated and shows a long-term life of over 9000 cycles at 1C with a capacity retention of 84.1%.

          Abstract

          Rechargeable Li-I 2 battery system is interesting due to high theoretical capacities but the insoluble discharge product at the conventional solid interface leads to poor performances. Here, by using a confined dissolution strategy the authors demonstrate a rechargeable all-solid-state Li-I 2 battery with extended cycle life.

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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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            Ordered mesoporous alpha-MoO3 with iso-oriented nanocrystalline walls for thin-film pseudocapacitors.

            Capacitive energy storage is distinguished from other types of electrochemical energy storage by short charging times and the ability to deliver significantly more power than batteries. A key limitation to this technology is its low energy density and for this reason there is considerable interest in exploring pseudocapacitive materials where faradaic mechanisms offer increased levels of energy storage. Here we show that the capacitive charge-storage properties of mesoporous films of iso-oriented alpha-MoO(3) are superior to those of either mesoporous amorphous material or non-porous crystalline MoO(3). Whereas both crystalline and amorphous mesoporous materials show redox pseudocapacitance, the iso-oriented layered crystalline domains enable lithium ions to be inserted into the van der Waals gaps of the alpha-MoO(3). We propose that this extra contribution arises from an intercalation pseudocapacitance, which occurs on the same timescale as redox pseudocapacitance. The result is increased charge-storage capacity without compromising charge/discharge kinetics in mesoporous crystalline MoO(3).
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              Challenges facing lithium batteries and electrical double-layer capacitors.

              Energy-storage technologies, including electrical double-layer capacitors and rechargeable batteries, have attracted significant attention for applications in portable electronic devices, electric vehicles, bulk electricity storage at power stations, and "load leveling" of renewable sources, such as solar energy and wind power. Transforming lithium batteries and electric double-layer capacitors requires a step change in the science underpinning these devices, including the discovery of new materials, new electrochemistry, and an increased understanding of the processes on which the devices depend. The Review will consider some of the current scientific issues underpinning lithium batteries and electric double-layer capacitors.
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                Author and article information

                Contributors
                pinghe@nju.edu.cn
                hszhou@nju.edu.cn
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                10 January 2022
                10 January 2022
                2022
                : 13
                : 125
                Affiliations
                [1 ]GRID grid.41156.37, ISNI 0000 0001 2314 964X, Center of Energy Storage Materials & Technology, College of Engineering and Applied Sciences, Jiangsu Key Laboratory of Artificial Functional Materials, National Laboratory of Solid State Microstructures and Collaborative Innovation Center of Advanced Microstructures, , Nanjing University, ; Nanjing, 210093 P. R. China
                [2 ]GRID grid.410752.5, Dalian National Lab for Clean Energy, State Key Laboratory of Catalysis, Dalian Institute of Chemical physics, Chinese Academy of Sciences, ; Dalian, 116023 P. R. China
                Author information
                http://orcid.org/0000-0001-8216-863X
                http://orcid.org/0000-0002-1498-8203
                Article
                27728
                10.1038/s41467-021-27728-0
                8748797
                35013285
                26c6a340-7fc3-4441-92f3-cab7e166d9d6
                © The Author(s) 2022

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 27 September 2021
                : 2 December 2021
                Funding
                Funded by: National Natural Science Foundation of China (21922508, 22179059)
                Funded by: National Natural Science Foundation of China (21922508, 21633003, and U1801251), the Natural Science Foundation of Jiangsu Province of China (BK20190009), and Key R&D Project funded by Department of Science and Technology of Jiangsu Province (BE2020003).
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