阳极
材料科学
桥接(联网)
解码方法
钠
碳纤维
纳米技术
光电子学
计算机科学
化学
算法
电极
冶金
复合材料
计算机网络
物理化学
复合数
作者
Laiqiang Xu,Yu Li,Yinger Xiang,Chengshuai Li,Chengshuai Li,Huali Zhu,Chuanchang Li,Chuanchang Li,Guoqiang Zou,Hongshuai Hou,Xiaobo Ji
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-04-09
卷期号:19 (15): 14627-14651
被引量:64
标识
DOI:10.1021/acsnano.5c02665
摘要
Amorphous carbon, particularly hard carbon (HC), is widely considered as the most promising anode material for sodium-ion batteries (SIBs) due to its high reversible capacity and cost-effectiveness. However, the complex and poorly defined structural properties of HC present challenges in understanding the underlying sodium storage mechanisms. To facilitate the rational design of high-performance HC anodes, a comprehensive understanding of the correlation between microstructure and sodium storage behavior is critical. This Review critically examines the interplay between the structural features of HC and its sodium storage capabilities, focusing on two key factors: pore structure and surface functional groups. It begins by outlining the fundamental sodium storage mechanisms in HC, followed by an in-depth discussion of how pore structure and surface chemistry influence sodium-ion storage. Finally, strategic insights are provided on how to manipulate these structural factors to optimize sodium storage performance. This Review aims to drive the development of next-generation high-performance HC anodes and support the commercialization of SIBs.
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