Water-Mediated Proton Hopping Mechanisms at the SnO<sub>2</sub>(110)/H<sub>2</sub>O Interface from Ab Initio Deep Potential Molecular Dynamics
Mei Jia, Yong‐Bin Zhuang, Feng Wang, Chao Zhang, Jun Cheng
Abstract
High Resolution Image Download MS PowerPoint Slide The interfacial proton transfer (PT) reaction on the metal oxide surface is an important step in many chemical processes including photoelectrocatalytic water splitting, dehydrogenation, and hydrogen storage. The investigation of the PT process, in terms of thermodynamics and kinetics, has received considerable attention, but the individual free energy barriers and solvent effects for different PT pathways on rutile oxide are still lacking. Here, by applying a combination of ab initio and deep potential molecular dynamics methods, we have studied interfacial PT mechanisms by selecting the rutile SnO 2 (110)/H 2 O interface as an example of an oxide with the characteristic of frequently interfacial PT processes. Three types of PT pathways among the interfacial groups are found, i.e., proton transfer from terminal adsorbed water to bridge oxygen directly (surface-PT) or via a solvent water (mediated-PT), and proton hopping between two terminal groups (adlayer PT). Our simulations reveal that the terminal water in mediated-PT prefers to point toward the solution and forms a shorter H-bond with the assisted solvent water, leading to the lowest energy barrier and the fastest relative PT rate. In particular, it is found that the full solvation environment plays a crucial role in water-mediated proton conduction, while having little effect on direct PT reactions. The PT mechanisms on aqueous rutile oxide interfaces are also discussed by comparing an oxide series composed of SnO 2, TiO 2, and IrO 2 . Consequently, this work provides valuable insights into the ability of a deep neural network to reproduce the ab initio potential energy surface, as well as the PT mechanisms at such oxide/liquid interfaces, which can help understand the important chemical processes in electrochemistry, photoelectrocatalysis, colloid science, and geochemistry.