Atomistic simulation of the glass transition of di-substituted polysilanes

Abstract

Molecular dynamics has been used to determine the glass transition temperature of the amorphous phase of five di-substituted polysilanes from plots of specific volume versus temperature. In each case, good agreement was obtained between the simulation values and the reported DSC results. The effect of amorphous cell dimensions and equilibration time on T_g has been investigated. The use of larger cells provides better agreement with experimental T_g and probably more accurate densities as suggested by earlier studies. The effect of pressure on the T_g of two different polysilanes was also investigated. Although experimental data for comparison is unavailable, values obtained for dT_g/dp are consistent with those reported for other polymers. Vectorial autocorrelation analysis was used to explore the mobility of the polysilane main chains and side groups relative to polyalkanes, polyphosphazenes, and polysiloxanes.