Abstract

The photovoltaic performance of perovskite solar cells is severely limited by the innate defects of perovskite films. Metal-organic framework (MOF)-based additives with luxuriant skeleton structures and tailored functional groups show a huge potential to solve these problems. Here, a multilateral passivation strategy is performed by introducing two alkyl-sulfonic acid functionalized MOFs, MIL-88B-1,3-SO3H and MIL-88B-1,4-SO3H, respectively, obtained from MIL-88B-NH2 through a post-synthetic process, for coordinating the lead defects and inhibiting non-radiative recombination. The flexible MIL-88B-type frameworks endow both functionalized MOFs with excellent electrical conductivity and preferable carrier transport in the hole-transport materials. Compared with the original MIL-88B-NH2 and MIL-88B-1,4-SO3H, MIL-88B-1,3-SO3H exhibits optimal steric hindrance and multiple passivation groups (-NH2, -NH-, and -SO3H), achieving the champion doped device with an enhanced power conversion efficiency (PCE) of 22.44% and excellent stability, which maintains 92.8% of the original PCE under ambient conditions (40% humidity and 25 °C) for 1200 h.

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