Probing High-Pressure Structural Evolution in Polyurea with In Situ Energy-Dispersive X-ray Diffraction and Molecular Dynamics Simulations

Polyurea, an elastomer with a phase-segregated microstructure, has been proven as an effective coating in defense applications. To gain a more complete understanding of the high-pressure atomic-level morphology of these phases and to validate molecular dynamics (MD) simulations, multi-angle energy-dispersive X-ray diffraction experiments were performed in situ up to pressures of similar to 6 GPa at room temperature. Structure factors were obtained and compared to MD simulations with an average error of less than 5% between major peak positions. The first sharp diffraction peak shifted from 4.56 A to lower d-spacing with pressure, indicating compression between hard segments. This was further supported by the behavior of a peak at similar to 3.86 A from the pair distribution function (PDF), suspected to represent p-stacking and separation between soft segments. Compression within the hard segments themselves is minimal as low-r peaks in the PDF are not greatly affected by pressure.

Automated summary

Polyurea, an elastomer with a phase-segregated microstructure, was studied under high pressure using multi-angle energy-dispersive X-ray diffraction experiments. The results indicate compression between hard segments and an increase in π-stacking separation between soft segments under pressure.