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Journal ArticleDOI

Bright and color-saturated emission from blue light-emitting diodes based on solution-processed colloidal nanocrystal quantum dots

02 Nov 2007-Nano Letters (Nano Lett)-Vol. 7, Iss: 12, pp 3803-3807
TL;DR: In this article, a multilayer solution-processed blue light-emitting diode based on colloidal core/shell CdS/ZnS nanocrystal quantum dots (QDs) is presented.
Abstract: We report a multilayer solution-processed blue light-emitting diode based on colloidal core/shell CdS/ZnS nanocrystal quantum dots (QDs). At a low-operating voltage of 5.5 V, the device emits spectrally pure blue radiation at 460 nm with a narrow full-width-at-half-maximum bandwidth of 20 nm and high brightness up to 1600 cd/m2. Broad-band, long-wavelength emission from the polymer components and deep traps in the QDs are minimized to less than 5% of the total emission.
Citations
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Journal ArticleDOI
TL;DR: In this paper, a solution-processed light-emitting diodes based on a quantum-dot emissive layer between an organic hole-transport layer and an electron transport layer of ZnO nanoparticles was demonstrated.
Abstract: Researchers demonstrate solution-processed light-emitting diodes based on a quantum-dot emissive layer between an organic hole-transport layer and an electron-transport layer of ZnO nanoparticles. The device achieves a luminance of 68,000 cd m−2 and power efficiencies of up to 8.2 lm W−1.

970 citations

Journal ArticleDOI
TL;DR: In this paper, the decoupling of quantum effects on excitation and emission is described, along with the use of quantum dots as sensitizers in phosphors, and the multimodal applications of quantum dot, including in electroluminescence device, solar cell and biological imaging.
Abstract: Semiconducting quantum dots, whose particle sizes are in the nanometer range, have very unusual properties. The quantum dots have band gaps that depend in a complicated fashion upon a number of factors, described in the article. Processing-structure-properties-performance relationships are reviewed for compound semiconducting quantum dots. Various methods for synthesizing these quantum dots are discussed, as well as their resulting properties. Quantum states and confinement of their excitons may shift their optical absorption and emission energies. Such effects are important for tuning their luminescence stimulated by photons (photoluminescence) or electric field (electroluminescence). In this article, decoupling of quantum effects on excitation and emission are described, along with the use of quantum dots as sensitizers in phosphors. In addition, we reviewed the multimodal applications of quantum dots, including in electroluminescence device, solar cell and biological imaging.

964 citations

Journal ArticleDOI
TL;DR: Highly bright and efficient inverted structure quantum dot (QD) based light-emitting diodes (QLEDs) by using solution-processed ZnO nanoparticles as the electron injection/transport layer and by optimizing energy levels with the organic hole transport layer are reported.
Abstract: We report highly bright and efficient inverted structure quantum dot (QD) based light-emitting diodes (QLEDs) by using solution-processed ZnO nanoparticles as the electron injection/transport layer and by optimizing energy levels with the organic hole transport layer. We have successfully demonstrated highly bright red, green, and blue QLEDs showing maximum luminances up to 23,040, 218,800, and 2250 cd/m(2), and external quantum efficiencies of 7.3, 5.8, and 1.7%, respectively. It is also noticeable that they showed turn-on voltages as low as the bandgap energy of each QD and long operational lifetime, mainly attributed to the direct exciton recombination within QDs through the inverted device structure. These results signify a remarkable progress in QLEDs and offer a practicable platform for the realization of QD-based full-color displays and lightings.

