Comparative Analysis of Recombination Dynamics in Perovskite Solar Cells via Steady-State and Transient Photoluminescence
Chris Dreessen a b, Ye Yuan a, Genghua Yan a, Markus Hülsbeck a, Benjamin Klingebiel a, Lidón Gil-Escrig b, Michele Sessolo b, Henk Bolink b, Uwe Rau a, Thomas Kirchartz a c
a IEK5-Photovoltaik, Forschungszentrum Jülich
b Instituto de Ciencia Molecular, ICMol, Universidad de Valencia
c Faculty of Engineering and CENIDE, University of Duisburg-Essen, Carl-Benz-Straße, 199, Duisburg, Germany
Proceedings of Device Physics Characterization and Interpretation in Perovskite and Organic Materials (DEPERO)
VALÈNCIA, Spain, 2023 October 3rd - 5th
Organizers: Sandheep Ravishankar, Juan Bisquert and Evelyne Knapp
Oral, Chris Dreessen, presentation 009
DOI: https://doi.org/10.29363/nanoge.DEPERO.2023.009
Publication date: 14th September 2023

Quantifying recombination in halide perovskites is essential for controlling and enhancing the performance of perovskite solar cells. Here, we present a comprehensive analysis of recombination dynamics in perovskite solar cells, focusing on the impact of transient measurement techniques on assessing steady-state performance. We emphasize that the decay times extracted from transient photoluminescence measurements cannot generally be reduced to a single value but rather depend strongly on the charge carrier concentration. It follows that the magnitude of the decay time relies on the measurement's sensitivity. We show photoluminescence decay curves with a large dynamic range of more than 10 orders of magnitude demonstrating decay times from tens of nanoseconds up to hundreds of microseconds in perovskite films. Assuming these high decay times correspond to a recombination lifetime in steady state, one would expect a material with perfect photoluminescence quantum yield, which does however not coincide with the experimental findings. Instead, the decay times in transient measurements are prolonged by capacitive effects resulting from charge trapping and detrapping. We quantitatively explain both the transient and steady-state photoluminescence with the presence of a high density of shallow traps without the influence of deep traps. The same characteristic of increasing decay times remains in the full device, indicating capacitive effects from either shallow traps or transport layers and electrodes. With the help of voltage-dependent steady-state photoluminescence measurements we extract the recombination lifetimes during steady-state operation of the device and compare these to the transient decay times. Furthermore, this experiment allows for the determination of the voltage-dependent collection efficiency which illustrates collection losses up to 10% due to recombination even at short circuit. In summary, this study offers a deeper understanding of recombination dynamics in halide perovskite solar cells by analyzing transient and steady-state measurements. Our findings underscore the importance of considering the influence of shallow traps and transport layers in interpreting decay times and optimizing device performance.

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