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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.

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At least 289 records · Page 16
All sourcesNASA NTRSDOE OSTI
DOE OSTI2016

The result of synthesis analysis of the powder TiO{sub 2}/ZnO as a layer of electrodes for dye sensitized solar cell applications

This study has been conducted synthesis of TiO{sub 2} nanoparticle powders and ZnO nanoparticle powder into a paste to be in this research, dye-sensitive solar cells (DSSC) was produced by TiO{sub 2} nanopowder and ZnO nanopowder synthesis to make paste that is applied as electrode. This electrode works based on photon absorbed by dye and transferred to different composition of TiO{sub 2}/ ZnO particle. Properties of DSSC are affected by fabrication method, parameter and dimension of TiO{sub 2} / ZnO nanoparticles, technique and composition of TiO{sub 2} / ZnO paste preparation is important to get the higher performance of DSSC. Doctor blade is a method for electrode coating on glass substrate. The electrode was immersed into dye solution of Z907 and ethanol. From the experiment, the effect of TiO{sub 2} and ZnO nanopowder mixture for electrode was investigated. XRD characterization show anatase and rutile phase, which sintered TiO{sub 2}/ZnO has intensity more than 11,000. SEM characterization shows the composition of 20% TiO{sub 2} / 80% ZnO has better porosity. Higher efficiency that is investigated by I-V measurement using Sun Simulator.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2016

To probe the equivalence and opulence of nanocrystal and nanotube based dye-sensitized solar cells

Dye-Sensitized solar cells based on TiO{sub 2} nanocrystal and TiO{sub 2} nanotubes have been fabricated by a simple sol-gel hydrothermal process and their performances have been compared. Current density and voltage (JV) characteristics and incident photon to current conversion efficiency (IPCE) plots have been set as criterion to check which one is better as a photoanode candidate in dye-sensitized solar cell. It has been observed that although open circuit voltage values for both type of cells do not differ much still, nanotube based dye-sensitized solar cells are more successful having an efficiency value of 7.28%.

30 DIRECT ENERGY CONVERSION↗
DOE OSTI2016

Photocatalytic behaviour of CdS/ZnS nanocomposite for dye degradation in presence of visible light

In the present work ZnS-CdS composite was prepared by hydrothermal method. The prepared samples were characterized by X-ray diffraction (XRD) to confirm formation of nano particles, Scanning electron microscopy (SEM) images exhibit nanoscale dimensions of as synthesized individual phases. UV/VIS spectra were recorded for evaluation of photophysical properties. The composite was explored as photocatalysts to study dye degradation using methylene blue in aqueous slurry under irradiation of 663 nm wavelength and congo red under irradiation of 493 nm wavelength. Under the same conditions the photocatalytic activity of the individual phases ZnS and CdS were also examined. The ZnS-CdS composite is found in enhancing the rate of photo degradation of toxic dyes as compare to ZnS and CdS individually in presence of visible light. This ZnS based metal sulphide/oxide semiconductor nanocomposites are high potential material for Photo-degradation of toxic dyes, and act as good photocatalyst in visible light.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2023

Probing DNA structural heterogeneity by identifying conformational subensembles of a bicovalently bound cyanine dye

DNA is a re-configurable, biological information-storage unit, and much remains to be learned about its heterogeneous structural dynamics. For example, while it is known that molecular dyes templated onto DNA exhibit increased photostability, the mechanism by which the structural dynamics of DNA affect the dye photophysics remains unknown. Here, we use femtosecond, two-dimensional electronic spectroscopy measurements of a cyanine dye, Cy5, to probe local conformations in samples of single-stranded DNA (ssDNA–Cy5), double-stranded DNA (dsDNA–Cy5), and Holliday junction DNA (HJ–DNA–Cy5). A line shape analysis of the 2D spectra reveals a strong excitation–emission correlation present in only the dsDNA–Cy5 complex, which is a signature of inhomogeneous broadening. Molecular dynamics simulations support the conclusion that this inhomogeneous broadening arises from a nearly degenerate conformer found only in the dsDNA–Cy5 complex. These insights will support future studies on DNA’s structural heterogeneity.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2011

