Engineering Papers⌕ Search

SEARCH · Engineering Papers

Results for “DYES”

Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,045 records · Page 58

Determination of effective optical gap in dye/TiO{sub 2} systems inspired by p-n junctions

The effective optical gap and device current limits of dye-sensitized solar cells (DSCs) were investigated. Optical gap determination was based on an approach that assumes the presence of a nanoscale p-n junction in the DSCs between the bulk TiO{sub 2} semiconductor and the dye-cluster with quantum size effect. On the basis of this approach, the effective optical gap of the dye-absorber was extracted from a relation between external quantum efficiency and photon energy. The short-circuit current density of the fabricated DSCs showed a current loss in the range from 3.7 to 5.1 mA cm{sup −2} compared to the device current limit. This current loss can be mainly attributed to the light reflection of the window layer and the native charge-transfer loss by device imperfections, including subsidiary charge-transfer loss by a nanoscale Schottky junction between TiO{sub 2} and the electrolyte.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Solid state photon upconversion utilizing thermally activated delayed fluorescence molecules as triplet sensitizer

The ability to upconvert light is useful for a range of applications, from biological imaging to solar cells. But modern technologies have struggled to upconvert incoherent incident light at low intensities. Here, we report solid state photon upconversion employing triplet-triplet exciton annihilation in an organic semiconductor, sensitized by a thermally activated-delayed fluorescence (TADF) dye. Compared to conventional phosphorescent sensitizers, the TADF dye maximizes the wavelength shift in upconversion due to its small singlet-triplet splitting. The efficiency of energy transfer from the TADF dye is 9.1%, and the conversion yield of sensitizer exciton pairs to singlet excitons in the annihilator is 1.1%. Our results demonstrate upconversion in solid state geometries and with non-heavy metal-based sensitizer materials.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

ZnO/TiO{sub 2} particles and their solar cell application

ZnO/TiO{sub 2} particles were investigated for dye-sensitized solar cells (DSSC). Nano-structured ZnO particles were produced by the hydrothermal method. TiO{sub 2} (P25) nanoparticles, was bought from the company of Degussa. Crystal structures and morphological properties of particles were examined by XRD and SEM. As an application, dye sensitized solar cells were fabricated from nano-structured produced metal oxide particles. The working electrodes of the DSSCs were obtained by mixture of ZnO and TiO{sub 2} powders. I-V characteristics of the cells were measured by using a solar simulator and the efficiency of the solar cells were obtained by using I-V graphs. ZnO cells sensitized with Ruthenium 535-bisTBA (N719) dyes yield higher efficiencies than corresponding TiO{sub 2} cells. By increasing TiO{sub 2} amount in the mixture of ZnO/TiO{sub 2}, it was observed that efficiencies of cells are getting lower.

14 SOLAR ENERGY↗

Effect of Förster-mediated triplet-polaron quenching and triplet-triplet annihilation on the efficiency roll-off of organic light-emitting diodes

We report the results of a systematic study of the interplay of triplet-polaron quenching (TPQ) and triplet-triplet annihilation (TTA) on the efficiency roll-off of organic light-emitting diodes (OLEDs) with increasing current density. First, we focus on OLEDs based on the green phosphorescent emitter tris[2-phenylpyridine]iridium(III) (Ir(ppy){sub 3}) and the red phosphorescent dye platinum octaethylporphyrin. It is found that the experimental data can be reproduced using kinetic Monte Carlo (kMC) simulations within which TPQ and TTA are due to a nearest-neighbor (NN) interaction, or due to a more long-range Förster-type process. Furthermore, we find a subtle interplay between TPQ and TTA: decreasing the contribution of one process can increase the contribution of the other process, so that the roll-off is not significantly reduced. Furthermore, we find that just analyzing the shape of the roll-off is insufficient for determining the relative role of TPQ and TTA. Subsequently, we investigate the wider validity of this picture using kMC simulations for idealized but realistic symmetric OLEDs, with an emissive layer containing a small concentration of phosphorescent dye molecules in a matrix material. Whereas for NN-interactions the roll-off can be reduced when the dye molecules act as shallow hole and electron traps, we find that such an approach becomes counterproductive for long-range TTA and TPQ. Developing well-founded OLED design rules will thus require that more quantitative information is available on the rate and detailed mechanism of the TPQ and TTA processes.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗

