Morhenn H, Busch S, Meyer H, Richter D, Petry W, Unruh T (2013)
Publication Status: Published
Publication Type: Journal article
Publication year: 2013
Publisher: AMER PHYSICAL SOC
Book Volume: 111
Journal Issue: 17
DOI: 10.1103/PhysRevLett.111.173003
Neutron scattering and extensive molecular dynamics simulations of an all atom C100H202 system were performed to address the short-time dynamics leading to center-of-mass self-diffusion. The simulated dynamics are in excellent agreement with resolution resolved time-of-flight quasielastic neutron scattering. The anomalous subdiffusive center-of-mass motion could be modeled by explicitly accounting for viscoelastic hydrodynamic interactions. A model-free analysis of the local reorientations of the molecular backbone revealed three relaxation processes: While two relaxations characterize local bond rotation and global molecular reorientation, the third component on intermediate times could be attributed to transient flowlike motions of atoms on different molecules. The existence of these collective motions, which are clearly visualized in this Letter, strongly contribute to the chain relaxations in molecular liquids.
APA:
Morhenn, H., Busch, S., Meyer, H., Richter, D., Petry, W., & Unruh, T. (2013). Collective Intermolecular Motions Dominate the Picosecond Dynamics of Short Polymer Chains. Physical Review Letters, 111(17). https://doi.org/10.1103/PhysRevLett.111.173003
MLA:
Morhenn, Humphrey, et al. "Collective Intermolecular Motions Dominate the Picosecond Dynamics of Short Polymer Chains." Physical Review Letters 111.17 (2013).
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