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Sample records for addition energy transfer

  1. Evidence of additional excitation energy transfer pathways in the phycobiliprotein antenna system of Acaryochloris marina.

    PubMed

    Nganou, A C; David, L; Adir, N; Pouhe, D; Deen, M J; Mkandawire, M

    2015-02-01

    To improve the energy conversion efficiency of solar organic cells, the clue may lie in the development of devices inspired by an efficient light harvesting mechanism of some aquatic photosynthetic microorganisms that are adapted to low light intensity. Consequently, we investigated the pathways of excitation energy transfer (EET) from successive light harvesting pigments to the low energy level inside the phycobiliprotein antenna system of Acaryochloris marina, a cyanobacterium, using a time resolved absorption difference spectroscopy with a resolution time of 200 fs. The objective was to understand the actual biochemical process and pathways that determine the EET mechanism. Anisotropy of the EET pathway was calculated from the absorption change trace in order to determine the contribution of excitonic coupling. The results reveal a new electron energy relaxation pathway of 14 ps inside the phycocyanin component, which runs from phycocyanin to the terminal emitter. The bleaching of the 660 nm band suggests a broader absorption of the terminal emitter between 660 nm and 675 nm. Further, there are trimer depolarization kinetics of 450 fs and 500 fs in high and low ionic strength, respectively, which arise from the relaxation of the β84 and α84 in adjacent monomers of phycocyanin. Under conditions of low ionic strength buffer solution, the evolution of the kinetic amplitude during the depolarization of the trimer is suggestive of trimer conservation within the phycocyanin hexamer. The anisotropy values were 0.38 and 0.40 in high and in low ionic strength, respectively, indicating that there is no excitonic delocalization in the high energy level of phycocyanin hexamers. PMID:25470281

  2. Additional correction for energy transfer efficiency calculation in filter-based Förster resonance energy transfer microscopy for more accurate results

    NASA Astrophysics Data System (ADS)

    Sun, Yuansheng; Periasamy, Ammasi

    2010-03-01

    Förster resonance energy transfer (FRET) microscopy is commonly used to monitor protein interactions with filter-based imaging systems, which require spectral bleedthrough (or cross talk) correction to accurately measure energy transfer efficiency (E). The double-label (donor+acceptor) specimen is excited with the donor wavelength, the acceptor emission provided the uncorrected FRET signal and the donor emission (the donor channel) represents the quenched donor (qD), the basis for the E calculation. Our results indicate this is not the most accurate determination of the quenched donor signal as it fails to consider the donor spectral bleedthrough (DSBT) signals in the qD for the E calculation, which our new model addresses, leading to a more accurate E result. This refinement improves E comparisons made with lifetime and spectral FRET imaging microscopy as shown here using several genetic (FRET standard) constructs, where cerulean and venus fluorescent proteins are tethered by different amino acid linkers.

  3. Backbone additivity in the transfer model of protein solvation

    PubMed Central

    Hu, Char Y; Kokubo, Hironori; Lynch, Gillian C; Bolen, D Wayne; Pettitt, B Montgomery

    2010-01-01

    The transfer model implying additivity of the peptide backbone free energy of transfer is computationally tested. Molecular dynamics simulations are used to determine the extent of change in transfer free energy (ΔGtr) with increase in chain length of oligoglycine with capped end groups. Solvation free energies of oligoglycine models of varying lengths in pure water and in the osmolyte solutions, 2M urea and 2M trimethylamine N-oxide (TMAO), were calculated from simulations of all atom models, and ΔGtr values for peptide backbone transfer from water to the osmolyte solutions were determined. The results show that the transfer free energies change linearly with increasing chain length, demonstrating the principle of additivity, and provide values in reasonable agreement with experiment. The peptide backbone transfer free energy contributions arise from van der Waals interactions in the case of transfer to urea, but from electrostatics on transfer to TMAO solution. The simulations used here allow for the calculation of the solvation and transfer free energy of longer oligoglycine models to be evaluated than is currently possible through experiment. The peptide backbone unit computed transfer free energy of −54 cal/mol/M compares quite favorably with −43 cal/mol/M determined experimentally. PMID:20306490

  4. Backbone Additivity in the Transfer Model of Protein Solvation

    SciTech Connect

    Hu, Char Y.; Kokubo, Hironori; Lynch, Gillian C.; Bolen, D Wayne; Pettitt, Bernard M.

    2010-05-01

    The transfer model implying additivity of the peptide backbone free energy of transfer is computationally tested. Molecular dynamics simulations are used to determine the extent of change in transfer free energy (ΔGtr) with increase in chain length of oligoglycine with capped end groups. Solvation free energies of oligoglycine models of varying lengths in pure water and in the osmolyte solutions, 2M urea and 2M trimethylamine N-oxide (TMAO), were calculated from simulations of all atom models, and ΔGtr values for peptide backbone transfer from water to the osmolyte solutions were determined. The results show that the transfer free energies change linearly with increasing chain length, demonstrating the principle of additivity, and provide values in reasonable agreement with experiment. The peptide backbone transfer free energy contributions arise from van der Waals interactions in the case of transfer to urea, but from electrostatics on transfer to TMAO solution. The simulations used here allow for the calculation of the solvation and transfer free energy of longer oligoglycine models to be evaluated than is currently possible through experiment. The peptide backbone unit computed transfer free energy of –54 cal/mol/Mcompares quite favorably with –43 cal/mol/M determined experimentally.

  5. Enhanced energy transfer between Co-dopants Pyronin-Y and Thionine incorporated into modified polymethyl methacrylate with addition of ZnO nanoparticles.

    PubMed

    Vijayaraghavan, G V; Basheer Ahamed, M

    2016-04-01

    Using a prism dye cell arrangement, the study investigated spectral energy transfer between co-dopants Pyronin-Y and Thionine incorporated into ethanol-modified polymethyl methacrylate. The spectral parameters of the absorption and fluorescence spectra of the donor and acceptor dyes in the so designed solid-state dye laser were calculated theoretically. Fluorescence lasing properties and slope efficiency of the solid-state dye laser were investigated both with and without addition of ZnO nanoparticles. The dye pair generally improved lasing efficiency and tunability in the range from 582 to 689nm. PMID:26803748

  6. Enhanced energy transfer between Co-dopants Pyronin-Y and Thionine incorporated into modified polymethyl methacrylate with addition of ZnO nanoparticles

    NASA Astrophysics Data System (ADS)

    Vijayaraghavan, G. V.; Basheer Ahamed, M.

    2016-04-01

    Using a prism dye cell arrangement, the study investigated spectral energy transfer between co-dopants Pyronin-Y and Thionine incorporated into ethanol-modified polymethyl methacrylate. The spectral parameters of the absorption and fluorescence spectra of the donor and acceptor dyes in the so designed solid-state dye laser were calculated theoretically. Fluorescence lasing properties and slope efficiency of the solid-state dye laser were investigated both with and without addition of ZnO nanoparticles. The dye pair generally improved lasing efficiency and tunability in the range from 582 to 689 nm.

  7. Solar Energy: Heat Transfer.

    ERIC Educational Resources Information Center

    Knapp, Henry H., III

    This module on heat transfer is one of six in a series intended for use as supplements to currently available materials on solar energy and energy conservation. Together with the recommended texts and references (sources are identified), these modules provide an effective introduction to energy conservation and solar energy technologies. The…

  8. Dexter energy transfer pathways.

    PubMed

    Skourtis, Spiros S; Liu, Chaoren; Antoniou, Panayiotis; Virshup, Aaron M; Beratan, David N

    2016-07-19

    Energy transfer with an associated spin change of the donor and acceptor, Dexter energy transfer, is critically important in solar energy harvesting assemblies, damage protection schemes of photobiology, and organometallic opto-electronic materials. Dexter transfer between chemically linked donors and acceptors is bridge mediated, presenting an enticing analogy with bridge-mediated electron and hole transfer. However, Dexter coupling pathways must convey both an electron and a hole from donor to acceptor, and this adds considerable richness to the mediation process. We dissect the bridge-mediated Dexter coupling mechanisms and formulate a theory for triplet energy transfer coupling pathways. Virtual donor-acceptor charge-transfer exciton intermediates dominate at shorter distances or higher tunneling energy gaps, whereas virtual intermediates with an electron and a hole both on the bridge (virtual bridge excitons) dominate for longer distances or lower energy gaps. The effects of virtual bridge excitons were neglected in earlier treatments. The two-particle pathway framework developed here shows how Dexter energy-transfer rates depend on donor, bridge, and acceptor energetics, as well as on orbital symmetry and quantum interference among pathways. PMID:27382185

  9. The Additive Property of Energy.

    ERIC Educational Resources Information Center

    Tsaoussis, Dimitris S.

    1995-01-01

    Presents exercises that analyze the additive property of energy. Concludes that if a body has more than one component of energy depending on the same physical quantity, the body's total energy will be the algebraic sum of the components if a linear relationship exists between the energy components and that physical quantity. (JRH)

  10. ENERGY-TRANSFER SYSTEMS

    DOEpatents

    Thonemann, P.C.; Cowhig, W.T.; Davenport, P.A.

    1963-04-01

    This patent relates to the transfer of energy in a traveling electromagnetic wave to direct-current electrical energy in a gaseous medium. The traveling wave is generated by means of a radio-frequency oscillator connected across a capacitance-loaded helix wound around a sealed tube enclosing the gaseous medium. The traveling wave causes the electrons within the medium to drift towards one end of the tube. The direct current appearing across electrodes placed at each end of the tube is then used by some electrical means. (AEC)

  11. Heat transfer in energy problems

    NASA Astrophysics Data System (ADS)

    Mizushina, T.; Yang, W. J.

