阳极
石墨烯
材料科学
硅
纳米颗粒
化学工程
电解质
纳米技术
电化学
光电子学
化学
电极
物理化学
工程类
作者
Jing-Zhou Chen,Mengxin Ren,Yun‐Lei Hou,Bo-Han Zhang,Wan‐Xin Wen,Huaying Wang,Dong‐Lin Zhao
标识
DOI:10.1016/j.jallcom.2023.169681
摘要
To cope with volume expansion, poor silicon conductivity and capacity decay due to solid electrolyte interface rupture, rational design of silicon negative electrode is an effective means to cope with the above challenges. We designed a graphene confined Si@Cu core-shell structure (Si@Cu@rGO) as integrated anode, in which the copper shell on the Si nanosurface enhances the electronic conductivity between the silicon particles and graphene. Meanwhile, the flexibility of the copper shell and graphene help suppress the change of electrode morphology during cycling and keep good contact between electrode material and collector. The graphene cladding not only effectively prevents the aggregation of Si@Cu nanoparticles, but also provides enough space for the expansion of silicon during lithiation, while the three-dimensional redox graphene layer builds a conductive structure that accelerates the reaction kinetics of the cell. Thanks to this design, Si@Cu@rGO has a satisfactory electrochemical performance. After 70 cycles in the rate performance test, the specific capacity of Si@Cu@rGO reached 2243.1 mAh g−1.
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