Abstract

Lead-free inorganic Cs2AgBiBr6 double perovskites have emerged as promising materials in perovskite solar cells (PSCs) to tackle the inferior stability and toxicity issues of organic–inorganic hybrid PSCs. However, the power conversion efficiencies (PCEs) of Cs2AgBiBr6 solar cells are remarkably restricted by the intrinsic and extrinsic defects of Cs2AgBiBr6 films. More specifically, the fast crystallization process in the formation of Cs2AgBiBr6 films strongly prevents the homogeneous growth of perovskite crystals, leading to inferior Cs2AgBiBr6 film quality. This work introduces a facile strategy to retard the crystallization of Cs2AgBiBr6 perovskites by introducing Lewis base additives into the precursor solution. The incorporation of a strongly coordinated thiourea additive with a sulfur donor leads to the generation of a Lewis acid base adduct, which retards the crystallization process for Cs2AgBiBr6 crystals, improves the quality of the Cs2AgBiBr6 film, decreases the defect density and inhibits charge carrier recombination. After optimization, the cell delivers a superior PCE of 3.07%, surpassing that reported for most Cs2AgBiBr6-based solar cells in the literature, and exhibits outstanding stability with a PCE retention rate of 95% after 20 days of storage in air. This work provides an effective strategy for further improvements in the performance of inorganic lead-free Cs2AgBiBr6-based photovoltaic cells.

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