Unveiling the Coexistence of Structural Isomers in the Hydrolysis of ZrO2: A Combined Computational and Photoelectron Spectroscopy Study

High-resolution anion photoelectron spectroscopy of the ZrO₃H₂^- and ZrO₃D₂^- anions and complementary electronic structure calculations are used to investigate the reaction between zirconium dioxide and a single water molecule, ZrO₂^0/- + H₂O. Experimental spectra of ZrO₃H₂^- and ZrO₃D₂^- were obtained using slow photoelectron velocity-map imaging (cryo-SEVI), revealing the presence of two dissociative adduct conformers and yielding insight into the vibronic structure of the corresponding neutral species. Franck-Condon simulations for both the \textit{cis}-- and \textit{trans}--dihydroxide structures are required to fully reproduce the experimental spectrum. Additionally, it was found that water-splitting is stabilized more by ZrO₂ than TiO₂, suggesting Zr-based catalysts are more reactive toward hydrolysis.