Currently, the most efficient perovskite solar cells (PSCs) mainly use planar and mesoporous titanium dioxide (TiO2) as an electron-transport layer (ETL). However, because of its intrinsic photocatalytic properties, TiO2 can decompose perovskite absorber and lead to poor stability under solar illumination (ultraviolet light). Herein, a simplified architectural ETL-free PSC with enhanced efficiency and outstanding photostability is produced by the facile deposition of a bathocuproine (BCP) interlayer. Power conversion efficiency of the ETL-free PSC improves from 15.56 to 19.07% after inserting the BCP layer, which is the highest efficiency reported for PSCs involving an ETL-free architecture, versus 19.03% for the n-i-p full device using TiO2 as an ETL. The BCP interlayer has been demonstrated to have several positive effects on the photovoltaic performances of devices, such as "modulation doping" of the perovskite layer, modification of FTO surface work function, and enhancing the charge-transfer efficiency between FTO and perovskite. Moreover, the BCP-based ETL-free devices exhibit outstanding photostability: the unencapsulated BCP-based ETL-free PSCs retain over 90% of their initial efficiencies after 1000 h of storage in air and maintain 92.2% after 450 h of exposure to full solar irradiation (without a UV filter), compared to only 14.1% in the n-i-p full cells under the same condition.
Keywords: bathocuproine; electron-transfer-layer-free; modulation doping; perovskite solar cell; photostability.