Advanced Materials, Journal Year: 2025, Volume and Issue: unknown
Published: April 25, 2025
Abstract Interfacial energy loss is a critical challenge in achieving high‐efficiency organic solar cells (OSCs), primarily due to mismatched levels and inefficient charge collection. Herein, bifunctional interface engineering strategy proposed, employing an ethanol/o‐difluorobenzene (EtOH/o‐DFB) dual‐solvent system for phosphotungstic acid (HPWO) processing. During film formation, o‐DFB regulates HPWO crystallization by suppressing excessive aggregation, while enabling situ ITO fluorination through the adsorbed o‐DFB. This synergistic approach simultaneously mitigates trap‐assisted nonradiative recombination at hole transport layer enhancing electrode work function, resulting better ohmic contact, minimized trap‐state densities, improved level alignment electrode/active interface. The effectiveness of this demonstrated across multiple active systems. Remarkable power conversion efficiencies 19.55%, 20.07%, 20.57% are achieved PM6/L8‐BO, D18/L8‐BO, D18/BTP‐eC9‐based OSCs, respectively. Notably, PCE represents one highest reported date highlighting potential advancing high‐performance photovoltaics.
Language: Английский