Filling the gaps: Introducing plasticizers into π-conjugated OPE-NH Langmuir layers for defect-free anisotropic interfaces and membranes towards unidirectional mass, charge, or energy transfer.

The construction of ultrathin membranes from linearly aligned π-electron systems is advantageous for targeted energy, charge, or mass transfer. The Langmuir-Blodgett (LB) technique enables the creation of such membranes, especially with amphiphilic π-electron systems. However, these systems often aggregate, forming rigid Langmuir monolayers with defects or holes. In this study we introduce plasticizers to effectively address this issue. To create anisotropic membranes, we used an oligo(phenylene ethynylene) derivative (OPE-NH) as an linear amphiphile and bisphenol A di-tert-butyl ester (BPAE) as a plasticizer. We analyzed surface pressure (mean molecular area) (Π(mma)) isotherms and characterized Langmuir monolayers with Brewster Angle Microscopy (BAM), to determine the optimal miscibility of OPE-NH with BPAE. Detailed analysis of hole areas filled was performed through image binarization. We identified an optimal BPAE concentration of 4 mol-% in the OPE-NH Langmuir monolayer. Our BAM image evaluation via binarization determined the difference between the mean molecular areas of close-packed Langmuir domains and those quantified via the Π(mma) isotherm. This study presents an automated method for BAM image analysis and a new approach for fabricating defect-free anisotropic molecular monolayers of π-conjugated amphiphiles.