Hole‐Boosted Cu(Cr,M)O₂ Nanocrystals for All‐Inorganic CsPbBr₃ Perovskite Solar Cells

Abstract

The all-inorganic CsPbBr₃ perovskite solar cell (PSC) is a promising solution to balance the high efficiency and poor stability of state-of-the-art organic-inorganic PSCs. Setting inorganic hole-transporting layers at the perovskite/electrode interface decreases charge carrier recombination without sacrificing superiority in air. Now, M-substituted, p-type inorganic Cu(Cr,M)O₂ (M=Ba²⁺ , Ca²⁺ , or Ni²⁺ ) nanocrystals with enhanced hole-transporting characteristics by increasing interstitial oxygen effectively extract holes from perovskite. The all-inorganic CsPbBr₃ PSC with a device structure of FTO/c-TiO₂ /m-TiO₂ /CsPbBr₃ /Cu(Cr,M)O₂ /carbon achieves an efficiency up to 10.18 % and it increases to 10.79 % by doping Sm³⁺ ions into perovskite halide, which is much higher than 7.39 % for the hole-free device. The unencapsulated Cu(Cr,Ba)O₂ -based PSC presents a remarkable stability in air in either 80 % humidity over 60 days or 80 °C conditions over 40 days or light illumination for 7 days.