The Readiness of Water Molecules to Split into Hydrogen + Oxygen: A Proposed New Aspect of Water Splitting

Author:

Schäfer Helmut1ORCID,Schuster Anja2,Kunis Stefan3,Bookholt Tom1,Hardege Jörg4,Rüwe Klara1,Brune Julia1

Affiliation:

1. University of Osnabrück The Electrochemical Energy and Catalysis Group Barbarastrasse 7 49076 Osnabrück Germany

2. University of Osnabrück Institute of Chemistry Inorganic Chemistry II Barbarastrasse 7 49076 Osnabrück Germany

3. Institute of Mathematics and Center for Cellular Nanoanalytics Osnabrück University 49076 Osnabrück Germany

4. University of Hull School of Natural Sciences Hull University Hull HU67RX UK

Abstract

AbstractThe potential of the anode, at which the evolution of oxygen begins, is a key parameter that describes how well water is split in water electrolyzers. Research efforts related to electrocatalytically initiated water splitting that aim at reducing the oxygen evolution reaction (OER) overpotential to date focus on the optimization of materials used to produce the electrodes. Descriptors for the readiness of the H2O molecule itself to break down into its components have not been considered in water electrolysis experiments so far. In a simple set of experiments, it is found that adding dioxane to aqueous solutions leads to a substantial blueshift of the frequency of the OH stretch vibration which is a sign of an increased strength of the OH bond (intramolecular bonding). This phenomenon coincides with a significant increase in the OER onset potential as derived from cyclic voltammetry experiments. Thus, the OH stretch frequency can be an ideal indicator for the readiness of water molecules to be split in its cleavage products. This is thought to be first example of a study into the relationship between structural features of water as derived from Fourier transform infrared (FTIR) spectroscopic studies and key results derived from water electrolysis experiments.

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

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