Ultrastable Glassy Polymer Films with an Ultradense Brush Morphology

Glassy polymer films with extreme stability could enable major advancements in a range of fields that require the use of polymers in confined environments. Yet, from a materials design perspective, we now know that the glass transition temperature (T-g) and thermal expansion of polymer thin films can be dramatically different from those characteristics of the bulk, i.e., exhibiting confinement-induced diminished thermal stability. Here, we demonstrate that polymer brushes with an ultrahigh grafting density, i.e., an ultradense brush morphology, exhibit a significant enhancement in thermal stability, as manifested by an exceptionally high T-g and low expansivity. For instance, a 5 nm thick polystyrene brush film exhibits an similar to 75 K increase in T-g and , similar to 90% reduction in expansivity compared to a spin-cast film of similar thickness. Our results establish how morphology can overcome confinement and interfacial effects in controlling thin-film material properties and how this can be achieved by the dense packing and molecular ordering in the amorphous state of ultradense brushes prepared by surface-initiated atom transfer radical polymerization in combination with a self-assembled monolayer of initiators.

Automated summary

This study demonstrates that polymer brushes with ultrahigh grafting density exhibit significantly improved thermal stability, overcoming confinement and interfacial effects to control thin-film material properties. The dense packing and molecular ordering in the amorphous state of ultradense brushes prepared by surface-initiated atom transfer radical polymerization in combination with a self-assembled monolayer of initiators play a crucial role in enhancing the thermal stability of polymer films.