Microstructural Investigation into Na-Ion Storage Behaviors of Cellulose-Based Hard Carbons for Na-Ion Batteries

纤维素 无定形固体 材料科学 化学工程 微观结构 碳纤维 微晶纤维素 无定形碳 微晶 分解 热分解 晶体结构 离子 电化学 有机化学 化学 结晶学 复合材料 物理化学 冶金 电极 复合数 工程类
作者
Jae-Bum Kim,Gi‐Hyeok Lee,Vincent Wing‐hei Lau,Jiliang Zhang,Feng Zou,Mingzhe Chen,Limin Zhou,Kyung‐Wan Nam,Yong‐Mook Kang
出处
期刊:Journal of Physical Chemistry C [American Chemical Society]
卷期号:125 (27): 14559-14566 被引量:39
标识
DOI:10.1021/acs.jpcc.1c03984
摘要

The physicochemical properties of hard carbon can vary significantly depending on the precursor used during its synthesis. Among various precursors for hard carbon, cellulose has been getting significant attention because of the excellent electrochemical performances of the hard carbon obtained from its decomposition. However, the correlation between the microstructure or crystal structure of the resultant hard carbons from cellulose and their electrochemical properties looks still elusive. Hence, this study compares the sodium-ion storage behaviors of fiber cellulose-based hard carbon composed of crystalline and amorphous grains with those of microcrystalline cellulose (MCC)-based hard carbon without any amorphous grains. The presence or absence of amorphous regions affects the pore size and distribution of hard carbons significantly. Particularly, the hard carbon obtained from a thermal decomposition of MCC exhibited a high capacity reaching 300 mA h g–1 thanks to plenty of open pores, whose size is primarily less than 2 nm. Additionally, 23Na MAS NMR analysis revealed that the characteristic pore structure from MCC played a key role in extending the reversible sodium storage of hard carbon. This study provides a meaningful insight into understanding the effect of the microstructure and crystal structure on the sodium storage mechanism of hard carbons with different cellulose precursors.
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