Browsing by Author "Adam, M."

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Open Access
Brightly luminescent Cu-Zn-In-S/ZnS Core/shell quantum dots in salt matrices
(De Gruyter, 2019) Lox, J. F. L.; Eichler, F.; Erdem, Talha; Adam, M.; Gaponik, N.; Demir, Hilmi Volkan; Lesnyak, V.; Eychmüller, A.
In the past decades cadmium-free quantum dots (QDs), among which are quaternary colloidal Cu-Zn-In-S/ZnS (CZIS/ZnS) core/shell nanocrystals (NCs), have attracted great scientific interest. Particularly, their low toxicity and the possibility to tune their photoluminescence (PL) properties by varying the composition in the multicomponent system make them highly attractive for applications in light-emitting diodes (LEDs). Thus, the demands for high quality CZIS/ZnS QDs and methods to process them into bulk materials stimulate investigations of these nanomaterials. Herein, we demonstrate the synthesis of CZIS/ZnS core/shell NCs via a surfactant induced nucleation process, which emit in various colors covering the range from 520 nm to 620 nm possessing high photoluminescence quantum yields (PLQYs) up to 47%. Furthermore, the as synthesized NCs were successfully integrated into two different salt matrices [Na2B4O7 (Borax) and LiCl] using two different approaches. The commonly used incorporation of the NCs into Borax salt led to salt crystals emitting from 540 nm to 600 nm with PLQYs up to 24%. By encapsulating the QDs into LiCl, brightly emitting NCs-in-LiCl powders with the PL covering a range from 520 nm to 650 nm with PLQYs of up to 14% were obtained. As a proof of concept, the fabrication of a color conversion LED using NCs encapsulated into LiCl demonstrated the applicability of the encapsulated NCs.
Open Access
Colloidal nanocrystals embedded in macrocrystals: methods and applications
(American Chemical Society, 2016) Adam, M.; Gaponik N.; Eychmüller A.; Erdem, T.; Soran-Erdem, Z.; Demir, Hilmi Volkan
Colloidal semiconductor nanocrystals have gained substantial interest as spectrally tunable and bright fluorophores for color conversion and enrichment solids. However, they suffer from limitations in processing their solutions as well as efficiency degradation in solid films. As a remedy, embedding them into crystalline host matrixes has stepped forward for superior photostability, thermal stability, and chemical durability while simultaneously sustaining high quantum yields. Here, we review three basic methods for loading the macrocrystals with nanocrystals, namely relatively slow direct embedding, as well as accelerated methods of vacuum-assisted and liquid-liquid diffusion-assisted crystallization. We discuss photophysical properties of the resulting composites and present their application in light-emitting diodes as well as their utilization for plasmonics and excitonics. Finally, we present a future outlook for the science and technology of these materials.
Open Access
Implementation of high-quality warm-white light-emitting diodes by a model-experimental feedback approach using quantum dot-salt mixed crystals
(American Chemical Society, 2015) Adam, M.; Erdem, T.; Stachowski, G.M.; Soran-Erdem Z.; Lox, J. F. L.; Bauer, C.; Poppe, J.; Demir, Hilmi Volkan; Gaponik N.; Eychmüller A.
