Single chain structure in thin polymer films: Corrections to Flory's and Silberberg's hypotheses
A. Cavallo, M. M\"uller, J.P. Wittmer, A. Johner, and K. Binder

TL;DR
This study uses Monte Carlo simulations to analyze how ultrathin polymer films deviate from classical theories, revealing logarithmic divergence in chain size and power-law decay in bond correlations, with implications for experimental interpretations.
Contribution
It provides the first detailed simulation-based analysis of chain conformations in ultrathin films, extending beyond Flory's and Silberberg's hypotheses with new quantitative insights.
Findings
Logarithmic divergence of chain size parallel to walls in ultrathin films.
Bond-bond correlation function decreases as a power law with exponent 1.
Deviations from classical scattering models increase as film thickness decreases.
Abstract
Conformational properties of polymer melts confined between two hard structureless walls are investigated by Monte Carlo simulation of the bond-fluctuation model. Parallel and perpendicular components of chain extension, bond-bond correlation function and structure factor are computed and compared with recent theoretical approaches attempting to go beyond Flory's and Silberberg's hypotheses. We demonstrate that for ultrathin films where the thickness, , is smaller than the excluded volume screening length (blob size), , the chain size parallel to the walls diverges logarithmically, with . The corresponding bond-bond correlation function decreases like a power law, with being the curvilinear distance between bonds and . % Upon increasing the film thickness, , we find -- in contrast to Flory's…
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