Plasmon - exciton coupling effects in light absorption and scattering by metal/J-aggregate bilayer nanoparticles

This paper examines plasmon - exciton coupling effects in light absorption and scattering by hybrid nanoparticles consisting of a metallic core and organic dye J-aggregate shell. The spectroscopic characteristics of such particles are calculated using generalised Mie theory for two concentric spheres in a wide spectral range for various geometric parameters of the system, core materials (Ag, Au, Cu and Al) and cyanine dyes (TC, OC and PIC). We determine the eigenfrequencies of hybrid modes in the system and photoabsorption peak heights as functions of the oscillator strength of the transition in the J-band of the dye, core radius and shell thickness, and demonstrate that the interactions of a Frenkel exciton with dipole and multipole plasmons have radically different effects on the optical properties of the composite nanoparticles. Varying the particle size and the optical constants of the core and shell materials influences the number of peaks in the spectra of the particles and leads to a significant redistribution of peak heights. We identify regions where the extinction spectrum of the particles is dominated by light absorption or scattering processes. (nanophotonics)

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗

A DNA Crystal Designed to Contain Two Molecules per Asymmetric Unit

We describe the self-assembly of a DNA crystal that contains two tensegrity triangle molecules per asymmetric unit. We have used X-ray crystallography to determine its crystal structure. In addition, we have demonstrated control over the colors of the crystals by attaching either Cy3 dye (pink) or Cy5 dye (blue-green) to the components of the crystal, yielding crystals of corresponding colors. Attaching the pair of dyes to the pair of molecules yields a purple crystal.

59 BASIC BIOLOGICAL SCIENCES↗

Two‐Dimensional Excitonic Networks Directed by DNA Templates as an Efficient Model Light‐Harvesting and Energy Transfer System

Abstract Photosynthetic organisms organize discrete light‐harvesting complexes into large‐scale networks to facilitate efficient light collection and utilization. Inspired by nature, herein, synthetic DNA templates were used to direct the formation of dye aggregates with a cyanine dye, K21, into discrete branched photonic complexes, and two‐dimensional (2D) excitonic networks. The DNA templates ranged from four‐arm DNA tiles, ≈10 nm in each arm, to 2D wireframe DNA origami nanostructures with different geometries and varying dimensions up to 100×100 nm. These DNA‐templated dye aggregates presented strongly coupled spectral features and delocalized exciton characteristics, enabling efficient photon collection and energy transfer. Compared to the discrete branched photonic systems templated on individual DNA tiles, the interconnected excitonic networks showed approximately a 2‐fold increase in energy transfer efficiency. This bottom‐up assembly strategy paves the way to create 2D excitonic systems with complex geometries and engineered energy pathways.

Zhou, Xu↗

Two–Dimensional Excitonic Networks Directed by DNA Templates as an Efficient Model Light–Harvesting and Energy Transfer System

Photosynthetic organisms organize discrete light-harvesting complexes into large-scale networks to facilitate efficient light collection and utilization. Inspired by nature, herein, synthetic DNA templates were used to direct the formation of dye aggregates with a cyanine dye, K21, into discrete branched photonic complexes, and two-dimensional (2D) excitonic networks. The DNA templates ranged from four-arm DNA tiles, ≈10 nm in each arm, to 2D wireframe DNA origami nanostructures with different geometries and varying dimensions up to 100×100 nm. These DNA-templated dye aggregates presented strongly coupled spectral features and delocalized exciton characteristics, enabling efficient photon collection and energy transfer. Compared to the discrete branched photonic systems templated on individual DNA tiles, the interconnected excitonic networks showed approximately a 2-fold increase in energy transfer efficiency. Lastly, this bottom-up assembly strategy paves the way to create 2D excitonic systems with complex geometries and engineered energy pathways.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

A scalable and autoclavable oxygen nanosensor platform for metabolic monitoring of Saccharomyces cerevisiae in a bioreactor and other in situ systems

