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The glass transition behavior and conformational
variations of polymer films are investigated
across bulk, confined, and free-standing states.
By spanning a wide range of film thicknesses,
this work captures how spatial confinement, free
surfaces, and entanglement densities modify
thermodynamic behaviors and chain conformation.
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"Glass transition temperature of (ultra-)thin polymer films", J. Chem. Phys. 159, 071104 (2023).
"Efficient equilibration of confined and free-standing films of highly entangled polymer melts", arXiv:2009.08999, J. Chem. Phys. 153, 144902 (2020).