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Effect of ion-specific water structures at metal surfaces on hydrogen production
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DOI：10.1038/s41467-024-52131-w.png)
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Abstract
En 中文
Water structures at electrolyte/electrode interfaces play a crucial role in determining the selectivity and kinetics of electrochemical reactions. Despite extensive experimental and theoretical efforts, atomic-level details of ion-specific water structures on metal surfaces remain unclear. Here we show, using scanning tunneling microscopy and noncontact atomic force microscopy, that we can visualize water layers containing alkali metal cations on a charged Au(111) surface with atomic resolution. Our results reveal that Li+ cations are elevated from the surface, facilitating the formation of an ice-like water layer between the Li+ cations and the surface. In contrast, K+ and Cs+ cations are in direct contact with the surface. We observe that the water network structure transitions from a hexagonal arrangement with Li+ to a distorted hydrogen-bonding configuration with Cs+. These observations are consistent with surface-enhanced infrared absorption spectroscopy data and suggest that alkali metal cations significantly impact hydrogen evolution reaction kinetics and efficiency. Our findings provide insights into ion-specific water structures on metal surfaces and underscore the critical role of spectator ions in electrochemical processes. Water structures at the electrolyte and electrode interfaces are crucial for electrochemical reactions. Here, the authors report that alkali metal cations can modify two-dimensional water networks at charged surfaces, impacting both reaction kinetics and efficiency.
Keywords:
ELECTRICAL DOUBLE-LAYER
INTERFACIAL WATER
ZERO CHARGE
EVOLUTION
GOLD
MOLECULES
OXIDATION
CATIONS
ELECTROREDUCTION
SPECTROSCOPY
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