Organic light-emitting devices based on solution-processable small molecular emissive layers doped with interface-engineering additives

In this study, we investigate small molecular organic light-emitting diodes (SM-OLEDs) consisting of emission layers (EMLs) fabricated using a solution-coating process of self-metered horizontal dip-(H-dip-) coating. The EML used was composed of a co-mixed small molecular host matrix of holetransporting 4,4',4 "-tris(9-carbazolyl)-triphenylamine (TcTa) and electron-transporting 2,7-bis (diphenyl phosphoryl)-9,90-spirobifluorene (SPPO13) doped with blue-, green-, and/or red-emitting phosphorescent iridium complexes. To improve the electron-injecting and hole-blocking properties at the cathode interface and to enhance the film-forming capabilities, an interface-engineering additive of poly(oxyethylene tridecyl ether) (PTE) was mixed with the small molecular EMLs. Using PTE additives was shown to reduce dramatically the formation of film defects such as nano-pinholes in the EMLs, resulting in thin and homogeneous PTE-mixed EMLs with smooth surface morphologies, even when using a single H-dip-coating process. The use of simple H-dip-coated EMLs mixed with PTEs in SM-OLEDs resulted in good device performance, with maximum luminance levels of 29 200 cd m(-2), 115 000 cd m(-2), and 16 400 cd m(-2), with corresponding peak current efficiencies of 18.8 cd A(-1), 31.2 cd A(-1), and 10.0 cd A(-1), for blue, green, and red SM-OLEDs, respectively. Furthermore, we demonstrated the feasibility of fabricating large-area and high-performance solution-processable SM-OLEDs using H-dipcoated EMLs doped with PTEs. These results clearly indicate that H-dip-coated small molecular EMLs mixed with PTE can be used to yield simple, bright, and efficient solution-processable SM-OLEDs.