Although carbon quantum dots (CQDs) are of great interest because of cost effectiveness and environmental compatibility with the facile tunability of their optical properties, poor photo‐ and electroluminescence (EL) of CQDs limits further implementation. Here, a novel bottom‐up synthetic route for fabricating highly crystalline CQDs suitable for high‐brightness blue light‐emitting diodes is demonstrated. The two‐step solution process is based on time‐controlled thermal carbonization of citric acid, followed by ligand exchange of the CQDs with oleylamine (OA) in solution. Carbonization allows for the nucleation and growth of crystalline CQDs, while OA treatment disperses the CQDs and stabilizes the solution, giving rise to CQDs with low structural defects and uniform sizes. The systematic study reveals the origin of the light emission of OA‐treated CQDs by photoluminescence (PL) analysis, which yields a high quantum efficiency of ≈30%. The photoluminescence‐optimized OA‐treated CQDs exhibit excellent blue EL performance with a low turn‐on voltage of ≈4 V and high brightness of 308 cd m−2; a negligible voltage‐dependent color shift when they are employed to an inverted light‐emitting diode. 相似文献
The temperature dependence of the current-voltage-luminescence characteristics in organic light-emitting diodes (OLEDs) with varying thickness of LiF layers are studied to understand the mechanism of the enhanced electron injection by inserting a thin insulating LiF layer at the tris(8-hydroxyquinoline) aluminum (Alq3)–Al interfaces. At room temperature, the LiF/Al cathode enhances the electron injection and the quantum efficiency (QE) of the electroluminescence (EL), implying that the LiF thin layer lowers the electron-injection barrier. However, at low temperatures it is observed that the injection-limited current dominates and the barrier height for the electron injection in the device with LiF/Al appears to be similar with the Al only device. Thus, our results suggest that at low temperatures the insertion of LiF does not cause a significant band bending of Alq3 or reduction of the Al work function. 相似文献
The efficiency droop behaviors of GaN-based green light-emitting diodes (LEDs) are studied as a function of temperature from 300 K to 480 K. The overall quantum efficiency of the green LEDs is found to degrade as temperature increases, which is mainly caused by activation of new non-radiative recombination centers within the LED active layer. Meanwhile, the external quantum efficiency of the green LEDs starts to decrease at low injection current level (<1 A/cm2 ) with a temperature-insensitive peak-efficiency-current. In contrast, the peak-efficiency-current of a control GaN-based blue LED shows continuous up-shift at higher temperatures. Around the onset point of efficiency droop, the electroluminescence spectra of the green LEDs also exhibit a monotonic blue-shift of peak energy and a reduction of full width at half maximum as injection current increases. Carrier delocalization is believed to play an important role in causing the efficiency droop in GaN-based green LEDs. 相似文献
In this paper, the green quantum dots capped with the ligand, tris(mercaptomethyl)nonane (TMMN), are fabricated as the light‐emitting layer for efficient and bright light‐emitting diodes. These TMMN‐capped quantum dots exhibit well‐preserved photoluminescence properties with quantum yields of ∼90% after ligand exchange. The light‐emitting diodes based on TMMN‐capped quantum dots are reported with a maximum external quantum efficiency of 16.5% corresponding to a power efficiency and current efficiency of 57.6 lm W–1 and 70.1 cd A–1, respectively. The devices exhibit high color stability that is not markedly affected by the increase of applied voltage, thus leading to a high color reproducibility. Most importantly, the devices exhibit high environmental stability. For the highest luminance devices (with emitting layer thickness of 25 nm) and the highest power efficiency devices (with emitting layer thickness of 38 nm), the lifetimes are > 480 000 h and > 110 000 h, respectively.
