4 research outputs found
Solution-Processed Self-Stratifying Layer with Controllable Dielectric Polarization for High-Luminance Organic Light-Emitting Diodes
Spin-coated
poly(3,4-ethylenedioxythiophene) polystyrene sulfonate
(PEDOT:PSS) layers are well known to show a PSS-rich surface layer.
Such a self-stratifying PEDOT:PSS layer has been applied for improving
maximum external quantum efficiency (EQE) of organic light-emitting
diodes (OLEDs). However, such devices typically show much reduced
high-luminance performance affecting practical applications of such
a self-stratifying interlayer (SSL). In this work, we demonstrate
that a simple ionization process can eliminate the adverse effects
at high luminance while maintaining high maximum EQE. It is shown
that ions of the salt can interact with hydroxyl groups of the PSS
polymer and thus disorder the orientation polarization. This implies
that the ionization process enables active tuning of the dielectric
properties of the PEDOT:PSS layer. It reduces carrier accumulation
caused by orientation polarization of the SSL and thus suppresses
both exciton annihilation and electric stress across the emitting
layer in OLEDs. With this strategy, the device using the self-stratifying
PEDOT:PSS layer shows a wide window of operating current density which
is nearly 6 times compared with that of the corresponding device without
the treatment. This enables 5 times of luminance and operation lifetime
enhancements
Ultrasonic Spray Processed, Highly Efficient All-Inorganic Quantum-Dot Light-Emitting Diodes
All-inorganic
and low-cost quantum-dot light-emitting diodes (QLEDs) are always
desired considering the easy processing and outstanding physical and
chemical stability of inorganic oxides. Herein, efficient all-inorganic
QLEDs are demonstrated by using NiO and ZnO as the charge transport
layers fabricated via ultrasonic spray processes. Excellent device
performance is achieved thanks to the introduction of an Al<sub>2</sub>O<sub>3</sub> interlayer between quantum dots (QDs) and an amorphous
NiO layer. Transient photoluminescence and electricity measurements
indicate that the Al<sub>2</sub>O<sub>3</sub> layer can suppress the
exciton quenching induced by the NiO layer and reduce the electron
leakage from QDs to NiO. In consequence, relative to that of a device
without an Al<sub>2</sub>O<sub>3</sub> layer, the efficiency of an
Al<sub>2</sub>O<sub>3</sub>-containing device is enhanced by a factor
of 539%, increasing from 3.8 cd/A to 20.5 cd/A, and it exhibits color-saturated
green emission (peak at 530 nm) and high luminescence (>20 000
cd/m<sup>2</sup>). These are the best performances for all-inorganic
QLEDs reported to date. Meanwhile, it is demonstrated that ultrasonic
spray is a feasible and cost-effective technology to construct efficient
all-inorganic QLEDs. We anticipate that these results will spur the
progress toward realization of high performance and mass production
of all-inorganic QLEDs as a platform for QD-based full-color displays
Coffee-Ring-Free Ultrasonic Spray Coating Single-Emission Layers for White Organic Light-Emitting Devices and Their Energy-Transfer Mechanism
Ultrasonic
spray coating (USC) process is an alternative for low-cost solution-processed
white organic light-emitting devices (OLEDs). However, complicated
flow behaviors in the thick liquid layer, especially in multicomponent
solution, result in the existence of ripples (coffee rings) in organic
films. The ripples keep the USC process from being generally recognized
as an efficient solution process for white OLEDs. Therefore, a slope
method is proposed to avoid the emergence of ripples during the USC
process. In the method, just like centrifugal force in a spin-coating
process, gravity is used to remove redundant solution so that the
remaining liquid layer can stay uniform under the control of substrate
surface forces. Based on this, uniform organic films consisting of
multiple components are obtained, and they are used as emitting layers
to realize efficient white OLEDs. The white OLEDs based on the USC
binary doping and ternary doping single-emission layer exhibit excellent
electroluminescent performances. Furthermore, to clarify the energy
transfer in the multicomponent emitting layers, their transient emission
spectra are built based on the transient photoluminescent decay curves.
And the detailed energy-transfer mechanism of the device is discussed
Cyanide-Bridged Rope-like Chains Based on Trigonal-Bipyramidal [Fe<sub>2</sub>Cu<sub>3</sub>] Subunits
Extending a selected cyanometalate block into a higher
dimensional
framework continues to present intriguing challenges in the fields
of chemistry and material science. Here, we prepared two rope-like
chain compounds of {[(Tp*Me)Fe(CN)3]2Cu2X2(L)}·sol (1, X = Cl,
L = (MeCN)0.5(H2O/MeOH)0.5, sol =
2MeCN·1.5H2O; 2, X = Br, L = MeOH, sol
= 2MeCN·0.75H2O; Tp*Me = tris(3, 4, 5-trimethylpyrazole)borate)
in which the cyanide-bridged trigonal-bipyramidal [Fe2Cu3] subunits were linked with the adjacent ones via two vertex
Cu(II) centers, providing a new cyanometallate chain archetype. Direct
current magnetic study revealed the presence of ferromagnetic couplings
between Fe(III) and Cu(II) ions and uniaxial anisotropy due to a favorable
alignment of the anisotropic tricyanoiron(III) units. Moreover, compound 1 exhibits single-chain magnet behavior with an appreciable
energy barrier of 72 K, while 2 behaves as a metamagnet,
likely caused by the subtle changes in the interchain interactions