Crystal
nucleation from solution plays an important role in environmental,
biological, and industrial processes and mainly occurs at interfaces,
although the mechanisms are not well understood. We performed nucleation
experiments on glycine aqueous solutions and found that an oil–solution
interface dramatically accelerates glycine nucleation compared to
an air–solution interface. This is surprising given that nonpolar,
hydrophobic oil (tridecane) would not be expected to favor heterogeneous
nucleation of highly polar, hydrophilic glycine. Molecular dynamics
simulations found significantly enhanced vs depleted glycine concentrations
at the oil–solution vs air–solution interfaces, respectively.
We propose that this interfacial concentration effect facilitates
heterogeneous nucleation, and that it is due to dispersion interactions.
This interface effect is distinct from previously described mechanisms,
including surface functionalization, templating, and confinement and
is expected to be present in a wide range of solution systems. This
work provides new insight that is essential for understanding and
controlling heterogeneous nucleation.