Polymer-encapsulated dye nanoparticle sensors are a valuable approach to achieving in situ analyte measurements with luminescence; however, typical emulsion-based nanosensors are poorly suited for large-scale biological samples due to limitations of synthesis scalability and stability. Branched polyethylenimine (PEI) is a versatile polymer scaffold ideal for constructing nanoparticles with various covalently conjugated moieties due to their high density of reactive primary amines, high water solubility, and biological stability. In this work, we used branched polyethylenimine as a scaffold-based approach for making a stable and scalable ratiometric oxygen sensor. Pt (II) tetracarboxyporphine was used as an oxygen-sensing dye and coumarin 343 as a reference dye, all covalently linked to the PEI scaffold producing a product that could withstand sterilization procedures and easily be scaled. To minimize toxicity from the PEI scaffold, we conjugated it with 2000 MW PEG. The applicability of the sensors was demonstrated in a 200 mL Saccharomyces cerevisiae yeast culture, using orthogonal luminescent and electrochemical oxygen measurements to validate sensor response and measure the metabolic activity of the yeast in our culture. Further, this approach was able to match the sensitivity of our electrochemical measurements while improving upon drawbacks of other luminescent methods of oxygen detection, demonstrating effective monitoring for at least 20 h. Our scaffold-based approach is a modular and easily translatable technology that could be useful in various biotechnological applications.

59 BASIC BIOLOGICAL SCIENCES↗

Comparison of the Optoelectronic Performance of Neutral and Cationic Forms of Riboflavin

The riboflavin dye 2,3,4,5-tetra-O-acetyl-1-[3-(6-bromohexyl)-7,8-dimethyl-2,4-dioxo-3,4-dihydrobenzo[g]pteridin-10(2H)-yl]-1-deoxypentitol and its pyridinium salt were synthesized, and studied by absorption and fluorescence spectroscopy in solutions and on thin film states. The first absorption band of riboflavin-pyridinium salt derivative is red-shifted by 10 nm compared to neutral one on film. Cationic riboflavin derivative shows significant wavelength changes on its fluorescence emission spectrum in the excited state depending on the solvent polarity and the electronic environment. The fluorescence quantum yields of cationic riboflavin gave much higher values as compared to that of its neutral form. The fluorescence lifetimes were found to be in the range of 5.5–6.6 ns with mono − exponential behavior. These dyes possess low-lying HOMO energy levels which are suitable to be able to inject holes to donor polymers so that they can be used as acceptor component in the active layer of bulk heterojunction solar cells (BHJ-SCs). Photovoltaic responses are reported for P3HT:riboflavin active layer wherein the synthesized dyes are used as acceptor component. Also, neutral riboflavin shows greater electron mobility value of 1.3 × 10{sup −3} cm{sup 2}/V∙s compared to its cationic derivative.

74 ATOMIC AND MOLECULAR PHYSICS↗

Fluorescent Labeling of Protein Using Blue-Emitting 8-Amino-BODIPY Derivatives

8-Amino-BODIPY (boron-dipyrromethane) dyes show bright blue fluorescence. Disclosed here are synthesis and characterization of the photophysical properties of a series of functionalized 8-Amino-BODIPY (BP1–4) for protein labeling. The compact structure and solvent-insensitive absorption property of the dye are desirable features for protein labeling. For the model protein, bovine serum albumin (BSA), the labeling proceeds under mild condition via amide bond formation or thiol-ene conjugation with maintaining the bright blue fluorescence. The chromatography and mass spectroscopy analysis clearly support the labeling of the BODIPY dye on the BSA. The protein labeling with blue-emitting BODIPY would be applicable for studying protein dynamics and fluorescence resonance energy transfer (FRET) with intrinsic biomolecules.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Removal of Congo Red from Aqueous Solution by Hydroxyapatite Nanoparticles Loaded on Zein as an Efficient and Green Adsorbent: Response Surface Methodology and Artificial Neural Network-Genetic Algorithm

