材料科学
阴极
电化学
离子
超级电容器
兴奋剂
多孔性
纳米技术
锂(药物)
碳纤维
电极
化学工程
光电子学
化学物理
复合材料
化学
复合数
有机化学
物理化学
工程类
内分泌学
医学
作者
Kexin Liang,Kaixiang Zou,Jinhai Liu,Yuanfu Deng,Guohua Chen
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-06-30
卷期号:8 (7): 3204-3213
被引量:10
标识
DOI:10.1021/acsenergylett.3c00924
摘要
Lithium-ion capacitors (LICs), by integrating the merits of batteries and supercapacitors, can improve energy/power density compatibly. However, the current understanding of the structure–property–performance relationship has limited the further development of carbon-based electrodes. Here we discuss how the architecture of interlayer channels influences the ion accessibility and selectivity in N-doped porous carbon (NDPC) cathodes. Electrochemical and spectroscopic measurements reveal that large interlayer channels provide high permeability for different anions and rearrange to buffer the volume variation. Conversely, narrow slits show high ion selectivity and suffer from distortion interacting with large anions. The turning point is the tuned channel size after the carbon layer rearrangement in the soaking process. Contrary to the popular opinion that pore size dominates capacitive behavior while d-spacing determines the intercalative process, we demonstrate the importance of interlayer spacing in electrical double-layer mechanism for NDPCs. This size effect is also successfully put into practice for developing advanced LICs.
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