Laura Bellini, Daniël Grosfeld, Bruno Branco, Guus J. W. Aalbers, Lana M. Kessels, Willemijn H. M. Remmerswaal, Nicolas Daub, Kunal Datta, Martijn M. Wienk, René A. J. Janssen
ABSTRACT Wide‐bandgap perovskite solar cells (PSCs) based on formamidinium lead bromide (FAPbBr 3 ) hold promise for unassisted solar‐driven water splitting using a single‐junction absorber. To meet the required thermodynamic voltage and overpotentials, nonradiative recombination in the PSC must be suppressed. Herein, a dual‐passivation strategy is used that combines formamidinium thiocyanate (FASCN) for bulk passivation and 1,3‐propane diammonium iodide (PDAI 2 ) for top surface passivation. FASCN promotes the growth of larger perovskite grains, while PDAI 2 mitigates surface defects, together leading to suppressed nonradiative recombination and improved charge extraction. Further optimization of the electron‐transport layer (ETL) using a ternary fullerene blend (PCBM, CMC, ICBA) in a 1:1:1 weight ratio improves energetic alignment and suppresses interfacial energy losses, resulting in an increase in open‐circuit voltage from 1.41 to 1.60 V and a power conversion efficiency of 9.4% in small‐area devices. After scaling up to a 1.0 cm 2 active area, the PSC is integrated into a coupled photovoltaic‐electrochemical (PV‐EC) system for continuous solar‐driven water splitting employing platinum (Pt) as the hydrogen evolution catalyst and ruthenium dioxide (RuO 2 ) as the oxygen evolution catalyst. The system achieves a solar‐to‐hydrogen (STH) efficiency of 6.5%, outperforming single‐absorber PV‐EC systems reported to date.