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在保持二硫化钼层状晶体结构的同时接近其锂化极限以改善锂存储性能。

Approaching the Lithiation Limit of MoS While Maintaining Its Layered Crystalline Structure to Improve Lithium Storage.

作者信息

Zhu Zhiqiang, Tang Yuxin, Leow Wan Ru, Xia Huarong, Lv Zhisheng, Wei Jiaqi, Ge Xiang, Cao Shengkai, Zhang Yanyan, Zhang Wei, Zhang Hongwei, Xi Shibo, Du Yonghua, Chen Xiaodong

机构信息

Innovative Centre for Flexible Devices (iFLEX), School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore, 639798, Singapore.

Institute of Chemical and Engineering Sciences, 1 Pesek Road, Jurong Island, Singapore, 627833, Singapore.

出版信息

Angew Chem Int Ed Engl. 2019 Mar 11;58(11):3521-3526. doi: 10.1002/anie.201813698. Epub 2019 Feb 20.

Abstract

MoS holds great promise as high-rate electrode for lithium-ion batteries since its large interlayer can allow fast lithium diffusion in 3.0-1.0 V. However, the low theoretical capacity (167 mAh g ) limits its wide application. Here, by fine tuning the lithiation depth of MoS , we demonstrate that its parent layered structure can be preserved with expanded interlayers while cycling in 3.0-0.6 V. The deeper lithiation and maintained crystalline structure endows commercially micrometer-sized MoS with a capacity of 232 mAh g at 0.05 A g and circa 92 % capacity retention after 1000 cycles at 1.0 A g . Moreover, the enlarged interlayers enable MoS to release a capacity of 165 mAh g at 5.0 A g , which is double the capacity obtained under 3.0-1.0 V at the same rate. Our strategy of controlling the lithiation depth of MoS to avoid fracture ushers in new possibilities to enhance the lithium storage of layered transition-metal dichalcogenides.

摘要

由于其较大的层间距能使锂离子在3.0 - 1.0伏的电压范围内快速扩散,二硫化钼作为锂离子电池的高倍率电极具有巨大潜力。然而,其较低的理论容量(167毫安每克)限制了它的广泛应用。在此,通过微调二硫化钼的锂化深度,我们证明了在3.0 - 0.6伏的电压范围内循环时,其母体层状结构能够得以保留,同时层间距增大。更深的锂化程度以及保持的晶体结构赋予了商业化微米尺寸的二硫化钼在0.05安每克的电流密度下232毫安每克的容量,并且在1.0安每克的电流密度下经过1000次循环后容量保持率约为92%。此外,增大的层间距使二硫化钼在5.0安每克的电流密度下能够释放出165毫安每克的容量,这是在相同倍率下3.0 - 1.0伏电压范围内所获容量的两倍。我们通过控制二硫化钼锂化深度以避免其破裂的策略为增强层状过渡金属二硫化物的锂存储性能带来了新的可能性。

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