Abstract
In a period of only a few years, the power conversion efficiency of organic–inorganic perovskite solar cells has surpassed a value of 24.2%. However, a major drawback is the lack of long-term stability, which is partially related to the dissociation of organic cations under prolonged illumination. This degradation mechanism is not limited to ambient temperatures. At low temperatures (T = 5 K), illumination of methyl ammonium lead iodide (CH3NH3PbI3) thin films with a photon energy of Eph = 3.4 eV results in the formation of localized trap states located about 100 meV within the bandgap. These light-induced defects are metastable, and annealing at T ≥ 15 K removes the localized states. Defect creation is not limited to polycrystalline perovskites but is also observed in single-crystal CH3NH3PbI3. The experimental data are discussed in terms of a two-level model where the metastable state is separated from the annealed state by an energy barrier.
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CITATION STYLE
Rappich, J., Lang, F., Brus, V. V., Shargaieva, O., Dittrich, T., & Nickel, N. H. (2020). Light-Induced Defect Generation in CH3NH3PbI3 Thin Films and Single Crystals. Solar RRL, 4(2). https://doi.org/10.1002/solr.201900216
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