Novel blue emitters based on π-

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• 作者：L.O. Pé ; res ; S.H. Wang ; J. Wé ; ry ; G. Froyer ; E. Faulques
• 关键词：Conjugated polymers ; Fluorene ; Copolymers ; Vibrational spectroscopy ; Photoluminescence ; Suzuki reaction
• 刊名：Materials Science and Engineering: C
• 出版年：2009
• 出版时间：1 March 2009
• 年：2009
• 卷：29
• 期：2
• 页码：372-376
• 全文大小：868 K

文摘

A series of new phenyl-based conjugated copolymers has been synthesized and investigated by vibrational and photoluminescence spectroscopy (PL). The materials are: poly(1,4-phenylene-alt-3,6-pyridazine) (COP-PIR), poly(9,9-dioctylfluorene)-co-quaterphenylene (COP-PPP) and poly[(1,4-phenylene-alt-3,6-pyridazine)-co-(1,4-phenylene-alt-9,9-dioctylfluorene)] (COP-PIR-FLUOR), with 3.5 % of fluorene. COP-PPP and COP-PIR-FLUOR have high fluorescence quantum yields in solution. Infrared and Raman spectra were used to check the chemical structure of the compounds. The copolymers exhibit blue emission ranging from 2.8 to 3.6 eV when excited at E_exc = 4.13 eV. Stokes-shift values were estimated on pristine samples in their condensed state from steady-state PL-emission and PL-excitation spectra. They suggest a difference in the torsional angle between the molecular configuration of the polymer blocks at the absorption and PL transitions and also in the photoexcitation diffusion. Additionally, the time-resolved PL of these materials has been investigated by using 100 fs laser pulses at E_exc = 4.64 eV and a streak camera. Results show very fast biexponential kinetics for the two fluorene-based polymers with decay times below 300 ps indicating both intramolecular, fast radiative recombination and migration of photogenerated electron–hole pairs. By contrast, the PL of COP-PIR is less intense and longer lived, indicating that excitons are confined to the chains in this polymer.