Abstract

A new series of soluble 3,6-carbazole–fluorene–silole copolymers (PCz–F–S) with Mw up to 52.1kDa were synthesized by Suzuki coupling reactions. Chemical structures and optoelectronic properties of the copolymers were characterized by elemental analysis, NMR, UV absorption, cyclic voltammetry, photoluminescence (PL), and electroluminescence (EL) spectra. The main absorption peaks of solutions and films of the copolymers are at 354nm and 347nm, respectively, showing the combined contribution from the 3,6-carbazole and fluorene blocks. The silole absorption is at wavelength range between 400nm and 500nm. Compared with the solution absorption, largely decreased relative absorption of the silole to the 3,6-carbazole and fluorene blocks can be found for the films of the copolymers. The copolymers possess HOMO levels of around −5.36eV, mainly from the contribution of 3,6-carbazole. Under excitation, the films of the copolymers show silole-dominated green emissions because of PL excitation energy transfer, with high absolute PL quantum yields up to 86%. EL devices with a configuration of ITO/PEDOT/PCz–F–S/Ba/Al only display a maximum external quantum efficiency of 0.48% whereas a device configuration of ITO/PEDOT/PCz–F–S/TPBI/Ba/Al with TPBI hole blocking layer greatly boosts the efficiency to 3.03% for a practical brightness of 236cd/m2. The improved EL efficiency suggests that more balanced charge injection and transport can be realized by inserting the TPBI hole blocking layer.

Full Text
Paper version not known

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 call

Disclaimer: 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.