    Results of recent research are presented concerning heat transfer in energy problems, including high-temperature heat transfer, high-flux heat transfer, high-performance heat transfer, heat transfer in nonconventional energy (power and propulsion) systems, and novel heat transfer techniques. Topics discussed include studies of full-coverage film cooling, radiative properties of metals and alloys at high temperature, critical heat flux conditions in high-quality boiling systems, heat transfer characteristics of the evaporation of a liquid droplet on heated surfaces, high-performance surfaces for non-boiling heat transfer, and high performance heat transfer surfaces for boiling and condensation. Also examined are high flux heat transfer in gaseous solid suspension flow, nuclear process heat applications of high temperature heat exchange, heat transfer considerations in the use of new energy resources, and high performance mist-cooled condensers for geothermal binary cycle plants. No individual items are abstracted in this volume

  12. Energy Transfer in Rotating Turbulence

    NASA Technical Reports Server (NTRS)

    Cambon, Claude; Mansour, Nagi N.; Godeferd, Fabien S.; Rai, Man Mohan (Technical Monitor)

    1995-01-01

    The influence or rotation on the spectral energy transfer of homogeneous turbulence is investigated in this paper. Given the fact that linear dynamics, e.g. the inertial waves regime tackled in an RDT (Rapid Distortion Theory) fashion, cannot Affect st homogeneous isotropic turbulent flow, the study of nonlinear dynamics is of prime importance in the case of rotating flows. Previous theoretical (including both weakly nonlinear and EDQNM theories), experimental and DNS (Direct Numerical Simulation) results are gathered here and compared in order to give a self-consistent picture of the nonlinear effects of rotation on tile turbulence. The inhibition of the energy cascade, which is linked to a reduction of the dissipation rate, is shown to be related to a damping due to rotation of the energy transfer. A model for this effect is quantified by a model equation for the derivative-skewness factor, which only involves a micro-Rossby number Ro(sup omega) = omega'/(2(OMEGA))-ratio of rms vorticity and background vorticity as the relevant rotation parameter, in accordance with DNS and EDQNM results fit addition, anisotropy is shown also to develop through nonlinear interactions modified by rotation, in an intermediate range of Rossby numbers (Ro(omega) = (omega)' and Ro(omega)w greater than 1), which is characterized by a marco-Rossby number Ro(sup L) less than 1 and Ro(omega) greater than 1 which is characterized by a macro-Rossby number based on an integral lengthscale L and the micro-Rossby number previously defined. This anisotropy is mainly an angular drain of spectral energy which tends to concentrate energy in tile wave-plane normal to the rotation axis, which is exactly both the slow and the two-dimensional manifold. In Addition, a polarization of the energy distribution in this slow 2D manifold enhances horizontal (normal to the rotation axis) velocity components, and underlies the anisotropic structure of the integral lengthscales. Finally is demonstrated the

  13. Microparticle Fluorimetry and Energy Transfer

    NASA Astrophysics Data System (ADS)

    Folan, Lorcan Michael

    1987-12-01

    The primary aims of this dissertation were to develop an aerosol particle fluorimeter, utilize the instrument to investigate electronic energy transfer in individual microparticles (liquid droplets approximately 10 microns in radius) and develop an electromagnetic model to explain the observed energy transfer. A spectrometer for measuring the fluorescence emission fron a single trapped aerosol particle is described. This device consists of a particle generator, an electrodynamic levitator, and excitation source and detection optics and electronics. Provision is made to cool the sample chamber and fluorescence emission spectra can be obtained in real time. The fluorimeter was used to investigate energy transfer between donor-acceptor pairs of laser dyes. Energy transfer between the dyes was found to be enhanced in the levitated particles over the same material in bulk solution by more than a factor of 100. The concentration dependence of the particle energy transfer and characteristic features identified in the emission spectra indicate that the natural electromagnetic resonances of the particle mediate the energy transfer. A model calculation supports the experimental conclusions and yields good qualitative agreement with the observed energy transfer magnitude and concentration dependence.

  14. Energy transfer in compressible turbulence

    NASA Technical Reports Server (NTRS)

    Bataille, Francoise; Zhou, YE; Bertoglio, Jean-Pierre

    1995-01-01

    This letter investigates the compressible energy transfer process. We extend a methodology developed originally for incompressible turbulence and use databases from numerical simulations of a weak compressible turbulence based on Eddy-Damped-Quasi-Normal-Markovian (EDQNM) closure. In order to analyze the compressible mode directly, the well known Helmholtz decomposition is used. While the compressible component has very little influence on the solenoidal part, we found that almost all of the compressible turbulence energy is received from its solenoidal counterpart. We focus on the most fundamental building block of the energy transfer process, the triadic interactions. This analysis leads us to conclude that, at low turbulent Mach number, the compressible energy transfer process is dominated by a local radiative transfer (absorption) in both inertial and energy containing ranges.

  15. Energy transfer mechanisms between molecules

    NASA Technical Reports Server (NTRS)

    Meador, W. E.

    1985-01-01

    Reliable rate coefficients for energy transfer and relaxation phenomena are needed in order to do the theoretical modeling which is necessary for accomplishing the following objectives: understanding and justifying proposed laser systems, determining limitations, identifying control parameters, and scaling to space-power requirements. Modeling also establishes the criteria to be followed for lasant selection. Lack of knowledge of rate coefficients is invariably the biggest obstacle to successful modeling. Existing theoretical methods are discussed, sources of error are identified, and transfer laser criteria suggested by the theory are listed. The emphasis is on vibrational-vibrational (V-V) energy transfer caused by both short range and long range interactions between molecules. Special attention is given to the importance of near-resonant collisional and dipole-dipole transfer. A technique is proposed for significantly improving the theoretical predictions of rate coefficients.

  16. Energy transfer processes in solar energy conversion

    SciTech Connect

    Fayer, M.D.

    1986-11-01

    By combining picosecond optical experiments and detailed statistical mechanics theory we continue to increase our understanding of the complex interplay of structure and dynamics in important energy transfer situations. A number of different types of problems will be focused on experimentally and theoretically. They are excitation transport among chromophores attached to finite size polymer coils; excitation transport among chromophores in monolayers, bilayers, and finite and infinite stacks of layers; excitation transport in large vesicle systems; and photoinduced electron transfer in glasses and liquids, focusing particularly on the back transfer of the electron from the photogenerated radical anion to the radical cation. 33 refs., 13 figs.

  17. Optimal Low Energy Earth-Moon Transfers

    NASA Technical Reports Server (NTRS)

    Griesemer, Paul Ricord; Ocampo, Cesar; Cooley, D. S.

    2010-01-01

    The optimality of a low-energy Earth-Moon transfer is examined for the first time using primer vector theory. An optimal control problem is formed with the following free variables: the location, time, and magnitude of the transfer insertion burn, and the transfer time. A constraint is placed on the initial state of the spacecraft to bind it to a given initial orbit around a first body, and on the final state of the spacecraft to limit its Keplerian energy with respect to a second body. Optimal transfers in the system are shown to meet certain conditions placed on the primer vector and its time derivative. A two point boundary value problem containing these necessary conditions is created for use in targeting optimal transfers. The two point boundary value problem is then applied to the ballistic lunar capture problem, and an optimal trajectory is shown. Additionally, the ballistic lunar capture trajectory is examined to determine whether one or more additional impulses may improve on the cost of the transfer.

  18. The electronic couplings in electron transfer and excitation energy transfer.

    PubMed

    Hsu, Chao-Ping

    2009-04-21

    The transport of charge via electrons and the transport of excitation energy via excitons are two processes of fundamental importance in diverse areas of research. Characterization of electron transfer (ET) and excitation energy transfer (EET) rates are essential for a full understanding of, for instance, biological systems (such as respiration and photosynthesis) and opto-electronic devices (which interconvert electric and light energy). In this Account, we examine one of the parameters, the electronic coupling factor, for which reliable values are critical in determining transfer rates. Although ET and EET are different processes, many strategies for calculating the couplings share common themes. We emphasize the similarities in basic assumptions between the computational methods for the ET and EET couplings, examine the differences, and summarize the properties, advantages, and limits of the different computational methods. The electronic coupling factor is an off-diagonal Hamiltonian matrix element between the initial and final diabatic states in the transport processes. ET coupling is essentially the interaction of the two molecular orbitals (MOs) where the electron occupancy is changed. Singlet excitation energy transfer (SEET), however, contains a Frster dipole-dipole coupling as its most important constituent. Triplet excitation energy transfer (TEET) involves an exchange of two electrons of different spin and energy; thus, it is like an overlap interaction of two pairs of MOs. Strategies for calculating ET and EET couplings can be classified as (1) energy-gap-based approaches, (2) direct calculation of the off-diagonal matrix elements, or (3) use of an additional operator to describe the extent of charge or excitation localization and to calculate the coupling value. Some of the difficulties in calculating the couplings were recently resolved. Methods were developed to remove the nondynamical correlation problem from the highly precise coupled cluster

  19. 'Green' reversible addition-fragmentation chain-transfer (RAFT) polymerization

    NASA Astrophysics Data System (ADS)

    Semsarilar, Mona; Perrier, Sébastien

    2010-10-01

    Reversible addition-fragmentation chain-transfer (RAFT) polymerization has revolutionized the field of polymer synthesis as a versatile tool for the production of complex polymeric architectures. As for all chemical processes, research and development in RAFT have to focus on the design and application of chemical products and processes that have a minimum environmental impact, and follow the principles of 'green' chemistry. In this Review, we summarize some of the green features of the RAFT process, and review the recent advances in the production of degradable polymers obtained from RAFT polymerization. Its use to modify biodegradable and renewable inorganic and organic materials to yield more functional products with enhanced applications is also covered. RAFT is a promising candidate for answering both the increasing need of modern society to employ highly functional polymeric materials and the global requirements for developing sustainable chemicals and processes.

