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受腱鞘启发的双网络粘合剂实现了硅电极卓越的循环性能。

An Endotenon Sheath-Inspired Double-Network Binder Enables Superior Cycling Performance of Silicon Electrodes.

作者信息

Jiang Meifang, Mu Pengzhou, Zhang Huanrui, Dong Tiantian, Tang Ben, Qiu Huayu, Chen Zhou, Cui Guanglei

机构信息

Qingdao Industrial Energy Storage Research Institute, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, No. 189 Songling Road, Qingdao, 266101, People's Republic of China.

Key Laboratory of Marine Chemistry Theory and Technology Ministry of Education, College of Chemistry and Chemical Engineering, Ocean University of China, No. 238 Songling Road, Qingdao, 266100, People's Republic of China.

出版信息

Nanomicro Lett. 2022 Apr 1;14(1):87. doi: 10.1007/s40820-022-00833-5.

DOI:10.1007/s40820-022-00833-5
PMID:35362872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8975975/
Abstract

Silicon (Si) has been regarded as an alternative anode material to traditional graphite owing to its higher theoretical capacity (4200 vs. 372 mAh g). However, Si anodes suffer from the inherent volume expansion and unstable solid electrolyte interphase, thus experiencing fast capacity decay, which hinders their commercial application. To address this, herein, an endotenon sheath-inspired water-soluble double-network binder (DNB) is presented for resolving the bottleneck of Si anodes. The as-developed binder shows excellent adhesion, high mechanical properties, and a considerable self-healing capability mainly benefited by its supramolecular hybrid network. Apart from these advantages, this binder also induces a LiN/LiF-rich solid electrolyte interface layer, contributing to a superior cycle stability of Si electrodes. As expected, the DNB can achieve mechanically more stable Si electrodes than traditional polyacrylic acid and pectin binders. As a result, DNB delivers superior electrochemical performance of Si/Li half cells and LiNiCoMnO/Si full cells, even with a high loading of Si electrode, to traditional polyacrylic acid and pectin binders. The bioinspired binder design provides a promising route to achieve long-life Si anode-assembled lithium batteries.

摘要

由于硅(Si)具有更高的理论容量(4200 vs. 372 mAh g),它被视为传统石墨的替代阳极材料。然而,硅阳极存在固有的体积膨胀和不稳定的固体电解质界面问题,因此容量快速衰减,这阻碍了它们的商业应用。为了解决这个问题,本文提出了一种受腱鞘启发的水溶性双网络粘合剂(DNB),以解决硅阳极的瓶颈问题。所开发的粘合剂表现出优异的粘附性、高机械性能和相当可观的自愈能力,这主要得益于其超分子混合网络。除了这些优点外,这种粘合剂还能诱导富含LiN/LiF的固体电解质界面层,有助于提高硅电极的循环稳定性。正如预期的那样,与传统的聚丙烯酸和果胶粘合剂相比,DNB可以使硅电极在机械上更稳定。因此,与传统的聚丙烯酸和果胶粘合剂相比,即使在硅电极高负载的情况下,DNB在硅/锂半电池和锂镍钴锰氧化物/硅全电池中也具有优异的电化学性能。这种受生物启发的粘合剂设计为实现长寿命硅阳极组装锂电池提供了一条有前景的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304a/8975975/ce10ae7daa74/40820_2022_833_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304a/8975975/dbbcb28b9d6f/40820_2022_833_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304a/8975975/149cc52afc18/40820_2022_833_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304a/8975975/b602ceeb06b1/40820_2022_833_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304a/8975975/16af921c54d0/40820_2022_833_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304a/8975975/ce10ae7daa74/40820_2022_833_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304a/8975975/dbbcb28b9d6f/40820_2022_833_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304a/8975975/149cc52afc18/40820_2022_833_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304a/8975975/b602ceeb06b1/40820_2022_833_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304a/8975975/16af921c54d0/40820_2022_833_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304a/8975975/ce10ae7daa74/40820_2022_833_Fig5_HTML.jpg

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