Role of Inorganic Cations in the Excitonic Properties of Lead Halide Perovskites
arXiv:2401.16093 · doi:10.1039/D2CP04288F
Abstract
We theoretically investigate lead iodide perovskites of general formula APbI for a series of metallic cations (namely Cs, Rb, K, Na and Li) by means of the density functional theory, GW method and Bethe-Salpeter equation including spin-orbit coupling. We demonstrate that the low-energy edges (up to 1.3 eV) of the absorption spectra are dominated by weakly bound excitons, with binding energies 30-80~meV, and the corresponding intensities grow as metallic %A cations become lighter. The middle parts of the spectra (1.8-2.4 eV), on the other hand, contain optical dipole transitions comprising more strongly bound excitons ( 150-200~meV) located at PbI. These parts of the spectra correspond to the optical-gain wavelengths which are experimentally achieved in optically-pumped perovskite lasers. Finally, the higher energy parts, from about 2.8~eV (LiPbI) to 4.3 eV (CsPbI), contain optical transitions with very strongly bound excitons ( 220-290~meV) located at the halide atoms and the empty states of the metallic cations.
References in corpus (5)
- Steric engineering of metal-halide perovskites with tunable optical band gaps
- Many-body perturbation theory calculations using the yambo code
- The impact of the halide cage on the electronic properties of fully inorganic caesium lead halide perovskites
- Efficient approach to solve the Bethe-Salpeter equation for excitonic bound states
- Phonon Screening of Excitons in Semiconductors: Halide Perovskites and Beyond