Evaluation of nanostructured silicon based anodes with enhanced cycling stability for all solid state lithium batteries

Herein, three representative silicon-based anode materials, namely pure nano-silicon (Si), ball-milled silicon/carbon composite (BM Si/C), and chemical vapor deposition silicon/carbon composite (CVD Si@C), were systematically investigated for their application in all-solid-state lithium batteries. X-ray diffraction and Raman spectroscopy analyses confirmed that BM Si/C maintained the crystalline structure of silicon with a defect-rich carbon network, while CVD Si@C exhibited an amorphous silicon phase uniformly distributed within porous carbon frameworks with Si–C covalent bonding. The initial reversible capacities for Si, BM Si/C and CVD Si@C were 2810.4, 1230.1 and 1648.2 mAh g − 1 , with Coulombic efficiencies of 65.97, 62.81 and 72.94%, respectively. The electrochemical performance of pure Si in this study was limited by capacity decay induced by volume expansion, while BM Si/C demonstrated an “activation-rising” behavior, stabilizing at approximately 900 mAh g − 1 after 100 cycles at 0.5 C. CVD Si@C exhibits outstanding cycling stability. Post-cycling characterizations reveal that despite a remarkable increase in electrode thickness, the surface contours of individual particles remain relatively intact. The porous carbon matrix may partially sustain electrode structural integrity via a combination of inward volume accommodation tendency, confinement effect from Si–C covalent bonds, and stress buffering derived from the amorphous silicon phase to a certain extent. Electrochemical impedance spectroscopy data analysis revealed that BM Si/C possessed the lowest charge transfer resistance, attributed to the three-dimensional conductive network formed by defect-induced carbon, whereas CVD Si@C showed higher resistance yet superior long-term stability. This study provides experimental insights into understanding how different silicon/carbon composite strategies affect the electrochemical performance of ASSLBs.

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Publication Details

Journal
Discover Electrochemistry.
Published
2026-07-25
DOI
https://doi.org/10.1007/s44373-026-00153-y
Primary Topic
Advancements in Battery Materials
Type
article
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article

Evaluation of nanostructured silicon based anodes with enhanced cycling stability for all solid state lithium batteries

Jingchao Chai, Lujia Guo, Yun Zheng, Xin Cheng et al.
Discover Electrochemistry.
Advancements in Battery Materials
article

Evaluation of nanostructured silicon based anodes with enhanced cycling stability for all solid state lithium batteries

Jingchao Chai, Lujia Guo, Yun Zheng, Xin Cheng, Qian Chen, Yu Peng, Zhihong Liu, Jiake Huo, Hua Cai, Bowen Li, Minghao Sun
article en

Abstract

Herein, three representative silicon-based anode materials, namely pure nano-silicon (Si), ball-milled silicon/carbon composite (BM Si/C), and chemical vapor deposition silicon/carbon composite (CVD Si@C), were systematically investigated for their application in all-solid-state lithium batteries. X-ray diffraction and Raman spectroscopy analyses confirmed that BM Si/C maintained the crystalline structure of silicon with a defect-rich carbon network, while CVD Si@C exhibited an amorphous silicon phase uniformly distributed within porous carbon frameworks with Si–C covalent bonding. The initial reversible capacities for Si, BM Si/C and CVD Si@C were 2810.4, 1230.1 and 1648.2 mAh g − 1 , with Coulombic efficiencies of 65.97, 62.81 and 72.94%, respectively. The electrochemical performance of pure Si in this study was limited by capacity decay induced by volume expansion, while BM Si/C demonstrated an “activation-rising” behavior, stabilizing at approximately 900 mAh g − 1 after 100 cycles at 0.5 C. CVD Si@C exhibits outstanding cycling stability. Post-cycling characterizations reveal that despite a remarkable increase in electrode thickness, the surface contours of individual particles remain relatively intact. The porous carbon matrix may partially sustain electrode structural integrity via a combination of inward volume accommodation tendency, confinement effect from Si–C covalent bonds, and stress buffering derived from the amorphous silicon phase to a certain extent. Electrochemical impedance spectroscopy data analysis revealed that BM Si/C possessed the lowest charge transfer resistance, attributed to the three-dimensional conductive network formed by defect-induced carbon, whereas CVD Si@C showed higher resistance yet superior long-term stability. This study provides experimental insights into understanding how different silicon/carbon composite strategies affect the electrochemical performance of ASSLBs.

Discover Electrochemistry.Vol. 3(1)
Jianghan University (CN)
Openalex Percentile: Top 15%
Advancements in Battery Materials
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