Simulation Study of the Effects of Polymer Network Dynamics and Mesh Confinement on the Diffusion and Structural Relaxation of Penetrants
arXiv:2301.05356 · doi:10.1063/5.0148247
Abstract
The diffusion of small molecular penetrants through polymeric materials represents an important fundamental problem, relevant to the design of materials for applications such as coatings and membranes. Polymer networks hold promise in these applications, because dramatic differences in molecular diffusion can result from subtle changes in the network structure. In this paper, we use molecular simulation to understand the role that crosslinked network polymers have in governing the molecular motion of penetrants. By considering the local, activated alpha relaxation time of the penetrant and its long-time diffusive dynamics, we can determine the relative importance of activated glassy dynamics on penetrants at the segmental scale versus entropic mesh confinement on penetrant diffusion. We vary several parameters, such as the crosslinking density, temperature, and penetrant size, to show that crosslinks primarily affect molecular diffusion through modification of the matrix glass transition, with local penetrant hopping at least partially coupled to the segmental relaxation of the polymer network. This coupling is very sensitive to the local activated segmental dynamics of the surrounding matrix, and we also show that penetrant transport is affected by dynamic heterogeneity at low temperatures. To contrast, only at high temperatures and for large penetrants or when the dynamic heterogeneity effect is weak does the effect of mesh confinement become significant, even though penetrant diffusion more broadly empirically follows similar trends as established models of mesh confinement-based transport.
arXiv commentIncluding a main text and a supporting information, for main text: 33 pages, 1 table, and 9 figures; for supporting information: 3 figures and 1 table. Totally, 35 pages, 2 tables, and 12 figures
References in corpus (11)
- Theoretical perspective on the glass transition and amorphous materials
- Testing Mode-Coupling Theory for a Supercooled Binary Lennard-Jones Mixture I: The van Hove Correlation Function
- Fractional Stokes-Einstein and Debye-Stokes-Einstein relations in a network forming liquid
- Nature of the Breakdown in the Stokes-Einstein Relationship in a Hard Sphere Fluid
- Investigating the influence of different thermodynamic paths on the structural relaxation in a glass forming polymer melt
- Collective dynamics effect transient subdiffusion of inert tracers in gel networks
- The origin of mechanical enhancement in polymer nanoparticle composites with ultra-high nanoparticle loading
- How Segmental Dynamics and Mesh Confinement Determine the Selective Diffusivity of Molecules in Crosslinked Dense Polymer Networks
- Soft interactions modify the diffusive dynamics of polymer-grafted nanoparticles in solutions of free polymer
- The microscopic origins of stretched exponential relaxation in two model glass-forming liquids as probed by simulations in the isoconfigurational ensemble
- Self-Consistent Hopping Theory of Activated Relaxation and Diffusion of Dilute Penetrants in Dense Crosslinked Polymer Networks