Near-surface defects break symmetry in water adsorption on CeO2−x(111)

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Water interactions with oxygen-deficient cerium dioxide (CeO2) surfaces are central to hydrogen production and catalytic redox reactions, but the atomic-scale details of how defects influence adsorption and reactivity remain elusive. Here, we unveil how water adsorbs on partially reduced CeO2−x(111) using atomic force microscopy (AFM) with chemically sensitive, oxygen-terminated probes, combined with first-principles calculations. Our AFM imaging reveals water molecules as sharp, asymmetric boomerang-like features radically departing from the symmetric triangular motifs previously attributed to molecular water. Strikingly, these features localize near subsurface defects. While the experiments are carried out at cryogenic temperatures, water was dosed at room temperature, capturing configurations relevant to initial adsorption events in catalytic processes. Density functional theory identifies Ce3+ sites adjacent to subsurface vacancies as the thermodynamically favored adsorption sites, where defect-induced symmetry breaking governs water orientation. Force spectroscopy and simulations further distinguish Ce3+ from Ce4+ centers through their unique interaction signatures. By resolving how subsurface defects control water adsorption at the atomic scale, this work demonstrates the power of chemically selective AFM for probing site-specific reactivity in oxide catalysts, laying the groundwork for direct investigations of complex systems such as single-atom catalysts, metal-support interfaces, and defect-engineered oxides. Water interactions with cerium dioxide surfaces are central to hydrogen production and catalytic redox reactions. Here, atomic force microscopy with oxygen-terminated probes and first principles calculations provide detailed mechanistic insight of the interactions at play.

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