阳极
材料科学
碳纤维
碳化
化学工程
钠离子电池
钠
电流密度
纳米技术
热解
电极
复合材料
复合数
化学
法拉第效率
扫描电子显微镜
工程类
物理
物理化学
量子力学
冶金
作者
Shreyasi Chattopadhyay,Atin Pramanik,Tymofii S. Pieshkov,Gautam Chandrasekhar,Salma Alhashim,Róbert Vajtai,Pulickel M. Ajayan
出处
期刊:Small
[Wiley]
日期:2025-04-17
卷期号:21 (28): e2500120-e2500120
被引量:16
标识
DOI:10.1002/smll.202500120
摘要
Hard carbon is a promising anode material for next-generation sodium-ion batteries (NIBs) due to its high specific capacity, low working potential, and excellent structural stability. This research focuses on synthesizing boron- and nitrogen-co-doped hard carbon (BNHC), which shows enhanced sodium storage properties in half and full-cell configurations. The BNHC is prepared using a simple, scalable sol-gel method followed by pyrolysis for carbonization. Its 3D nano-sponge structure provides abundant active sites for sodium storage, while the low surface area and optimal interlayer distance minimize volume expansion during high-rate charge/discharge cycles, ensuring exceptional cycling stability. Compared to undoped hard carbon, BNHC demonstrates significantly improved sodium storage performance. The BNHC electrode achieves a reversible capacity of ≈310 mAh g⁻¹ with ultra-long cycling stability at high current rates and robust rate capability. It delivers ≈115 mAh g⁻¹ at an exceptionally high current density of 10 A g⁻¹. Further, BNHC//NaFePO4 full cell demonstrates excellent cycling stability with ≈206 mAh g⁻¹ at a 150 mA g⁻¹ current rate. This study paves the way to commercializing hard carbon as an anode material for sodium-ion batteries.
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