Synergistic effect of two hydrochlorides resulting in significantly enhanced performance of tin-based perovskite solar cells with 3D to quasi-2D structural transition

The development of tin (Sn)-based perovskite solar cells has attracted extensive attention due to their strong infrared absorption and non-toxicity properties. However, the self-doping effect of Sn 2+ oxidation leads to the generation of abundant vacancies of Sn, and the excessively fast crystallization rate also produces serious pinholes in the film. This hinders the further development of Sn-based perovskite devices. In this study, hydrazine monohydrochloride (HMCl) and diethylamine hydrochloride (DEACl) were simultaneously introduced into the precursor solution to suppress the oxidation of Sn 2+ and decelerate the crystallization rate of the film, and thus, a high-quality quasi-2D DEA 2 FA n −1 Sn n I 3 n +1 film was obtained (FA: formamidinium). Additionally, DEA + is confirmed as more beneficial for carrier transfer than BA + and PEA + via density functional theory calculations and experimental evidence in the quasi-2D perovskite films. Consequently, under the synergistic effect of two hydrochlorides, a champion power conversion efficiency of 9.5% with ultra-high stability was realized due to a significant increase in V OC . This study demonstrated a new strategy to evidently enhance the performance and stability of Sn-based perovskite devices by causing the 3D to 2D structure transition via two functional additives. Hydrazine monohydrochloride (HMCl) inhibits Sn 2+ oxidation, and diethylamine hydrochloride (DEACl) leads to a 2D structure. Under the synergistic effect of the two hydrochlorides, PCE and the V OC are largely enhanced for stable Sn-based devices.