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      Ultrafast lithium energy storage enabled by interfacial construction of interlayer-expanded MoS 2/N-doped carbon nanowires

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          Abstract

          Edge-oriented and interlayer-expanded MoS 2 nanosheets/N-doped carbon nanowires are prepared and exhibit ultrafast and durable Li + storage performance.

          Abstract

          Two-dimensional (2D) molybdenum disulfide (MoS 2) has been extensively regarded as a promising host material for lithium ion batteries due to the reversible insertion of Li + into the layered structures. However, achieving ultrafast and durable Li + storage has a challenge of designing largely exposed edge-oriented and kinetically favorable MoS 2-based nanostructures. Herein, we report an interfacial synthesis strategy for facile construction of ultrathin MoS 2/N-doped carbon nanowires (MoS 2/N–C NWs) ( ca. 10 μm in length) with a largely expanded (002) plane of MoS 2 ( d = 1.03 nm, vs. bulk 0.62 nm). This hierarchical nanowire configuration composed of edge-oriented and interlayer-expanded MoS 2 nanosheets can not only effectively decrease the diffusion energy barriers for Li + intercalation and improve the number of electrochemically active sites, but also provide fast electron pathways. As an anode for LIBs, the MoS 2/N–C NWs demonstrate excellent rate capabilities (600 mA h g −1 at 5 A g −1 and 453 mA h g −1 at 10 A g −1) and long-term durability (86.7% retention at 5 A g −1 over 500 cycles). This study demonstrates the great potential of the MoS 2/N–C NWs as promising anode materials for ultrafast lithium energy storage.

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          Most cited references48

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          Pseudocapacitive oxide materials for high-rate electrochemical energy storage

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            Is Open Access

            Controlled Scalable Synthesis of Uniform, High-Quality Monolayer and Few-layer MoS2 Films

            Two dimensional (2D) materials with a monolayer of atoms represent an ultimate control of material dimension in the vertical direction. Molybdenum sulfide (MoS2) monolayers, with a direct bandgap of 1.8 eV, offer an unprecedented prospect of miniaturizing semiconductor science and technology down to a truly atomic scale. Recent studies have indeed demonstrated the promise of 2D MoS2 in fields including field effect transistors, low power switches, optoelectronics, and spintronics. However, device development with 2D MoS2 has been delayed by the lack of capabilities to produce large-area, uniform, and high-quality MoS2 monolayers. Here we present a self-limiting approach that can grow high quality monolayer and few-layer MoS2 films over an area of centimeters with unprecedented uniformity and controllability. This approach is compatible with the standard fabrication process in semiconductor industry. It paves the way for the development of practical devices with 2D MoS2 and opens up new avenues for fundamental research.
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              MoS2Nanoflowers with Expanded Interlayers as High-Performance Anodes for Sodium-Ion Batteries

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                Author and article information

                Contributors
                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2018
                2018
                : 6
                : 27
                : 13419-13427
                Affiliations
                [1 ]State Key Laboratory of Solidification Processing
                [2 ]Center for Nano Energy Materials
                [3 ]School of Materials Science and Engineering
                [4 ]Northwestern Polytechnical University and Shaanxi Joint Lab of Graphene (NPU)
                [5 ]Xi'an 710072
                [6 ]Department of Chemical and Biomolecular Engineering
                [7 ]The Hong Kong University of Science & Technology
                [8 ]Kowloon
                [9 ]China
                Article
                10.1039/C8TA04852E
                25e66c50-1083-45d7-bf46-74097f919817
                © 2018

                http://rsc.li/journals-terms-of-use

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