Charge Carrier Dynamics in Methylammonium Lead Iodide Perovskite Solar Cells
Vidmantas Gulbinas a, Marius Franckevičius a, Ramūnas Augulis a, Shaik Mohammed Zakeeruddin b, Michael Grätzel b
a Center for Physical Sciences and Technology, LT, Savanorių prospektas, 231, Vilnius, Lithuania
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, Marius Franckevičius, 302
Publication date: 28th March 2016

Methylammonium lead halide perovskite-based solar cells eventually exceeding revolutionary power conversion efficiencies of 20% [1] show radical change in solar energy research. Despite rapid progress in the device efficiencies, understanding of the factors contributing to such a high photovoltaic (PV) performance is still insufficient and therefore further development of perovskite solar cell technology inevitably requires deeper fundamental knowledge of device operation especially at initial steps after photoexcitation.Here, we aim to elucidate the nature and dynamics of photogenerated charge carriers in methylammonium lead iodide perovskites by employing time-resolved photoluminescence spectroscopy with up to several picoseconds time resolution. We show that PL dynamics features two distinct decay components: the fast one, with decay rate on the order of several to tens of psand the slow one decaying on the nanosecond time-scale. The two componential PL relaxation was observed for many different sample architectures, which shows that this behavior is an universal property of MAPbI3 perovskites. Measurements performed by varying photoexcitation densities over four orders of magnitude, enabled separation of photoluminescence components related to recombination of geminate and non-geminate charge-pairs. PL decay kinetics of the geminate recombination weakly depends on temperature and is remarkably independent of the material properties. The non-geminate recombination causes photoluminescence decay on a nanosecond time scale and is determined by charge extraction [2] and by recombination rate at very high intensities.

Acknowledgement: M.F. and V.G. thanks the financial support from the Research Council of Lithuania (a grant No. MIP-085/2015).

References:

[1] Bi, D. et al. Efficient luminescent solar cells based on tailored mixed-cation perovskites, Sci. Adv. 2, e1501170 (2016).

[2] Xing, G. et al. Long-range balanced electron and hole-transport lengths in organic-inorganic CH3NH3PbI3. Science 342, 344-347 (2013).



© 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