电解质
惰性
作文(语言)
化学
化学工程
热力学
物理
物理化学
工程类
有机化学
电极
哲学
语言学
作者
Xing Ding,Batyr Garlyyev,Sebastian Watzele,Theophilus Kobina Sarpey,Aliaksandr S. Bandarenka
标识
DOI:10.1002/chem.202101537
摘要
The influence of electrolyte pH, the presence of alkali metal cations (Na+ , K+ ), and the presence of O2 on the interfacial water structure of polycrystalline gold electrodes has been experimentally studied in detail. The potential of maximum entropy (PME) was determined by the laser-induced current transient (LICT) technique. Our results demonstrate that increasing the electrolyte pH and introducing O2 shift the PME to more positive potentials. Interestingly, the PME exhibits a higher sensitivity to the pH change in the presence of K+ than Na+ . Altering the pH of the K2 SO4 solution from 4 to 6 can cause a drastic shift in the PME. These findings reveal that, for example, K2 SO4 and Na2 SO4 cannot be considered as equal supporting electrolytes: it is not a viable assumption. This can likely be extrapolated to other common "inert" supporting electrolytes. Beyond this, knowledge about the near-ideal electrolyte composition can be used to optimize electrochemical devices such as electrolyzers, fuel cells, batteries, and supercapacitors.
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