Quantification of Ion Migration in CH3NH3PbI3 Perovskite Solar Cells by Deep Level Transient Spectroscopy
Moritz Futscher a, Jumin Lee a, Tianyi Wang a, Azhar Fakharuddin b, Lukas Schmidt-Mende b, Bruno Ehrler a
a Center for Nanophotonics, AMOLF, The Netherlands, Science Park, 104, Amsterdam, Netherlands
b Department of Physics, University of Konstanz, POB 680, Konstanz, 78457, Germany
Asia-Pacific International Conference on Perovskite, Organic Photovoltaics and Optoelectronics
Proceedings of International Conference Asia-Pacific Hybrid and Organic Photovoltaics 2018 (AP-HOPV18)
Kitakyūshū-shi, Japan, 2018 January 28th - 30th
Organizers: Shuzi Hayase, Juan Bisquert and Hiroshi Segawa
Poster, Moritz Futscher, 138
Publication date: 27th October 2017

Solar cells based on organic-inorganic halide perovskites already reach efficiencies close to highly optimized silicon solar cells. However, perovskite solar cells suffer from current-voltage hysteresis impeding large-scale commercial applications. Hysteresis is commonly attributed to ion migration within the perovskite layer due to the presence of vacancies, defects, or substitutions. We use admittance spectroscopy and deep-level transient spectroscopy to measure activation energy, density, and attempt-to-escape frequency for ion migration in methylammonium lead triiodide (MAPI) perovskite solar cells. We identify three mobile ion species with activation energies of 0.8, 0.6, and 0.4 eV. We attribute this to vacancy-assisted migration of iodide (I and II) and methylammonium ions respectively. We find that the ion migration is strongly correlated with the observed current-voltage hysteresis. This quantification of mobile ions in MAPI will help to develop a better understanding of ion migration, which will help to develop hysteresis-free perovskite solar cells.

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