Phase-Pure α-FAPbI<sub>3</sub> Perovskite Solar Cells via Activating Lead-Iodine Frameworks.

Niu, Tingting; Chao, Lingfeng; Xia, Yingdong; Wang, Kaiyu; Ran, Xueqin; Huang, Xiao; Chen, Changshun; Wang, Jinpei et al. · Adv Mater · 2024

basic_science · Level V

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Abstract

Narrow bandgap cubic formamidine perovskite (α-FAPbI<sub>3</sub>) 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-FAPbI<sub>3</sub> lattice is to replace intrinsic FA<sup>+</sup> or I<sup>-</sup> with smaller ions of MA<sup>+</sup>, Cs<sup>+</sup>, Rb<sup>+</sup>, and Br<sup>-</sup>, whereas this generally leads to broadened optical bandgap and phase separation. Studies show that ions substitution-free phase-pure α-FAPbI<sub>3</sub> 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<sup>+</sup>, Cs<sup>+</sup>, Rb<sup>+</sup>, and Br<sup>-</sup>-free phase-pure α-FAPbI<sub>3</sub> 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-FAPbI<sub>3</sub> 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.