  20. Energy transfer in nanostructured materials

    NASA Astrophysics Data System (ADS)

    Haughn, Chelsea

    Energy transport and loss are critical to the performance of optoelectronic devices such as photovoltaics and terahertz imaging devices. Nanostructured materials provide many opportunities to tailor transport and loss parameters for specific device applications. However, it has been very difficult to correlate specific nanoscale structural parameters with changes in these performance metrics. I report the development of new ways of using time-resolved photoluminescence (TRPL) to probe charge and energy transport and loss dynamics. These techniques are applied to several types of nanostructured materials, including bulk semiconductors with defects, self-assembled quantum dots and colloidal quantum dots. First, GaAs/InP double heterostructures grown via metal organic chemical vapor deposition (MOCVD) were characterized with TRPL. TRPL is typically used to extract minority carrier lifetimes, but we discovered that the measured lifetime depended critically on the intensity of the exciting laser. We developed a Shockley-Read-Hall model to extract trap state densities from intensity-dependent TRPL measurements. Second, we characterized energy and charge transfer between InAs quantum dots and ErAs nanoinclusions within III-V heterostructures. Using intensity- and temperature-dependent TRPL, we confirmed tunneling as the dominant mechanism of charge transport and characterized the electronic structure of the ErAs nanoparticles. Finally, we characterized energy transport in colloidal quantum dot cascade structures. These cascade structures utilize Forster Resonance Energy Transfer and trap state recycling to funnel excitons from donor layers to acceptor layers and suggest a promising method for avoiding losses associated with surface trap states. Collectively, the analysis of these disparate material types advances our understanding of energy dynamics in nanostructured materials and improves our ability to design the next generation of photovoltaic and optoelectronic

  1. Vibrational energy transfer in fluids

    NASA Astrophysics Data System (ADS)

    Miller, David W.; Adelman, Steven A.

    A review of several of the available theories of vibrational energy transfer (VET) in the gas and liquid phases is presented. First the classical theory of gas phase VET mainly due to Landau and Teller, to Jackson and Mott and to Zener is developed in some detail. Next the Schwartz-Slawsky-Herzfeld theory, a framework for analysing VET data based on the classical theory, is outlined. Experimental tests of the classical theory and theoretical critiques of its assumptions are then described. Next a brief review of the modern ab-initio quantum approach to gas phase VET rates, taking as an example the work of Banks, Clary and Werner, is given. Theories of VET at elevated densities are then discussed. The isolated binary collision model is reviewed and a new molecular approach to the density, temperature and isotope dependences of vibrational energy relaxation rates, due to Adelman and co-workers, is outlined.

  2. Energy Transfer Involving Diatomic Molecules.

    NASA Astrophysics Data System (ADS)

    Gibbons, John Paul

    A three-dimensional, Monte Carlo model for the calculation of vibrational energy relaxation and transfer rates for both diatomic-monatomic and diatomic-diatomic systems was developed, analyzed and implemented. Mediation by internal angular momentum was demonstrated to be important in these energy transfer processes. This was named the TLV mechanism for translation to vibration flow through changes in angular momentum. The equations for the component of vibrational energy change due to the TLV mechanism for the two extreme cases of very hard or very soft collisions were derived. Results of using these equations were compared with those obtained by direct integration of the differential equations of motion and in many cases were found to agree. This mechanism was incorporated into the model in order to achieve statistically significant results within reasonable computer running times. When this was done the variance of a result was frequently reduced by a factor of thirty to fifty or more with little or no increase in the computer times required. This made possible a meaningful study of the full three-dimensional diatomic-diatomic collisional processes and also permitted extension of the mono-diatomic model calculations to much lower temperatures than had been previously investigated. After this calculational procedure was developed for Ar - O(,2) collisions, it was also applied to He - O(,2) and to the near resonant vibration energy exchange process:. CO ((nu)=0)+N(,2)((nu)=1)(--->)CO((nu)=1)+N(,2)((nu)=0). These three processes were investigated at several temperatures between room temperature and 4000K. Exponential repulsive intermolecular potentials were used. The values for the coefficients and characteristic lengths for these potentials were obtained from independent sources both experimental and theoretical. In general, the results, when compared to experiment, are very consistent relative to their dependence on the potential parameters. In every case for all

  3. Coherence in Energy Transfer and Photosynthesis

    NASA Astrophysics Data System (ADS)

    Chenu, Aurélia; Scholes, Gregory D.

    2015-04-01

    Ultrafast energy transfer is used to transmit electronic excitation among the many molecules in photosynthetic antenna complexes. Recent experiments and theories have highlighted the role of coherent transfer in femtosecond studies of these proteins, suggesting the need for accurate dynamical models to capture the subtle characteristics of energy transfer mechanisms. Here we discuss how to think about coherence in light harvesting and electronic energy transfer. We review the various fundamental concepts of coherence, spanning from classical phenomena to the quantum superposition, and define coherence in electronic energy transfer. We describe the current status of experimental studies on light-harvesting complexes. Insights into the microscopic process are presented to highlight how and why this is a challenging problem to elucidate. We present an overview of the applicable dynamical theories to model energy transfer in the intermediate coupling regime.

  4. Reversible addition-fragmentation chain transfer polymerization in microemulsion.

    PubMed

    O'Donnell, Jennifer M

    2012-04-21

    This tutorial review first details the uncontrolled microemulsion polymerization mechanism, and the RAFT polymerization mechanism to provide the necessary background for examining the RAFT microemulsion polymerization mechanism. The effect of the chain transfer agent per micelle ratio and the chain transfer agent aqueous solubility on the RAFT microemulsion polymerization kinetics, polymer molecular weight and polydispersity, and polymer nanoparticle size are discussed with a focus on oil-in-water microemulsions. Modeling of RAFT microemulsion polymerization kinetics and the resulting final polymer molecular weight are presented to assist with the analysis of observed experimental trends. Lastly, the current significance of RAFT microemulsion polymerization and the future directions are discussed. PMID:22246214

  5. Geo energy research and development: technology transfer

    SciTech Connect

    Traeger, R.K.

    1982-03-01

    Sandia Geo Energy Programs related to geothermal, coal, oil and gas, and synfuel resources have provided a useful mechanism for transferring laboratory technologies to private industry. Significant transfer of hardware, computer programs, diagnostics and instrumentation, advanced materials, and in situ process understanding has occurred through US/DOE supported programs in the past five years. The text briefly reviews the technology transfer procedures and summarizes 32 items that have been transferred and another 20 technologies that are now being considered for possible transfer to industry. A major factor in successful transfer has been personal interactions between Sandia engineers and the technical staff from private industry during all aspects of the technology development.

  6. Transferability and additivity of dihedral parameters in polarizable and nonpolarizable empirical force fields.

    PubMed

    Zgarbová, Marie; Rosnik, Andreana M; Luque, F Javier; Curutchet, Carles; Jurečka, Petr

    2015-09-30

    Recent advances in polarizable force fields have revealed that major reparameterization is necessary when the polarization energy is treated explicitly. This study is focused on the torsional parameters, which are crucial for the accurate description of conformational equilibria in biomolecules. In particular, attention is paid to the influence of polarization on the (i) transferability of dihedral terms between molecules, (ii) transferability between different environments, and (iii) additivity of dihedral energies. To this end, three polarizable force fields based on the induced point dipole model designed for use in AMBER are tested, including two recent ff02 reparameterizations. Attention is paid to the contributions due to short range interactions (1-2, 1-3, and 1-4) within the four atoms defining the dihedral angle. The results show that when short range 1-2 and 1-3 polarization interactions are omitted, as for instance in ff02, the 1-4 polarization contribution is rather small and unlikely to improve the description of the torsional energy. Conversely, when screened 1-2 and 1-3 interactions are included, the polarization contribution is sizeable and shows potential to improve the transferability of parameters between different molecules and environments as well as the additivity of dihedral terms. However, to reproduce intramolecular polarization effects accurately, further fine-tuning of the short range damping of polarization is necessary. PMID:26224547

  7. Fundamental Interactions Leading to Energy Transfer

    NASA Astrophysics Data System (ADS)

    di Bartolo, Baldassare

    2001-11-01

    The purpose of the lectures reported in this article is to investigate the basic interactions that lead to processes by which excitation energy, initially localized in a particular constituent or restricted region of a material, transfers itself to other parts or degrees of freedom of the system. Energy transfer processes are relevant to such various and important fields as spectroscopy, laser technology, phosphors, artificial solar energy conversion, and photobiology. The subject of the interactions among atoms is introduced by considering first the static and then the dynamic effects of these interactions in a two-atom system. Subsequently the different types of interactions (multipolar, exchange and electromagnetic) in a two-atom system are examined. After reviewing the different modes of excitation of a solid containing both donors and acceptors, a statistical treatment of energy transfer is presented. Firstly the case of energy transfer without migration among donors, and secondly the case of energy transfer in the presence of such migration are considered.

  8. Ultrafast Energy Transfer in Biomimetic Multistrand Nanorings

    PubMed Central

    2014-01-01

    We report the synthesis of LH2-like supramolecular double- and triple-stranded complexes based upon porphyrin nanorings. Energy transfer from the antenna dimers to the π-conjugated nanoring occurs on a subpicosecond time scale, rivaling transfer rates in natural light-harvesting systems. The presence of a second nanoring acceptor doubles the transfer rate, providing strong evidence for multidirectional energy funneling. The behavior of these systems is particularly intriguing because the local nature of the interaction may allow energy transfer into states that are, for cyclic nanorings, symmetry-forbidden in the far field. These complexes are versatile synthetic models for natural light-harvesting systems. PMID:24878362

  9. Nonradiative resonance energy transfer between semiconductor quantum dots

    SciTech Connect

    Samosvat, D. M. Chikalova-Luzina, O. P.; Zegrya, G. G.

    2015-07-15

    A microscopic analysis of the mechanisms of nonradiative energy transfer in a system of two semiconductor QDs caused by Coulomb interaction of donor and acceptor electrons is performed. The energy transfer rate is calculated for QDs based on III–V compounds using the Kane model. Conditions are analyzed under which energy transfer from a donor to an acceptor is possible. The mixing in of the p states of the valence band to the s states of the conduction band is found to give rise to additional contributions to the matrix element of energy transfer. It is shown that these additional contributions play a considerable role in the energy transfer process at distances between QDs close to contact distances or much greater. The influence of the exchange interaction on the energy transfer mechanism is analyzed, and it is shown that this interaction should be taken into account for a quantitative description of the energy transfer when QDs are separated by a distance close to the contact distance.

