Morphology engineering of biomass-derived porous carbon from 3D to 2D towards boosting capacitive charge storage capability

假电容 超级电容器 电容 电容感应 材料科学 形态学(生物学) 多孔性 碳纤维 纳米技术 电容器 生物量(生态学) 化学工程 复合材料 化学 电极 电压 复合数 计算机科学 电气工程 生态学 工程类 物理化学 操作系统 生物 遗传学
作者
Beichen Xue,Jiahuan Xu,Yi Feng,Jing Wang,Rui Xiao,Xiaofeng Wang
出处
期刊:Journal of Colloid and Interface Science [Elsevier BV]
卷期号:642: 736-746 被引量:15
标识
DOI:10.1016/j.jcis.2023.03.200
摘要

Carbon morphology significantly affects the capacitive performance of porous carbons. Biomass-derived porous carbons are usually restricted by inferior capacitive performance owing to their inherently three-dimensional (3D) blocked morphologies. Fabricating two-dimensional (2D) sheet-like morphology is expected to expose more inner space for better electrochemical performance, however, it needs to overcome the self-aggregation of biomass. The comprehensive understanding of how 2D morphology boosts capacitive performance remains challenging. Herein, we provide a morphology-regulating strategy to prepare 2D and 3D porous carbons and investigate the morphology effect on charge storage capability via both experimental data and theoretical simulations. 2D carbon exhibits better capacitance than 3D carbon in both electric double-layer capacitors (254 versus 211F g-1) and zinc-ion hybrid supercapacitors (320 versus 232F g-1), because the 2D carbon morphology not only improves the pore accessibility for higher double-layer capacitance, but also facilitates the exposure of active functional groups for more pseudocapacitance. Moreover, 2D morphology shortens pore length, leading to better anti-self-discharge capability. This study is beneficial to understanding the relationship between carbon morphology and capacitive performance and provides a facile strategy to upgrade biomass-derived porous carbons via morphology engineering.
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