Abstract
The microscopic details of the flow of energy in a single chain of polyethylene containing 300 atoms is discussed. The intramolecular dynamics of the polyethylene molecule is studied as a function of CH stretch excitation, temperature, and pressure. The rate of energy flow from CH stretching modes is found to be very rapid and irreversible, occurring on a timescale of less than 0.5 ps at low temperatures, and increases with temperature. A general characteristic two-phase energy flow behavior is observed, where there is initially a very rapid flow (due to the decay of the initial excitation) followed by a slower flow (due to energy redistribution throughout the system). The mechanism for the initial facile energy flow is shown to involve strong resonant pathways. In particular, a CH stretch/HCH bend Fermi (1:2) resonance is shown to dominate the short-time dynamics and facilitates the overall process of energy redistribution. The increase in the rate of energy flow as a function of the backbone temperature is found to be due to the increase in the density of the bath states for energy redistribution which subsequently results in the formation of new low-order resonant interactions (1:1, etc). The long-time dynamics, associated to complete redistribution of the initial CH stretch energy with all of the 894 available vibrational modes, occurs within a time of 2 ps. This timescale corresponds to the time for intramolecular redistribution. A comparison of the intramolecular redistribution time to that of intermolecular redistribution (redistribution in the condensed or solid phase as opposed to a single chain) is also made. A preliminary study of energy flow in a crystal of polyethylene (system containing 19 polyethylene chains) shows that the energy flow exhibits two very different time behaviors. The first is for the intramolecular redistribution as in the single chain study and the second is for intermolecular (chain-to-chain) redistribution. The timescale for intermolecular redistribution is found to be on the order of 0.2 ns at room temperature and pressure, about two orders of magitude larger than the intramolecular timescale.
| Original language | English |
|---|---|
| Pages (from-to) | 393-403 |
| Number of pages | 11 |
| Journal | Chemical Physics |
| Volume | 160 |
| Issue number | 3 |
| DOIs | |
| State | Published - Mar 15 1992 |
Funding
This work was supportedb y the Office of Basic Energy Sciences,U S Department of Energy, under Contract No. DE-AC05-840R2 1400 with Martin Marietta Energy Systems, Inc., and by the Polymer Program of the National Science Foundation, present Grant No. DMR-88 1841 2.B GS acknowledgesth e support provided by the Direction General de Investigation Cientilica y Ttcnica of the Ministry of Education and Science (MEC) of Spain for his stay at the Universidad Complutense de Madrid during the summer of 1991 . The computations were performed on the IBM 3081 and 3090 at the University of Tennessee,t he CRAY-YMP/48 at the National Center for Supercomputing Applications at the University of Illinois (grant CHE890025N), and the CRAY YMP at the NSF Pittsburgh Supercomputing Center (grant CHE9 1OOOPC ray sponsored research). We would like to thank E.L. Sibert III and S.K. Gray for useful suggestions on the use of cross-correlation functions and Langevin dynamics. We also thank Coral Getino for many discussions on energyt ransfer in polyatomic molecules.