Abstract
By combining the iridium(III) ppy-type complex (Hppy=2-phenylpyridine) with a square-planar platinum(II) unit, some novel phosphorescent oligometallaynes bearing dual metal centers (viz. Ir(III) and Pt(II)) were developed by combining trans-[Pt(PBu(3))(2)Cl(2)] with metalloligands of iridium possessing bifunctional pendant acetylene groups. Photophysical and computational studies indicated that the phosphorescent excited states arising from these oligometallaynes can be ascribed to the triplet emissive Ir(III) ppy-type chromophore, owing to the obvious trait (such as the longer phosphorescent lifetime at 77 K) also conferred by the Pt(II) center. So, the two different metal centers show a synergistic effect in governing the photophysical behavior of these heterometallic oligometallaynes. The inherent nature of these amorphous materials renders the fabrication of simple solution-processed doped phosphorescent organic light-emitting diodes (PHOLEDs) feasible by effectively blocking the close-packing of the host molecules. Saliently, such a synergistic effect is also important in affording decent device performance for the solution-processed PHOLEDs. A maximum brightness of 3,356 cd m(-2) (or 2,708 cd m(-2)), external quantum efficiency of 0.50% (or 0.67%), luminance efficiency of 1.59 cd A(-1) (or 1.55 cd A(-1)), and power efficiency of 0.60 Lm W(-1) (or 0.55 Lm W(-1)) for the yellow (or orange) phosphorescent PHOLEDs can be obtained. These results show the great potential of these bimetallic emitters for organic light-emitting diodes.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
