A major efficiency limit for solution-processed perovskite optoelectronic devices (e.g. light-emitting diodes, LEDs) is trap-mediated non-radiative losses. Defect passivation using organic molecules has been identified as an attractive approach to tackle this issue. However, implementation of this approach has been hindered by a lack of deep understanding of how the molecular structures affect the passivation effectiveness. We show that the so far largely ignored hydrogen bonds play a critical role. By weakening the hydrogen bonding between the passivating functional moieties and the organic cation featuring the perovskite, we significantly enhance the interaction with defects sites and minimize non-radiative recombination losses. Consequently, we achieve exceptionally high-performance near infrared perovskite LEDs (PeLEDs) with a record external quantum efficiency (EQE) of 21.6%. In addition, our passivated PeLEDs maintain a high EQE of 20.1% and a wall-plug efficiency of 11.0% at a high current density of 200 mA cm-2 , making them more attractive than the most efficient organic and quantum-dot LEDs at high excitations.

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We reveal an iodine vapor-induced degradation mechanism in formamidinium–lead-iodide-based perovskite solar cells stressed under combined heat and light illumination.