This study is based on the application of hydroxyapatite nanoparticles loaded on Zein (Zein/nHAp) as an efficient adsorbent for the removal of Congo red from aqueous solutions. The properties of the adsorbent were characterized using various techniques including FT-IR, XRD, FE-SEM, and BET. The influence of five parameters such as pH, temperature, contact time, initial dye concentration, and adsorbent dosage on the removal percentage of the dye was investigated. The optimum conditions of 5.83, 34.32 °C, 5.20 min, 392.10 ppm, and 0.007 g were achieved for pH, temperature, contact time, initial dye concentration, and adsorbent dosage, respectively. The maximum removal percentage of 99.48% was obtained under the optimum condition that exhibited high adsorption potential of the used adsorbent. Central composite design (CCD) under response surface methodology and artificial neural network-genetic algorithm (ANN-GA) were utilized for optimization of parameters. Comparison of the results of the two models in terms of coefficient of determination (R{sup 2}) and mean absolute percentage error confirmed the prediction potential of CCD and ANN-GA. Higher ability and accuracy of ANN-GA in prediction was found based on given results. The experimental equilibrium data were studied by Langmuir, Freundlich, Temkin and Dubinin-Radushkevic isotherm models and explored that the data well presented by Langmuir model with maximum adsorption capacity of 416.66 mg/g. The adsorption kinetic was well-fitted by the pseudo-second-order model. The thermodynamics of the adsorption displayed spontaneous and endothermic nature of the process. Regeneration investigation showed that Zein/nHAp can impressively be reused, indicating that the adsorbent was a promising one for the removal of Congo red from aqueous solution. Graphical Abstract: .

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Chitosan–Gelatin @ Tin (IV) Tungstatophosphate Nanocomposite Ion Exchanger: Synthesis, Characterization and Applications in Environmental Remediation

The present study reported the synthesis of novel organic–inorganic hybrid nanocomposite by incorporating tin (IV) based ion exchanger into the hybrid polymer network of chitosan and gelatin prepared under vacuum for the efficient removal of heavy metal ions and toxic dyes from an aqueous fluid. The physicochemical studies such as ion exchange capacity (IEC), chemical stability, thermal stability, pH titration and distribution behaviour studies were also carried out to determine the cation exchange behaviour of the material. The surface morphology and structural properties were studied by the techniques such as FTIR, FESEM, EDS, TEM and XRD. Distribution studies confirmed the synthesized CG/STPNC had the highest selectivity for Pb{sup 2+} ions (85.3 mL/g). Maximum adsorption of methylene blue (82%) was achieved within 240 min at 500 mg of adsorbent dose, 10 mg/L of the initial concentration of dye, pH of 7 and 30 °C of temperature. Adsorption kinetic data fitted well with pseudo-second order rate model with R{sup 2} = 0.995. The correlation value 0.95 and favourable R{sub L} = 0.21 of adsorption data suggested better fit for Langmuir adsorption. Thus the synthesized nanocomposite ion exchanger was found to be a promising cation exchanger as well as an adsorbent for heavy metal ion and dye removal from textile industrial effluents. Graphical abstract: .

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Microfluidic Fabrication of Nanoparticles Based on Ethyl Acrylate-Functionalized Chitosan for Adsorption of Methylene Blue from Aqueous Solutions

The adsorption of nanoparticle (NP)-based adsorbents especially those made of polymers to remove dyes as toxic substances from pollutants is yet remained as a critical issue. The objective of this work was to prepare microfluidic (MF) fabrication of NPs based on ethyl acrylate (EA)-functionalized chitosan (CS) for methylene blue (MB) dye removal from aqueous solutions. For this purpose, a series of experiments such as FTIR, SEM alongside DLS, and UV–vis spectrophotometry were carried out to investigate the physicochemical properties of the samples. The FTIR spectra showed that the amine (–NH{sub 2}) and hydroxyl (–OH) groups on CS structure were replaced with EA, appropriately. The SEM and DLS results depicted that EA-functionalized CS NPs fabricated using MF technique had uniform shapes, and the diameters as small as 70 nm compared to those samples produced via bulk mixing (BM) method (~ 300 nm). Moreover, the surface charge of MF-assisted CS NPs after functionalization exhibited the lower zeta potential value (~ + 11) than that of samples based on BM (~ + 14) due to occurring the laminar flow through the micro-channels embedded in the MF chip, leading to an increase in the MB adsorption. Subsequently, at the optimized amounts of the dye concentration (89.12 mg L{sup −1}), the adsorbent concentration (1.38 g L{sup −1}), and pH (10.58) by means of Box-Behnken design (BBD) method, the maximum percentage of MB removal by the use of MF-fabricated EA-functionalized CS NPs was 98.4%. By fitting the obtained adsorption data to the isotherm models such as Lagmuir, Freundlich, and Temkin, it has been found that the adsorption mechanism followed the Langmuir model (maximum capacity of the adsorption 384.61 mg/g), which assumed a monolayer coverage of MB molecules as adsorbates over a homogeneous adsorbent surface.

