Composition dependence of photo-induced chemical changes in mixed-ion perovskite materials
Ute Cappel a, Sebastian Svanström b, Håkan Rensmo b
a Department of Chemistry, Division of Applied Physical Chemistry, KTH Royal Institute of Technology, Sweden, SE-10044 Stockholm, Sweden
b Department of Physics and Astronomy, Uppsala University, Sweden, Uppsala, Sweden
International Conference on Hybrid and Organic Photovoltaics
Proceedings of International Conference on Hybrid and Organic Photovoltaics (HOPV18)
Benidorm, Spain, 2018 May 28th - 31st
Organizers: Emilio Palomares and Rene Janssen
Oral, Ute Cappel, presentation 164
DOI: https://doi.org/10.29363/nanoge.hopv.2018.164
Publication date: 21st February 2018

Lead halide perovskites have developed from the initially used methylammonium lead iodide (MAPbI3) to structures containing anion (e.g. Br- and I-) and cation (e.g. formamidinium (FA), MA, Cs+ and Rb+) mixtures. Many aspects related to these materials still need to be understood including the materials’ photo-stability. Processes such as ion migration are likely to play a role in the photon to electron conversion mechanism and for the long-term stability. It is therefore of high importance to understand how the exact composition of the perovskite influences these properties.

We have recently developed a photoelectron spectroscopy-based methodology in which the chemical changes at the surface of the perovskite can be studied under visible light illumination [1]. These measurements are carried out at the LowDose PES beamline at the synchrotron Bessy II, where a X-ray low photon flux is combined with a highly efficient spectrometer. This enables us to study the electronic structure of the perovskite surface without any X-ray degradation. In our first study, we demonstrated that ion movement of halides can be observed through intensity changes of the halides at the surface for an MAFA-based perovskite during visible laser illumination [1]. Furthermore, we observed the reduction of a fraction of Pb2+ at the perovskite surface to Pb0, which was partially reversible in the dark.

We now have used the same methodology to study photo-induced processes in perovskites with different compositions including different I/Br ratios and Cs ions. This presentation will summarise the results of this study. We show that the presence of Cs ions can lead to a strong suppression of halide ion migration at high I/Br ratios, while other aspects of the photo-stability of the perovskite can be enhanced independent of I/Br ratio. Our results give therefore an indication of the mechanism with which Cs ions enhance the stability of perovskite solar cells.

[1] Ute B. Cappel, et al. ACS Appl. Mater. Interfaces 9, 34970-34978 (2017).

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