储能
钠
碳捕获和储存(时间表)
碳纤维
领域(数学分析)
化学
材料科学
纳米技术
环境科学
化学工程
物理
工程类
热力学
数学
有机化学
生物
气候变化
复合材料
功率(物理)
数学分析
复合数
生态学
作者
Zhidong Hou,Mingwei Jiang,Da Lei,Xiang Zhang,Yuyang Gao,Jian‐Gan Wang
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2024-02-01
卷期号:17 (6): 5188-5196
被引量:58
标识
DOI:10.1007/s12274-024-6448-1
摘要
Hard carbon anode has shown extraordinary potentials for sodium-ion batteries (SIBs) owing to the cost-effectiveness and advantaged microstructure. Nevertheless, the widespread application of hard carbon is still hindered by the insufficient sodium storage capacity and depressed rate property, which are mainly induced by the undesirable pseudographitic structure. Herein, we develop a molten-salt-mediated strategy to regulate the pseudographitic structure of hard carbon with suitable interlayer spacing and enlarged pseudographitic domain, which is conducive to the intercalation capacity and diffusion kinetics of sodium ions. Impressively, the optimized hard carbon anode delivers a high reversible capacity of 320 mAh·g−1, along with superior rate property (138 mAh·g−1 at 2 A·g−1) and stable cyclability over 1800 cycles. Moreover, the in situ Raman spectroscopic study and full-cell assembly further investigate the sodium storage mechanism and practical implement of obtained hard carbon. This work pioneers a low-cost and effective route to regulate the pseudographitic structure of hard carbon materials for advanced SIBs.
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