Browsing by Subject "Solid state lighting"

Now showing 1 - 6 of 6

Open Access
Förster resonance energy transfer enhanced color-conversion using colloidal semiconductor quantum dots for solid state lighting
(American Institute of Physics, 2009-10-15) Nizamoglu, S.; Demir, Hilmi Volkan
In this paper, we present Förster resonance energy transfer (FRET)-enhanced color-conversion using colloidal semiconductor quantum dot nanocrystals (NCs) to make reddish-orange light-emitting diodes for use in ultraefficient solid state lighting. To achieve FRET enhancement at 614 nm, we use an energy gradient hybrid structure made of cyan- and orange-emitting CdSe/ZnS NCs (λPL =492 and 588 nm in solution, respectively). This enables recycling of trapped excitons using FRET and achieves a relative quantum efficiency enhancement of 15.1% in reddish-orange full color-conversion for the integrated hybrid cyan-orange NC layer with respect to the case of full color-conversion using only orange NCs without FRET.
Open Access
High-stability, high-efficiency organic monoliths made of oligomer nanoparticles wrapped in organic matrix
(American Chemical Society, 2016) Soran-Erdem Z.; Erdem, T.; Gungor K.; Pennakalathil, J.; Tuncel, D.; Demir, Hilmi Volkan
Oligomer nanoparticles (OL NPs) have been considered unsuitable for solid-state lighting due to their low quantum yields and low temperature stability of their emission. Here, we address these problems by forming highly emissive and stable OL NPs solids to make them applicable in lighting. For this purpose, we incorporated OL NPs into sucrose matrix and then prepared their all-organic monoliths. We show that wrapping the OL NPs in sucrose significantly increases their quantum yield up to 44%, while the efficiency of their dispersion and direct solid-film remain only at ∼6%. We further showed ∼3-fold improved temperature stability of OL NP emission within these monoliths. Our experiments revealed that a physical passivation mechanism is responsible from these improvements. As a proof-of-concept demonstration, we successfully employed these high-stability, high-efficiency monoliths as color converters on a blue LED chip. Considering the improved optical features, low cost, and simplicity of the presented methodology, we believe that this study holds great promise for a ubiquitous use of organic OL NPs in lighting and possibly in other photonic applications.
Open Access
Highly flexible, electrically driven, top-emitting, quantum dot light-emitting stickers
(American Chemical Society, 2014) Yang X.; Mutlugun, E.; Dang, C.; Dev, K.; Gao, Y.; Tan, S.T.; Sun X.W.; Demir, Hilmi Volkan
Flexible information displays are key elements in future optoelectronic devices. Quantum dot light-emitting diodes (QLEDs) with advantages in color quality, stability, and cost-effectiveness are emerging as a candidate for single-material, full color light sources. Despite the recent advances in QLED technology, making high-performance flexible QLEDs still remains a big challenge due to limited choices of proper materials and device architectures as well as poor mechanical stability. Here, we show highly efficient, large-area QLED tapes emitting in red, green, and blue (RGB) colors with top-emitting design and polyimide tapes as flexible substrates. The brightness and quantum efficiency are 20 000 cd/m2 and 4.03%, respectively, the highest values reported for flexible QLEDs. Besides the excellent electroluminescence performance, these QLED films are highly flexible and mechanically robust to use as electrically driven light-emitting stickers by placing on or removing from any curved surface, facilitating versatile LED applications. Our QLED tapes present a step toward practical quantum dot based platforms for high-performance flexible displays and solid-state lighting. © 2014 American Chemical Society.
Open Access
Highly luminescent CB[7]-based conjugated polyrotaxanes embedded into crystalline matrices
(Wiley-VCH Verlag, 2017) Erdem, T.; Idris, M.; Demir, Hilmi Volkan; Tuncel, D.
π-Conjugated polymers suffer from low quantum yields (QYs) due to chain–chain interactions. Furthermore, their emission in solid films is significantly quenched due to aggregation leading further decrease in QY. These are the two main issues of these materials hampering their widespread use in optoelectronic devices. To address these issues, here the backbone of poly(9,9′-bis(6″-(N,N,N-trimethylammonium)hexyl)fluorene-alt-co-thiophenelene) is isolated by threading with cucurbit[7]uril (CB7). Subsequently, the conjugated polyrotaxanes are incorporated into organic crystalline matrices to obtain highly efficient color-converting solids suitable for solid-state lighting. Upon threading the polymer backbone with CB7s, although the QY of the resulting polyrotaxane in solution state increases, the quenching problem in their solid state is not completely tackled. To solve this problem, these conjugated polyrotaxanes are embedded into various crystalline matrices and their remarkably high QYs (>50%) in the solution are successfully maintained in the solid state. To demonstrate the suitability of these aforementioned materials for solid-state lighting, a proof-of-concept light-emitting diode is constructed by employing their powders as color converters.
Open Access
Nanocrystal integrated light emitting diodes based on radiative and nonradiative energy transfer for the green gap
(IEEE, 2009) Nizamoğlu, Sedat; Sarı, Emre; Baek J.-H.; Lee I.-H.; Demir, Hilmi Volkan
Recently the photometric conditions for ultra-efficient solid-state lighting have been discussed [1-2]. These studies show that a luminous efficacy of optical radiation at 408 lm/Wopt and a color rendering index (CRI) of 90 at a correlated color temperature (CCT) of 3000 K are achievable at the same time. For this purpose light emitting diodes (LEDs) emitting in blue, green, yellow, and red colors at 463, 530, 573, and 614 nm with relative optical power levels of 1/8, 2/8, 2/8, and 3/8, are required, respectively [1-2]. Although InxGa1-xN material system is capable to cover the whole visible by changing the In composition (x), it is technically extremely challenging to obtain efficient green/yellow light emitting diodes especially at those wavelengths (i.e., at 530 nm and 573 nm, respectively) due to reduced internal quantum efficiency [2-4]. Furthermore, by using the (Al xGa1-x)1-yInyP quaternary alloy it is also possible to cover from 650 nm to 580 nm. However, the efficiencies significantly decrease towards green. Therefore, there exists a significant gap in the green-yellow spectral regions (known as "the green gap") to make efficient light emitting diodes. To address this green gap problem, we propose and demonstrate proof-of-concept nanocrystal (NCs) hybridized green/yellow light emitting diodes that rely on both radiative energy transfer and nonradiative energy transfer (i.e., FRET-Förster resonance energy transfer) for color conversion on near-ultraviolet (near-UV) LEDs.
Open Access
Quantum dot integrated LEDs using photonic and excitonic color conversion
(Elsevier, 2011-11-23) Demir, Hilmi Volkan; Nizamoglu, S.; Erdem, T.; Mutlugun, E.; Gaponik N.; Eychmüller A.
This review summarizes advantages, recent progress and challenges related to the quickly evolving research field of colloidal quantum dot integrated LEDs based on color conversion. We start with presenting a short general introduction to the field of solid state lighting and color conversion phenomena, which are essential for defining the requirements for high-quality general lighting. Subsequently we continue with a brief description of the synthesis of nanocrystal quantum dots and their optical properties together with the advantages of utilizing them in LEDs as color convertors. Following this basic background, we review the recent efforts on quantum dot integrated color-conversion LEDs, Förster resonance energy transfer (FRET) converted LEDs and FRET-enhanced LEDs. Finally, we conclude with a future outlook on semiconductor lighting and quantum dot integrated LEDs.