4 research outputs found
Benzophenones as Generic Host Materials for Phosphorescent Organic Light-Emitting Diodes
Despite
the fact that benzophenone has traditionally served as a prototype
molecular system for establishing triplet state chemistry, materials
based on molecular systems containing the benzophenone moiety as an
integral part have not been exploited as generic host materials in
phosphorescent organic light-emitting diodes (PhOLEDs). We have designed
and synthesized three novel host materials, i.e., BP2–BP4,
which contain benzophenone as the active triplet sensitizing molecular
component. It is shown that their high band gap (3.91–3.93
eV) as well as triplet energies (2.95–2.97 eV) permit their
applicability as universal host materials for blue, green, yellow,
and red phosphors. While they serve reasonably well for all types
of dopants, excellent performance characteristics observed for yellow
and green devices are indeed the hallmark of benzophenone-based host
materials. For example, maximum external quantum efficiencies of the
order of 19.2% and 17.0% were obtained from the devices fabricated
with yellow and green phosphors using BP2 as the host material. White
light emission, albeit with rather poor efficiencies, has been demonstrated
as a proof-of-concept by fabrication of co-doped and stacked devices
with blue and yellow phosphors using BP2 as the host material
Amorphous Host Materials Based on Tröger’s Base Scaffold for Application in Phosphorescent Organic Light-Emitting Diodes
Tröger’s bases (<b>TB</b>s) functionalized
with carbazoles (<b>TB-Cz</b>s) and phosphine oxides (<b>TB-PO</b>s) were designed and synthesized as host materials for
application in phosphorescent organic light-emitting diodes. The <b>TB</b> scaffold is shown to impart thermal stability with high <i>T</i><sub>g</sub> values (171–211 °C) as well as
high triplet energies in the range of 2.9–3.0 eV. With a limited
experimentation of the devices, it is shown that the <b>TB</b>s doped with a green phosphor, namely, IrÂ(ppy)<sub>3</sub>, permit
impressive external efficiencies on the order of ca. 16% with a high
brightness of ca. 3000–4000 cd/m<sup>2</sup>. Better device
performance results are demonstrated by a small structural manipulation
of the <b>TB</b> scaffold involving substitution of methyl groups
in the core scaffold
Nitrogen-Free Bifunctional Bianthryl Leads to Stable White-Light Emission in Bilayer and Multilayer OLED Devices
White organic light-emitting
diodes (WOLEDs) are at the center
stage of OLED research today because of their advantages in replacing
the high energy-consuming lighting technologies in vogue for a long
time. New materials that emit white light in simple devices are much
sought after. We have developed two novel electroluminescent materials,
referred to as <b>BABZF</b> and <b>BATOMe</b>, based on
a twisted bianthryl core, which are brilliantly fluorescent, thermally
highly stable with high <i>T</i><sub>d</sub> and <i>T</i><sub>g</sub>, and exhibit reversible redox property. Although
inherently blue emissive, <b>BABZF</b> leads to white-light
emission (CIE ≈ 0.28, 0.33) with a moderate power efficiency
of 2.24 lm/W and a very high luminance of 15 600 cd/m<sup>2</sup> in the fabricated multilayer nondoped OLED device. This device exhibited
excellent color stability over a range of applied potential. Remarkably,
similar white-light emission was captured even from a double-layer
device, attesting to the innate hole-transporting ability of <b>BABZF</b> despite it being non-nitrogenous, that is, lacking any
traditional hole-transporting di-/triarylamino group(s). Similar studies
with <b>BATOMe</b> led to inferior device performance results,
thereby underscoring the importance of dibenzofuryl groups in <b>BABZF</b>. Experimental as well as theoretical studies suggest
the possibility of emission from multiple species involving <b>BABZF</b> and its exciplex and electroplex in the devices. The
serendipitously observed white-light emission from a double-layer
device fabricated with an unconventional hole-transporting material
(HTM) opens up new avenues to create new non-nitrogenous HTMs that
may lead to more efficient white-light emission in simple double-layer
devices