Ionic liquids (ILs)salts
in a liquid stateplay
a crucial role in various applications, such as green solvents for
chemical synthesis and catalysis, lubricants, especially for micro-
and nanoelectromechanical systems, and electrolytes in solar cells.
These applications critically rely on unique or tunable bulk properties
of ionic liquids, such as viscosity, density, and surface tension.
Furthermore, their interactions with different solid surfaces of various
roughness and structures may uphold other promising applications,
such as combustion, cooling, and coating. However, only a few systematic
studies of IL wetting and interactions with solid surfaces exist.
Here, we experimentally and theoretically investigate the dynamic
wetting and contact angles (CA) of water and three kinds of ionic
liquid droplets on hydrophobic microstructures of surface roughness
(r = 2.61) and packing fraction (ϕ = 0.47)
formed by micropillars arranged in a periodic pattern. The results
show that, except for water, higher-viscosity ionic liquids have greater
advancing and receding contact angles with increasing contact line
velocity. Water drops initially form a gas-trapping, CB wetting state,
whereas all three ionic liquid drops are in a Wenzel wetting state,
where liquids penetrate and completely wet the microstructures. We
find that an existing model comparing the global surface energies
between a CB and a Wenzel state agrees well with the observed wetting
states. In addition, a molecular dynamic model well predicts the experimental
data and is used to explain the observed dynamic wetting for the ILs
and superhydrophobic substrate. Our results further show that energy
dissipation occurs more significantly in the three-phase contact line
region than in the liquid bulk.