Bright Multicolor Bandgap Fluorescent Carbon Quantum Dots for Electroluminescent Light-Emitting Diodes
15 Apr 2017-Iss: 12, pp 826-826
TL;DR: For the first time, monochrome electroluminescent light-emitting diodes (LEDs) with MCBF-CQDs directly as an active emission layer are fabricated and the maximum luminance of blue LEDs reaches 136 cd m-2, which is the best performance for CQD-based monochrominescent LEDs.
Abstract: Multicolor bandgap fluorescent carbon quantum dots (MCBF-CQDs) from blue to red with quantum yield up to 75% are synthesized using a solvothermal method. For the first time, monochrome electroluminescent light-emitting diodes (LEDs) with MCBF-CQDs directly as an active emission layer are fabricated. The maximum luminance of blue LEDs reaches 136 cd m-2 , which is the best performance for CQD-based monochrome electroluminescent LEDs.
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TL;DR: In this article , a review of pre-and post-synthetic approaches for the preparation of carbon dots and their derivatives or composites is presented, and examples to correlate structure, composition and function are used to discuss future development of this class of nanomaterials.
Abstract: Photoluminescent carbon nanoparticles, or carbon dots, are an emerging class of materials that has recently attracted considerable attention for biomedical and energy applications. They are defined by characteristic sizes of <10 nm, a carbon-based core and the possibility to add various functional groups at their surface for targeted applications. These nanomaterials possess many interesting physicochemical and optical properties, which include tunable light emission, dispersibility and low toxicity. In this Review, we categorize how chemical tools impact the properties of carbon dots. We look for pre- and postsynthetic approaches for the preparation of carbon dots and their derivatives or composites. We then showcase examples to correlate structure, composition and function and use them to discuss the future development of this class of nanomaterials. This Review discusses synthetic strategies to functionalize photoluminescent carbon nanomaterials, or carbon dots, for targeted applications.
197 citations
TL;DR: In this article , the use of solar energy as the driving force of the photocatalysts as a starting point, the factors affecting photocatalyst performance in the preparation process, and the catalytic mechanism of the photochemical degradation of dyes.
61 citations
TL;DR: In this article , the authors used 2,3-diaminopyridine as a single precursor to synthesize colorful CDs in different pH conditions, by simply regulating the reaction media from alkali to neutral to acid, bright CDs emitting violet, green, and orange fluorescence, respectively.
51 citations
07 Apr 2022
TL;DR: In this review, the various mass transfer display technologies and color conversion strategies which are being used for the realization of a full‐color display are discussed.
Abstract: The demand for high‐performance displays is continuously increasing because of their wide range of applications in smart devices (smartphones/watches), augmented reality, virtual reality, and naked eye 3D projection. High‐resolution, transparent, and flexible displays are the main types of display to be used in future. In the above scenario, the micro‐LEDs (light‐emitting diodes) display which has outstanding features, such as low power consumption, wider color gamut, longer lifetime, and short response‐time, can replace traditional liquid crystal displays and organic LEDs‐based display technologies. However, to attain a remarkable position in future display technology, the micro‐LEDs need to overcome problems associated with mass transfer and its high cost of manufacturing. Besides micro‐LEDs, the other option for future displays includes the usage of color conversion medium (phosphor/ quantum dots) to convert some of the blue light into other colors. In this review, the various mass transfer display technologies and color conversion strategies which are being used for the realization of a full‐color display are discussed.
45 citations
References
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TL;DR: In this paper, a simple route to the production of high-quality CdE (E=S, Se, Te) semiconductor nanocrystallites is presented, based on pyrolysis of organometallic reagents by injection into a hot coordinating solvent.
Abstract: A simple route to the production of high-quality CdE (E=S, Se, Te) semiconductor nanocrystallites is presented. Crystallites from ∼12 A to ∼115 A in diameter with consistent crystal structure, surface derivatization, and a high degree of monodispersity are prepared in a single reaction. The synthesis is based on the pyrolysis of organometallic reagents by injection into a hot coordinating solvent. This provides temporally discrete nucleation and permits controlled growth of macroscopic quantities of nanocrystallites. Size selective precipitation of crystallites from Portions of the growth solution isolates samples with narrow size distributions (<5% rms in diameter). High sample quality results in sharp absorption features and strong «band-edge» emission which is tunable with particle size and choice of material
8,374 citations
TL;DR: It is reported that nanoscale carbon particles (carbon dots) upon simple surface passivation are strongly photoluminescent in both solution and the solid state.
Abstract: We report that nanoscale carbon particles (carbon dots) upon simple surface passivation are strongly photoluminescent in both solution and the solid state. The luminescence emission of the carbon dots is stable against photobleaching, and there is no blinking effect. These strongly emissive carbon dots may find applications similar to or beyond those of their widely pursued silicon counterparts.
