阳极
石墨烯
材料科学
聚偏氟乙烯
碳纤维
锂(药物)
化学工程
氧化物
电容器
热解
纳米技术
复合数
复合材料
电极
化学
电压
聚合物
电气工程
医学
物理化学
内分泌学
工程类
冶金
作者
Yibo Ma,Kai Wang,Yanan Xu,Xudong Zhang,Qunjia Peng,Shani Li,Xiong Zhang,Xianzhong Sun,Yanwei Ma
出处
期刊:Carbon
[Elsevier]
日期:2023-01-01
卷期号:202: 175-185
被引量:12
标识
DOI:10.1016/j.carbon.2022.11.030
摘要
The sluggish kinetics of battery-type anode limits the realization of high capacitance especially at elevated charge-discharge rates for lithium-ion capacitors (LICs). In this work, graphene wrapped carbon cages (GxPy) are obtained via a facile physical-confined pyrolysis approach from graphene oxide (GO)/polyvinylidene fluoride (PVDF), which exhibits great promise as a fast and large-capacity anode for LICs. The thermal degradation process analysis reveals that carbon cages with abundant mesopores derived from the dehalogenation of PVDF are formed spontaneously due to the HF releasing in the pyrolysis process with the aid of physical confined GO template. Hollow carbon cages could ameliorate the Li+ transport path, while 2D graphene serves as a conducting bridge connecting the isolated carbon cages to minimize the barrier of charge transfer. As a result, a LIC pouch-cell based on GxPy hierarchical carbon anode demonstrates high energy density and superior power density, as well as remarkable cycle life. This study may open a unique avenue for designing fast and large-capacity carbon anode and push the development of high-performance LICs.
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