Premelting layer during ice growth: role of clusters.

The premelting layer plays an important role in ice growth, but there is a significant gap in our knowledge between the atomistic premelting surface structure and the macroscopic growth mechanism. In this work, using large-scale molecular dynamics simulation, we reveal the existence of clusters on the premelting surface, as an intermediate feature bridging the gap. We show the spontaneous formation and evolution of clusters, and they form a stable distribution determined by the growth rate. We demonstrate how this stable distribution is related to the growth mode of ice, connected by the growth of clusters. We come to a bilayer-by-bilayer growth mode at simulation-reachable high growth rates, but another mechanism, namely "cluster stacking", is speculated to exist at lower growth rates. This work builds a connection between the microscopic structure of the premelting layer and the macroscopic growth of ice, making a step forward toward the full understanding of premelting and ice growth.

Probing structural superlubricity of two-dimensional water transport with atomic resolution.

Low-dimensional water transport can be drastically enhanced under atomic-scale confinement. However, its microscopic origin is still under debate. In this work, we directly imaged the atomic structure and transport of two-dimensional water islands on graphene and hexagonal boron nitride surfaces using qPlus-based atomic force microscopy. The lattice of the water island was incommensurate with the graphene surface but commensurate with the boron nitride surface owing to different surface electrostatics. The area-normalized static friction on the graphene diminished as the island area was increased by a power of ~-0.58, suggesting superlubricity behavior. By contrast, the friction on the boron nitride appeared insensitive to the area. Molecular dynamic simulations further showed that the friction coefficient of the water islands on the graphene could reduce to <0.01.

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).