Preferentially coordinating tin ions to suppress composition segregation for high-performance tin-lead mixed perovskite solar cells

Abstract

Tin-lead mixed perovskites (TLPs) with a tunable and ideal bandgap exhibit great potential in approaching the Shockley–Queisser limit of power conversion efficiency (PCE). However, two critical issues are necessary to be addressed, including the oxidation of Sn2+ and negligible composition and phase segregation. The latter derives from the unbalanced crystallization rate between Sn- and Pb-based perovskites. Here, we report a strategy to address the above critical issues by introducing 3,4-Dihydroxybenzylamine hydrobromide (DHBABr) in the TLP precursor solution. DHBABr was revealed to promote the crystallization of FAPbI3 perovskite by suppressing the formation of crystalline DMSO-FA-Pb-I intermediates and retard the crystallization rate of FASnI3 by preferentially forming a steady amorphous DHBA-FA-Sn-I intermediate. This, therefore, balances the crystallization rate between Sn- and Pb-based perovskites. As a result, the spatial distribution of Sn/Pb ratio is much more uniform across the whole TLP film, which benefits the upscaling of the manufacturing process. Relying on this doping strategy accompanied by the surface passivation with DHBABr, which reduces the defect density of TLP, inhibits the oxidation of Sn2+, and optimizes the band alignment of the device, we have achieved a PCE of 22.44 % with Voc of 0.853 V and FF of 80.0 %, along with an enhanced long-term stability of T80 = 476 h under continuously light illumination in the champion device.