3,817 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
TL;DR: A facile and highoutput strategy for the fabrication of CDs, which is suitable for industrial-scale production and is almost equal to fluorescent dyes, is discussed.
Abstract: Fluorescent carbon-based materials have drawn increasing attention in recent years owing to exceptional advantages such as high optical absorptivity, chemical stability, biocompatibility, and low toxicity. These materials primarily include carbon dots (CDs), nanodiamonds, carbon nanotubes, fullerene, and fluorescent graphene. The superior properties of fluorescent carbon-based materials distinguish them from traditional fluorescent materials, and make them promising candidates for numerous exciting applications, such as bioimaging, medical diagnosis, catalysis, and photovoltaic devices. Among all of these materials, CDs have drawn the most extensive notice, owing to their early discovery and adjustable parameters. However, many scientific issues with CDs still await further investigation. Currently, a broad series of methods for obtaining CD-based materials have been developed, but efficient one-step strategies for the fabrication of CDs on a large scale are still a challenge in this field. Current synthetic methods are mainly deficient in accurate control of lateral dimensions and the resulting surface chemistry, as well as in obtaining fluorescent materials with high quantum yields (QY). Moreover, it is important to expand these kinds of materials to novel applications. Herein, a facile and highoutput strategy for the fabrication of CDs, which is suitable for industrial-scale production (yield is ca. 58%), is discussed. The QY was as high as ca. 80%, which is the highest value recorded for fluorescent carbon-based materials, and is almost equal to fluorescent dyes. The polymer-like CDs were converted into carbogenic CDs by a change from low to high synthesis temperature. The photoluminescence (PL) mechanism (high QY/PL quenching) was investigated in detail by ultrafast spectroscopy. The CDs were applied as printing ink on the macro/micro scale and nanocomposites were also prepared by polymerizing CDs with certain polymers. Additionally, the CDs could be utilized as a biosensor reagent for the detection of Fe in biosystems. The CDs were prepared by a hydrothermal method, which is described in the Supporting Information (Figure 1a; see also the Supporting Information, Figure S1). The reaction was conducted by first condensing citric acid and ethylenediamine, whereupon they formed polymer-like CDs, which were then carbonized to form the CDs. The morphology and structure of CDs were confirmed by analysis. Figure 1b shows transmission electron microscopy (TEM) images of the CDs, which can be seen to have a uniform dispersion without apparent aggregation and particle diameters of 2–6 nm. The sizes of CDs were also measured by atomic force microscopy (AFM; Figure S2), and the average height was 2.81 nm. From the high-resolution TEM, most particles are observed to be amorphous carbon particles without any lattices; rare particles possess well-resolved lattice fringes. With such a low carbon-lattice-structure content, no obvious D or G bands were detected in the Raman spectra of the CDs (Figure S3). The XRD patterns of the CDs (Figure 1c) also displayed a broad peak centered at 258 (0.34 nm), which is also attributed to highly disordered carbon atoms. Moreover, NMR spectroscopy (H and C) was employed to distinguish sp-hybridized carbon atoms from sp-hybridized carbon atoms (Figure S4). In the H NMR spectrum, sp carbons were detected. In the C NMR spectrum, signals in the range of 30–45 ppm, which correspond to aliphatic (sp) carbon atoms, and signals from 100–185 ppm, which are indicative of sp carbon atoms, were observed. Signals in the range of 170– 185 ppm, which correspond to carboxyl/amide groups, were also present. In the FTIR analysis of CDs, the following were observed: stretching vibrations of C OH at 3430 cm 1 and C H at 2923 cm 1 and 2850 cm , asymmetric stretching vibrations of C-NH-C at 1126 cm , bending vibrations of N H at 1570 cm , and the vibrational absorption band of C=O at 1635 cm 1 (Figure S5). Moreover, the surface groups were also investigated by XPS analysis (Figure 1d). C1s analysis revealed three different types of carbon atoms: graphitic or aliphatic (C=C and C C), oxygenated, and nitrous (Table S1). In the UV/Vis spectra, the peak was focused on 344 nm in an aqueous solution of CDs. In the fluorescence spectra, CDs have optimal excitation and emission wavelengths at 360 nm and 443 nm, and show a blue color under a hand-held UV lamp (Figure 2a). Excitation-dependent PL behavior was [*] S. Zhu, Q. Meng, Prof. J. Zhang, Y. Song, Prof. K. Zhang, Prof. B. Yang State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University Changchun, 130012 (P. R. China) E-mail: byangchem@jlu.edu.cn
3,095 citations
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