Predicting glass transition of amorphous polymers by application of cheminformatics and molecular dynamics simulations

摘要

Predicting the glass-transition temperatures (T-g) of glass-forming polymers is of critical importance as it governs the thermophysical properties of polymeric materials. The cheminformatics approaches based on machine learning algorithms are becoming very useful in predicting the quantitative relationships between key molecular descriptors and various physical properties of materials. In this work, we developed a modeling framework by integrating the cheminformatics approach and coarse-grained molecular dynamics (CG-MD) simulations to predict T-g of a diverse set of polymers. The developed machine learning-based QSPR model identified the most prominent molecular descriptors influencing the T-g of a hundred of polymers. Informed by the QSPR model, CG-MD simulations are performed to further delineate mechanistic interpretation and systematic dependence of these influential molecular features on T-g by investigating three major CG model parameters, namely the cohesive interaction, chain stiffness, and grafting density. The CG-MD simulations reveal that the higher intermolecular interaction and chain stiffness increase the T-g of CG polymers, where their relative influences are coupled with the existence of side chains grafted on the backbone. This synergistic modeling framework provides valuable insights into the roles of key molecular features influencing the T-g of polymers, paving the way to establishing a materials-by-design framework for polymeric materials via molecular engineering.