Previous
work has shown that photoisomerization of dopant molecules
in a polystyrene film can either enhance or suppress its adhesion
to a polar glass surface (MostafaviS. H.
Mostafavi, S. H.
Macromolecules20185123882394; MostafaviS. H.
Mostafavi, S. H.
Macromolecules20195263116317). In this paper, a different polymer host,
Zeonex (ZX), is used in conjunction with the photochrome spiropyran.
Nonpolar ZX has a higher glass transition temperature that makes it
resistant to nanoscale mechanical deformations, while the spiropyran
(SP) → merocyanine (MC) photoisomerization is a reversible
reaction with a large polarity change. Ultraviolet light isomerizes
SP to the polar MC form, increasing both the shear and pull-off adhesion
forces to a clean glass surface by a factor of 5. Visible irradiation
switches it back to the nonpolar SP form and returns the film back
to its original weak adhesion, in contrast to the previously studied
polystyrene films. The ability of visible light to switch off the
polymer–glass adhesion is harnessed to make a light-controlled
payload release device as well as to accelerate the polymer film delamination
rate in water by a factor of 100. The kinetics of the water delamination,
as well as the origin of residual adhesion after switching back to
the SP form, are investigated. This work demonstrates how light-controlled
noncovalent adhesion can be used as a solvent-free method to remove
protective coatings or to disassemble structures.