Highly efficient lepidine‐based phosphorescent iridium(III) complexes with pentane‐2,4‐dione or triazolpyridine as ancillary ligands have been designed and prepared by a newly developed facile synthetic route. Fluorine atoms and trifluoromethyl groups have been introduced into the different positions of ligand, and their influence on the photophysical properties of complexes has been investigated in detail. All the triazolpyridine‐based complexes display the blueshifted dual‐peak emission compared to the pentane‐2,4‐dione‐based ones with a broad single‐peak emission. The complexes show emission with broad full width at half maximum (FWHM) over 100 nm, and the emissions are ranges from greenish–yellow to orange region with the absolute quantum efficiency (ΦPL) of 0.21–0.92 in solution, i.e., ΦPL = 0.92 (18), which is the highest value among the reported neutral yellow iridium(III) complexes. Furthermore, high‐performance yellow and complementary‐color‐based white organic light‐emitting diodes (OLEDs) have been fabricated. The FWHMs of the yellow, greenish–yellow OLEDs are in the range of 94–102 nm, which are among the highest values of the reported yellow or greenish–yellow‐emitting devices without excimer emission. The maximum external quantum efficiency of monochrome OLEDs can reach 24.1%, which is also the highest value among the reported yellow or greenish–yellow devices. The color rendering indexes of blue and complementary yellow‐based white OLED is as high as 78.

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An effective and simple method has been explored to construct an efficient ultraviolet organic light-emitting diode (OLED) by incorporating poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS)/MoOx double-stacked hole injection layer (HIL) and slightly retarding electron injection for achieving extremely balanced charge carriers. The device produces 4.6% external quantum efficiency with an attractive ultraviolet emission peak of 377 nm and full width at half maximum of 35 nm. Ultraviolet photoelectron spectroscopy and impedance spectroscopy analysis determine the substantially enhanced hole injection capacity of PEDOT:PSS/MoOx double-stacked HIL, which accordingly contributes to optimizing carrier balance. The results pave a way to advancing OLED in potential application towards short wavelength emission.

A significant enhancement in ultraviolet (UV) durable indium tin oxide (ITO)-free flexible nonfullerene organic solar cells (OSCs) has been demonstrated using a hybrid nanostructured flexible transparent electrode (FTE), comprising a mixture of 0D silver nanoparticles (AgNPs), 1D Ag nanowires (AgNWs) and 2D exfoliated graphene sheets. The FTE exhibits high optical transparency and electric conductivity, good air stability and full-solution fabrication capability at a low processing temperature. An average power convention efficiency (PCE) of 8.15% has been obtained for the flexible nonfullerene OSCs, based on the blend of poly[(2,6-(4, 8-bis(5-(2-ethylhexyl)thiophen-2-yl)-benzo[1,2-b:4,5-b']dithiophene))-alt-(5,5-(1',3'-di-2-thi enyl-5',7'-bis(2-ethylhexyl)benzo[1',2'-c:4',5'-c'] dithiophene-4,8-dione)] (PBDB-T): 3,9bis(2-methylene-(3-(1,1-dicyanomethylene)-indanone))-5,5,11,11-tetrakis(4-hexylphenyl)-dit hieno[2,3-d:2',3'-d']-s-indaceno[1,2-b:5,6-b'] dithiophene (ITIC). The flexible PBDB-T:ITIC OSCs exhibit an excellent UV durability compared to the ITO-based control cell, realized by the tailored FTE absorption in wavelength < 380 nm. The novel FTE developed in this work provides a promising alternative to ITO for use in UV durable flexible OSCs, serving as a UV filter to impede an unavoidable UV-induced degradation in ITO-based OSCs.

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