RESUMO
We used single-molecule tracking experiments to observe the motion of small hydrophobic fluorescent molecules at the interface between water and a solid surface that exhibited periodic chemical patterns. The dynamics were characterized by non-ergodic, continuous time random walk statistics. The step-size distributions displayed enhanced probability of steps to periodic distances, consistent with theoretical predictions for diffusion in an atomic/molecular scale periodic potential. Surprisingly, this general behavior was observed here for surfaces exhibiting characteristic length scales three orders of magnitude larger than atomic/molecular dimensions, and may provide a new way to understand and control solid-liquid interfacial diffusion for molecular targeting applications.