  10. Phosphorescence and Energy Transfer in Rigid Solutions.

    ERIC Educational Resources Information Center

    Enciso, E.; Cabello, A.

    1980-01-01

    Describes an experiment which illustrates the general aspects of intermolecular energy transfer between triplet states in rigid solutions of organic compounds solved in an ethanol-ether mixture. Measurements of quenching and energy transfer processes are made using the chemicals of benzophenone and naphthalene. (CS)

  11. Classical Approach to Multichromophoric Resonance Energy Transfer

    NASA Astrophysics Data System (ADS)

    Duque, Sebastián; Brumer, Paul; Pachón, Leonardo A.

    2015-09-01

    A classical formulation of the quantum multichromophoric theory of resonance energy transfer is developed on the basis of classical electrodynamics. The theory allows for the identification of a variety of processes of different order in the interactions that contribute to the energy transfer in molecular aggregates with intracoupling in donors and acceptor chromophores. Enhanced rates in multichromophoric resonance energy transfer are shown to be well described by this theory. Specifically, in a coupling configuration between NA acceptors and ND donors, the theory correctly predicts an enhancement of the energy transfer rate dependent on the total number of donor-acceptor pairs. As an example, the theory, applied to the transfer rate in light harvesting II, gives results in excellent agreement with experiment. Finally, it is explicitly shown that as long as linear response theory holds, the classical multichromophoric theory formally coincides with the quantum formulation.

  12. Classical approach to multichromophoric resonance energy transfer.

    PubMed

    Duque, Sebastián; Brumer, Paul; Pachón, Leonardo A

    2015-09-11

    A classical formulation of the quantum multichromophoric theory of resonance energy transfer is developed on the basis of classical electrodynamics. The theory allows for the identification of a variety of processes of different order in the interactions that contribute to the energy transfer in molecular aggregates with intracoupling in donors and acceptor chromophores. Enhanced rates in multichromophoric resonance energy transfer are shown to be well described by this theory. Specifically, in a coupling configuration between N_{A} acceptors and N_{D} donors, the theory correctly predicts an enhancement of the energy transfer rate dependent on the total number of donor-acceptor pairs. As an example, the theory, applied to the transfer rate in light harvesting II, gives results in excellent agreement with experiment. Finally, it is explicitly shown that as long as linear response theory holds, the classical multichromophoric theory formally coincides with the quantum formulation. PMID:26406811

  13. Energy transfer processes in solar energy conversion

    SciTech Connect

    Fayer, M.D.

    1992-01-01

    During the past year, we have been working in three general areas: electronic excitation transport in clustered chromophore systems and other complex systems, photo-induced electron transfer and back transfer in liquid solutions in which diffusion and charge interactions are important, and the construction of a new two color dye laser system to enhance our experimental capability.

  14. Resonance energy transfer: Dye to metal nanoparticles

    SciTech Connect

    Wari, M. N.; Pujar, G. H.; Inamdar, S. R.

    2015-06-24

    In the present study, surface energy transfer (SET) from Coumarin 540A (C540 A) to Gold nanoparticle (Au) is demonstrated. The observed results show pronounced effect on the photoluminescence intensity and shortening of the lifetime of Coumarin 540A upon interaction with the spherical gold nanoparticle, also there are measured effects on radiative rate of the dye. Experimental results are analyzed with fluorescence resonance energy transfer (FRET) and SET theories. The results obtained from distance-dependent quenching provide experimental evidence that the efficiency curve slope and distance of quenching is best modeled by surface energy transfer process.

  15. Resonance energy transfer: Dye to metal nanoparticles

    NASA Astrophysics Data System (ADS)

    Wari, M. N.; Pujar, G. H.; Inamdar, S. R.

    2015-06-01

    In the present study, surface energy transfer (SET) from Coumarin 540A (C540 A) to Gold nanoparticle (Au) is demonstrated. The observed results show pronounced effect on the photoluminescence intensity and shortening of the lifetime of Coumarin 540A upon interaction with the spherical gold nanoparticle, also there are measured effects on radiative rate of the dye. Experimental results are analyzed with fluorescence resonance energy transfer (FRET) and SET theories. The results obtained from distance-dependent quenching provide experimental evidence that the efficiency curve slope and distance of quenching is best modeled by surface energy transfer process.

  16. Dynamics of excitation energy transfer in phycobiliproteins

    NASA Astrophysics Data System (ADS)

    Zheng, Xiguang; Wang, He Z.; Zhao, Fuli; Gao, Zhaolan; Yu, Zhenxin

    1994-08-01

    Theoretical descriptions of excitation energy transfer between chromophores in allophycocyanin are presented, including bilateral energy transfer paths between chromophores, and are expressed, based on Foster interaction mechanism, as Pauli master equations. Group analysis in C3 symmetry is performed to carry out analytic expressions for fluorescence decays which is generally of triexponential with effects of chromophore coupling and exciton splitting taken account. It is pointed out that the time constant of each decay component contains mixed information of different energy transfer paths, and therefore show its dependence on subtle configuration of chromophores, probably related to site heterogeneity and thus to inhomogeneous broadening previously observed.

  17. Compost addition reduces porosity and chlordecone transfer in soil microstructure.

    PubMed

    Woignier, Thierry; Clostre, Florence; Fernandes, Paula; Rangon, Luc; Soler, Alain; Lesueur-Jannoyer, Magalie

    2016-01-01

    Chlordecone, an organochlorine insecticide, pollutes soils and contaminates crops and water resources and is biomagnified by food chains. As chlordecone is partly trapped in the soil, one possible alternative to decontamination may be to increase its containment in the soil, thereby reducing its diffusion into the environment. Containing the pesticide in the soil could be achieved by adding compost because the pollutant has an affinity for organic matter. We hypothesized that adding compost would also change soil porosity, as well as transport and containment of the pesticide. We measured the pore features and studied the nanoscale structure to assess the effect of adding compost on soil microstructure. We simulated changes in the transport properties (hydraulic conductivity and diffusion) associated with changes in porosity. During compost incubation, the clay microstructure collapsed due to capillary stresses. Simulated data showed that the hydraulic conductivity and diffusion coefficient were reduced by 95 and 70% in the clay microstructure, respectively. Reduced transport properties affected pesticide mobility and thus helped reduce its transfer from the soil to water and to the crop. We propose that the containment effect is due not only to the high affinity of chlordecone for soil organic matter but also to a trapping mechanism in the soil porosity. PMID:26250815

  18. Conformational Disorder in Energy Transfer: Beyond Forster Theory

    NASA Astrophysics Data System (ADS)

    Nelson, Tammie; Fernandez-Alberti, Sebastian; Roitberg, Adrian; Tretiak, Sergei

    2013-03-01

    Energy transfer in donor/acceptor chromophore pairs, where the absorption of each species is well separated, can be understood through a Förster resonance energy transfer model. The picture is more complex for organic conjugated polymers, where the total absorption spectrum can be described as a sum of the individual contributions from each subunit, whose absorption is not well separated. Although excitations in these systems tend to be well localized, traditional donors and acceptors cannot be defined and energy transfer can occur through various pathways. In addition, fast torsional motions between individual monomers can break conjugation and lead to reordering of excited state energy levels. Energy transfer in these systems can be induced by both electronic transitions and by fast torsional fluctuations where both mechanisms occur simultaneously. We use non-adiabatic excited state molecular dynamics (NA-ESMD) to simulate energy transfer between two poly-phenylene vinylene (PPV) segments composed of 3-rings and 4-rings separated by varying distances. The transition density decay represents the transfer rate, and can be decomposed into contributions from various transfer pathways.

  19. Environment assisted energy transfer in dimer system

    SciTech Connect

    Khan, Salman; Ibrahim, M.; Khan, M.K.

    2014-02-15

    The influence of collective and multilocal environments on the energy transfer between the levels of a dimer is studied. The dynamics of energy transfer are investigated by considering coupling of collective environment with the levels of the dimer in the presence of both two individuals and mutually correlated multilocal environments. It is shown that every way of coupling we consider assists, though differently, the probability of transition between the levels of dimer. The probability of transition is strongly enhanced when the two local environments are mutually correlated. -- Highlights: • The dynamics of energy transfer between the levels of a dimer are studied. • Coupling of collective as well as individual environments are considered. • The environments are in spin star configurations. • The environment assists the energy transfer between the levels. • For correlated multilocal environments, the transition probability is almost 100%.

  20. Optical Energy Transfer and Conversion System

    NASA Technical Reports Server (NTRS)

    Stone, William C. (Inventor); Hogan, Bartholomew P. (Inventor)

    2015-01-01

    An optical power transfer system comprising a fiber spooler, a fiber optic rotary joint mechanically connected to the fiber spooler, and an electrical power extraction subsystem connected to the fiber optic rotary joint with an optical waveguide. Optical energy is generated at and transferred from a base station through fiber wrapped around the spooler, through the rotary joint, and ultimately to the power extraction system at a remote mobility platform for conversion to another form of energy.

  1. Targeting Low-Energy Ballistic Lunar Transfers

    NASA Technical Reports Server (NTRS)

    Parker, Jeffrey S.

    2010-01-01

    Numerous low-energy ballistic transfers exist between the Earth and Moon that require less fuel than conventional transfers, but require three or more months of transfer time. An entirely ballistic lunar transfer departs the Earth from a particular declination at some time in order to arrive at the Moon at a given time along a desirable approach. Maneuvers may be added to the trajectory in order to adjust the Earth departure to meet mission requirements. In this paper, we characterize the (Delta)V cost required to adjust a low-energy ballistic lunar transfer such that a spacecraft may depart the Earth at a desirable declination, e.g., 28.5(white bullet), on a designated date. This study identifies the optimal locations to place one or two maneuvers along a transfer to minimize the (Delta)V cost of the transfer. One practical application of this study is to characterize the launch period for a mission that aims to launch from a particular launch site, such as Cape Canaveral, Florida, and arrive at a particular orbit at the Moon on a given date using a three-month low-energy transfer.

