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Transporter layers for greater stability
Although perovskite solar cells (PSCs) can have power conversion efficiencies exceeding 20%, they can have limited stability under ultraviolet irradiation. This is in part because the mesoporous TiO2 used as an electron-transporting layer can photocatalyze unwanted reactions in the perovskite layer. Shin et al. report a low-temperature colloidal method for depositing La-doped BaSnO3 films as a replacement for TiO2 to reduce such ultraviolet-induced damage. Solar cells retained over 90% of their initial performance after 1000 hours of full sun illumination.
Science, this issue p. 167
Perovskite solar cells (PSCs) exceeding a power conversion efficiency (PCE) of 20% have mainly been demonstrated by using mesoporous titanium dioxide (mp-TiO2) as an electron-transporting layer. However, TiO2 can reduce the stability of PSCs under illumination (including ultraviolet light). Lanthanum (La)–doped BaSnO3 (LBSO) perovskite would be an ideal replacement given its electron mobility and electronic structure, but LBSO cannot be synthesized as well-dispersible fine particles or crystallized below 500°C. We report a superoxide colloidal solution route for preparing a LBSO electrode under very mild conditions (below 300°C). The PSCs fabricated with LBSO and methylammonium lead iodide (MAPbI3) show a steady-state power conversion efficiency of 21.2%, versus 19.7% for a mp-TiO2 device. The LBSO-based PSCs could retain 93% of their initial performance after 1000 hours of full-Sun illumination.