Reactive Passivation of Wide-Bandgap Organic–Inorganic Perovskites with Benzylamine

Abstract

While amines are widely used as additives in metal-halide perovskites, our understanding of the way amines in perovskite precursor solutions impact the resultant perovskite film is still limited. In this paper, we explore the multiple effects of benzylamine (BnAm), also referred to as phenylmethylamine, used to passivate both FA_0.75Cs_0.25Pb(I_0.8Br_0.2)₃ and FA_0.8Cs_0.2PbI₃ perovskite compositions. We show that, unlike benzylammonium (BnA⁺) halide salts, BnAm reacts rapidly with the formamidinium (FA⁺) cation, forming new chemical products in solution and these products passivate the perovskite crystal domains when processed into a thin film. In addition, when BnAm is used as a bulk additive, the average perovskite solar cell maximum power point tracked efficiency (for 30 s) increased to 19.3% compared to the control devices 16.8% for a 1.68 eV perovskite. Under combined full spectrum simulated sunlight and 65 °C temperature, the devices maintained a better T₈₀ stability of close to 2500 h while the control devices have T₈₀ stabilities of <100 h. We obtained similar results when presynthesizing the product BnFAI and adding it directly into the perovskite precursor solution. These findings highlight the mechanistic differences between amine and ammonium salt passivation, enabling the rational design of molecular strategies to improve the material quality and device performance of metal-halide perovskites.