阳极
材料科学
相容性(地球化学)
纳米技术
电化学
电导率
电池(电)
电极
碳纤维
多孔性
结构稳定性
碳纳米管
碳纳米纤维
纳米纤维
工作(物理)
分子动力学
电化学储能
机制(生物学)
储能
化学物理
化学工程
纳米结构
石墨
纤维素
科技与社会
作者
Hieu Trung Luong,Alexis Front,Tigani Zarrouk,Seyedabolfazl Mousavihashemi,Vasuki Durairaj,Katri S. Kontturi,Tekla Tammelin,Miguel A. Caro,Tomi T. Laurila
标识
DOI:10.1021/acs.jpcc.5c08259
摘要
High Resolution Image Download MS PowerPoint Slide Unlike lithium-ion batteries (LIBs), sodium-ion battery (SIB) technology is still in an early stage of development, where the pursuit of cost-effective and sustainable active materials is critical. Hard carbon (HC) is the most extensively studied anode material thanks to its compatibility with sodium-ion insertion. In this study, several cellulose-derived HCs were further evaluated as potential SIB anodes by using experimental and computational methods. Among them, the HC prepared from cellulose nanofibers delivers outstanding rate capability and cycling stability (∼210 mAh g –1 at 1000 mA g –1 ), exceeding the performance of its commercial counterpart. The excellent electrochemical performance is attributed to multiple merits: enlarged interplanar spacing, a hierarchical porous architecture, abundant defective sites, and enhanced conductivity arising from graphitic ribbon-like networks throughout the carbon matrix. Atomistic simulations using machine learning interatomic potentials further support these findings. Overall, this work offers new insights into the fundamental sodium-ion storage mechanisms in high-performance HC electrodes and highlights a sustainable route to next-generation SIB anodes.
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