Constructing Robust Cross-Linked Binder Networks for Silicon Anodes with Improved Lithium Storage Performance

材料科学 阳极 电解质 化学工程 锂(药物) X射线光电子能谱 阴极 电极 纳米技术 光电子学 医学 工程类 内分泌学 物理化学 化学
作者
Zhiming Zheng,Haowen Gao,Chengzhi Ke,Miao Li,Yong Cheng,Dong‐Liang Peng,Qiaobao Zhang,Ming‐Sheng Wang
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:13 (45): 53818-53828 被引量:50
标识
DOI:10.1021/acsami.1c14907
摘要

Despite the high specific capacity of silicon as a promising anode material for the next-generation high-capacity Li-ion batteries (LIBs), its practical applications are impeded by the rapid capacity decay during cycling. To tackle the issue, herein, a binder-grafting strategy is proposed to construct a covalently cross-linked binder [carboxymethyl cellulose/phytic acid (CMC/PA)], which builds a robust branched network with more contact points, allowing stronger bonds with Si nanoparticles by hydrogen bonding. Benefitting from the enhanced mechanical reliability, the resulting Si-CMC/PA electrodes exhibit a high reversible capacity with improved long-term cycling stability. Moreover, an assembled full cell consisting of the as-obtained Si-CMC/PA anode and commercial LiFePO4 cathode also exhibits excellent cycling performance (120.4 mA h g-1 at 1 C for over 100 cycles with 88.4% capacity retention). In situ transmission electron microscopy was employed to visualize the binding effect of CMC/PA, which, unlike the conventional CMC binder, can effectively prevent the lithiated Si anodes from cracking. Furthermore, the combined ex situ microscopy and X-ray photoelectron spectroscopy analysis unveils the origin of the superior Li-ion storage performance of the Si-CMC/PA electrode, which arises from its excellent structural integrity and the stabilized solid-electrolyte interphase films during cycling. This work presents a facile and efficient binder-engineering strategy for significantly improving the performance of Si anodes for next-generation LIBs.
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