Year: 2025
Type: article
Abstract: Compatibilized polymer blends are a complex yet versatile and widespread category of materials. When the components of a binary blend are immiscible, they are typically driven toward a macrophase-separated state, but with the introduction of electrostatic interactions, they can be either homogenized or shifted to microphase separation. However, both experimental and simulation approaches face significant challenges in efficiently exploring the vast design space of charge-compatibilized polymer blends, encompassing chemical interactions, architectural properties, and composition. In this work, we introduce a white-box machine learning approach integrated with polymer field theory to predict the phase behavior of these systems, which is significantly more accurate than conventional black-box machine learning approaches. The random phase approximation (RPA) calculation is used as a testbed to determine polymer phases. Instead of directly predicting the polymer phase output of RPA calculations from a large input space by a machine learning model, we build a parallel partial Gaussian process model to predict the most computationally intensive component of the RPA calculation that involves only polymer architecture parameters as inputs. This approach substantially reduces the computational cost of the RPA calculation across a vast input space with nearly 100% accuracy for the out-of-sample prediction, enabling rapid screening of polymer blend charge-compatibilization designs. More broadly, the white-box machine learning strategy offers a promising approach for the dramatic acceleration of polymer field-theoretic methods for mapping out polymer phase behavior.
Source: Macromolecules
Authors: Clayton Ellis, Xinyi Fang, Christopher Balzer, Timothy Quah, M. Scott Shell, Glenn H. Fredrickson, Mengyang Gu
Language: English
Subfield: Materials Chemistry
Field: Materials Science
Domain: Physical Sciences
Open Access status: green
Funder: National Science Foundation
OpenAlex ID: W4417436849