Silver‐nanoicosahedron particles (AgNIPs) are produced by chemical reduction and photochemical methods and doped into the hole transport layer (HTL) or emissive layer (EML) of blue‐emitting polymer light‐emitting diodes (PLEDs) to improve their luminous efficiency. The optimal distributed‐densities of the AgNIPs are determined from current density–voltage–luminance measurements at different doping concentrations. The AgNIP dopant doses that maximize the average luminous efficiency of the proposed PLED are 6.71 µg cm?2 in EML (achieving 3.48 cd A?1) and 6.88 µg cm?2 in HTL (achieving 3.35 cd A?1). Although the luminous efficiencies of the blue‐emitting PLEDs fabricated by both doping methods are not significantly different, the maximum plasmonic enhancement (around 30‐fold) of the blue‐emitting PLED with AgNIPs in EML is red‐shifted to the green region (≈530 nm in the electroluminescence spectrum), seriously degrading the luminescent monochromaticity of the blue‐emitting PLED. The maximum plasmonic enhancement (around 33‐fold) of blue‐emitting PLED with AgNIPs in HTL occurred at 430 nm, overlapping the localized surface‐plasmon resonance extinctions of the AgNIPs in HTL (425 nm), thus favoring the enhancement of fluorescence emission. Therefore, to enhance the large‐area emission of blue‐emitting PLEDs, the AgNIPs should be doped in the HTL rather than the EML. 相似文献
Color tunable microcavity organic light-emitting diodes (OLEDs) with structure of distributed Bragg reflectors (DBR)/indium-tin-oxide
(ITO)/N,N′-di(naphthalene-1-yl)-N,N′-diphenyl-benzidine (NPB)/tris(8-hydroxyquinoline) aluminum (Alq3)/LiF/Al were fabricated. Orange red and green light emissions with full width at half maximum (FWHM) of less than 20 nm were
obtained through simply changing the thickness of NPB layer. Furthermore, due to the effective modification of the spontaneous
emission within microcavity, the brightness and electroluminescent (EL) efficiency of the microcavity OLEDs were significantly
enhanced. The maximum brightness and current efficiency, respectively, reached 31000 cd/m2 at a current density of 480.0 mA/cm2 and 8.3 cd/A at a current density of 110.0 mA/cm2 for green devices, and 9700 cd/m2 at a current density of 180.0 mA/cm2 and 6.6 cd/A at a current density of 36.4 mA/cm2 for red devices, which are over 1.5 times higher than those of noncavity OLEDs.
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Growths of blue and green multi-quantum wells (MQWs) and light-emitting diodes (LEDs) are realized on lateral epitaxial overgrowth
(LEO) GaN, and compared with identical structures grown on conventional GaN. Atomic force microscopy is used to confirm the
significant reduction of dislocations in the wing region of our LEO samples before active-region growth. Differences between
surface morphologies of blue and green MQWs are analyzed. These MQWs are integrated into LEDs. All devices show a blue shift
in the electroluminescence (EL) peak and narrowing in EL spectra with increasing injection current, both characteristics attributed
to the band-gap renormalization. Green LEDs show a larger EL peak shift and a broader EL spectrum due to larger piezoelectric
field and more indium segregation in the MQWs, respectively. Blue LEDs on LEO GaN show a higher performance than those on
conventional GaN; however, no performance difference is observed for green LEDs on LEO GaN versus conventional GaN. The performance
of the green LEDs is shown to be primarily limited by the active layer growth quality. 相似文献
The parameters of silicon light-emitting diodes (LEDs) prepared through boron implantation into n-Si, followed by annealing at 700–1200°C, were studied. The maximum room-temperature internal quantum efficiency of electroluminescence (EL) in the region of band-to-band transitions was estimated as 0.4% and reached at an annealing temperature of 1100°C. This value did not vary more than twofold within the operating temperature range 80–500 K. The EL growth and decay kinetics was studied at various currents. Following an initial current range of nonlinear dependence, the EL intensity scaled linearly with the current. It is shown that interpretation of this result will apparently require a revision of some present-day physical concepts concerning carrier recombination in silicon diodes.
Bottom emitting organic light emitting diodes (OLEDs) can suffer from lower external quantum efficiencies (EQE) due to inefficient out‐coupling of the generated light. Herein, it is demonstrated that the current efficiency and EQE of red, yellow, and blue fluorescent single layer polymer OLEDs is significantly enhanced when a MoOx(5 nm)/Ag(10 nm)/MoOx(40 nm) stack is used as the transparent anode in a top emitting OLED structure. A maximum current efficiency and EQE of 21.2 cd/A and 6.7%, respectively, was achieved for a yellow OLED, while a blue OLED achieved a maximum of 16.5 cd/A and 10.1%, respectively. The increase in light out‐coupling from the top‐emitting OLEDs led to increase in efficiency by a factor of up to 2.2 relative to the optimised bottom emitting devices, which is the best out‐coupling reported using solution processed polymers in a simple architecture and a significant step forward for their use in large area lighting and displays. 相似文献