阳极
多孔性
酰胺
表面改性
电化学
锂(药物)
材料科学
化学工程
碳纤维
化学
无机化学
电极
有机化学
复合材料
复合数
物理化学
内分泌学
工程类
医学
作者
Dong‐Geon Lee,Taeeun Yim,Sang‐Gil Woo,Ji‐Sang Yu
出处
期刊:ChemPhysChem
[Wiley]
日期:2019-01-10
卷期号:20 (5): 752-756
被引量:3
标识
DOI:10.1002/cphc.201801018
摘要
Abstract Porous carbonaceous anode materials have received considerable attention as an alternative anode material, however, there is a critical bottleneck as it suffers from a large irreversible specific capacity loss over several initial cycles owing to undesired surface reactions. In order to suppress undesired surface reactions of porous carbonaceous anode material, here, we suggest a simple and convenient two‐step surface modification approach that allows the embedding of an amide functional group on the surface of a porous carbonaceous anode, which effectively improves the surface stability. In this approach, the porous carbonaceous anode material is firstly activated by means of strong acid treatment comprising a combination of H 2 SO 4 and HNO 3 , and it is subjected to further modification by means of an amide coupling reaction. Our additional systematic analyses confirm that the acid functional group effectively transforms into the amide functional group. The resulting amide‐functionalized porous carbon exhibits an improved electrochemical performance: the initial discharge specific capacity is greatly reduced to less than 2,620 mA h g −1 and charge specific capacity is well still remained, indicating stabling cycling performance of the cell.
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