  2. Wireless energy transfer between anisotropic metamaterials shells

    SciTech Connect

    Díaz-Rubio, Ana; Carbonell, Jorge; Sánchez-Dehesa, José

    2014-06-15

    The behavior of strongly coupled Radial Photonic Crystals shells is investigated as a potential alternative to transfer electromagnetic energy wirelessly. These sub-wavelength resonant microstructures, which are based on anisotropic metamaterials, can produce efficient coupling phenomena due to their high quality factor. A configuration of selected constitutive parameters (permittivity and permeability) is analyzed in terms of its resonant characteristics. The coupling to loss ratio between two coupled resonators is calculated as a function of distance, the maximum (in excess of 300) is obtained when the shells are separated by three times their radius. Under practical conditions an 83% of maximum power transfer has been also estimated. -- Highlights: •Anisotropic metamaterial shells exhibit high quality factors and sub-wavelength size. •Exchange of electromagnetic energy between shells with high efficiency is analyzed. •Strong coupling is supported with high wireless transfer efficiency. •End-to-end energy transfer efficiencies higher than 83% can be predicted.

  3. Quantum electrodynamics of resonance energy transfer in nanowire systems

    NASA Astrophysics Data System (ADS)

    Weeraddana, Dilusha; Premaratne, Malin; Andrews, David L.

    2016-02-01

    Nonradiative resonance energy transfer (RET) provides the ability to transfer excitation energy between contiguous nanowires (NWs) with high efficiency under certain conditions. Nevertheless, the well-established Förster formalism commonly used to represent RET was developed for energy transfer primarily between molecular blocks (i.e., from one molecule, or part of a molecule, to another). Although deviations from Förster theory for functional blocks such as NWs have been studied previously, the role of the relative distance, the orientation of transition dipole moment pairs, and the passively interacting matter on electronic energy transfer are to a large extent unknown. Thus, a comprehensive theory that models RET in NWs is required. In this context, analytical insights to give a deeper and more intuitive understanding of the distance and orientation dependence of RET in NWs is presented within the framework of quantum electrodynamics. Additionally, the influence of an included intermediary on the rate of excitation energy transfer is illustrated, embracing indirect energy transfer rate and quantum interference. The results deliver equations that afford new intuitions into the behavior of virtual photons. In particular, results indicate that RET efficiency in a NW system can be explicitly expedited or inhibited by a neighboring mediator, depending on the relative spacing and orientation of NWs.

  4. Excitation energy transfer in the photosystem I

    SciTech Connect

    Webber, Andrew N

    2012-09-25

    Photosystem I is a multimeric pigment protein complex in plants, green alage and cyanobacteria that functions in series with Photosystem II to use light energy to oxidize water and reduce carbon dioxide. The Photosystem I core complex contains 96 chlorophyll a molecules and 22 carotenoids that are involved in light harvesting and electron transfer. In eucaryotes, PSI also has a peripheral light harvesting complex I (LHCI). The role of specific chlorophylls in excitation and electron transfer are still unresolved. In particular, the role of so-called bridging chlorophylls, located between the bulk antenna and the core electron transfer chain, in the transfer of excitation energy to the reaction center are unknown. During the past funding period, site directed mutagenesis has been used to create mutants that effect the physical properties of these key chlorophylls, and to explore how this alters the function of the photosystem. Studying these mutants using ultrafast absorption spectroscopy has led to a better understanding of the process by which excitation energy is transferred from the antenna chlorophylls to the electron transfer chain chlorophylls, and what the role of connecting chlorophylls and A_0 chlorophylls is in this process. We have also used these mutants to investigate whch of the central group of six chlorophylls are involved in the primary steps of charge separation and electron transfer.

  5. Exciton Transfer in Carbon Nanotube Aggregates for Energy Harvesting Applications

    NASA Astrophysics Data System (ADS)

    Davoody, Amirhossein; Karimi, Farhad; Knezevic, Irena

    Carbon nanotubes (CNTs) are promising building blocks for organic photovoltaic devices, owing to their tunable band gap, mechanical and chemical stability. We study intertube excitonic energy transfer between pairs of CNTs with different orientations and band gaps. The optically bright and dark excitonic states in CNTs are calculated by solving the Bethe-Salpeter equation. We calculate the exciton transfer rates due to the direct and exchange Coulomb interactions, as well as the second-order phonon-assisted processes. We show the importance of phonons in calculating the transfer rates that match the measurements. In addition, we discuss the contribution of optically inactive excited states in the exciton transfer process, which is difficult to determine experimentally. Furthermore, we study the effects of sample inhomogeneity, impurities, and temperature on the exciton transfer rate. The inhomogeneity in the CNT sample dielectric function can increase the transfer rate by about a factor of two. We show that the exciton confinement by impurities has a detrimental effect on the transfer rate between pairs of similar CNTs. The exciton transfer rate increases monotonically with increasing temperature. Support by the U.S. Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering under Award DE-SC0008712.

  6. Rotational Energy Transfer in N2

    NASA Technical Reports Server (NTRS)

    Huo, Winifred M.

    1994-01-01

    Using the N2-N2 intermolecular potential of van der Avoird et al. rotational energy transfer cross sections have been calculated using both the coupled state (CS) and infinite order sudden (IOS) approximations. The rotational energy transfer rate constants at 300 K, calculated in the CS approximation, are in reasonable agreement with the measurements of Sitz and Farrow. The IOS approximation qualitatively reproduces the dependence of the rate constants on the rotational quantum numbers, but consistently overestimates their magnitudes. The treatment of exchange symmetry will be discussed.

  7. Intramolecular energy transfer reactions in polymetallic

    SciTech Connect

    Petersen, J.

    1990-11-01

    This report is concerned with intramolecular, energy-transfer reactions. The concept of preparing synthetically a complex molecular species, capable of absorbing a photon at one metal center (antenna fragment), transferring that energy to a second metal center (reactive fragment) via a bridging ligand was first reported by our group in 1979. It is now apparent that a major emphasis in inorganic chemistry in the future will involve these types of molecular ensembles. Complexes discussed include Rh, Ru, and Cu complexes. 23 refs., 14 tabs.

  8. 36 CFR 1235.40 - What records are covered by additional transfer requirements?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... additional transfer requirements? 1235.40 Section 1235.40 Parks, Forests, and Public Property NATIONAL ARCHIVES AND RECORDS ADMINISTRATION RECORDS MANAGEMENT TRANSFER OF RECORDS TO THE NATIONAL ARCHIVES OF THE..., architectural, and electronic records to the National Archives of the United States. In general, such...

  9. Plasmon-induced resonance energy transfer for solar energy conversion

    NASA Astrophysics Data System (ADS)

    Li, Jiangtian; Cushing, Scott K.; Meng, Fanke; Senty, Tess R.; Bristow, Alan D.; Wu, Nianqiang

    2015-09-01

    In Förster resonance energy transfer (FRET), energy non-radiatively transfers from a blue-shifted emitter to a red-shifted absorber by dipole-dipole coupling. This study shows that plasmonics enables the opposite transfer direction, transferring the plasmonic energy towards the short-wavelength direction to induce charge separation in a semiconductor. Plasmon-induced resonance energy transfer (PIRET) differs from FRET because of the lack of a Stoke's shift, non-local absorption effects and a strong dependence on the plasmon's dephasing rate and dipole moment. PIRET non-radiatively transfers energy through an insulating spacer layer, which prevents interfacial charge recombination losses and dephasing of the plasmon from hot-electron transfer. The distance dependence of dipole-dipole coupling is mapped out for a range of detuning across the plasmon resonance. PIRET can efficiently harvest visible and near-infrared sunlight with energy below the semiconductor band edge to help overcome the constraints of band-edge energetics for single semiconductors in photoelectrochemical cells, photocatalysts and photovoltaics.

  10. Resonant vibrational energy transfer in ice Ih

    SciTech Connect

    Shi, L.; Li, F.; Skinner, J. L.

    2014-06-28

    Fascinating anisotropy decay experiments have recently been performed on H{sub 2}O ice Ih by Timmer and Bakker [R. L. A. Timmer, and H. J. Bakker, J. Phys. Chem. A 114, 4148 (2010)]. The very fast decay (on the order of 100 fs) is indicative of resonant energy transfer between OH stretches on different molecules. Isotope dilution experiments with deuterium show a dramatic dependence on the hydrogen mole fraction, which confirms the energy transfer picture. Timmer and Bakker have interpreted the experiments with a Förster incoherent hopping model, finding that energy transfer within the first solvation shell dominates the relaxation process. We have developed a microscopic theory of vibrational spectroscopy of water and ice, and herein we use this theory to calculate the anisotropy decay in ice as a function of hydrogen mole fraction. We obtain very good agreement with experiment. Interpretation of our results shows that four nearest-neighbor acceptors dominate the energy transfer, and that while the incoherent hopping picture is qualitatively correct, vibrational energy transport is partially coherent on the relevant timescale.

  11. Low-energy ballistic lunar transfers

    NASA Astrophysics Data System (ADS)

    Parker, Jeffrey S.

