Multichannel Strategies to Produce Stabilized Azaphenalene Diradicals: A Predictable Model to Generate Self-Doped Cathode Interfacial Layers for Organic Photovoltaics

摘要

Self-doped cathode interfacial layers (CILs) are crucial to enable Ohmic-like contact between the electrode and organic functional layers and thus profoundly promote the performances of organic optoelectronic devices. Herein, multifarious azaphenalene-embedded organic salts with variable counterions, substituent groups, and repeating units are prepared, and their impacts on producing homologous diradicals are established. Electron paramagnetic resonance and X-ray photoelectron spectroscopy studies reveal the existence of free radicals of these azaphenalene salts in the solid state. Density functional theory simulations indicate that the thermal energy of counterion-induced proton transfer is crucial to produce diradicaloids, which can be manipulated in tailoring the azaphenalene backbones. Noticeably, the formed diradicaloids that are delocalized over the pi-conjugated systems will be beneficial to enhance the carrier density of the matrix and remarkably decrease the work functions of the Al electrode. The all-solution-processed bulk heterojunction organic solar cells are fabricated by employing them as CILs, which results in high power conversion efficiency of 10.24% in contrast to the 7.34% of the reference device without CILs.