Abstract

We isolated the key substrate–polymer interactions responsible for the propagation of substrate surface field effects in block polymer (BP) thin films through a modified approach to the Owens and Wendt interfacial energy formalism. This modification captured the influence of long-range surface energy components on through-film nanostructure orientation in BP thin films, and it provides a framework for manipulating BP thin film behavior without the need for extensive parameter space exploration. Optical microscopy (OM) of gradient thickness films on chlorosilane-modified substrates provided a high-throughput approach for identifying the critical propagation depth of substrate–polymer interfacial energy effects. Atomic force microscopy (AFM) was combined with OM to verify changes in free surface nanostructure as a function of film thickness. Using a model poly(methyl methacrylate-b-n-butyl acrylate) BP thin films system, we mapped the critical propagation depth as a function of interfacial energy difference...

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