802 citations

Journal ArticleDOI
TL;DR: The epitaxial deposition of a compressive shell onto a soft nanocrystalline core to form a lattice-mismatched quantum dot can dramatically change the conduction and valence band energies of both the core and the shell.
Abstract: Lattice strain is a structural parameter that has been exploited in microelectronic devices with great success, but its role in colloidal nanocrystals is still poorly understood. Here we have developed strain-tunable colloidal nanocrystals by using lattice-mismatched heterostructures that are grown by epitaxial deposition of a compressive shell (e.g., ZnSe or CdS) onto a soft and small nanocrystalline core (e.g., CdTe). This combination of a “squeezed” core and a “stretched” shell causes dramatic changes in both the conduction and valence band energies. As a result, we show that core-shell QDs with standard type-I behavior are converted into type-II nanostructures, leading to spatial separation of electrons and holes, extended excited state lifetimes, and giant spectral shifting. This new class of strain-tunable QDs exhibits narrow light emission with high quantum yield across a broad range of visible and near-infrared wavelengths (500 nm to 1050 nm).

699 citations

Journal ArticleDOI
TL;DR: In this article, a blue-violet quantum-dot-based light-emitting diodes (QD-LEDs) with 1-octanethiol capped ligands have been shown to achieve a maximum luminance of 7600 cd/m2 and a maximum external quantum efficiency (ηEQE) of (10.3 ± 0.9)% with an electroluminescence peak at 443 nm.
Abstract: We report high-efficiency blue-violet quantum-dot-based light-emitting diodes (QD-LEDs) by using high quantum yield ZnCdS/ZnS graded core–shell QDs with proper surface ligands. Replacing the oleic acid ligands on the as-synthesized QDs with shorter 1-octanethiol ligands is found to cause a 2-fold increase in the electron mobility within the QD film. Such a ligand exchange also results in an even greater increase in hole injection into the QD layer, thus improving the overall charge balance in the LEDs and yielding a 70% increase in quantum efficiency. Using 1-octanethiol capped QDs, we have obtained a maximum luminance (L) of 7600 cd/m2 and a maximum external quantum efficiency (ηEQE) of (10.3 ± 0.9)% (with the highest at 12.2%) for QD-LEDs devices with an electroluminescence peak at 443 nm. Similar quantum efficiencies are also obtained for other blue/violet QD-LEDs with peak emission at 455 and 433 nm. To the best of our knowledge, this is the first report of blue QD-LEDs with ηEQE > 10%. Combined with ...

361 citations

References
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Journal ArticleDOI
04 Aug 1994-Nature
TL;DR: In this article, a hybrid organic/inorganic electroluminescent device was constructed based on the recombination of holes injected into a layer of semiconducting p-paraphenylene vinylene (PPV) with electrons injected into the multilayer film of cadmium selenide nanocrystals.
Abstract: ELECTROLUMINESCENT devices have been developed recently that are based on new materials such as porous silicon1 and semiconducting polymers2,3. By taking advantage of developments in the preparation and characterization of direct-gap semiconductor nanocrystals4–6, and of electroluminescent polymers7, we have now constructed a hybrid organic/inorganic electroluminescent device. Light emission arises from the recombination of holes injected into a layer of semiconducting p-paraphenylene vinylene (PPV)8–10 with electrons injected into a multilayer film of cadmium selenide nanocrystals. Close matching of the emitting layer of nanocrystals with the work function of the metal contact leads to an operating voltage11 of only 4V. At low voltages emission from the CdSe layer occurs. Because of the quantum size effect19–24 the colour of this emission can be varied from red to yellow by changing the nanocrystal size. At higher voltages green emission from the polymer layer predominates. Thus this device has a degree of voltage tunability of colour.

3,783 citations

Journal Article
TL;DR: In this article, a hybrid organic/inorganic electroluminescent device was constructed based on the recombination of holes injected into a layer of semiconducting p-paraphenylene vinylene (PPV) with electrons injected into the multilayer film of cadmium selenide nanocrystals.
Abstract: ELECTROLUMINESCENT devices have been developed recently that are based on new materials such as porous silicon' and semiconducting polymers 2,3 . By taking advantage of developments in the preparation and characterization of direct-gap semiconductor nanocrystals 4-6 , and of electroluminescent polymers7, we have now constructed a hybrid organic/inorganic electroluminescent device. Light emission arises from the recombination of holes injected into a layer of semiconducting p-paraphenylene vinylene (PPV) 2-10 with electrons injected into a multilayer film of cadmium selenide nanocrystals. Close matching of the emitting layer of nanocrystals with the work function of the metal contact leads to an operating voltage" of only 4 V. At low voltages emission from the CdSe layer occurs. Because of the quantum size effect 19-24 the colour of this emission can be varied from red to yellow by changing the nanocrystal size. At higher voltages green emission from the polymer layer predominates. Thus this device has a degree of voltage tunability of colour.