    A systematic method is developed that uses dynamical systems theory to model, analyze, and construct low-energy ballistic lunar transfers (BLTs). It has been found that low-energy BLTs may be produced by intersecting the stable manifold of an unstable Earth-Moon three-body orbit with the Earth. A spacecraft following such a trajectory is only required to perform a single maneuver, namely, the Trans-Lunar Injection maneuver, in order to complete the transfer. After the Trans-Lunar Injection maneuver, the spacecraft follows an entirely ballistic trajectory that asymptotically approaches and arrives at the target lunar three-body orbit. Because these orbit transfers require no orbit insertion maneuver at the three-body orbit, the transfers may be used to send spacecraft 25--40% more massive than spacecraft sent to the same orbits via conventional, direct transfers. From the targeted three-body orbits, the spacecraft may transfer to nearly any region within the Earth-Moon system, including any location on the surface of the Moon. The systematic methods developed in this research allow low-energy BLTs to be characterized by six parameters. It has been found that BLTs exist in families, where a family of BLTs consists of transfers whose parameters vary in a continuous fashion from one end of the family to the other. The families are easily identified and studied using a BLT State Space Map (BLT Map). The present research studies BLT Maps and has surveyed a wide variety of BLTs that exist in the observed families. It has been found that many types of BLTs may be constructed between 185-km low Earth parking orbits and lunar three-body orbits that require less than 3.27 km/s and fewer than 120 days of transfer time. Under certain conditions, BLTs may be constructed that require less than 3.2 km/s and fewer than 100 days of transfer time. It has been found that BLTs may implement LEO parking orbits with nearly any combination of altitude and inclination; they may depart from

  12. Angular momentum conservation in dipolar energy transfer.

    PubMed

    Guo, Dong; Knight, Troy E; McCusker, James K

    2011-12-23

    Conservation of angular momentum is a familiar tenet in science but has seldom been invoked to understand (or predict) chemical processes. We have developed a general formalism based on Wigner's original ideas concerning angular momentum conservation to interpret the photo-induced reactivity of two molecular donor-acceptor assemblies with physical properties synthetically tailored to facilitate intramolecular energy transfer. Steady-state and time-resolved spectroscopic data establishing excited-state energy transfer from a rhenium(I)-based charge-transfer state to a chromium(III) acceptor can be fully accounted for by Förster theory, whereas the corresponding cobalt(III) adduct does not undergo an analogous reaction despite having a larger cross-section for dipolar coupling. Because this pronounced difference in reactivity is easily explained within the context of the angular momentum conservation model, this relatively simple construct may provide a means for systematizing a broad range of chemical reactions. PMID:22194572

  13. Energy Efficient Storage and Transfer of Cryogens

    NASA Technical Reports Server (NTRS)

    Fesmire, James E.

    2013-01-01

    Cryogenics is globally linked to energy generation, storage, and usage. Thermal insulation systems research and development is an enabling part of NASA's technology goals for Space Launch and Exploration. New thermal testing methodologies and materials are being transferred to industry for a wide range of commercial applications.

  14. Energy transfer of nucleic acid products

    NASA Astrophysics Data System (ADS)

    Jung, Paul M.; Hu, Hsiang-Yun; Khalil, Omar S.

    1995-04-01

    Fluorescence energy transfer was investigated as a homogeneous detection method for the gapped ligase chain reaction (G-LCR). Oligonucleotides of a Chlamydia trachomatic G-LCR probe set were labeled with fluorescein as the donor and Texas Red as the acceptor fluorophore. Amplification and detection of 10 molecules of synthetic target was demonstrated in spiked urine samples.

  15. Effect of polymer additives on hydrodynamics and oxygen transfer in a bubble column bioreactor.

    PubMed

    Kawase, Y

    1993-01-01

    The influence of polymer additives (polyethylene oxide and polyacrylamide) on the hydrodynamics and oxygen transfer in a bubble column bioreactor was examined. The addition of small amounts of these polymers has been known to cause significant drag reduction in turbulent flow circumstances. The gas hold-up was slightly decreased and the liquid-phase mixing was somewhat enhanced due to the addition of the polymers. The addition of polymer additives brought about a reduction of the volumetric oxygen transfer coefficient by about 40%. In dilute polymer solutions, large bubbles formed by bubble coalescence moved with high rise velocities in the presence of many small bubbles and the bubble size distributions were less uniform compared with those in water. The complicated changes in bubble hydrodynamic characteristics were examined to give possible explanations for oxygen transfer reduction. PMID:7763940

  16. Can an energy balance model provide additional constraints on how to close the energy imbalance?

    PubMed

    Wohlfahrt, Georg; Widmoser, Peter

    2013-02-15

    Elucidating the causes for the energy imbalance, i.e. the phenomenon that eddy covariance latent and sensible heat fluxes fall short of available energy, is an outstanding problem in micrometeorology. This paper tests the hypothesis that the full energy balance, through incorporation of additional independent measurements which determine the driving forces of and resistances to energy transfer, provides further insights into the causes of the energy imbalance and additional constraints on energy balance closure options. Eddy covariance and auxiliary data from three different biomes were used to test five contrasting closure scenarios. The main result of our study is that except for nighttime, when fluxes were low and noisy, the full energy balance generally did not contain enough information to allow further insights into the causes of the imbalance and to constrain energy balance closure options. Up to four out of the five tested closure scenarios performed similarly and in up to 53% of all cases all of the tested closure scenarios resulted in plausible energy balance values. Our approach may though provide a sensible consistency check for eddy covariance energy flux measurements. PMID:24465072

  17. Risk transfer via energy savings insurance

    SciTech Connect

    Mills, Evan

    2001-10-01

    Among the key barriers to investment in energy efficiency improvements are uncertainties about attaining projected energy savings and apprehension about potential disputes over these savings. The fields of energy management and risk management are thus intertwined. While many technical methods have emerged to manage performance risks (e.g. building commissioning), financial risk transfer techniques are less developed in the energy management arena than in other more mature segments of the economy. Energy Savings Insurance (ESI) - formal insurance of predicted energy savings - is one method of transferring financial risks away from the facility owner or energy services contractor. ESI offers a number of significant advantages over other forms of financial risk transfer, e.g. savings guarantees or performance bonds. ESI providers manage risk via pre-construction design review as well as post-construction commissioning and measurement and verification of savings. We found that the two mos t common criticisms of ESI - excessive pricing and onerous exclusions - are not born out in practice. In fact, if properly applied, ESI can potentially reduce the net cost of energy savings projects by reducing the interest rates charged by lenders, and by increasing the level of savings through quality control. Debt service can also be ensured by matching loan payments to projected energy savings while designing the insurance mechanism so that payments are made by the insurer in the event of a savings shortfall. We estimate the U.S. ESI market potential of $875 million/year in premium income. From an energy-policy perspective, ESI offers a number of potential benefits: ESI transfers performance risk from the balance sheet of the entity implementing the energy savings project, thereby freeing up capital otherwise needed to ''self-insure'' the savings. ESI reduces barriers to market entry of smaller energy services firms who do not have sufficiently strong balance sheets to self

  18. Heat transfer characteristics for some coolant additives used for water cooled engines

    SciTech Connect

    Abou-Ziyan, H.Z.; Helali, A.H.B.

    1996-12-31

    Engine coolants contain certain additives to prevent engine overheating or coolant freezing in cold environments. Coolants, also, contain corrosion and rust inhibitors, among other additives. As most engines are using engine cooling solutions, it is of interest to evaluate the effect of engine coolants on the boiling heat transfer coefficient. This has its direct impact on radiator size and environment. This paper describes the apparatus and the measurement techniques. Also, it presents the obtained boiling heat transfer results at different parameters. Three types of engine coolants and their mixtures in distilled water are evaluated, under sub-cooled and saturated boiling conditions. A profound effect of the presence of additives in the coolant, on heat transfer, was clear since changes of heat transfer for different coolants were likely to occur. The results showed that up to 180% improvement of boiling heat transfer coefficient is experienced with some types of coolants. However, at certain concentrations other coolants provide deterioration or not enhancement in the boiling heat transfer characteristics. This investigation proved that there are limitations, which are to be taken into consideration, for the composition of engine coolants in different environments. In warm climates, ethylene glycol should be kept at the minimum concentration required for dissolving other components, whereas borax is beneficial to the enhancement of the heat transfer characteristics.

  19. Light Increases Energy Transfer Efficiency in a Boreal Stream

    PubMed Central

    Lesutienė, Jūratė; Gorokhova, Elena; Stankevičienė, Daiva; Bergman, Eva; Greenberg, Larry

    2014-01-01

    Periphyton communities of a boreal stream were exposed to different light and nutrient levels to estimate energy transfer efficiency from primary to secondary producers using labeling with inorganic 13C. In a one-day field experiment, periphyton grown in fast-flow conditions and dominated by opportunistic green algae were exposed to light levels corresponding to sub-saturating (forest shade) and saturating (open stream section) irradiances, and to N and P nutrient additions. In a two-week laboratory experiment, periphyton grown in low-flow conditions and dominated by slowly growing diatoms were incubated under two sub-saturating light and nutrient enrichment levels as well as grazed and non-grazed conditions. Light had significant positive effect on 13C uptake by periphyton. In the field experiment, P addition had a positive effect on 13C uptake but only at sub-saturating light levels, whereas in the laboratory experiment nutrient additions had no effect on the periphyton biomass, 13C uptake, biovolume and community composition. In the laboratory experiment, the grazer (caddisfly) effect on periphyton biomass specific 13C uptake and nutrient content was much stronger than the effects of light and nutrients. In particular, grazers significantly reduced periphyton biomass and increased biomass specific 13C uptake and C:nutrient ratios. The energy transfer efficiency, estimated as a ratio between 13C uptake by caddisfly and periphyton, was positively affected by light conditions, whereas the nutrient effect was not significant. We suggest that the observed effects on energy transfer were related to the increased diet contribution of highly palatable green algae, stimulated by higher light levels. Also, high heterotrophic microbial activity under low light levels would facilitate energy loss through respiration and decrease overall trophic transfer efficiency. These findings suggest that even a small increase in light intensity could result in community-wide effects on

