© 1996 Nature Publishing Group
Transparent light-emitting devices
SIR - Organic light-emitting devices
(OLEDs), which emit in the redl, green
2
and blue
3
spectral regions, have recently
become promising candidates for colour
flat-panel display pixels owing to their
high luminosity and low operating voltage.
Furthermore, long device lifetimes
4
(exceeding 1,000 hours at a video bright-
ness of -100 cd m-
2
) have been demon-
strated. One unique property of
vacuum-deposited OLEDs is that the
luminescence band is substantially red-
shifted from the absorption band
5
, render-
ing the organic layers highly transparent
to their own luminescence and throughout
most of the visible spectrum.
Here we demonstrate a new class of
OLEDs, which are greater than 70% trans-
parent when turned off, and emit light
from both top and bottom surfaces with up
to 0.75% quantum efficiency when turned
on. Such transparency offers the potential
for very high-definition, full-colour displays
in which the red (R), green (G) and blue
(B) emission layers are placed in a vertical-
ly stacked geometry, providing a simple,
low-temperature fabrication process, as
well as minimum R-G-B pixel size and
maximum fill factor. Further applications
a
EL ½ig ht
ITO
Mg-Ag
V
Alq
3
+
TPD
ITO
Glass
EL Light
F IG. 1 a, Schematic diagram of the TOLED
structure (ITO, indium tin oxide). b, An array of
TOLEDs with one device turned on (green
spot) against a backdrop of the eastern US
coastline. Typical operating conditions for the
1-mm-diameter devices are 10-
4
A and 10 V
drive voltage . The emission spectra from both
surfaces are similar to t hose of conventional
Alq3-b ased devices
2
·
5
, after accounting for
absorption in the Mg- Ag layer. The total quan-
tum eff iciency of light emission from this
devi ce is 0. 75%. Approximately 10% higher
intensity is emitted from the substrate than
from the top contact surface . c, The same
array with all devices turned off, demonstrat-
ing the device transparency.
NATURE · VOL 380 · 7 MARCH 1996
of this device include low-voltage, semi-
transparent displays for helmet-mounted,
windscreen-mounted or other 'head-up'
applications.
The transparent OLED (TOLED)
structure is shown in Fig. la. The device
is grown on a glass substrate pre-coated
with a thin film of transparent indium tin
oxide, with a sheet resistivity of 20 n per
square. Before deposition of the organic
films, the substrates were pre-cleaned as
discussed elsewhere
5
• Deposition was
performed by sublimation, in a vacuum
of < 10-
6
torr, of a 200-A-thick layer
of the hole-conducting compound N,N '-
diphenyl-N,N' -bis(3-methylphenyl)-1-
1 '-biphenyl-4,4' -diamine (TPD), fol-
lowed by a 400-A-thick layer of the
electron-conducting and highly elec-
troluminescent tris(8-hydroxyquinoline)
aluminium (Alq3).
Figure la shows how electron-injecting
contact to the device was made by deposi-
tion through a shadow mask of a thin
layer (50--400 A) of Mg-Ag alloy (in an
approximate atomic ratio of 40 Mg:1 Ag).
Finally, the device was capped by a second
400-A-thick layer of indium tin oxide,
sputter-deposited onto the Mg-Ag sur-
face to provide a continuous, transparent
conducting surface. The sheet resistance
of this layer is 400 n per square, which
acts in parallel to the Mg- Ag sheet resis-
tance and is adequate to serve as an
injecting contact for a display pixel.
Figure 1 shows a photograph of a
TOLED array with a 100-A-thick Mg-Ag
layer. In Fig. lb, one TOLED array ele-
ment is switched on (arrow) and the inac-
tive devices are only faintly visible. They
reduce the light from the background by
only - 3 dB, even though these images are
taken under the condition that the light
illuminating the background must pass
twice through the TOLED. In Fig. le, all
the elements are switched off. The trans-
parency as a function of a TOLED from
this array is shown in detail in Fig. 2. The
device becomes non-transmissive at short
wavelengths owing to a combination of
Mg- Ag absorption and the strong molecu-
lar transitions to the
1
La and
1
Bb states
6
of
Alq3, and at long wavelengths due to absor-
ption by the Mg- Ag. However, the device
is 63 % transparent at the peak (530 nm)
emission wavelength of Alq3, and this
transpare ncy extends across the visible
spectrum.
The inset to Fig. 2 shows the transmis-
sion of the Mg-Ag contact at a wave-
length of 530 nm, with Mg-Ag film
thicknesses ranging from (50± 10) A to
(400± 10) A. The thinnest Mg-Ag layer
used thus far in a working device is 75 A
thick, corresponding to a contact trans-
CORRESPONDENCE
70
C: 50
0
'iii
"'
E
"' C: 30
10
/2- rs 0
o .!!! 10
o E
# 1
I
.= 0 200 400
Mg-Ag thickness (A)
O 300 500 700
Wavelength (nm)
900
FIG. 2 Transmission spectrum of a TOLED with
a 100-A-thick Mg-Ag electrode as a function of
wavelength. Inset, Transmission as a function
of Mg-Ag contact thickness at a wavelength of
530 nm. The slope of the straight line fit to the
data gives an optical absorption coefficient of
the Mg-Ag of a=1.1x10
6
cm- 1, consistent
with a calculated skin depth of 125 A.
parency of 81 % and a total device trans-
parency of 71 %. The real and imaginary
coefficients of the refractive index of Mg
at 530 nm are n=0.57 and k=3.47, respec-
tively7. Neglecting the small amount of Ag
in the electrode, we calculate that an 81 %
transmissive film of Mg should be 15 A
thick. This suggests that approximately
(60±10) A of the Mg-Ag electrode is
compositionally changed in the deposition
process, presumably due to a redox reac-
tion with indium tin oxide during sputter-
ing. This explains the higher measured
transparency, the departure of our trans-
mission versus thickness data from a
straight line, and our inability to produce
working devices with less than a 75-A-
thick layer of Mg-Ag.
In conclusion, we have demonstrated
the first transparent, thin-film organic
light-emitting devices. This is the crucial
first step towards realizing high-definition,
full-colour and head-up displays using
organic materials.
V. Bulovic
G.Gu
P. E. Burrows
S. R. Forrest
Advanced Technology Center for Photonics
and Optoelectronic Mat er ials,
Department of Electrical Engineering,
Princeton University, Princeton,
New Jersey 08544, USA
M. E. Thompson
Department of Chemistry,
University of Southern California,
Los Angeles, California 90089, USA
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