Abstract
The vibrational density of states (VDOS), electronic structure and optical properties of bulk organo lead-halide perovskites, CH(3)NH(3)PbX(3) (where X = Cl, I and Br), very promising and exciting candidate materials for solar-energy applications, have been studied by means of (hybrid) Density Functional Theory (DFT), with and without spin-orbit coupling, and equilibrium Born-Oppenheimer molecular dynamics (BOMD) in the constant-volume, isothermal (NVT) ensemble at 298 K. Particular emphasis has been directed towards the detailed characterisation of optimal hybrid-DFT strategies to reproduce faithfully the band gap, band structure and optical properties vis-à-vis both experiment and more computationally demanding GW calculations (i.e., those involving the single-particle Green's function, G, and the screened Coulomb interaction, W). The VDOS was found to feature intimate coupling between the lead and halide atoms, and was dominated by acoustic phonon modes - particularly so for chlorine, suggesting this as the more effective candidate material of the considered halides. Bulk optical properties were also determined. In view of promising 'hybrid' architectures of perovskites adsorbed on titania substrates, further simulations of lead iodide in contact with titania have been performed to assess thermal stability, as well as dynamical and structural properties of these systems. It was found that lattice strain led to some atomic layers in perovskite further from the interface adopting less crystal-like structure and less pronounced phonon spectra.