Prospects of Colloidal Nanocrystals for Electronic - Computer Science
Prospects of Colloidal Nanocrystals for Electronic - Computer Science
Prospects of Colloidal Nanocrystals for Electronic - Computer Science
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<strong>Colloidal</strong> <strong>Nanocrystals</strong> in <strong>Electronic</strong> Applications Chemical Reviews, 2010, Vol. 110, No. 1 421<br />
Figure 36. White light emitting LED utilizing a mixture <strong>of</strong> red, green, and blue emitting semiconductor nanocrystals. (a) Normalized EL<br />
spectra <strong>of</strong> devices containing only blue-, green-, and red-emitting nanocrystals. (b) Device cross section, and (c) photograph <strong>of</strong> white<br />
QD-LED. Reprinted with permission from ref 93. Copyright 2007 American Chemical Society.<br />
core in emitting CdSe/ZnS core-shell NCs from 3.2 to 5.8<br />
nm; ηext was improved to ∼1.1% by optimizing the thickness<br />
<strong>of</strong> ZnS shell. 407 Optimization <strong>of</strong> packing and ordering <strong>of</strong> NCs<br />
allowed enhancing ηext to over 2% (>1 lmW -1 ) with a<br />
maximum brightness <strong>of</strong> over 7000 cd m -2 . 402 The electroluminescence<br />
spectrum was dominated by the NC emission<br />
with excellent color purity. 402 Steckel et al. reported LEDs<br />
utilizing CdxZn1-xSe/CdyZn1-yS core-shell NCs integrated<br />
into a four-layered HTL/QDs/HBL/ETL structure. 403 The<br />
color saturated green emission was achieved with a peak ηext<br />
<strong>of</strong> 0.5% at low operating voltages (1100 cd m -2 ). 405 Uni<strong>for</strong>m and defect-free<br />
EL emission from the QDs over a large surface area (1.5<br />
cm × 2.5 cm) was displayed, promising <strong>for</strong> the application<br />
<strong>of</strong> QD-LEDs in large-area displays.<br />
Other potential areas <strong>of</strong> application <strong>for</strong> thin film LEDs<br />
are large area lighting systems and backlighting <strong>for</strong> liquid<br />
crystal displays. Such applications require LEDs emitting<br />
white light. Here, colloidal NCs with their tunable emission<br />
colors and the possibility <strong>of</strong> inexpensive solution-based<br />
device fabrication have a potential to successfully compete<br />
with other technologies such as OLEDs. Li et al. fabricated<br />
white organic/NCs LEDs by combining blue emitting poly[(9,9dihexyloxyfluoren-2,7-diyl)-alt-co-(2-methoxy-5-phenylen-<br />
1,4-diyl)] (PFH-MEH) polymer doped with red-emitting QDs<br />
and green-emitting Alq3. 413 The key <strong>for</strong> balanced white<br />
emission in the hybrid ternary systems PFH-MEH/QDs/Alq3<br />
was the charge-transfer processes from PFH-MEH and Alq3<br />
to the QDs. Maximum external quantum efficiency <strong>of</strong> 0.24%<br />
at1mAcm -2 and 11 V during operation in air was reported.<br />
Anikeeva et al. reported white QD-LEDs with the emitting<br />
layer assembled <strong>of</strong> a balanced mixture <strong>of</strong> red, green, and<br />
blue emitting NCs integrated into ITO/PEDOT:PSS/TPD/<br />
QDs/TAZ/Alq3 device (Figure 36). 93 The mixed-monolayer<br />
QD-LED revealed uni<strong>for</strong>mly white luminescence with the<br />
international commission on illumination (CIE) coordinates<br />
(0.35, 0.41) at an applied voltage <strong>of</strong> 9 V. At 5 V applied<br />
bias (1.51 mA/cm 2 ), the peak ηext <strong>of</strong> white QD-LED was<br />
0.36%, corresponding to 0.9 cd A -1 . The independent<br />
processing <strong>of</strong> HTL and emitting layer <strong>of</strong> NCs provided<br />
precise tuning <strong>of</strong> the emission spectrum by simply changing<br />
the color ratio <strong>of</strong> QDs without altering the device structure.<br />
In contrast to significant efficiency improvements <strong>of</strong> QD-<br />
LEDs, the lifetime <strong>of</strong> hybrid organic/NC devices is limited<br />
by the instability <strong>of</strong> the metal contacts and degradation <strong>of</strong><br />
organic components under high current operation conditions.<br />
In an attempt to overcome these limitations, the organic hole<br />
transport and electron transport layers have been replaced<br />
with much more robust inorganic materials. Caurge et al.<br />
reported QD-LEDs with p-type inorganic NiO films as<br />
HTL. 266 Inorganic NiO films demonstrated higher chemical,<br />
thermal, and electrical stability as compared to TPD and other<br />
tested organic materials. A maximum ηext ≈ 0.18% and<br />
brightness ∼3000 cd m -2 were achieved by optimizing<br />
resistivity <strong>of</strong> the NiO layer. In the next step toward<br />
all-inorganic QD LEDs, same authors fabricated inorganic<br />
ETL by replacing TAZ and Alq3 layers with sputtered<br />
amorphous ZnO:SnO2 semiconductor. 266 The all-inorganic<br />
QD-LED combined HTL <strong>of</strong> p-type NiO, luminescent<br />
Cd1-xZnxSe NCs as the emitting layer, and n-type ZnO:SnO2<br />
ETL as shown in Figure 37. These devices demonstrated<br />
pure QD emission with the peak luminance <strong>of</strong> 1950 cd m -2<br />
and enabled very high injection currents <strong>of</strong> 3.5A cm -2 . The<br />
maximum ηext was about 0.1%. The ability <strong>of</strong> inorganic HTL<br />
and ETL to drive high currents into QD layers may one day<br />
open up bright perspectives <strong>for</strong> electrically pumped lasers<br />
on colloidal NCs.<br />
Highly luminescent spectrally tunable core-shell NCs can<br />
also be coupled to bright and efficient single-crystal LEDs.<br />
This approach utilizes NCs as the down-converting medium,<br />
which efficiently absorbs blue light emitted by, <strong>for</strong> example,