Photoinduced translational molecular mobility in solid nanostructured azo dye films

A new mechanism controlling the molecular motion in thin azo-containing films during a photoinduced change in the surface nanorelief is found. It is shown experimentally that exposure of a solid AD-1 azo dye, deposited on a glass substrate, to incoherent linearly polarised light leads to formation of nanostructures with a characteristic size of 200 nm, which are similar to droplets of melt of this dye on the same substrate. It is shown that photoinduced mass transport in a solid AD-1 azo dye film can be explained by the mobility of molecules related to their trans-cis-photoisomerisation, which leads to film softening with subsequent formation of spherical protrusions under surface tension forces.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2015

Light absorption and plasmon – exciton interaction in three-layer nanorods with a gold core and outer shell composed of molecular J- and H-aggregates of dyes

Optical properties of hybrid rod-like nanoparticles, consisting of a gold core, an intermediate passive organic layer (spacer) and outer layer of ordered molecular cyanine dye aggregates, are experimentally and theoretically investigated. It is shown that these dyes can form not only ordered J-aggregates but also H-aggregates (differing by the packing angle of dye molecules in an aggregate and having other spectral characteristics) in the outer shell of the hybrid nanostructure. Absorption spectra of synthesised three-layer nanorods are recorded, and their sizes are determined. The optical properties of the composite nanostructures under study are found to differ significantly, depending on the type of the molecular aggregate formed in the outer shell. The experimental data are quantitatively explained based on computer simulation using the finite-difference time-domain (FDTD) method, and characteristic features of the plasmon – exciton interaction in the systems under study are revealed. (nanophotonics)

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗
DOE OSTI2016

New efficient laser dyes for the red spectral range. Part 2. Pyrone derivatives

We report the generation characteristics of ethanol solutions of some dyes belonging to the derivatives of 2H- and 4H- pyrones, as well as of some structurally similar model fluorophores. The tuning curves of these dyes generating light in the orange and red spectral regions are measured, and the wavelength tuning ranges are determined. The dependences of the generated energy on the pump energy in a non-selective cavity are also measured. It is shown that some of the studied compounds possess better characteristics than those of widely used laser dyes in these spectral regions. (paper)

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2018

Optical and photoelectric properties of multichromic cyanine dye J-aggregates

We report the results of investigation of spectra and kinetics of photoluminescence as well as of photoabsorption and photoelectric properties for multichromic molecular crystals consisting of J-aggregates of three cyanine dyes with various structures. An original ‘self-assembly’ method is used for fabricating such prolate ordered structures with a thickness of 5 – 100 nm, width of 0.1 – 5 μm, and length of 50 – 300 μm. The method is based on the formation of the anionic platform in a water solution, which absorbs light in the blue spectrum range and comprises J-aggregates of magnesium complexes of anionic cyanine dye. Then the ‘matrix synthesis’ is used for coating its surface with J-aggregates of the two cationic dyes that have the absorption maxima in the green and red spectral ranges. It is shown that each of the multichromic organic crystals produced in this way is a multilayer photoelement, which possesses photoconductivity in three excitonic absorption maxima (in the blue, green, and red spectral ranges) with the external quantum efficiency varying from 2.7 % to 6.1 %. The results obtained provide a basis for technological development of highly-ordered molecular structures, which are promising for using in organic and hybrid photonics and optoelectronics including thin-film photo-converters operating in wide spectral ranges.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2011

Correlating Titania Morphology and Chemical Composition with Dye-sensitized Solar Cell Performance

We have investigated the use of various morphologies, including nanoparticles, nanowires, and sea-urchins of TiO{sub 2} as the semiconducting material used as components of dye-sensitized solar cells (DSSCs). Analysis of the solar cells under AM 1.5 solar irradiation reveals the superior performance of hydrothermally derived nanoparticles, by comparison with two readily available commercial nanoparticle materials, within the DSSC architecture. The sub-structural morphology of films of these nanostructured materials has been directly characterized using SEM and indirectly probed using dye desorption. Furthermore, the surfaces of these nanomaterials were studied using TEM in order to visualize their structure, prior to their application within DSSCs. Surface areas of the materials have been quantitatively analyzed by collecting BET adsorption and dye desorption data. Additional investigation using open circuit voltage decay measurements reveals the efficiency of electron conduction through each TiO{sub 2} material. Moreover, the utilization of various chemically distinctive titanate materials within the DSSCs has also been investigated, demonstrating the deficiencies of using these particular chemical compositions within traditional DSSCs.

