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构建具有改善锂存储性能的用于硅阳极的坚固交联粘结剂网络。

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

作者信息

Zheng Zhiming, Gao Haowen, Ke Chengzhi, Li Miao, Cheng Yong, Peng Dong-Liang, Zhang Qiaobao, Wang Ming-Sheng

机构信息

State Key Lab of Physical Chemistry of Solid Surfaces, College of Materials, Xiamen University, Xiamen 361005, China.

出版信息

ACS Appl Mater Interfaces. 2021 Nov 17;13(45):53818-53828. doi: 10.1021/acsami.1c14907. Epub 2021 Nov 3.

DOI:10.1021/acsami.1c14907
PMID:34730928
Abstract

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 LiFePO cathode also exhibits excellent cycling performance (120.4 mA h g 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.

摘要

尽管硅作为下一代高容量锂离子电池(LIBs)的一种有前景的负极材料具有高比容量,但其实际应用却受到循环过程中快速的容量衰减的阻碍。为了解决这个问题,本文提出了一种粘合剂接枝策略,以构建一种共价交联的粘合剂[羧甲基纤维素/植酸(CMC/PA)],它能构建一个具有更多接触点的坚固分支网络,通过氢键与硅纳米颗粒形成更强的键。得益于增强的机械可靠性,所得的硅-CMC/PA电极表现出高可逆容量以及改善的长期循环稳定性。此外,由所制备的硅-CMC/PA负极和商用磷酸铁锂正极组成的组装全电池也表现出优异的循环性能(在1C下120.4 mA h g,超过100次循环,容量保持率为88.4%)。采用原位透射电子显微镜来观察CMC/PA的结合效果,与传统的CMC粘合剂不同,它能有效防止锂化硅负极开裂。此外,结合非原位显微镜和X射线光电子能谱分析揭示了硅-CMC/PA电极优异的锂离子存储性能的来源,这源于其优异的结构完整性以及循环过程中稳定的固体电解质界面膜。这项工作提出了一种简便有效的粘合剂工程策略,可显著提高下一代LIBs中硅负极的性能。

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A Multifunctional Interlocked Binder with Synergistic In Situ Covalent and Hydrogen Bonding for High-Performance Si Anode in Li-ion Batteries.
一种具有协同原位共价和氢键作用的多功能互锁粘结剂,用于锂离子电池中的高性能硅阳极。
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