Crystal Structure Ideality Impact on Bimolecular, Auger, and Diffusion Coefficients in Mixed-Cation CsxMA1–xPbBr3 and CsxFA1–xPbBr3 Perovskites

Nonlinear nonradiative recombination processes are considered as a main obstacle to efficient lead halide perovskite light emitters as light emitting diodes and lasers. In this work, crystal structure ideality, described by the Goldschmidt tolerance factor, impact on Auger and bimolecular recombination rates in spin-coated mixed-cation CsxMA1–xPbBr3 and CsxFA1–xPbBr3 perovskite layers was investigated. The excitation-dependent carrier lifetime and diffusion coefficient were determined using optical pump–probe techniques: time-resolved photoluminescence and light-induced transient grating. Layers with a Goldschmidt tolerance factor closer to unity revealed Auger and bimolecular recombination rates smaller by up to an order of magnitude. The bimolecular coefficient (0.6–5 × 10–10 cm3/s) increased simultaneously with the Auger coefficient (0.05–2 × 10–27 cm6/s) upon increase of x and simultaneous decrease of tolerance factor, due to variation in the localized carrier population and Rashba splitting. A larger fraction of cesium in the perovskite layers also favored a larger carrier diffusion coefficient at low excitations. Meanwhile, an optimal cesium content in the cubic phase (x < 0.25) revealed maximum values of diffusion length and internal quantum efficiency.