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由MoS纳米片构建的具有增强储钠性能的分级微管。

Hierarchical Microtubes Constructed by MoS Nanosheets with Enhanced Sodium Storage Performance.

作者信息

Wang Peiyuan, Sun Shumin, Jiang Yu, Cai Qiong, Zhang Yong-Hui, Zhou Liming, Fang Shaoming, Liu Jian, Yu Yan

机构信息

Henan Provincial Key Laboratory of Surface and Interface Science, Department of Materials and Chemical Engineering, Zhengzhou University of Light Industry, Zhengzhou 450002, People's Republic of China.

Hefei National Laboratory for Physical Sciences at the Microscale, Department of Materials Science and Engineering, CAS Key Laboratory of Materials for Energy Conversion, University of Science and Technology of China, Hefei, Anhui 230026, People's Republic of China.

出版信息

ACS Nano. 2020 Nov 24;14(11):15577-15586. doi: 10.1021/acsnano.0c06250. Epub 2020 Oct 27.

Abstract

Emerging sodium-ion batteries (SIBs) have aroused great attention in large-scale energy storage. However, it is still a great challenge to develop suitable electrode materials due to the large radius of Na. This work demonstrates a strategy to synthesize hierarchical tubular MoS a facial hydrothermal method with the assistance of tetramethylammonium bromide (TMAB). The results show that sufficient amounts of TMA ions are necessary to form the hierarchical tubular structures of MoS. The obtained tubular MoS displays a high diffusion coefficient of Na ions, a high specific capacity of 652.5 mAh/g at the current density of 100 mA/g after 50 cycles, and a good cycling stability (94.2% of the initial capacity can be retained after 100 cycles at 1000 mA/g). XRD during the discharge/charge process displays a reversible intercalation/deintercalation of Na into MoS layers followed by a conversion-type reaction. Systematic analyses reveal that the enhanced electrochemical performance is attributed to its tubular hierarchical structures with the wall composed of loosely stacked nanosheets, which can provide nearly unobstructed ion transportation paths, sufficient active sites, and enough space to mitigate the effects of the volume change during the discharge/charge process. This synthetic approach can be easily extended to other metal oxides and metal sulfides with hierarchical structures for versatile applications.

摘要

新兴的钠离子电池(SIBs)在大规模储能领域引起了极大关注。然而,由于钠离子半径较大,开发合适的电极材料仍然是一个巨大的挑战。这项工作展示了一种通过在四甲基溴化铵(TMAB)辅助下的简易水热法合成分级管状二硫化钼(MoS₂)的策略。结果表明,需要足够量的TMA离子来形成MoS₂的分级管状结构。所制备的管状MoS₂显示出高的钠离子扩散系数,在100 mA/g的电流密度下经过50次循环后具有652.5 mAh/g的高比容量,以及良好的循环稳定性(在1000 mA/g下经过100次循环后可保留初始容量的94.2%)。充放电过程中的XRD显示钠离子可逆地嵌入/脱嵌到MoS₂层中,随后发生转化型反应。系统分析表明,其电化学性能的增强归因于其管状分级结构,其管壁由松散堆叠的纳米片组成,这可以提供几乎无阻碍的离子传输路径、足够的活性位点以及足够的空间来减轻充放电过程中体积变化的影响。这种合成方法可以很容易地扩展到其他具有分级结构的金属氧化物和金属硫化物,以实现多种应用。

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