微分电容
电容
电荷密度
分子动力学
亥姆霍兹自由能
化学物理
从头算
电场
化学
双层电容
极化(电化学)
水溶液
密度泛函理论
表面电荷
双层(生物学)
材料科学
计算化学
电化学
纳米技术
电极
图层(电子)
物理化学
热力学
物理
量子力学
介电谱
有机化学
作者
Xue Wang,Yongbo Kuang,Jiabo Le
标识
DOI:10.1016/j.coelec.2023.101341
摘要
The surface charge density is a crucial property of the electric double layer. It determines the strength of the electric field, the water orientation, and ion hydration structure at interface and thus has strong impact on the performance of electrocatalytic reactions. While surface charge density cannot be directly controlled in electrochemical experiments, it can be estimated from the potential of zero charge and the differential double layer capacitance curve. In this mini-review, taking the metal/aqueous solution interface as the study case, we summarize the recent advances in determining their potential of zero charge and Helmholtz capacitance with ab initio molecular dynamics simulations. By comparing computational and theoretical results, we also discuss factors that influence the potential of zero charge and Helmholtz capacitance, including metal surface work function, metal-solvent chemical interactions, electrode polarization, and ion hydration structure at the interface. These insights provide a more detailed microscopic understanding of the electric double layer.
科研通智能强力驱动
Strongly Powered by AbleSci AI