In this work, a model-experimental feedback approach is developed and applied to fabricate high-quality, warm-white light-emitting diodes based on quantum dots (QDs) as color-conversion materials. Owing to their unique chemical and physical properties, QDs offer huge potential for lighting applications. Nevertheless, both emission stability and processability of the QDs are limited upon usage from solution. Incorporating them into a solid ionic matrix overcomes both of these drawbacks, while preserving the initial optical properties. Here borax (Na2B4O7·10H2O) is used as a host matrix because of its lower solubility and thereby reduced ionic strength in water in comparison with NaCl. This guarantees the stability of high-quality CdSe/ZnS QDs in the aqueous phase during crystallization and results in a 3.4 times higher loading amount of QDs within the borax crystals compared to NaCl. All steps from the synthesis via mixed crystal preparation to the warm-white LED preparation are verified by applying the model-experimental feedback, in which experimental data and numerical results provide feedback to each other recursively. These measures are taken to ensure a high luminous efficacy of optical radiation (LER) and a high color rendering index (CRI) of the final device as well as a correlated color temperature (CCT) comparable to an incandescent bulb. By doing so, a warm-white LED with a LER of 341 lm/Wopt, a CCT of 2720 K and a CRI of 91.1 is produced. Finally, we show that the emission stability of the QDs within the borax crystals on LEDs driven at high currents is significantly improved. These findings indicate that the proposed warm-white light-emitting diodes based on QDs-in-borax hold great promise for quality lighting. © 2015 American Chemical Society.
Open Access
Liquid-liquid diffusion ‐ assisted crystallization: a fast and versatile approach toward high quality mixed quantum dot ‐ salt crystals
(Wiley-VCH Verlag, 2015) Adam, M.; Wang, Z.; Dubavik, A.; Stachowski, G. M.; Meerbach, C.; Soran-Erdem, Z.; Rengers, C.; Demir, Hilmi Volkan; Gaponik N.; Eychmuller, A.
Here, a new, fast, and versatile method for the incorporation of colloidal quantum dots (QDs) into ionic matrices enabled by liquid-liquid diffusion is demonstrated. QDs bear a huge potential for numerous applications thanks to their unique chemical and physical properties. However, stability and processability are essential for their successful use in these applications. Incorporating QDs into a tight and chemically robust ionic matrix is one possible approach to increase both their stability and processability. With the proposed liquid-liquid diffusion-assisted crystallization (LLDC), substantially accelerated ionic crystallization of the QDs is shown, reducing the crystallization time needed by one order of magnitude. This fast process allows to incorporate even the less stable colloids including initially oil-based ligand-exchanged QDs into salt matrices. Furthermore, in a modified two-step approach, the seed-mediated LLDC provides the ability to incorporate oil-based QDs directly into ionic matrices without a prior phase transfer. Finally, making use of their processability, a proof-of-concept white light emitting diode with LLDC-based mixed QD-salt films as an excellent color-conversion layer is demonstrated. These findings suggest that the LLDC offers a robust, adaptable, and rapid technique for obtaining high quality QD-salts.
Open Access
Stable and efficient colour enrichment powders of nonpolar nanocrystals in LiCl
(Royal Society of Chemistry, 2015) Erdem, T.; Soran-Erdem Z.; Sharma, V. K.; Keleştemur, Y.; Adam, M.; Gaponik N.; Demir, Hilmi Volkan
In this work, we propose and develop the inorganic salt encapsulation of semiconductor nanocrystal (NC) dispersion in a nonpolar phase to make a highly stable and highly efficient colour converting powder for colour enrichment in light-emitting diode backlighting. Here the wrapping of the as-synthesized green-emitting CdSe/CdZnSeS/ZnS nanocrystals into a salt matrix without ligand exchange is uniquely enabled by using a LiCl ionic host dissolved in tetrahydrofuran (THF), which simultaneously disperses these nonpolar nanocrystals. We studied the emission stability of the solid films prepared using NCs with and without LiCl encapsulation on blue LEDs driven at high current levels. The encapsulated NC powder in epoxy preserved 95.5% of the initial emission intensity and stabilized at this level while the emission intensity of NCs without salt encapsulation continuously decreased to 34.7% of its initial value after 96 h of operation. In addition, we investigated the effect of ionic salt encapsulation on the quantum efficiency of nonpolar NCs and found the quantum efficiency of the NCs-in-LiCl to be 75.1% while that of the NCs in dispersion was 73.0% and that in a film without LiCl encapsulation was 67.9%. We believe that such ionic salt encapsulated powders of nonpolar NCs presented here will find ubiquitous use for colour enrichment in display backlighting. © The Royal Society of Chemistry 2015.