A better understanding
of the dynamic behavior of polymer chains
on solid surfaces is indispensable for the design and construction
of high-performance polymer composites. We herein visualized the in-plane
movement of isolated poly(methyl methacrylate) (PMMA) and poly(tert-butyl methacrylate) (PtBMA) single
chains on hydrophilic silicon wafers under ambient conditions by atomic
force microscopy. Isolated PMMA chains adsorbed to the substrate,
whereas PtBMA chains diffused, the degree of which
was dependent on the humidity. Neutron reflectivity revealed the formation
of a layer of condensed water on the substrate. All-atomistic molecular
dynamics simulations implied that the diffusivity difference of the
two polymers was based on the submerged depth in which a part of a
chain existed. That is, the interaction of a polymer with the surface
of the hydrophilic substrate primarily governs its lateral movement,
or adsorption behavior, facilitated by the presence of water.