Illumination Enhanced Crystallization and Defect Passivation for High Performance CsPbI 3 Perovskite Solar Cells by Sacrificing Dye

All‐inorganic perovskite solar cells (PSCs) have been the research focus due to their high thermal stability and proper band gap for tandem solar cells. However, their power conversion efficiency (PCE) is still lower than that of organic‐inorganic hybrid PSCs. Herein, a sacrificing dye (Rhodamine B...

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Veröffentlicht in:Advanced functional materials 2023-12, Vol.33 (49)
Hauptverfasser: Zhang, Na, Wang, Jungang, Duan, Yuwei, Yang, Shaomin, Xu, Dongfang, Lei, Xuruo, Wu, Meizi, Yuan, Ningyi, Ding, Jianning, Cui, Jian, Liu, Zhike
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Sprache:eng
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Zusammenfassung:All‐inorganic perovskite solar cells (PSCs) have been the research focus due to their high thermal stability and proper band gap for tandem solar cells. However, their power conversion efficiency (PCE) is still lower than that of organic‐inorganic hybrid PSCs. Herein, a sacrificing dye (Rhodamine B isothiocyanate, RBITC) is developed to regulate the growth of perovskite film by in situ release of ethylammonium cations, isothiocyanate anions and benzoic acid molecules upon annealing and illumination. The ethylammonium cations can efficiently passivate surface defects. The isothiocyanate anions incorporate with uncoordinated Pb to regulate the crystallization process. The benzoic acid molecules facilitate the nucleation of the perovskite crystals. Especially, the illumination can accelerate the release of these beneficial ions/molecules to improve the quality of perovskite films further. After optimization with RBITC, a high open circuit voltage ( V OC ) of 1.24 V and a champion PCE of 20.95% are obtained, which are among the highest V oc and PCE values of CsPbI 3 PSCs. Accordingly, the operational stability of the PSC devices is significantly improved. The results provide an efficient chemical strategy to regulate the formation of perovskite films in whole crystallization process for high performance all‐inorganic PSCs.
ISSN:1616-301X
1616-3028
DOI:10.1002/adfm.202303873