Institute of Engineering Thermodynamics, Computational Electrochemistry, German Aerospace Center (DLR), 70569 Stuttgart, Germany.
Phys Chem Chem Phys. 2018 Nov 14;20(44):27804-27821. doi: 10.1039/c8cp05113e.
We deduce a generic interface theory to describe charge and electron transfer reactions at electrified interfaces based on fundamental principles. Considering the contact between a solid electrode and a liquid electrolyte, the model allows the consistent determination of emerging electric fields and space charge layers at the interface. The interaction between charge transport and the electrochemical double layer at the boundary between the electrode and electrolyte is investigated. Time scales of interfacial reaction and transport processes are analyzed. Further, we present a reduced bulk model of the electrochemical interface, which allows us to incorporate properties of the electrochemical double layer as extended boundary conditions in transport models of lithium-ion batteries. Numerically less intensive, the reduced model builds a bridge between our detailed description of reactions at electrified interfaces and commonly used modeling approaches for electrode reactions. With both the full and the reduced model, we simulate the impedance response of an electrochemical cell.
我们基于基本原理推导出一种通用的界面理论,以描述在带电界面处的电荷和电子转移反应。考虑到固体电极与液体电解质之间的接触,该模型允许在界面处一致地确定新兴的电场和空间电荷层。我们研究了电荷输运与电极和电解质之间边界处电化学双层之间的相互作用。分析了界面反应和输运过程的时间尺度。此外,我们提出了电化学界面的简化体模型,该模型允许我们将电化学双层的性质作为锂离子电池输运模型的扩展边界条件纳入其中。简化模型的数值计算强度较低,它在我们对带电界面反应的详细描述与电极反应常用的建模方法之间建立了桥梁。我们使用全模型和简化模型都对电化学池的阻抗响应进行了模拟。