Affiliation:
1. Department of Chemistry Oregon State University Corvallis OR 97331–4003 United States
2. Department of Chemical and Biomolecular Engineering Vanderbilt University Nashville TN 37235 United States
3. Materials Science and Engineering University of California Riverside Riverside CA 92521 United States
Abstract
AbstractThe electrochemical stability window of water is known to vary with the type and concentration of dissolved salts. However, the underlying influence of ions on the thermodynamic stability of aqueous solutions has not been fully understood. Here, we investigated the electrolytic behaviors of aqueous electrolytes as a function of different ions. Our findings indicate that ions with high ionic potentials, i.e., charge density, promote the formation of their respective hydration structures, enhancing electrolytic reactions via an inductive effect, particularly for small cations. Conversely, ions with lower ionic potentials increase the proportion of free water molecules—those not engaged in hydration shells or hydrogen‐bonding networks—leading to greater electrolytic stability. Furthermore, we observe that the chemical environment created by bulky ions with lower ionic potentials impedes electrolytic reactions by frustrating the solvation of protons and hydroxide ions, the products of oxygen evolution reaction (OER) and hydrogen evolution reaction (HER), respectively. We found that the solvation of protons plays a more substantial role than that of hydroxide, which explains a greater shift for OER than for HER, a puzzle that cannot be rationalized by the notion of varying O−H bond strengths of water. These insights will help the design of aqueous systems.
Funder
Division of Materials Research
Division of Chemical, Bioengineering, Environmental, and Transport Systems
Division of Chemistry
Cited by
1 articles.
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