阳极
动能
材料科学
碳纤维
离子
钠
煤
化学工程
化学
冶金
废物管理
复合材料
电极
物理化学
物理
有机化学
工程类
量子力学
复合数
作者
Xinyu Wang,Kai-Yang Zhang,Meng‐Yuan Su,Han‐Hao Liu,Zhen‐Yi Gu,Dongmei Dai,Bao Li,Jiawei Wang,HE Xiao-yan,Xing‐Long Wu
出处
期刊:Carbon
[Elsevier BV]
日期:2024-08-06
卷期号:229: 119526-119526
被引量:3
标识
DOI:10.1016/j.carbon.2024.119526
摘要
Hard carbon (HC) has demonstrated a significant potential in anode for sodium-ion batteries (SIBs) due to its superior electrochemical properties. Coal is considered a promising hard carbon precursor due to its high carbon yield. However, the widespread adoption of coal-derived HC faces challenges such as limited storage capacity and decreased rate performance, primarily attributed to the dense structure of coal. In this study, a molten salt-assisted approach was developed to adjust the microstructure of coal-derived HC. The dense coal is etched into a flaky structure by molten salt, which is conducive to the diffusion and transport of sodium ions. The optimized HC materials possess large interlayer spacing and abundant pseudo-graphitic domains, exhibiting a remarkable reversible capacity of 303.6 mA h g−1 at 30 mA g−1 and 82.1 mA h g−1 at 500 mA g−1. Besides, a full cell with the configuration of as-prepared coal derived HC versus Na3V2(PO4)2O2F (NVPOF) is presented with a high initial coulombic efficiency of 76.15 % and capacity of 100.7 mA h g−1. The results indicate that our synthesis strategy is feasible for the application of coal derived carbon materials in SIBs.
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