Inhomogeneous Broadening of Photoluminescence Spectra and Kinetics of Nanometer-Thick (Phenethylammonium)2PbI4 Perovskite Thin Films: Implications for Optoelectronics

Abstract

An outstanding potentiality of layered two-dimensional (2D) organic–inorganic hybrid perovskites (2DHPs) is in the development of solar cells, photodetectors, and light-emitting diodes. In 2DHPs, an exciton is localized in an atomically thin lead(II) halide inorganic layer of sub-nanometer thickness as in a quantum well sandwiched between organic layers as energetic and dielectric barriers. In previous years, versatile optical characterization of 2DHPs has been carried out mainly for thin flakes of single crystals and ultrathin (of the order of 20 nm) polycrystalline films, whereas there is a lack of optical characterization of thick (hundreds of nanometers) polycrystalline films, fundamentals for fabrication of devices. Here, with the use of photoluminescence (PL) and absorption spectroscopies, we studied the exciton behavior in ∼200 nm polycrystalline thin films of 2D perovskite (PEA)2PbI4, where PEA is phenethylammonium. Contrary to the case of ultrathin films, we have found that peak energies and line width of the excitonic bands in our films demonstrate unusual extremely weak sensitivity to temperature in 20–300 K diapason. The excitonic PL band is characterized by a significant (∼30 meV) Stokes shift with respect to the corresponding absorption band as well as by a full absence of the exciton fine structure at cryogenic temperatures. We suggest that the observed effects are due to the large inhomogeneous broadening of the excitonic PL and absorption bands resulting from the (PEA)2PbI4 band gap energy dependence on the number of lead(II) halide layers of individual crystallites. The characteristic time of the exciton energy funneling from higher- to lower-energy crystallites within (PEA)2PbI4 polycrystalline thin films is about 100 ps.