ABSTRACT
The defect accumulation mechanism of amorphization has been studied for the La2Zr2O7 pyrochlore by means of classical molecular dynamic simulations. Present calculations show that the accumulation of cation Frenkel pairs is the main driving parameter for the amorphization process, while the oxygen atoms simply rearrange around cations. Under Frenkel pair accumulation, the structure follows the pyrochlore-fluorite-amorphous sequence. Present results consequently provide atomic-level interpretation to previous experimental irradiation observations of the two-step phase transition.
ABSTRACT
We have studied self-trapped excitons in alpha-quartz using density functional theory (DFT), both in the crystal and at the (0001) surface. The excitons are triplet excited states that distort the crystal locally. They have a long lifetime, of the order of a millisecond, and become thermally equilibrated. We have calculated the drop in the exciton energy as it approaches the surface from the interior of the crystal. In the subsurface layer of the -OH terminated (0001) surface, the energy has dropped by 0.7 eV. Another 0.4 eV drop occurs as the exciton enters the surface layer, where it breaks off an OH radical. The drop in energy can be understood from the greater ease of structural distortion at the surface. These calculations illustrate that excitons formed in the bulk could migrate out to the surface and form chemically active surface species. Molecules adsorbed at the surface could also serve as traps for the excitons and could, in principle, be induced to undergo structural or chemical transitions.
