Visualizing Eigen/Zundel cations and their interconversion in monolayer water on metal surfaces

The nature of hydrated proton on solid surfaces is of vital importance in electrochemistry, proton channels, and hydrogen fuel cells but remains unclear because of the lack of atomic-scale characterization. We directly visualized Eigen-and Zundel-type hydrated protons within the hydrogen bonding water network on Au(111) and Pt(111) surfaces, using cryogenic qPlus-based atomic force microscopy under ultrahigh vacuum. We found that the Eigen cations self-assembled into monolayer structures with local order, and the Zundel cations formed long-range ordered structures stabilized by nuclear quantum effects. Two Eigen cations could combine into one Zundel cation accompanied with a simultaneous proton transfer to the surface. Moreover, we revealed that the Zundel configuration was preferred over the Eigen on Pt(111), and such a preference was absent on Au(111).

Automated summary

The nature of hydrated proton on solid surfaces has been visualized using cryogenic qPlus-based atomic force microscopy. Eigen cations self-assemble into monolayer structures with local order, while Zundel cations form long-range ordered structures stabilized by nuclear quantum effects. It is found that Zundel configuration is preferred over Eigen on Pt(111), but such preference is absent on Au(111).