阳极
机制(生物学)
钠
碳纤维
离子
化学物理
材料科学
纳米技术
工程物理
计算机科学
化学
物理
物理化学
冶金
复合材料
有机化学
电极
量子力学
复合数
作者
Zhaoming Wang,Guanghui Shi,Guanghui Wang,Man Wang,Xiao Wang,Feng Ding
标识
DOI:10.48550/arxiv.2412.00340
摘要
Sodium-ion batteries (SIBs) have garnered significant attention in recent years as a promising alternative to lithium-ion batteries (LIBs) due to their low cost, abundant sodium resources, and excellent cycling performance. Hard carbon materials, characterized by their high specific capacity, outstanding cycling stability, and low cost, have emerged as potential candidates for SIB anodes. However, the sodium storage mechanism in hard carbon anodes remains highly complex, especially in disordered structures, and is yet to be fully understood. To address this, we employed relative machine learning force fields (MLFFs) in conjunction with multiscale simulation techniques to systematically investigate the sodium storage behavior in hard carbon. By integrating simulations, this study provides a detailed exploration of sodium adsorption, intercalation, and filling mechanisms. High-precision, large-scale simulations reveal the dynamic behavior and distribution patterns of sodium ions in hard carbon. The findings not only deepen our understanding of sodium storage mechanisms in hard carbon anodes, but also offer a theoretical foundation for optimizing future SIB designs, while introducing novel simulation methodologies and technical frameworks to enhance battery performance.
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