3,285 citations

Journal ArticleDOI
19 Dec 2002-Nature
TL;DR: A hybrid light-emitting diode (LED) that combines the ease of processability of organic materials with the narrow-band, efficient luminescence of colloidal quantum dots (QDs) is demonstrated and a 25-fold improvement in luminescent efficiency is observed.
Abstract: The integration of organic and inorganic materials at the nanometre scale into hybrid optoelectronic structures enables active devices that combine the diversity of organic materials with the high-performance electronic and optical properties of inorganic nanocrystals. The optimization of such hybrid devices ultimately depends upon the precise positioning of the functionally distinct materials. Previous studies have already emphasized that this is a challenge, owing to the lack of well-developed nanometre-scale fabrication techniques. Here we demonstrate a hybrid light-emitting diode (LED) that combines the ease of processability of organic materials with the narrow-band, efficient luminescence of colloidal quantum dots (QDs). To isolate the luminescence processes from charge conduction, we fabricate a quantum-dot LED (QD-LED) that contains only a single monolayer of QDs, sandwiched between two organic thin films. This is achieved by a method that uses material phase segregation between the QD aliphatic capping groups and the aromatic organic materials. In our devices, where QDs function exclusively as lumophores, we observe a 25-fold improvement in luminescence efficiency (1.6 cd A(-1) at 2,000 cd m(-2)) over the best previous QD-LED results. The reproducibility and precision of our phase-segregation approach suggests that this technique could be widely applicable to the fabrication of other hybrid organic/inorganic devices.

2,438 citations

Journal ArticleDOI
TL;DR: The SILAR technique reported here can also be used for the growth of complex colloidal semiconductor nanostructures, such as quantum shells and colloidal quantum wells.
Abstract: Successive ion layer adsorption and reaction (SILAR) originally developed for the deposition of thin films on solid substrates from solution baths is introduced as a technique for the growth of high-quality core/shell nanocrystals of compound semiconductors. The growth of the shell was designed to grow one monolayer at a time by alternating injections of air-stable and inexpensive cationic and anionic precursors into the reaction mixture with core nanocrystals. The principles of SILAR were demonstrated by the CdSe/CdS core/shell model system using its shell-thickness-dependent optical spectra as the probes with CdO and elemental S as the precursors. For this reaction system, a relatively high temperature, about 220−240 °C, was found to be essential for SILAR to fully occur. The synthesis can be readily performed on a multigram scale. The size distribution of the core/shell nanocrystals was maintained even after five monolayers of CdS shell (equivalent to about 10 times volume increase for a 3.5 nm CdSe na...

1,502 citations

Journal ArticleDOI
TL;DR: The electroluminescence of CdSe nanocrystallites (quantum dots) incorporated into thin films (1000 A) of polyvinyl carbazole (PVK) and an oxadiazole derivative (t‐Bu‐PBD) and sandwiched between ITO and Al electrodes was studied in this article.
Abstract: Electroluminescence is obtained from nearly monodisperse CdSe nanocrystallites (quantum dots) incorporated into thin films (1000 A) of polyvinylcarbazole (PVK) and an oxadiazole derivative (t‐Bu‐PBD) and sandwiched between ITO and Al electrodes. The electroluminescence and photoluminescence spectra (bandwidths ≤40 nm) are nearly identical at room temperature and are tunable from ∼530 to ∼650 nm by varying the size of the dots. Voltage studies at 77 K indicate that while only the dots electroluminesce at the lower voltages, both the dots and the PVK matrix electroluminesce at higher applied voltages. Variable temperature studies indicate that the electroluminescence efficiency increases substantially as the films are cooled down to cryogenic temperatures.

1,032 citations