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一种部分硫化策略衍生的用于超稳定钾/钠/锂离子存储的多壳层蛋黄结构

A Partial Sulfuration Strategy Derived Multi-Yolk-Shell Structure for Ultra-Stable K/Na/Li-ion Storage.

作者信息

Shi Xiuling, Gan Yanmei, Zhang Qixin, Wang Chaoying, Zhao Yi, Guan Lunhui, Huang Wei

机构信息

Fujian Cross Strait Institute of Flexible Electronics (Future Technologies), Fujian Normal University, Fuzhou, 350117, China.

CAS Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Key Laboratory of Nanomaterials, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, 350108, China.

出版信息

Adv Mater. 2021 Aug;33(33):e2100837. doi: 10.1002/adma.202100837. Epub 2021 Jul 9.

Abstract

Metal sulfides are attractive anodes for alkali metal ion batteries due to the high theoretical capacity, while their practical implementation is hampered by the inherent poor conductivity and vast volume variation during cycles. Approaching rational designed microstructures with good stability and fast charge transfer is of great importance in response to these issues. Herein, a partial sulfuration strategy for the rational construction of multi-yolk-shell (m-Y-S) structures, from which multiple Fe S nanoparticles are confined within hollow carbon nanosheet with tunable interior void space is reported. As anode materials, the m-Y-S Fe S@C composite can display high capacity and excellent rate capability (134, 365, and 447 mA h g for K , Na , and Li storage at 20 A g ). Remarkably, it exhibits ultra-stable potassium storage up to 1200, 6000, and 20 000 cycles under current densities of 0.1, 0.5, and 1 A g , which is much superior to previous yolk-shell structures and metal-sulfide anodes. Based on comprehensive experimental analysis and theoretical calculations, the exceptional performance of m-Y-S structure can be ascribed to the optimized interior void space for good structure stability, as well as the multiple connection points and conductive carbon layer for superior electron/ion transportation.

摘要

金属硫化物因其高理论容量而成为碱金属离子电池颇具吸引力的阳极材料,然而其实际应用受到固有低导电性和循环过程中巨大体积变化的阻碍。构建具有良好稳定性和快速电荷转移的合理设计微观结构对于解决这些问题至关重要。在此,报道了一种用于合理构建多壳层(m-Y-S)结构的部分硫化策略,其中多个FeS纳米颗粒被限制在具有可调内部空隙空间的中空碳纳米片中。作为阳极材料,m-Y-S FeS@C复合材料在20 A g时对钾、钠和锂存储可分别展现出高容量和优异的倍率性能(134、365和447 mA h g)。值得注意的是,在0.1、0.5和1 A g的电流密度下,它在高达1200、6000和20000次循环中表现出超稳定的钾存储性能,这远优于先前的壳层结构和金属硫化物阳极。基于全面的实验分析和理论计算,m-Y-S结构的优异性能可归因于优化的内部空隙空间以实现良好的结构稳定性,以及多个连接点和导电碳层以实现卓越的电子/离子传输。

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