All-inorganic quantum dot assisted enhanced charge extraction across the interfaces of bulk organo-halide perovskites for efficient and stable pin-hole free perovskite solar cells

In spite of achieving high power conversion efficiency (PCE), organo-halide perovskites suffer from long term stability issues. Especially the grain boundaries of polycrystalline perovskite films are considered as giant trapping sites for photo-generated carriers and therefore play an important role in charge transportation dynamics. Surface engineering via grain boundary modification is the most promising way to resolve this issue. A unique antisolvent-cum-quantum dot (QD) assisted grain boundary modification approach has been employed for creating monolithically grained, pin-hole free perovskite films, wherein the choice of all-inorganic CsPbBr x I 3 x ( x = 12) QDs is significant. The grain boundary filling by QDs facilitates the formation of compact films with 12 m perovskite grains as compared to 300500 nm grains in the unmodified films. The solar cells fabricated by CsPbBr 1.5 I 1.5 QD modification yield a PCE of 16.5% as compared to 13% for the unmodified devices. X-ray photoelectron spectral analyses reveal that the sharing of electrons between the PbI 6 framework in the bulk perovskite and Br ions in CsPbBr 1.5 I 1.5 QDs facilitates the charge transfer process while femtosecond transient absorption spectroscopy (fs-TAS) suggests quicker trap filling and enhanced charge carrier recombination lifetime. Considerable ambient stability up to 720 h with