阳极
锂(药物)
材料科学
储能
电化学
硅
纳米复合材料
化学工程
纳米技术
电极
光电子学
化学
医学
物理
工程类
内分泌学
物理化学
功率(物理)
量子力学
作者
Tariq Bashir,Xiangyi Li,Shiqi Yang,Yuheng Song,Shaowen Zhou,Jiaqi Wang,Wenhao Zhu,Jie Yang,Jianqing Zhao,Lijun Gao
标识
DOI:10.1016/j.jallcom.2022.166213
摘要
High-energy lithium-ion batteries (LIBs) have been actively pursued for practical applications in advanced electric vehicles and large-scale energy storage systems. The silicon (Si) material has been considered as a promising anode candidate due to its impressive lithium storage capacity, but is facing the challenge to ameliorate its cycling and rate performance. We here report a structure integration strategy to overcome major issues of poor capacity retention and slow kinetics during the lithium storage of Si anode, through in situ embedding Si nanoparticles into V2C MXene nanosheets. The MXene-supported [email protected]2C nanocomposite anode reveals significantly enhanced cycling stability and improved lithium storage kinetics compared to that of the pristine Si anode. A high capacity exceeding to 430 mAh g−1 can be retained for 150 cycles at 200 mA g−1 current density. In addition, the conductive MXene supporter has been demonstrated to facilitate lithiation/delithiation processes for the Si by enhancing the charge transfer kinetics, as it is demonstrated by in situ electrochemical impedance spectroscopic (EIS) and Galvanostatic Intermittent Titration Technique (GITT) measurements. Findings from this work may inspire feasible structural designs for the practical deployment of MXene composited Si anode materials for next-generation lithium-ion batteries.
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