Abstract
Charge recombination at grain-boundary interfaces and charge extraction loss at perovskite-carrier transport layer interfaces are the two main causes for the performance deficiency in perovskite solar cells. Herein we reported the synthesis of an ionic liquid compound 9-bromo-6,7-diphenylpyrido[2,1-a]isoquinolin-5-ium hexafluorophosphate (DPPIQ+PF6−), which can synchronously react with perovskites at these two essential interfaces. Specifically, the PF6− anions are incorporated into the perovskite film bulk, immobilizing organic amine ions via hydrogen bonding, while the DPPIQ+ cations are mainly accumulated at the top film surface, binding the [PbI3]− through anion-π interactions. Reduced defect density and improved energy level alignment are achieved in the resultant perovskite solar cells. The best-performing DPPIQ+PF6− incorporated device shows a high power conversion efficiency of 23.41% and demonstrates 90% efficiency retention upon maximum-power-point tracking for 1260 h under continuous one-sun-intensity illumination.
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