| Autor: |
Dinpajooh M; Department of Chemistry and Biochemistry, University of Oregon, Eugene, Oregon 97403, United States., Millis J; Department of Physics, University of Oregon, Eugene, Oregon 97403, United States., Donley JP; Material Science Institute, University of Oregon, Eugene, Oregon 97403, United States., Guenza MG; Department of Chemistry and Biochemistry, University of Oregon, Eugene, Oregon 97403, United States.; Department of Physics, University of Oregon, Eugene, Oregon 97403, United States.; Material Science Institute, University of Oregon, Eugene, Oregon 97403, United States.; Institute for Fundamental Science, University of Oregon, Eugene, Oregon 97403, United States. |
| Abstrakt: |
While the excess chemical potential is the key quantity in determining phase diagrams, its direct computation for high-density liquids of long polymer chains has posed a significant challenge. Computationally, the excess chemical potential is calculated using the Widom insertion method, which involves monitoring the change in internal energy as one incrementally introduces individual molecules into the liquid. However, when dealing with dense polymer liquids, inserting long chains requires generating trial configurations with a bias that favors those at low energy on a unit-by-unit basis: a procedure that becomes more challenging as the number of units increases. Thus, calculating the excess chemical potential of dense polymer liquids using this method becomes computationally intractable as the chain length exceeds N ≥ 30. Here, we adopt a coarse-grained model derived from the integral equation theory for which inserting long polymer chains becomes feasible. The integral equation theory of coarse graining (IECG) represents a polymer as a sphere or a collection of blobs interacting through a soft potential. We employ the IECG approach to compute the excess chemical potential using Widom's method for polymer chains of increasing lengths, extending up to N = 720 monomers, and at densities reaching up to ρ = 0.767 g/cm 3 . From a fundamental perspective, we demonstrate that the excess chemical potentials remain nearly constant across various levels of coarse graining, offering valuable insights into the consistency of this type of procedure. Ultimately, we argue that current Monte Carlo algorithms, originally designed for atomistic simulations, such as configurational bias Monte Carlo (CBMC) methods, can significantly benefit from the integration of the IECG approach, thereby enhancing their performance in the study of phase diagrams of polymer liquids. |