36 MATERIALS SCIENCE↗

Oxygen and relative humidity monitoring with films tailored for enhanced photoluminescence

In this study, approaches to generate porous or doped sensing films, which significantly enhance the photoluminescence (PL) of oxygen optical sensors, and thus improve the signal-to-noise (S/N) ratio, are presented. Tailored films, which enable monitoring the relative humidity (RH) as well, are also presented. Effective porous structures, in which the O 2 -sensitive dye Pt octaethylporphyrin (PtOEP) or the Pd analog PdOEP was embedded, were realized by first generating blend films of polyethylene glycol (PEG) with polystyrene (PS) or with ethyl cellulose (EC), and then immersing the dried films in water to remove the water-soluble PEG. This approach creates pores (voids) in the sensing films. The dielectric contrast between the films’ constituents and the voids increases photon scattering, which in turn increases the optical path of the excitation light within the film, and hence light absorption by the dye, and its PL. Optimized sensing films with a PEG:PS ratio of 1:4 (PEG’s molecular weight M w ~8000) led to ~4.4× enhancement in the PL (in comparison to PS films). Lower M w ~200 PEG with a PEG:EC ratio of 1:1 led to a PL enhancement of ~4.7×. Film-dependent PL enhancements were observed at all oxygen concentrations. The strong PL enhancement enables (i) using lower dye (luminophore) concentrations, (ii) reducing power consumption and enhancing the sensor’s operational lifetime when using organic light emitting diodes (OLEDs) as excitation sources, (iii) improving performance when using compact photodetectors with no internal gain, and (iv) reliably extending the dynamic range.

47 OTHER INSTRUMENTATION↗

Nanoadsorbents based on conducting polymer nanocomposites with main focus on polyaniline and its derivatives for removal of heavy metal ions/dyes: A review

Highlights: • Nanoadsorbents based on conductive polymers can remove heavy metal ions/dye. • Contact time, pH, adsorbent dosage and temperature are effective adsorption factors. • Chemical structures of nanoadsorbents play an important role in adsorption. • Adsorption of metal ions on PANI based nanocomposites is of physical type. Water contamination by toxic heavy metal ions and dyes remains a serious public health problem for humans, so attention on specific methods and technologies to remove heavy metal ions and dyes from wastewaters/aqueous solutions are desired. Numerous adsorbents have been reported for the removal of heavy metal ions/dyes from wastewaters/aqueous solutions. Polyaniline (PANI) and its derivatives, as conducting polymers, are good adsorbents to remove various kinds of heavy metal ions and dyes from wastewaters/aqueous solutions. The nanoadsorbents based on PANI and its derivatives have received much consideration, and are extensively reported in literature. This review focuses on the PANI and its derivatives based on nanoadsorbents for water purification. Various types of these nanoadsorbents used for the removal of heavy metal ions/dyes from wastewaters/aqueous solutions are also briefly compared in this review.

54 ENVIRONMENTAL SCIENCES↗

Donor-fullerene dyads for energy cascade organic solar cells

Organic bulk hetero junction (BHJ) solar cells require broad absorption of the incident solar spectrum by the donor and acceptor in the blend. Fullerene derivatives with covalently linked dyes, referred to as dyads, were designed to have strong optical absorption and appropriate electronic levels for electron transfer with common donor polymers in BHJs. Dyads with dyes based on diketopyrrolopyrrole and benzothiadiazole were synthesized using either a methanofullerene or a fulleropyrrolidine linkage. Here, the performance of these dyad acceptors in BHJ solar cells with poly(3-hexylthiophene) (P3HT) and a low optical gap co-polymer of thiophene and diketopyrrolopyrrole (PDPP2FT) were examined. Although the solar power conversion efficiencies were low, charge generation from the molecular dye in the dyad could be observed in BHJs with PDPP2FT. The low power conversion efficiency was attributed to the morphology of the BHJs based on grazing incidence wide angle X-ray scattering patterns. Density functional theory was used to examine the charge transfer states between the donor and the dyad. The lowest energy charge-transfer state was found to be a transition from the donor polymer to the fullerene portion of the dyad.

14 SOLAR ENERGY↗