RESUMO
The growing demand for organic electronic devices warrants further development of the scalability and green solvent processibility of π-conjugated materials. Perylene diimide (PDI)-based materials have shown impressive performance as interlayers for electronic devices due to a low ELUMO energy and high charge mobility in films. The next step in the development of these materials is the transition toward scalable production and the fabrication of devices under ambient conditions. Here, we develop a green synthetic methodology to prepare a series of PDI-based electronically active materials (X2-5), which can be slot-die-coated into uniform thin films from green solvents in air. Compounds X2-5 comprised a monomeric PDI core with a functional cyclic secondary amine appended to the bay region. Bromine or cyano moieties are incorporated into the molecular scaffold to systematically tune optoelectronic properties. The utility of these materials is demonstrated by slot-die coating them from ethanol to serve as cathode interlayers in prototype air-processed conventional organic photovoltaics. Using a PM6:Y6 active layer, device power conversion efficiencies reached 10%, among the best reported under these conditions.
RESUMO
Commercialization of organic solar cells (OSC) is imminent. Interlayers between the photoactive film and the electrodes are critical for high device efficiency and stability. Here, the applicability of SnO2 nanoparticles (SnO2 NPs) as the electron transport layer (ETL) in conventional OSCs is evaluated. A commercial SnO2 NPs solution in butanol is mixed with ethanol (EtOH) as a processing co-solvent to improve film formation for spin and slot-die coating deposition procedures. When processed with 200% v/v EtOH, the SnO2 NPs film presents uniform film quality and low photoactive layer degradation. The optimized SnO2 NPs ink is coated, in air, on top of two polymer:fullerene-based systems and a nonfullerene system, to form an efficient ETL film. In every case, addition of SnO2 NPs film significantly enhances photovoltaic performance, from 3.4 and 3.7% without the ETL to 6.0 and 5.7% when coated on top of PBDB-T:PC61BM and PPDT2FBT:PC61BM, respectively, and from 3.7 to 7.1% when applied on top of the PTQ10:IDIC system. Flexible, all slot-die-coated devices, in air, are also fabricated and tested, demonstrating the versatility of the SnO2 NPs ink for efficient ETL formation on top of organic photoactive layers, processed under ambient condition, ideal for practical large-scale production of OSCs.