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      Three-dimensional hierarchically porous MoS 2 foam as high-rate and stable lithium-ion battery anode

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          Abstract

          Architected materials that actively respond to external stimuli hold tantalizing prospects for applications in energy storage, wearable electronics, and bioengineering. Molybdenum disulfide, an excellent two-dimensional building block, is a promising candidate for lithium-ion battery anode. However, the stacked and brittle two-dimensional layered structure limits its rate capability and electrochemical stability. Here we report the dewetting-induced manufacturing of two-dimensional molybdenum disulfide nanosheets into a three-dimensional foam with a structural hierarchy across seven orders of magnitude. Our molybdenum disulfide foam provides an interpenetrating network for efficient charge transport, rapid ion diffusion, and mechanically resilient and chemically stable support for electrochemical reactions. These features induce a pseudocapacitive energy storage mechanism involving molybdenum redox reactions, confirmed by in-situ X-ray absorption near edge structure. The extraordinary electrochemical performance of molybdenum disulfide foam outperforms most reported molybdenum disulfide-based Lithium-ion battery anodes and state-of-the-art materials. This work opens promising inroads for various applications where special properties arise from hierarchical architecture.

          Abstract

          The stacked and brittle 2D layered structure of molybdenum disulphide limits its practical application in lithium ion batteries. Here, authors report a dewetting-induced manufacture strategy to create the interpenetrating network and induce the pseudocapacity to improve the electrochemical performance.

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          The chemistry of two-dimensional layered transition metal dichalcogenide nanosheets.

          Ultrathin two-dimensional nanosheets of layered transition metal dichalcogenides (TMDs) are fundamentally and technologically intriguing. In contrast to the graphene sheet, they are chemically versatile. Mono- or few-layered TMDs - obtained either through exfoliation of bulk materials or bottom-up syntheses - are direct-gap semiconductors whose bandgap energy, as well as carrier type (n- or p-type), varies between compounds depending on their composition, structure and dimensionality. In this Review, we describe how the tunable electronic structure of TMDs makes them attractive for a variety of applications. They have been investigated as chemically active electrocatalysts for hydrogen evolution and hydrosulfurization, as well as electrically active materials in opto-electronics. Their morphologies and properties are also useful for energy storage applications such as electrodes for Li-ion batteries and supercapacitors.
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            Stretching and breaking of ultrathin MoS2.

            We report on measurements of the stiffness and breaking strength of monolayer MoS(2), a new semiconducting analogue of graphene. Single and bilayer MoS(2) is exfoliated from bulk and transferred to a substrate containing an array of microfabricated circular holes. The resulting suspended, free-standing membranes are deformed and eventually broken using an atomic force microscope. We find that the in-plane stiffness of monolayer MoS(2) is 180 ± 60 Nm(-1), corresponding to an effective Young's modulus of 270 ± 100 GPa, which is comparable to that of steel. Breaking occurs at an effective strain between 6 and 11% with the average breaking strength of 15 ± 3 Nm(-1) (23 GPa). The strength of strongest monolayer membranes is 11% of its Young's modulus, corresponding to the upper theoretical limit which indicates that the material can be highly crystalline and almost defect-free. Our results show that monolayer MoS(2) could be suitable for a variety of applications such as reinforcing elements in composites and for fabrication of flexible electronic devices.
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              Stable cycling of double-walled silicon nanotube battery anodes through solid-electrolyte interphase control.

              Although the performance of lithium ion-batteries continues to improve, their energy density and cycle life remain insufficient for applications in consumer electronics, transport and large-scale renewable energy storage. Silicon has a large charge storage capacity and this makes it an attractive anode material, but pulverization during cycling and an unstable solid-electrolyte interphase has limited the cycle life of silicon anodes to hundreds of cycles. Here, we show that anodes consisting of an active silicon nanotube surrounded by an ion-permeable silicon oxide shell can cycle over 6,000 times in half cells while retaining more than 85% of their initial capacity. The outer surface of the silicon nanotube is prevented from expansion by the oxide shell, and the expanding inner surface is not exposed to the electrolyte, resulting in a stable solid-electrolyte interphase. Batteries containing these double-walled silicon nanotube anodes exhibit charge capacities approximately eight times larger than conventional carbon anodes and charging rates of up to 20C (a rate of 1C corresponds to complete charge or discharge in one hour).
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                Author and article information

                Contributors
                hanyi.chen@mx.nthu.edu.tw
                vincent@g.ecc.u-tokyo.ac.jp
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                12 October 2022
                12 October 2022
                2022
                : 13
                : 6006
                Affiliations
                [1 ]GRID grid.45672.32, ISNI 0000 0001 1926 5090, Physical Science and Engineering Division, , King Abdullah University of Science and Technology, ; Thuwal, 23955-6900 Saudi Arabia
                [2 ]GRID grid.38348.34, ISNI 0000 0004 0532 0580, Department of Materials Science and Engineering, , National Tsing Hua University, ; Hsinchu, 300 Taiwan
                [3 ]GRID grid.184769.5, ISNI 0000 0001 2231 4551, Molecular Foundry, , Lawrence Berkeley National Lab, Berkeley, ; California, 94720 USA
                [4 ]GRID grid.116068.8, ISNI 0000 0001 2341 2786, Department of Electrical Engineering, , Massachusetts Institute of Technology, Cambridge, ; Massachusetts, 02139 USA
                [5 ]GRID grid.26999.3d, ISNI 0000 0001 2151 536X, Department of Chemical System Engineering, , School of Engineering, The University of Tokyo, ; Tokyo, 113-8656 Japan
                [6 ]GRID grid.454873.9, ISNI 0000 0000 9113 8494, Saudi Aramco, , Chemicals R&D Lab at KAUST, Research and Development Center, ; Thuwal, 23955-6900 Saudi Arabia
                [7 ]GRID grid.411851.8, ISNI 0000 0001 0040 0205, Guangdong Provincial Key Laboratory of Plant Resources Biorefinery, School of Chemical Engineering and Light Industry, , Guangdong University of Technology (GDUT), 100 Waihuan Xi Road, Panyu District, ; Guangzhou, 510006 China
                Author information
                http://orcid.org/0000-0002-3180-7582
                http://orcid.org/0000-0001-7417-9857
                http://orcid.org/0000-0002-4031-0156
                http://orcid.org/0000-0002-0745-2945
                http://orcid.org/0000-0003-0551-1208
                http://orcid.org/0000-0001-8146-7101
                http://orcid.org/0000-0003-3230-0932
                Article
                33790
                10.1038/s41467-022-33790-z
                9556660
                36224249
                3d0b6c5b-9ebd-43d3-8ae7-a2a8143661c3
                © 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
                : 20 April 2022
                : 3 October 2022
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100004663, Ministry of Science and Technology, Taiwan (Ministry of Science and Technology of Taiwan);
                Award ID: MOST 111-2628-E-007-018
                Award Recipient :
                Categories
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                © The Author(s) 2022

                Uncategorized
                batteries,two-dimensional materials
                Uncategorized
                batteries, two-dimensional materials

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