Le Jia-Bo, Chen Ao, Kuang Yongbo, Cheng Jun
Key Laboratory of Advanced Fuel Cells and Electrolyzers Technology of Zhejiang Province, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo 315201, China.
State Key Laboratory of Physical Chemistry of Solid Surfaces, iChEM, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.
Natl Sci Rev. 2023 Apr 20;10(9):nwad105. doi: 10.1093/nsr/nwad105. eCollection 2023 Sep.
Cation effects have been shown in numerous experiments to play a significant role in electrocatalysis. To understand these effects at the molecular level, we systematically investigate the structures and capacitances of electric double layers with a variety of cations as counter charges at Pt(111)-CO/water interfaces with molecular dynamics. It is encouraging to find that the computed Helmholtz capacitances for different cations are in quantitative agreement with experiments, and that the trend of cation effects on capacitances shows clear correlation with the structures of interface cations of differing sizes and hydration energies. More importantly, we demonstrate the Helmholtz capacitance as the key descriptor for measuring the activity of CO-CO dimerization, the rate-determining step for C formation in electroreduction of CO and CO. Our work provides atomistic insights into cation effects on electric double layers and electrocatalysis that are crucial for optimizing electrode and electrolyte materials.
在众多实验中已表明阳离子效应在电催化中起着重要作用。为了在分子水平上理解这些效应,我们利用分子动力学系统地研究了在Pt(111)-CO/水界面上以各种阳离子作为反电荷的双电层的结构和电容。令人鼓舞的是,发现计算得到的不同阳离子的亥姆霍兹电容与实验结果在数量上一致,并且阳离子对电容的影响趋势与不同大小和水合能的界面阳离子结构呈现出明显的相关性。更重要的是,我们证明了亥姆霍兹电容是测量CO-CO二聚化活性的关键描述符,而CO-CO二聚化是CO和CO电还原生成C过程中的速率决定步骤。我们的工作为阳离子对双电层和电催化的影响提供了原子层面的见解,这对于优化电极和电解质材料至关重要。