MXenes公司
阳极
材料科学
二硫化钼
化学工程
电极
纳米技术
堆积
储能
合理设计
锂(药物)
动力学
电池(电)
化学
复合材料
有机化学
工程类
医学
功率(物理)
物理
物理化学
量子力学
内分泌学
作者
Jiachen Han,Wenbin Xu,Zhimin Liu,Zhaoyang Gao,Song Tao,Huihua Min,Hao Yang,Jin Wang
标识
DOI:10.1016/j.jallcom.2023.170282
摘要
Sodium-ion batteries (SIBs) have evolved into the most potential alternatives to lithium-ion batteries (LIBs) especially for large-scale energy storage applications. However, the large radius of sodium ion inevitably causes large volume change and sluggish ion diffusion kinetics. Molybdenum disulfide (MoS2) as a rising star of anode for SIBs has raised concern because of its high theoretical capacity. Nevertheless, MoS2 suffers from low electronic conductivity and serious re-stacking, resulting in declined cycling stability and poor rate capability. Herein, we reported an electrostatic self-assembly process to synthesize three-dimensional (3D) crumpled MXene-bonded MoS2 nanosheets. The MoS2/MXene heterostructure not only avoids the serious self-aggregation of MoS2 nanoparticles but only maintains the chemical and mechanical stability of MoS2/MXene hybrids during sodiation and desodiation. Strong chemical interactions were validated on the interface of MXene and MoS2, favoring fast charge transfer kinetics and durable structural stability. The developed MoS2/MXene electrode exhibits a high specific capacity (509 mAh g−1 at 0.05 A g−1) and considerable cyclability (326 mAh g−1 at 1 A g−1 after 900 cycles), manifesting a promising application prospect for SIBs. Our work can provide a rational strategy for the electrode design strategy for SIBs.
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