Summary
Along with the rapidly-developed power conversion efficiencies (PCEs), operational stability of perovskite solar cells (PSCs) becomes the bottleneck for further commercialization. The instability mainly comes from the unstable organic components in the whole devices and the responsive metal electrode to the halogens from perovskites. In this work, we develop a carbide-titanium oxide (C-TiO2) hybrid electron-transporting layer (ETL) and a halogen-resistant Sb electrode on top of the inorganic CsPbI2Br layer to solve the unstable issues. The hybrid C-TiO2 presents uniform and pinhole-free morphology, adequate band structure and electronic property, and observably strong stability. On the other hand, Sb is demonstrated to be effective to restrict inferior ions diffusion and further perovskite decomposition. As a result, our well-designed PSCs achieve both high efficiencies (14.8% for the champion device) and long-term stabilities (< 6% decline @ 85 degrees C, dark; < 10% decline @ 60 degrees C, continuous illumination) of 1000 h.