  20. Collisional energy transfer in highly excited molecules.

    PubMed

    Houston, Paul L; Conte, Riccardo; Bowman, Joel M

    2014-09-11

    The excitation/de-excitation step in the Lindemann mechanism is investigated in detail using model development and classical trajectory studies based on a realistic potential energy surface. The model, based on a soft-sphere/line-of-centers approach and using elements of Landau-Teller theory and phase space theory, correctly predicts most aspects of the joint probability distribution P(ΔE,ΔJ) for the collisional excitation and de-excitation process in the argon-allyl system. The classical trajectories both confirm the validity of the model and provide insight into the energy transfer. The potential employed was based on a previously available ab initio intramolecular potential for the allyl fit to 97418 allyl electronic energies and an intermolecular potential fit to 286 Ar-allyl energies. Intramolecular energies were calculated at the CCSD(T)/AVTZ level of theory, while intermolecular energies were calculated at the MP2/AVTZ level of theory. Trajectories were calculated for each of four starting allyl isomers and for an initial rotational level of Ji = 0 as well as for Ji taken from a microcanonical distribution. Despite a dissimilarity in Ar-allyl potentials for fixed Ar-allyl geometries, energy transfer properties starting from four different isomers were found to be remarkably alike. A contributing factor appears to be that the orientation-averaged potentials are almost identical. The model we have developed suggests that most hydrocarbons should have similar energy transfer properties, scaled by differences in the potential offset of the atom-hydrogen interaction. Available data corroborate this suggestion. PMID:25116732

  1. Micro-Plasma Transferred Arc Additive Manufacturing for Die and Mold Surface Remanufacturing

    NASA Astrophysics Data System (ADS)

    Jhavar, Suyog; Paul, Christ Prakash; Jain, Neelesh Kumar

    2016-07-01

    Micro-plasma transferred arc ( µPTA) additive manufacturing is one of the newest options for remanufacturing of dies and molds surfaces in the near-millimeter range leading to extended usage of the same. We deployed an automatic micro-plasma deposition setup to deposit a wire of 300 µm of AISI P20 tool steel on the substrate of same material for the potential application in remanufacturing of the die and mold surface. Our present research effort is to establish µPTA additive manufacturing as a viable economical and cleaner methodology for potential industrial applications. We undertook the optimization of single weld bead geometry as the first step in our present study. Bead-on-plate trials were conducted to deposit single bead geometry at various processing parameters. The bead geometry (shape and size) and dilution were measured and the parametric dependence was derived. A set of parameters leading to reproducible regular and smooth single bead geometry were identified and used to prepare a thin wall for mechanical testing. The deposits were subjected to material characterization such as microscopic studies, micro-hardness measurements and tensile testing. The process was compared qualitatively with other deposition processes involving high-energy density beams and was found to be advantageous in terms of low initial and running costs with comparable properties. The outcome of the study confirmed the process capability of µPTA deposition leading to deployment of cost-effective and environmentally friendlier technology for die and mold remanufacturing.

  2. Micro-Plasma Transferred Arc Additive Manufacturing for Die and Mold Surface Remanufacturing

    NASA Astrophysics Data System (ADS)

    Jhavar, Suyog; Paul, Christ Prakash; Jain, Neelesh Kumar

    2016-05-01

    Micro-plasma transferred arc (µPTA) additive manufacturing is one of the newest options for remanufacturing of dies and molds surfaces in the near-millimeter range leading to extended usage of the same. We deployed an automatic micro-plasma deposition setup to deposit a wire of 300 µm of AISI P20 tool steel on the substrate of same material for the potential application in remanufacturing of the die and mold surface. Our present research effort is to establish µPTA additive manufacturing as a viable economical and cleaner methodology for potential industrial applications. We undertook the optimization of single weld bead geometry as the first step in our present study. Bead-on-plate trials were conducted to deposit single bead geometry at various processing parameters. The bead geometry (shape and size) and dilution were measured and the parametric dependence was derived. A set of parameters leading to reproducible regular and smooth single bead geometry were identified and used to prepare a thin wall for mechanical testing. The deposits were subjected to material characterization such as microscopic studies, micro-hardness measurements and tensile testing. The process was compared qualitatively with other deposition processes involving high-energy density beams and was found to be advantageous in terms of low initial and running costs with comparable properties. The outcome of the study confirmed the process capability of µPTA deposition leading to deployment of cost-effective and environmentally friendlier technology for die and mold remanufacturing.

  3. Wireless Energy Transfer Through Magnetic Reluctance Coupling

    NASA Astrophysics Data System (ADS)

    Pillatsch, P.

    2014-11-01

    Energy harvesting from human motion for body worn or implanted devices faces the problem of the wearer being still, e.g. while asleep. Especially for medical devices this can become an issue if a patient is bed-bound for prolonged periods of time and the internal battery of a harvesting system is not recharged. This article introduces a mechanism for wireless energy transfer based on a previously presented energy harvesting device. The internal rotor of the energy harvester is made of mild steel and can be actuated through a magnetic reluctance coupling to an external motor. The internal piezoelectric transducer is consequently actuated and generates electricity. This paper successfully demonstrates energy transfer over a distance of 16 mm in air and an achieved power output of 85 μW at 25 Hz. The device functional volume is 1.85 cm3. Furthermore, it was demonstrated that increasing the driving frequency beyond 25 Hz did not yield a further increase in power output. Future research will focus on improving the reluctance coupling, e.g. by investigating the use of multiple or stronger magnets, in order to increase transmission distance.

  4. Addition Laws for Intensities of Radiation Emerging from Scattering Atmospheres Containing Energy Sources

    NASA Astrophysics Data System (ADS)

    Nikoghossian, A. G.; Kapanadze, N. G.

    2016-03-01

    A group theoretical approach is developed for solving astrophysical radiative transfer problems described in a previous series of papers. Addition laws for observed radiative intensities are derived for the case in which atmospheres not only absorb and scatter radiation incident on them, but radiate themselves because of energy sources contained within them. As an illustration of the application of these laws, several special radiative transfer problems which we believe are of practical interest are discussed.

  5. Investigation of Vibrational Energy Transfer in Connected Structures

    NASA Technical Reports Server (NTRS)

    Hwang, C.; Pi, W. S.

    1973-01-01

    The results are reported of an analytical and experimental investigation on the vibrational energy transfer between connected substructures under random excitation. In the analytical area, the basic foundation and assumptions of the statistical energy analysis (SEA) method, a major tool in random response analysis of structures, were examined and reviewed. A new SEA formulation based on the strong coupling condition of the substructures was carried out and presented. Also presented were the results of vibration energy transfer study based on the wave equations applied to connected structures. In the experimental phase, three simple structural models were fabricated and tested. Additional tests were performed on selected substructures which formed parts of the test models. The test results were presented and evaluated against the analytical data.

  6. Linear energy transfer spectrum measurement experiment (P0006)

    SciTech Connect

    Benton, E.V.; Parnell, T.A.

    1984-02-01

    The linear energy transfer (LET) is the energy deposited per unit path length of charged particle traversing matter. For estimating the rate of damage from single-hit phenomena, the quantity that best combines the radiation environment, orbital situation, and spacecraft shielding is the linear energy transfer (LET) spectrum at the device location. This experiment will measure the LET spectrum behind different shielding configurations for approxmately 1 year. The shielding will be increased in increments of approximately 1 G/sq cm up to a maximum shieldng of 16 G/sq cm. In addition to providing critical information to future spacecraft designers, these measurements will also provide data that will be extremely valuable to other experiments on LDEF.

  7. Linear energy transfer spectrum measurement experiment (P0006)

    NASA Technical Reports Server (NTRS)

    Benton, E. V.; Parnell, T. A.

    1984-01-01

    The linear energy transfer (LET) is the energy deposited per unit path length of charged particle traversing matter. For estimating the rate of damage from single-hit phenomena, the quantity that best combines the radiation environment, orbital situation, and spacecraft shielding is the linear energy transfer (LET) spectrum at the device location. This experiment will measure the LET spectrum behind different shielding configurations for approximately 1 year. The shielding will be increased in increments of approximately 1 G/sq cm up to a maximum shieldng of 16 G/sq cm. In addition to providing critical information to future spacecraft designers, these measurements will also provide data that will be extremely valuable to other experiments on LDEF.

  8. Intramolecular energy transfer in fullerene pyrazine dyads

    SciTech Connect

    Guldi, D.M.; Torres-Garcia, G.; Mattay, J.

    1998-11-26

    Excited-state properties of three different pyrazine derivatives 4--6 were probed by emission and transient absorption spectroscopy. They display emission maxima at 464 (4), 417 (5), and 515 nm (6) that are red-shifted with respect to their strong UV ground-state absorption and formed with overall quantum yields ({Phi}) of 0.156, 0.22, and 0.13, respectively. Once photoexcited, these triplet excited pyrazines undergo rapid intermolecular energy transfer to a monofunctionalized fullerene derivative (7) with bimolecular rate constants ranging from 3.64 {times} 10{sup 9} M{sup {minus}1} s{sup {minus}1} (6) to 1.1 {times} 10{sup 10} M{sup {minus}1} s{sup {minus}1} (4). The product of these bimolecular energy-transfer reactions is in all cases the fullerene triplet excited state. Functionalization of pristine C{sub 60} with the investigated pyrazine derivatives promotes the UV-vis absorption characteristics and, in turn, improves the light-harvesting efficiency of the resulting dyads 1--3 relative to pristine C{sub 60}. Photoexcitation of the pyrazine moieties in dyads 1--3 leads to the formation of their singlet excited states. In contrast to the pyrazine models, photoexcitation of dyad 1--3 is followed by rapid intramolecular deactivation processes of the latter via energy transfer to the fullerene ground state with half-lives between 37 and 100 ps. In turn, energy transfer transforms the short-lived and moderately redox-active singlet excited states of pyrazine into the highly reactive fullerene triplet excited state. The latter is found to produce effectively singlet oxygen ({sup 1}O{sub 2}) with quenching rate constants for 1--3 of (1--1.5) {times} 10{sup 9} M{sup {minus}1} s{sup {minus}1}. Similarly, reductive quenching of the triplet excited states in dyads 1--3 via electron transfer with diazabicyclooctane (DABCO) occurs with rate constants of 5.2--9.4 {times} 10{sup 7} M{sup {minus}1} s{sup {minus}1}.

