Understanding the Role of Cesium and Rubidium Additives in Perovskite Solar Cells: Trap States and Charge Carrier Mobility
Yinghong Hu a, Eline M. Hutter b, Philipp Rieder c, Irene Grill a, Jonas Hanisch d, Meltem F. Aygüler a, Alexander G. Hufnagel a, Matthias Handloser e, Thomas Bein a, Achim Hartschuh a, Kristofer Tvingstedt c, Vladimir Dyakonov c, Andreas Baumann f, Tom J. Savenije b, Michiel L. Petrus a, Pablo Docampo g
a University of Munich (LMU), Department of Chemistry and Center for Nanoscience (CeNS), 81377 Múnich, Alemania, Múnich, Germany
b Delft University of Technology, The Netherlands, Julianalaan, 136, Delft, Netherlands
c Experimental Physics VI, Julius Maximillian University of Würzburg, 97074 Würzburg, Germany
d Zentrum für Sonnenenergie- und Wasserstoff-Forschung Baden-Württemberg (ZSW), Stuttgart, Meitnerstraße, 1, Stuttgart, Germany
e TOPTICA Photonics AG, Lochhamer Schlag 19, 81266 Gräfelfing, Germany
f Bavarian Center for Applied Energy Research, Magdalene-Schoch-Str. 3, 97074 Würzburg, Germany
g Physics Department, School of Electrical and Electronic Engineering, Newcastle University, United Kingdom, Merz Court, Newcastle upon Tyne NE1 7RU, Reino Unido, United Kingdom
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, Yinghong Hu, presentation 083
DOI: https://doi.org/10.29363/nanoge.hopv.2018.083
Publication date: 21st February 2018

The introduction of cesium (Cs) and/or rubidium (Rb) cations to the FA0.83MA0.17Pb(I0.83Br0.17)3 perovskite has recently shown to result in remarkable enhancements in solar cell performance. However, the origin of these improvements has not been fully understood yet. In order to elucidate the impact of the inorganic cation additives on the trap landscape and charge transport properties within perovskite solar cells, Time-of-Flight (ToF), Time-Resolved Microwave Conductivity (TRMC), and Thermally Stimulated Current (TSC) measurements were performed.[1] By combining these complementary experimental techniques we can assess both local features within the perovskite crystals and macroscopic properties of perovskite thin films and full devices. Most importantly, our results show that Cs-incorporation significantly reduces the trap density in the perovskite layer and removes deep trap states. This is in good agreement with the observed improvements in Voc and fill factor of Cs-containing devices. In comparison, Rb-addition results in an increased charge carrier mobility, which is accompanied by a minor increase in device efficiency and reduced current-voltage hysteresis. We found indications for an inhomogeneous distribution of Rb within the perovskite layer and therefore hypothesize that the effect of Rb is mainly present in surface passivation. By mixing Cs and Rb, the advantages of both inorganic cations can be found in the resulting state-of-the-art quadruple cation perovskite (Cs–Rb–FA–MA) devices, showing the lowest trap density, the highest charge mobility and the most stable power output. Our in-depth study provides insights into the role of these additives in multiple-cation perovskite solar cells, which are essential for the future optimization of high-performance devices.

 

[1]        Hu, Y.; Hutter, E. M.; Rieder, P.; Grill, I.; Hanisch, J.; Aygüler, M. F.; Hufnagel, A. G.; Handloser, M.; Bein, T.; Hartschuh, A.; Tvingstedt, K.; Dyakonov, V.; Baumann, A.; Savenije, T. J.; Petrus, M. L.; Docampo, P. Adv. Energy Mater. 2018, in press.

© FUNDACIO DE LA COMUNITAT VALENCIANA SCITO
We use our own and third party cookies for analysing and measuring usage of our website to improve our services. If you continue browsing, we consider accepting its use. You can check our Cookies Policy in which you will also find how to configure your web browser for the use of cookies. More info