9 research outputs found

    Configuration effect of novel bipolar triazole/carbazole-based host materials on the performance of phosphorescent OLED devices

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    <p id="sp0010"> A series of structurally isomeric carbazole/triazole (TAZ)-based bipolar host materials <strong class="boldFont">1</strong>&ndash;<strong class="boldFont">4</strong> were designed and synthesized. These new materials were found to exhibit wide energy gaps (<em>E</em><sub>g</sub>: 3.29&ndash;3.52&nbsp;eV), high triplet energies (<em>E</em><sub>T</sub>: 2.56&ndash;2.76&nbsp;eV), high thermal stability (<em>T</em><sub>d</sub>: 426&ndash;454&nbsp;&deg;C), high glass-transition temperatures (<em>T</em><sub>g</sub>: 116&ndash;156&nbsp;&deg;C) and excellent film-forming property. Green and blue emitting devices with <em>fac</em>-tris(2-phenylpyridine)iridium (Ir(ppy)<sub>3</sub>) and iridium(III) bis(4,6-(di-fluorophenyl)pyridinato-<em>N</em>,C<sup>2&prime;</sup>)picolinate (FIrpic) as phosphorescent dopants have been fabricated. The measurements of turn-on voltages, efficiencies and luminance suggested that the practice of combining carbazole&rsquo;s high triplet energy and excellent hole-transporting ability with TAZ&rsquo;s electron-transporting ability at the molecular level was effectively translated into better performance at the device level. The molecular structure of compound <strong class="boldFont">4</strong> is well-correlated with its efficiencies, which (32.7 and 21.1&nbsp;cd/A for green and blue devices, respectively) were the best among the four materials.</p> <!--VALIDHTML--> <hr /

    Substituent effect of ancillary ligands on the luminescence of bis[4,6-(di-fluorophenyl)-pyridinato-N,C2]iridium(III) complexes

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    <p> Two series of (dfppy)<sub><font size="2">2</font></sub>Ir(L<sub><font size="2">N^O</font></sub>) with different substituents were designed and successfully synthesized and the effect of substitution at the ancillary ligand on the photophysical and electrochemical properties of (dfppy)<sub><font size="2">2</font></sub>Ir(L<sub><font size="2">N^O</font></sub>) were investigated. The results indicate that the electron-donating group of &ndash;OMe at L<sub><font size="2">N^O</font></sub> increases the PL quantum efficiencies of (dfppy)<sub><font size="2">2</font></sub>Ir(L<sub><font size="2">N^O</font></sub>) and the electron-withdrawing groups of &ndash;CF<sub><font size="2">3</font></sub> and &ndash;F lower the PL quantum efficiencies.</p> <br /
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