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调控多孔硅碳负极稳定性:碳/碳化硅半透层减轻硅氟反应并增强锂离子传输。

Modulating porous silicon-carbon anode stability: Carbon/silicon carbide semipermeable layer mitigates silicon-fluorine reaction and enhances lithium-ion transport.

作者信息

Zhang Baoguo, Wu Lin, Hu Ya, Yang Xiaoyu, Liu Ying, Li Jingwang, Tang Ming, Chen Rongsheng, Ma Feng, Wang Jiayi, Wang Xin

机构信息

Key Laboratory of Hubei Province for Coal Conversion and New Carbon Materials, School of Chemistry and Chemical Engineering, Wuhan University of Science and Technology, Wuhan 430081, China.

Key Laboratory of Hubei Province for Coal Conversion and New Carbon Materials, School of Chemistry and Chemical Engineering, Wuhan University of Science and Technology, Wuhan 430081, China; Academy of Green Manufacturing Engineering, Wuhan University of Science and Technology, Wuhan 430081, China.

出版信息

J Colloid Interface Sci. 2024 Nov 15;674:643-652. doi: 10.1016/j.jcis.2024.06.223. Epub 2024 Jun 28.

DOI:10.1016/j.jcis.2024.06.223
PMID:38950463
Abstract

Silicon-based material is regarded as one of the most promising anodes for next-generation high-performance lithium-ion batteries (LIBs) due to its high theoretical capacity and low cost. Harnessing silicon carbide's robustness, we designed a novel porous silicon with a sandwich structure of carbon/silicon carbide/Ag-modified porous silicon (Ag-PSi@SiC@C). Different from the conventional SiC interface characterized by a frail connection, a robust dual covalent bond configuration, dependent on SiC and SiOC, has been successfully established. Moreover, the innovative sandwich structure effectively reduces detrimental side reactions on the surface, eases volume expansion, and bolsters the structural integrity of the silicon anode. The incorporation of silver nanoparticles contributes to an improvement in overall electron transport capacity and enhances the kinetics of the overall reaction. Consequently, the Ag-PSi@SiC@C electrode, benefiting from the aforementioned advantages, demonstrates a notably elevated lithium-ion mobility (2.4 * 10 cm·s), surpassing that of silicon (5.1 * 10 cm·s). The half-cell featuring Ag-PSi@SiC@C as the anode demonstrated robust rate cycling stability at 2.0 A/g, maintaining a capacity of 1321.7 mAh/g, and after 200 cycles, it retained 962.6 mAh/g. Additionally, the full-cell, featuring an Ag-PSi@SiC@C anode and a LiFePO (LFP) cathode, exhibits outstanding longevity. Hence, the proposed approach has the potential to unearth novel avenues for the extended exploration of high-performance silicon-carbon anodes for LIBs.

摘要

硅基材料因其高理论容量和低成本,被视为下一代高性能锂离子电池(LIBs)最有前景的负极材料之一。利用碳化硅的坚固性,我们设计了一种新型多孔硅,其具有碳/碳化硅/银改性多孔硅(Ag-PSi@SiC@C)的三明治结构。与以脆弱连接为特征的传统碳化硅界面不同,一种依赖于碳化硅和硅氧碳的强大双共价键结构已成功建立。此外,创新的三明治结构有效减少了表面的有害副反应,缓解了体积膨胀,并增强了硅负极的结构完整性。银纳米颗粒的掺入有助于提高整体电子传输能力,并增强整个反应的动力学。因此,受益于上述优势的Ag-PSi@SiC@C电极表现出显著提高的锂离子迁移率(2.4×10⁻⁵cm²·s⁻¹),超过了硅(5.1×10⁻⁶cm²·s⁻¹)。以Ag-PSi@SiC@C为负极的半电池在2.0 A/g下表现出强大的倍率循环稳定性,保持容量为1321.7 mAh/g,经过200次循环后,仍保留962.6 mAh/g。此外,以Ag-PSi@SiC@C为负极和LiFePO₄(LFP)为正极的全电池表现出出色的寿命。因此,所提出的方法有可能为高性能锂离子电池的硅碳负极的进一步探索开辟新途径。

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