Water‐Splitting “Without Water”: Splitting of the Crystallised Water of Hydrated Salts

In contrast to the liquid phase of water, the structural molecular realities of H<sub>2</sub>O molecules embedded in crystallised salts vary little and can be precisely determined. However, this water, which is neither in the liquid nor in the gas phase, has not yet been used in water electrolysis. Here, we demonstrate that water electrolysis can be achieved without the addition of (liquid) water through experiments with a wide range of hydrated salts and organic solvent suspensions. We obtain an excellent correlation between the position of the FTIR O─H stretch vibration of the hydrated salts and the onset of the OER potential from CV measurements. Together with first-principles density functional theory calculations, we demonstrate that intramolecular bonds in crystallised water can be effectively controlled through choice of the inorganic salt. Targeted manipulation of the bonds in the H<sub>2</sub>O molecule is a promising new approach to more efficient hydrogen production.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-12-06
DOI
https://doi.org/10.1002/anie.202520018
Citations
1
Primary Topic
Spectroscopy and Quantum Chemical Studies
Type
article
Field-Weighted Citation Impact
1.25
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Water‐Splitting “Without Water”: Splitting of the Crystallised Water of Hydrated Salts

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article

Water‐Splitting “Without Water”: Splitting of the Crystallised Water of Hydrated Salts

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article en
1 citations

Abstract

In contrast to the liquid phase of water, the structural molecular realities of H<sub>2</sub>O molecules embedded in crystallised salts vary little and can be precisely determined. However, this water, which is neither in the liquid nor in the gas phase, has not yet been used in water electrolysis. Here, we demonstrate that water electrolysis can be achieved without the addition of (liquid) water through experiments with a wide range of hydrated salts and organic solvent suspensions. We obtain an excellent correlation between the position of the FTIR O─H stretch vibration of the hydrated salts and the onset of the OER potential from CV measurements. Together with first-principles density functional theory calculations, we demonstrate that intramolecular bonds in crystallised water can be effectively controlled through choice of the inorganic salt. Targeted manipulation of the bonds in the H<sub>2</sub>O molecule is a promising new approach to more efficient hydrogen production.

Angewandte Chemie International EditionVol. 65(4)
Osnabrück University (DE), London Biofoundry (GB), Hochschule Osnabrück (DE)
Openalex Percentile: Top 15%
Spectroscopy and Quantum Chemical Studies
1.25
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