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• W4386156514 abstract "The comprehensive interpretation of the measured differential Helmholtz capacitance curve is vital for advancing our understanding of the interfacial structure. While several possible physical effects contributing to the Helmholtz capacitance have been proposed theoretically, combining those factors to explain the experimentally observed potential-dependent capacitance profile remains a significant challenge. In this study, we employ ab initio molecular dynamics simulations to model various metal/solution interfaces. Our investigation primarily emphasizes the substantial effect of water chemisorption on the potential-dependent behavior of the Helmholtz capacitance. Additionally, we identify other critical factors that profoundly impact the Helmholtz capacitance: (1) Ions with low hydration energy hinder the availability of surface sites for water adsorption, resulting in a diminished enhancement of capacitance from water chemisorption. (2) Using large-sized ions leads to an expansion of the Helmholtz layer, causing a decrease in the Helmholtz capacitance. (3) Metal surfaces with higher affinity for water attract water adsorption at lower potentials, resulting in a lower peak potential for the differential Helmholtz capacitance curve." @default.
• W4386156514 created "2023-08-26" @default.
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• W4386156514 date "2023-08-25" @default.
• W4386156514 modified "2023-10-14" @default.
• W4386156514 title "Understanding the Effects of Electrode Material, Single Crystal Facet, and Electrolyte Ion on the Helmholtz Capacitance of Metal/Aqueous Solution Interfaces" @default.
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• W4386156514 doi "https://doi.org/10.1021/acs.jpclett.3c02108" @default.
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