Abstract
Narrow bandgap cubic formamidine perovskite (α-FAPbI3) is widely studied for its potential to achieve record‑breaking efficiency. However, its high preparation difficulty caused by lattice instability is criticized. A popular strategy for stabilizing the α-FAPbI3 lattice is to replace intrinsic FA+ or I− with smaller ions of MA+, Cs+, Rb+, and Br−, whereas this generally leads to broadened optical bandgap and phase separation. Studies show that ions substitution-free phase-pure α-FAPbI3 can achieve intrinsic phase stability. However, the challenging preparation of high-quality films has hindered its further development. Here, a facile synthesis of high-quality MA+, Cs+, Rb+, and Br−-free phase-pure α-FAPbI3 perovskite film by a new solution modification strategy is reported. This enables the activation of lead–iodine (Pb─I) frameworks by forming the coated Pb⋯O network, thus simultaneously promoting spontaneous homogeneous nucleation and rapid phase transition from δ to α phase. As a result, the efficient and stable phase-pure α-FAPbI3 PSC is obtained through a one-step method without antisolvent treatment, with a record efficiency of 23.15% and excellent long-term operating stability for 500 h under continuous light stress.
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Niu, T., Chao, L., Xia, Y., Wang, K., Ran, X., Huang, X., … Chen, Y. (2024). Phase-Pure α-FAPbI3 Perovskite Solar Cells via Activating Lead–Iodine Frameworks. Advanced Materials, 36(13). https://doi.org/10.1002/adma.202309171
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