纳米孔
超级电容器
电解质
材料科学
纳米孔
化学物理
分子动力学
电极
纳米技术
储能
振荡(细胞信号)
离子
电容
功率(物理)
化学
计算化学
物理
物理化学
热力学
生物化学
有机化学
作者
Tangming Mo,Jianguo Zhou,Haoyu He,Bingzheng Zhu
标识
DOI:10.1021/acsami.3c12913
摘要
Nanopore electrodes have the potential to enhance the energy density of supercapacitors but tend to reduce charging dynamics, consequently impacting power density. A comprehensive understanding of their charging mechanisms can provide insights into how to boost charging dynamics. In this work, we conducted constant-potential-based molecular dynamics simulations to explore the charging mechanism of nanopore supercapacitors with organic electrolytes. Contrary to the traditional understanding associating larger pore sizes with faster charging, our results found a complex oscillatory behavior of the charging rate, correlating with nanopore size in organic electrolytes. An anomalously increased charging dynamics was found in the 0.9 nm pore. This anomalous enhancement can be attributed to the improved in-pore ion diffusion and reduced desolvation energy, owing to the orientation transition of the solvate molecules. These results pave a new way for innovative designs of nanoporous electrode supercapacitors that can enlarge both power and energy densities.
科研通智能强力驱动
Strongly Powered by AbleSci AI