材料科学
阳极
化学工程
锂(药物)
聚丙烯酸
涂层
硅
瓜尔胶
电化学
电极
复合材料
纳米技术
聚合物
化学
工程类
内分泌学
物理化学
冶金
医学
生物化学
作者
Hui Xu,Xiaoxi Liu,Wenlu Sun,Guanghui Xu,Yihong Tong,Hongyuan Xu,Jia Li,Kaile Zhao,Yong Wang,Zhiyong Lin,Hong Jin,Hongwei Chen
出处
期刊:Nanoscale
[The Royal Society of Chemistry]
日期:2022-12-08
卷期号:15 (2): 791-801
被引量:3
摘要
Currently, a variety of binders are developed to inhibit the rapid capacity fading of Si. The Si anodes are mainly enhanced by the chemical bonding effect on the surface of conventional solid-state binders. However, with a huge volume change of silicon, solid binders are easily deactivated. Herein, a semi-fluid binder termed GPC is designed based on a viscoelastic crosslinking network with abundant active sites and self-healing performance. The backbone of the binder network is in situ synthesized using guar gum (GG), polyacrylic acid (PAA), and citric acid (CA). Serving as the flexible joints and the plasticizer of the network, CA small molecules remarkably improve the viscoelasticity of the binder to tolerate the volume change of Si via rearranging particles in the network during cycling. Moreover, CA can form a layer of surface coating on Si to stabilize the SEI for long-term electrochemical performance. As a result, the Si@GPC electrode shows excellent cycling stability and exhibits a superb capacity of 1292 mA h g-1 after 1000 cycles at 2 A g-1. This work illustrates the advantages and prospects of designing semi-fluid binders for high-performance batteries.
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