In-Situ Electron Microscopy Examines Atomic Adsorption on Surfaces of Solid-Liquid Interfaces

In-Situ Electron Microscopy Examines Atomic Adsorption on Surfaces of Solid-Liquid Interfaces

**Groundbreaking In-Situ Microscopy Method Reveals Gold Atom Dynamics on Graphene**

A significant advancement in chemical microscopy has surfaced, enabling scientists to witness how gold atoms engage with graphene in various solvents. By enhancing the exploration of solid-liquid interfaces, this innovative technique carries potential for the enhancement of catalysts, fuel cells, and batteries.

Conventional methods such as transmission electron microscopy (TEM) necessitate a vacuum, complicating the study of atomic behavior within a solution context. To overcome this hurdle, researchers have utilized nanosized cells that trap liquids between two sheets of graphene. Although promising, these cells frequently encounter contamination from sealing adhesives, and solvent evaporation during cell assembly can lead to fluctuations in solution concentration.

The groundbreaking method, as explained by Sarah Haigh from the University of Manchester, immerses the cells in a solution, sealing them with a silicon nitride cantilever, which ultimately detaches like a “Post-it note”. This technique has been applied to monitor the adsorption behaviors of gold atoms on graphene in five distinct solvents: acetone, ethanol, water, butanol, and cyclohexanone.

The research team employed an artificial intelligence tool to analyze over a million gold atoms captured in images of the cells. Their results demonstrated that in acetone, gold atoms appeared predominantly as isolated entities due to the solvent’s low polarity, resulting in heightened repulsive forces among the gold ions. In contrast, polar solvents like water and cyclohexanone promoted the emergence of large gold nanoparticles through atom aggregation.

Sarah Haigh underscores the importance of this novel technique, shifting from indirect inference toward direct visualization of surface interactions at the solid-liquid interface. In agreement, Alex Robertson from the University of Warwick commends the achievement as a “technical tour de force”, highlighting the insights gathered regarding atomic interactions with 2D materials in solution, pertinent for catalytic uses.

Looking forward, Haigh aspires to investigate dynamic reactions at solid-liquid interfaces and foresees the technique’s application in advancing studies on materials critical to energy solutions such as batteries and fuel cells.