Modeling of Charge Injection, Recombination, and Diffusion in Complete Perovskite Solar Cells on Short Time Scales

Abstract

A model of charge population decay upon ultrafast optical pulse excitation in complete, working perovskite solar cells is proposed. The equation, including charge injections (extractions) from perovskite to contact materials, charge diffusion, and charge recombination via first-, second-, and third-order processes, is solved using numerical simulations. Results of simulations are positively verified by broadband transient absorption results of mixed halide, triple-cation perovskite (FA0.76MA0.19Cs0.05Pb(I0.81Br0.19)3). The combined analytical and experimental findings reveal the best approaches for the proper determination of the crucial parameters that govern charge transfer dynamics in perovskite solar cells on picosecond and single nanosecond time scales. Measurements from both electron and hole transporting layer sides under different applied bias potentials (zero and close to open circuit potential) and different pump fluence (especially below 5 μJ/cm2), followed by fitting of parameters using numerical modeling, are proposed as the optimal methodology for describing the processes taking place in efficient devices.

MXenes as a hole transport interfacial layer for efficient and air-stable quasi-2D perovskite solar cells

“…This decay at high pump fluence (25 μJ cm −2 ) reflects mainly the effect of second-order (radiative) recombination, while at low pump fluence (1 μJ cm −2 and 2.5 μJ cm −2 ) – also the contribution of charge extraction to contact materials (hole injection processes in this case). 66 It indicates that both the above processes (rate constants of recombination and hole extraction from the bulk phase to HTM) are not affected by the presence of MXene.…”