14 SOLAR ENERGY↗
DOE OSTI2018

Manganese Doped Zinc Sulfide Quantum Dots as Efficient Photocatalyst for Dye Decolorization

A simple aqueous based synthesis technique at room temperature was performed for preparation of pure and manganese (Mn{sup 2+}) doped ZnS quantum dots in the presence of glutathione as the capping agent. Under UV-excitation quantum dots show photoluminescence bands at 2.13 and 3.0 eV corresponded to Mn{sup 2+} and intrinsic ZnS emission respectively. ZnS quantum dots were used as the photocatalyst to remove organic dyes in aqueous solution, with methylene blue as a model dye. The influence of the Mn{sup 2+} concentration on the dye degradation efficiency was studied. The highest photocatalytic degradation rate of methylene blue was obtained for ZnS quantum dots in glutathione shell doped with 0.125 at % of Mn{sup 2+}.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2024

Anomalous Dispersion in Reflection and Emission of Dye Molecules Strongly Coupled to Surface Plasmon Polaritons

We have studied dispersion of surface plasmon polaritons (SPPs) in the Kretschmann geometry (prism/Ag/dye-doped polymer) in weak, intermediate, and ultra-strong exciton–plasmon coupling regimes. The dispersion curves obtained in the reflection experiment were in good agreement with the simple model predictions at small concentrations of dye (Rhodamine 590, Rh590) in the polymer (Poly(methyl methacrylate), PMMA). At the same time, highly unusual multi-segment “staircase-like” dispersion curves were observed at extra-large dye concentrations, also in agreement with the simple theoretical model predicting large, small, and negative group velocities featured by different polariton branches. In a separate experiment, we measured angular dependent emission of Rh590 dye and obtained the dispersion curves consisting of two branches, one nearly resembling the SPP dispersion found in reflection and the second one almost horizontal. The results of our study pave the road to unparalleled fundamental science and future applications of weak and strong light—matter interactions.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
NASA NTRS2004

Detection of microlesions induced by heavy ions using liposomes filled with fluorescent dye

In cells irradiation by heavy ions has been hypothesized to produce microlesions, regions of local damage. In cell membranes this damage is thought to manifest itself in the form of holes. The primary evidence for microlesions comes from morphological studies of cell membranes, but this evidence is still controversial, especially since holes also have been observed in membranes of normal, nonirradiated, cells. However, it is possible that damage not associated with histologically discernable disruptions may still occur. In order to resolve this issue, we developed a system for detecting microlesions based on liposomes filled with fluorescent dye. We hypothesized that if microlesions form in these liposomes as the result of irradiation, then the entrapped dye will leak out into the surrounding medium in a measurable way. Polypropylene vials containing suspensions of vesicles composed of either dipalmitoyl phosphatidylcholine, or a combination of egg phosphatidylcholine and cholesterol were irradiated at the Brookhaven National Laboratory using 56Fe ions at 1 GeV/amu. In several cases we obtained a significant loss of the entrapped dye above the background level. Our results suggest that holes may form in liposomes as the result of heavy ion irradiation, and that these holes are large enough to allow leakage of cell internal contents that are at least as large as a 1 nm diameter calcein molecule. c2004 COSPAR. Published by Elsevier Ltd. All rights reserved.

