RESUMEN
The solution-processed zinc oxide (ZnO) electron transport layer (ETL) always exhibits ubiquitous defects, and its photocatalytic activity is detrimental for the organic solar cell (OSC) to achieve high efficiency and stability. Herein, an organic dye molecule, PDINN-S is introduced, to dope ZnO, constructing a hybrid ZnO:PDINN-S ETL. This hybrid ETL exhibits improved electron mobility and conductivity, particularly post-light exposure. The catalytic activity of ZnO is also effectively suppressed.Consequently, the efficiency and photo-stability of inverted non-fullerene OSCs are synergistically enhanced. The devices based on PM6:Y6/PM6:BTP-eC9 active layer with ZnO:PDINN-S as ETL give impressive power conversion efficiencies (PCEs) of 16.78%/17.59%, significantly higher than those with pure ZnO as ETL (PCEs = 15.31%/16.04%). Moreover, ZnO:PDINN-S-based device shows exceptional long-term stability under continuous AM 1.5G illumination (T80 = 1130 h) , overwhelming the reference device (T80 = 455 h). In addition, Incorporating PDINN-S into ZnO alleviate mechanical stress within the inorganic lattice, making ZnO:PDINN-S ETL more suitable for the fabrication of flexible devices. Overall, doping ZnO with organic dye molecules offers an innovative strategy for developing multifunctional and efficient hybrid ETL of the non-fullerene OSCs with excellent efficiency and photo-stability.
RESUMEN
Electron transport layers (ETLs) generally contain polar groups for enhancing performance and reducing the work function. Nevertheless, the polar group with high surface energy may cause inferior interfacial compatibility, which challenges the ETLs to balance stability and performance. Here, two conjugated small molecules of ETLs with low surface energy siloxane, namely PDI-Si and PDIN-Si, are synthesized. The siloxane with low surface energy not only enhances the interfacial compatibility between ETLs and active layers but also improves the moisture-proof stability of the device. Impressively, the amine-functionalized PDIN-Si can simultaneously exhibit conspicuous n-type self-doping properties and outstanding moisture-proof stability. The optimization of interfacial contact and morphology enables the PM6:Y6-based OSC with PDIN-Si to achieve a power conversion efficiency (PCE) of 15.87%, which is slightly superior to that of classical ETL PDINO devices (15.27%), and when the PDIN-Si film thickness reaches 28 nm, the PCE remains at 13.19% (≈83%), which indicates that PDIN-Si has satisfactory thickness insensitivity to facilitate roll-to-roll processing. Excitingly, after 120 h of storage in an environment with humidity above 45%, the unencapsulated device with PDIN-Si as ETL remains at 75% of the initial PCE value, while the device with PDINO as ETL is only 50%.
RESUMEN
The field of organic solar cells (OSCs) has acquired rapid progress with the development of nonfullerene acceptors. Interfacial engineering is also significant for the enhancement of the power conversion efficiency (PCE) in OSCs. Among the cathode interfacial materials (CIMs), perylene diimide (PDI) small molecules are promising owing to the excellent electron affinity and electron mobility. Although the well-known PDINN molecule has excellent properties, it has a high planarity formed by an extensive rigid π-conjugated backbone. Because the PDI molecular backbone has a strong tendency to aggregate, it causes the problem of excessive molecular aggregation and stacking, which directly leads to excessive crystallinity. Proper accumulation is beneficial for charge transport, but oversized crystals formed by overaggregation will hinder charge transport, ultimately affecting the film morphology and charge transport efficiency. Modifying the bay position of PDINN is an effective strategy to reduce the planarity, modulate the molecular aggregation, optimize the morphology, and enhance the charge-collecting efficiency. Therefore, PDINN-S was synthesized from PDINN by substituting the hydrogen with thiophene. The optimal PCE in the PM6:Y6 active layer was 16.18% and remained at 80% of the initial value after 720 h in a glovebox. This provides some guidance for exploring CIMs and preparing large-scale OSCs in the future.