Abstract
The crystalline-to-vitreous phase transformation of a SiO(2) bilayer supported on Ru(0001) was studied by time-dependent LEED, local XPS, and DFT calculations. The silica bilayer system has parallels to 3D silica glass and can be used to understand the mechanism of the disorder transition. DFT simulations show that the formation of a Stone-Wales-type of defect follows a complex mechanism, where the two layers show decoupled behavior in terms of chemical bond rearrangements. The calculated activation energy of the rate-determining step for the formation of a Stone-Wales-type of defect (4.3 eV) agrees with the experimental value. Charge transfer between SiO(2) bilayer and Ru(0001) support lowers the activation energy for breaking the Si-O bond compared to the unsupported film. Pre-exponential factors obtained in UHV and in O(2) atmospheres differ significantly, suggesting that the interfacial ORu underneath the SiO(2) bilayer plays a role on how the disordering propagates within the film.