阳极
电容器
法拉第效率
阴极
锂(药物)
材料科学
碳纤维
功率密度
储能
电极
化学工程
无定形碳
纳米技术
无定形固体
电气工程
化学
功率(物理)
复合材料
物理
工程类
电压
热力学
有机化学
复合数
物理化学
医学
内分泌学
作者
So Hyun Jeon,Sehee lm,Inyeong Kang,Dongki Shin,Seung‐Ho Yu,Minah Lee,Jihyun Hong
出处
期刊:Small
[Wiley]
日期:2024-02-27
卷期号:20 (30): e2401295-e2401295
被引量:10
标识
DOI:10.1002/smll.202401295
摘要
Lithium-ion capacitors (LICs) exhibit superior power density and cyclability compared to lithium-ion batteries. However, the low initial Coulombic efficiency (ICE) of amorphous carbon anodes (e.g., hard carbon (HC) and soft carbon (SC)) limits the energy density of LICs by underutilizing cathode capacity. Here, a solution-based deep prelithiation strategy for carbon anodes is applied using a contact-ion pair dominant solution, offering high energy density based on a systematic electrode balancing based on the cathode capacity increased beyond the original theoretical limit. Increasing the anode ICE to 150% over 100%, the activated carbon (AC) capacity is doubled by activating Li+ cation storage, which unleashes rocking-chair LIC operation alongside the dual-ion-storage mechanism. The increased AC capacity results in an energy density of 106.6 Wh kg-1 AC+SC, equivalent to 281% of that of LICs without prelithiation. Moreover, this process lowers the cathode-anode mass ratio, reducing the cell thickness by 67% without compromising the cell capacity. This solution-based deep chemical prelithiation promises high-energy LICs based on transition metal-free, earth-abundant active materials to meet the practical demands of power-intensive applications.
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