Abstract
Inorganic CsPbI2Br perovskite has a substantial potential for triple-junction tandem solar cells as a top subcell, however it exhibits relative instability in the air compared with organic-inorganic perovskites as well as significantly lower efficiency than the theoretical efficiency limit. To further enhance the air-stability and efficiency of CsPbI2Br-based perovskite solar cells (PSCs), it is vitally crucial to improve the crystallinity and passivate the defects within films that accelerate the phase transformation to the photo-inactive phase in the air. Here, it is reported that crystallization management via incorporating sodium formate (NaFo) in a CsPbI2Br perovskite solution effectively leads to enlarged grain size and the reduced trap density. The Na+ cation and HOOC− anion produce a synergistic effect for engineering the defects by acting as cation and pseudo-halide anion passivators, respectively. As a result, the NaFo-incorporating device shows an improved power conversion efficiency (PCE) of 17.7% with a fill factor (FF) of 84.5%. To the best of the authors' knowledge, this progressive FF value is the highest value among CsPbI2Br-based PSCs reported thus far. In addition, the NaFo-incorporated device shows improved air stability compared to the control device, retaining over 95% of its initial PCE for 1000 hours under 10% relative humidity at room temperature without any encapsulation.
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Jeong, M. J., Jeon, S. W., Kim, S. Y., & Noh, J. H. (2023). High Fill Factor CsPbI2Br Perovskite Solar Cells Via Crystallization Management. Advanced Energy Materials, 13(23). https://doi.org/10.1002/aenm.202300698
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