Perovskite solar cells (PSCs) have reached an impressive efficiency over 23%. One of its promising characteristics is the low-cost solution printability, especially for flexible solar cells. However, printing large area uniform electron transport layers on rough and soft plastic substrates without hysteresis is still a great challenge. Herein, we demonstrate slot-die printed high quality tin oxide films for high efficiency flexible PSCs. The inherent hysteresis induced by the tin oxide layer is suppressed using a universal potassium interfacial passivation strategy regardless of fabricating methods. Results show that the potassium cations, not the anions, facilitate the growth of perovskite grains, passivate the interface, and contribute to the enhanced efficiency and stability. The small size flexible PSCs achieve a high efficiency of 17.18% and large size (5 × 6 cm²) flexible modules obtain an efficiency over 15%. This passivation strategy has shown great promise for pursuing high performance large area flexible PSCs.

Suppressing nucleation over large areas: Although formamidinium-based lead iodide (PbI ₂ ) perovskites have a favorable bandgap and good thermal stability, the difficulty in controlling nucleation makes it difficult to grow high-quality, large-area films compared with methylammonium counterparts. Bu et al. show that adding N -methyl-2-pyrrolidone to the perovskite precursors forms an adduct with PbI ₂ that promotes the formation of the desired black α-phase at room temperature. The addition of potassium hexafluorophosphate eliminated hysteresis by passivating interfacial defects and promoted long-term thermal stability at 85°C in unencapsulated devices. Large-area modules (17 square centimeters) achieved power conversion efficiencies of 20.4%. Science , abh1035, this issue p. 1327

Organic–inorganic metal halide perovskite solar cells (PSCs) have made a striking breakthrough with a power conversion efficiency (PCE) over 22%. However, before moving to commercialization, the hysteresis of PSCs, characterized as an inconsistent photovoltaic conversion property at varied electric fields, should be eliminated for stable performance. Herein, we present a novel quadruple-cation perovskite absorber, K_xCs_0.05(FA_0.85MA_0.15)_0.95Pb(I_0.85Br_0.15)₃ (labeled as KCsFAMA), with which the hysteresis in PSCs can be fully eliminated irrespective of the electron transportation layers. The incorporation of potassium intensively promotes the crystallization of the perovskite film with a grain size up to ∼1 μm, doubled compared to the K free counterparts. Further characterization revealed that a lower interface defect density, longer carrier lifetime and fast charge transportation have all made contributions to the hysteresis-free, stable and high PCE (20.56%) of the KCsFAMA devices. Moreover, we present a 6 × 6 cm² sub-module with the KCsFAMA composition achieving a high efficiency of 15.76% without hysteresis. This result suggests that the quadruple-cation perovskite is a highly attractive candidate for future developments of efficient and stable PSC modules.