Non-NASA Center↗
DOE OSTI2022

Dicyanobenzothiadiazole (DCBT) Organic Dye as a Visible Light Absorbing Strong Photoinduced Oxidant with a 16 Microsecond Long–Lived Excited State

Strong photoinduced oxidants are important to organic synthesis and solar energy conversion, to chemical fuels or electric. For these applications, visible light absorption is important to solar energy conversion and long–lived excited states are needed to drive catalysis. With respect to these desirable qualities, a series of five 5,6–dicyano[2,1,3]benzothiadiazole (DCBT) dyes are examined as organic chromophores that can serve as strong photooxidants in catalytic systems. The series utilizes a DCBT core with aryl groups on the periphery with varying electron donation strengths relative to the core. The dyes are studied via both steady–state and transient absorption and emission studies. Additionally, computational analysis, voltammetry, crystallography, and absorption spectroelectrochemistry are also used to better understand the behavior of these dyes. Ultimately, a strong photooxidant is arrived at with an exceptionally long excited state lifetime for an organic chromophore of 16 µs. Finally, the long–lived excited state photosensitizer is well–suited for use in catalysis, and visible light driven photosensitized water oxidation is demonstrated using a water–soluble photosensitizer.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2023

Effects of Anionic Polymer Modification of Dye‐Sensitized Niobate Photocatalysts on Solar‐Driven Z‐Scheme Overall Water Splitting

Pt‐intercalated calcium niobate nanosheets (Pt/HCa 2 Nb 3 O 10 ) sensitized by a Ru(II) complex dye are good photocatalysts for producing H 2 from aqueous solutions containing I − as a reversible electron donor. These materials are applicable to Z‐scheme overall water splitting in combination with a WO 3 ‐based O 2 ‐evolving photocatalyst under simulated sunlight. In this work, the effects of anionic polymer modification of the dye‐sensitized nanosheets are examined by adsorbing sodium poly(styrenesulfonate) (PSS), sodium polyacrylate, sodium polymethacrylate (PMA), or sodium poly(4‐styrenesulfonic‐ co ‐maleic acid) onto the dye‐sensitized nanosheet surface. For half‐cell H 2 ‐evolution reaction in the presence of NaI, all of the polymers have a positive impact on the activity under visible light at lower light intensity, whereas only PMA is effective under high light‐intensity condition. For Z‐scheme overall water splitting with PtO x /H‐Cs‐WO 3 , PSS and PMA give almost the same solar‐to‐hydrogen energy conversion efficiencies (0.12% ± 0.01%) under optimized conditions. However, PMA operates better than PSS at relatively low and high NaI concentrations, which are in general disadvantageous for the H 2 ‐ and O 2 ‐evolving components of the Z‐scheme, respectively.

Energy & Fuels↗
DOE OSTI2018

Fluorescence Quenching of Dyes by Graphene Oxide

Fluorescence quenching of four dyes [acridine orange (AO), rhodamine B (Rd B), rhodamine 110 (Rd 110), and rhodamine 640 (Rd 640)] by colloidal graphene oxide (GO) in phosphate buffer (pH 6.0) was studied. Dynamic and static quenching were analyzed using the Stern–Volmer equation. Static quenching by graphene oxide was observed for AO, Rd 640, and Rd B whereas mixed dynamic and static quenching was characteristic of Rd 110. The Stern–Volmer constant of dynamic quenching was 10 times less than that of static quenching. The measured association constants of the dyes with GO fell in the order 2540 (AO) > 495 (Rd 640) > 260 (Rd 110) > 144 L/g (Rd B). The value of the π–π-stacking interaction was strongly influenced by the phthalic fragment oriented perpendicular to the xanthene in the rhodamine dyes and the four alkyl groups of Rd B as a result of their torsional vibrations and rotational motions.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2018

Modulation of the Photophysical Properties of β-substituted BODIPY Dyes

Photophysical properties of BODIPY dyes containing acetyl acetone and benzoyl acetone BF2 unit as an electron accepting substituent at beta position linked via double bond have been investigated using a wide range of solvents of different polarities. The substitution effect at beta position of the BODIPY dyes on their absorption, emission and quantum yield of fluorescence have been the aim of present study. For the synthesized BODIPY dyes fluorescence quantum yields and lifetimes show very sharp decrease with an increase in the solvent polarity, suggesting the involvement of highly polar ICT state de-excitation mechanism along with the local excitation process. The polarity dependent changes in average fluorescence life time and quantum yield values rationalize the formation of ICT states.

