A dendritic molecule of poly(propylene imine) whose periphery
is
modified with photoresponsive mesogenic azobenzene units was synthesized.
This compound exhibited highly ordered smectic B or smectic A layer
structure orienting parallel to the substrate in the film state. When
this film of 90 nm thickness on a hydrophilic substrate was exposed
to UV (365 nm) light, the initial flat film morphology started to
form holes followed by a drastic transformation to form separated
dome structure of micrometer levels. Upon continuous UV light irradiation,
the domain height increased and reached to a level of ca. 8-fold higher
than that of the initial thickness, which can be correlated with the
disordering of layer structures as revealed by grazing angle incidence
X-ray diffraction measurements. This phototriggered dewetting behavior
depended on the film thickness. The thinner film resulted in local
migrations to form the smaller and more homogeneous domes. The dewetting
was observed below a threshold thickness of 100 nm. By UV light irradiation
through a photomask, phototriggered migration at micrometer distances
also occurred. By the combination of phototriggered migration and
concerted dewetting, characteristic hierarchical morphologies were
formed, depending on the initial film thickness. This work proposes
a new possibility to control and design the dewetting processes of
thin films using the dendritic material.