Bandgap-Tunable Caesium Lead Halide Perovskites with High Thermal Stability for Efficient Solar Cells
Maximilian Hörantner a, Henry Snaith a, David Moore a, Amir Abbas Haghighirad a, Michael Johnston a, Rebecca Sutton a, Giles Eperon a, Jay Patel a, Elizabeth Parrott a, Laura Miranda b, Brett Kamino b
a University of Oxford, Clarendon Laboratory, Parks rd, Oxford, 0, United Kingdom
International Conference on Hybrid and Organic Photovoltaics
Proceedings of International Conference on Hybrid and Organic Photovoltaics (HOPV16)
Swansea, United Kingdom, 2016 June 29th - July 1st
Organizers: James Durrant, Henry Snaith and David Worsley
Poster, Rebecca Sutton, 323
Publication date: 28th March 2016

Lead-halide perovskite solar cells have been the subject of much research in the last few years due to their excellent absorption and ambipolar conduction [1–3]. Most of the research has used methylammonium and/or formamidinium as the cation to make hybrid organic-inorganic perovskite materials [4–6]. In contrast, fully inorganic caesium lead-halide perovskites have been known since 1893 [7], and have been prepared as crystals [8], nanocrystals [9], and in thin films by thermal evaporation [10]. The caesium lead mixed halide perovskites are known to form solid solutions [11], and exhibit a range of colours (see Figure 1) and hence a tuneable absorption onset. Here we present a detailed comparison between caesium and methylammonium lead-halide perovskite materials and show that the caesium materials have potential for use in tandem solar cells.

References [1] M. Liu, M. B. Johnston, and H. J. Snaith, Nature (2013), 501, 395–8. [2] A. Kojima, K. Teshima, Y. Shirai, and T. Miyasaka, J. Am. Chem. Soc. (2009), 131, 6050–6051, [3] M. Grätzel, Nat. Mater. (2014), 13, 838–842. [4] M. A. Green, A. Ho-Baillie, and H. J. Snaith, Nat. Photonics (2014), 8, 506–514. [5] S. N. Habisreutinger, T. Leijtens, G. E. Eperon, S. D. Stranks, R. J. Nicholas, and H. J. Snaith, J. Phys. Chem. Lett. (2014), 5, 4207–4212. [6] G. E. Eperon, S. D. Stranks, C. Menelaou, M. B. Johnston, L. M. Herz, and H. J. Snaith, Energy Environ. Sci. (2014), 7, 982. [7] H. L. Wells, Zeitschrift fur Anorg. Chemie (1893), 3, 195–210. [8] C. K. Moller, Nature (1958), 182, 1436. [9] L. Protesescu, S. Yakunin, M. I. Bodnarchuk, F. Krieg, R. Caputo, et al., Nano Lett. (2015) 15, 3692−3696. [10] S. Kondo and T. Saito, Phys. status solidi (2005), 202, 455–461. [11] S. Sharma, N. Weiden, and A. Weiss, Zeitschrift für Phys. Chemie (1992), 175, 63–80.



© 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