74 ATOMIC AND MOLECULAR PHYSICS↗
DOE OSTI2018

A New Candidate Laser Dye Based 1,4-Bis[β-(2-Naphthothiazolyle)Vinyl]Benzene. Spectroscopic Behavior, Laser Parameters and Excitation Energy Transfer

A new candidate laser dye based 1,4-bis[β-(2-naphthothisolyl) vinyl] benzene (BNTVB) were prepared, and characterized in various organic solvents. The center polarity is less sensitive than electronic absorption. A red shift was noticed in the fluorescence spectra (ca. 40 nm) with increment in the solvent’s polarity, this means that BNTVB’s polarity appreciates upon excitation. The dipole moment of ground state (μ{sub g}) and the excited singlet state dipole moment (μ{sub e}) are determined from Kawski – Chamma and Bakshiev–Viallet equations using the disparity of Stokes shift with solvent polarity function of ε (dielectric constant) and n (refractive index) of the solvent. The result was found to be 0.019D and 5.13D for ground and exited state, in succession. DFT/TD-DFT manners were used to understand the electronic structures and geometric of BNTVB in other solvents. The experimental and theoretical results showed a good agreement. The photochemical quantum yield (Ф{sub c}) of BNTVB was calculated in variable organic reagents such as Dioxane, CHCl{sub 3}, EtOH and MeOH at room temperature. The values of φ{sub c} were calculated as 2.3 × 10{sup −4}, 3.3 × 10{sup −3}, 9.7 × 10{sup −5} and 6.2 × 10{sup −5} in Dioxane, CHCl{sub 3}, EtOH and MeOH, respectively. The dye solutions (2 × 10{sup −4} M) in DMF, MeOH and EtOH give laser emission in the blue-green region. The green zone is excited by nitrogen pulse 337.1 nm. The tuning range, gain coefficient (α) and cross – section emission (σ{sub e}) of laser were also estimated. Excitation energy transfer from BNTVB to rhodamine-6G (R6G) and N,N-bis(2,6-dimethyphenyl)-3,4:9,10-perylenebis-(dicarboximide) (BDP) was also studied in EtOH to increase the laser emission output from R6G and BDP when excited by nitrogen laser. The dye-transfer power laser system (ETDL) obeys the Foster Power Transmission (FERT) mechanism with a critical transmission distance, R{sub o} of 40 and 32 A and k{sub ET} equals 2.6 × 10{sup 13} and 1.06 × 10{sup 13} M{sup −1} s{sup −1} for BNTVB / R6G and BNTVB / BDP pair, respectively.

74 ATOMIC AND MOLECULAR PHYSICS↗
DOE OSTI2017

Single-unit-cell layer established Bi 2 WO 6 3D hierarchical architectures: Efficient adsorption, photocatalysis and dye-sensitized photoelectrochemical performance

Single-layer catalysis sparks huge interests and gains widespread attention owing to its high activity. Simultaneously, three-dimensional (3D) hierarchical structure can afford large surface area and abundant reactive sites, contributing to high efficiency. Herein, we report an absorbing single-unit-cell layer established Bi2WO6 3D hierarchical architecture fabricated by a sodium dodecyl benzene sulfonate (SDBS)-assisted assembled strategy. The DBS- long chains can adsorb on the (Bi2O2)2+ layers and hence impede stacking of the layers, resulting in the single-unit-cell layer. We also uncovered that SDS with a shorter chain is less effective than SDBS. Due to the sufficient exposure of surface O atoms, single-unit-cell layer 3D Bi2WO6 shows strong selectivity for adsorption on multiform organic dyes with different charges. Remarkably, the single-unit-cell layer 3D Bi2WO6 casts profoundly enhanced photodegradation activity and especially a superior photocatalytic H2 evolution rate, which is 14-fold increase in contrast to the bulk Bi2WO6. Systematic photoelectrochemical characterizations disclose that the substantially elevated carrier density and charge separation efficiency take responsibility for the strengthened photocatalytic performance. Additionally, the possibility of single-unit-cell layer 3D Bi2WO6 as dye-sensitized solar cells (DSSC) has also been attempted and it was manifested to be a promising dye-sensitized photoanode for oxygen evolution reaction (ORR). Our work not only furnish an insight into designing single-layer assembled 3D hierarchical architecture, but also offer a multi-functional material for environmental and energy applications.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