  9. Metal Linkage Effects on Ultrafast Energy Transfer.

    PubMed

    Dekkiche, Hervé; Buisson, Antoine; Langlois, Adam; Karsenti, Paul-Ludovic; Ruhlmann, Laurent; Ruppert, Romain; Harvey, Pierre

    2016-07-18

    We report the preparation of several new porphyrin homodimers bridged by a platinum(II) ion in which very intense electronic communication through the coordination link occurs. Moreover, the synthesis of a new porphyrin dyad and its photophysical properties are reported. This dyad exhibits the fastest singlet energy transfer ever reported for synthetic systems between a zinc(II) porphyrin and a porphyrin free base. This extremely fast transfer (∼100 femtoseconds) is in the same range as the fastest one measured in natural systems. This feature is due to the platinum(II) linker, which allows for strong MO couplings between the two porphyrin units as experimentally supported by electrochemistry and corroborated by DFT computations. PMID:27333487

  10. Local energy transfer in hybrid nanoplasmonics

    NASA Astrophysics Data System (ADS)

    Bachelot, Renaud; Zhou, Xuan; Plain, Jérome; Adam, Pierre-Michel; Baudrion, Anne-Laure; Gray, Stephen K.; Wiederrecht, Gary P.

    2014-05-01

    Incorporating resonant optical properties of metal nanostructures into nanoscale applications such as ultrahigh density storage devices, nanoelectronics, and nanophotonics has gained considerable interest within the last years. Recent advances in hybrid and molecular plasmonics are presented. The approach relies on near-field energy transfer between metal nanoparticles and other molecular material, and is not diffraction-limited. We will see that optical nanosources supported by metal nanoparticles can be used for controlling/triggering photochemical and photo physical processes involving photons, charges and motion transfers at the nanoscale. In particular, three examples will be presented and commented: free radical photopolymerization, photo isomerization and nanoscale strong coupling. These examples open new routes including optical near-field photography of ultra confined fields, mode hybridizing in single nanoparticles, molecular optical nanomotors, and new anisotropic nanoemitters.

  11. Air Storage System Energy Transfer (ASSET) plants

    NASA Astrophysics Data System (ADS)

    Stys, Z. S.

    1983-09-01

    The design features and performance capabilities of Air Storage System Energy Transfer (ASSET) plants for transferring off-peak utility electricity to on-peak hours are described. The plant operations involve compressing ambient air with an axial flow compressor and depositing it in an underground reservoir at 70 bar pressure. Released during a peaking cycle, the pressure is reduced to 43 bar, the air is heated to 550 C, passed through an expander after a turbine, and passed through a low pressure combustion chamber to be heated to 850 C. A West German plant built in 1978 to supply over 300 MW continuous power for up to two hours is detailed, noting its availability factor of nearly 98 percent and power delivery cost of $230/kW installed. A plant being constructed in Illinois will use limestone caverns as the air storage tank.

  12. Chill water additive controls transfer of Salmonella and Campylobacter by improved chlorine efficacy

    Technology Transfer Automated Retrieval System (TEKTRAN)

    In earlier work, we showed that a proprietary additive (T-128) maintains chlorine activity in the presence of organic material such as broiler parts. T-128 improves the efficacy of chlorine to control transfer of Campylobacter and Salmonella from inoculated wings to un-inoculated wings during immer...

  13. 27 CFR 479.83 - Transfer tax in addition to import duty.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 3 2011-04-01 2010-04-01 true Transfer tax in addition to import duty. 479.83 Section 479.83 Alcohol, Tobacco Products, and Firearms BUREAU OF ALCOHOL, TOBACCO, FIREARMS, AND EXPLOSIVES, DEPARTMENT OF JUSTICE FIREARMS AND AMMUNITION MACHINE GUNS, DESTRUCTIVE...

  14. 27 CFR 479.83 - Transfer tax in addition to import duty.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 3 2013-04-01 2013-04-01 false Transfer tax in addition to import duty. 479.83 Section 479.83 Alcohol, Tobacco Products, and Firearms BUREAU OF ALCOHOL, TOBACCO, FIREARMS, AND EXPLOSIVES, DEPARTMENT OF JUSTICE FIREARMS AND AMMUNITION MACHINE GUNS,...

  15. 27 CFR 479.83 - Transfer tax in addition to import duty.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 3 2010-04-01 2010-04-01 false Transfer tax in addition to import duty. 479.83 Section 479.83 Alcohol, Tobacco Products, and Firearms BUREAU OF ALCOHOL, TOBACCO, FIREARMS, AND EXPLOSIVES, DEPARTMENT OF JUSTICE FIREARMS AND AMMUNITION MACHINE GUNS,...

  16. 27 CFR 479.83 - Transfer tax in addition to import duty.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 3 2014-04-01 2014-04-01 false Transfer tax in addition to import duty. 479.83 Section 479.83 Alcohol, Tobacco Products, and Firearms BUREAU OF ALCOHOL, TOBACCO, FIREARMS, AND EXPLOSIVES, DEPARTMENT OF JUSTICE FIREARMS AND AMMUNITION MACHINE GUNS,...

  17. 27 CFR 479.83 - Transfer tax in addition to import duty.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 3 2012-04-01 2010-04-01 true Transfer tax in addition to import duty. 479.83 Section 479.83 Alcohol, Tobacco Products, and Firearms BUREAU OF ALCOHOL, TOBACCO, FIREARMS, AND EXPLOSIVES, DEPARTMENT OF JUSTICE FIREARMS AND AMMUNITION MACHINE GUNS, DESTRUCTIVE...

  18. Low-Energy Ballistic Transfers to Lunar Halo Orbits

    NASA Technical Reports Server (NTRS)

    Parker, Jeffrey S.

    2009-01-01

    Recent lunar missions have begun to take advantage of the benefits of low-energy ballistic transfers between the Earth and the Moon rather than implementing conventional Hohmann-like lunar transfers. Both Artemis and GRAIL plan to implement low-energy lunar transfers in the next few years. This paper explores the characteristics and potential applications of many different families of low-energy ballistic lunar transfers. The transfers presented here begin from a wide variety of different orbits at the Earth and follow several different distinct pathways to the Moon. This paper characterizes these pathways to identify desirable low-energy lunar transfers for future lunar missions.

  19. Nanoparticles for heat transfer and thermal energy storage

    DOEpatents

    Singh, Dileep; Cingarapu, Sreeram; Timofeeva, Elena V.; Moravek, Michael

    2015-07-14

    An article of manufacture and method of preparation thereof. The article of manufacture and method of making the article includes an eutectic salt solution suspensions and a plurality of nanocrystalline phase change material particles having a coating disposed thereon and the particles capable of undergoing the phase change which provides increase in thermal energy storage. In addition, other articles of manufacture can include a nanofluid additive comprised of nanometer-sized particles consisting of copper decorated graphene particles that provide advanced thermal conductivity to heat transfer fluids.

  20. Outcome following addition of peroneus brevis tendon transfer to treatment of acquired posterior tibial tendon insufficiency.

    PubMed

    Song, S J; Deland, J T

    2001-04-01

    The flexor digitorum longus, the tendon most often used for transfer in posterior tibial tendon insufficiency, is one-half to one-third the size of the posterior tibial tendon. Occasionally it may be particularly small or may have been previously used for transfer. In these cases, the senior author has felt that the addition of a transfer of the Peroneus Brevis (PBr) tendon may be helpful in maintaining sufficient tendon and muscle mass to rebalance the foot. Thirteen patients who underwent this procedure were retrospectively identified and matched by age and length of follow-up to patients who underwent a more standard tendon transfer operation minus the addition of the PBr transfer. Pain and functional status were then assessed by the American Orthopaedic Foot and Ankle Society's ankle/hindfoot rating scale. Each patient was tested by an independent physical therapist to evaluate inversion and eversion strength. The mean duration of follow-up was 20.6 months (12 to 34 months). The average AOFAS score of the PBr group was 75.8 compared to 71.5 for the standard control group. There was no significant difference between the groups when inversion or eversion strengths were compared. Inversion strength and eversion strength was rated good or excellent (4 or 5) in 12 out of 13 of the PBr transfer group patients. No major complications were encountered in either group. Although it does not increase inversion strength, a PBr transfer can be used to augment a small FDL without causing significant eversion weakness. This can be useful when the FDL is particularly small or in revision surgery. PMID:11354442

  1. Energy Transfer in the Earth-Sun System

    NASA Astrophysics Data System (ADS)

    Lui, A. T. Y.; Kamide, Y.

    2007-02-01

    Conference on Earth-Sun System Exploration: Energy Transfer; Kailua-Kona, Hawaii, USA, 16-20 January 2006; The goal of this conference, which was supported by several agencies and organizations, was to provide a forum for physicists engaged in the Earth-Sun system as well as in laboratory experiments to discuss and exchange knowledge and ideas on physical processes involving energy transfer. The motivation of the conference stemmed from the following realization: Space assets form an important fabric of our society, performing functions such as television broadcasting, cell- phone communication, navigation, and remote monitoring of tropospheric weather. There is increasing awareness of how much our daily activities can be adversely affected by space disturbances stretching all the way back to the Sun. In some of these energetic phenomena, energy in various forms can propagate long distances from the solar surface to the interplanetary medium and eventually to the Earth's immediate space environment, namely, its magnetosphere, ionosphere, and thermosphere. In addition, transformation of energy can take place in these space disturbances, allowing charged-particle energy to be transformed to electromagnetic energy or vice versa. In- depth understanding of energy transformation and transmission in the Earth-Sun system will foster the identification of physical processes responsible for space disturbances and the prediction of their occurrences and effects. Participants came from 15 countries.

  2. Additives

    NASA Technical Reports Server (NTRS)

    Smalheer, C. V.

    1973-01-01

    The chemistry of lubricant additives is discussed to show what the additives are chemically and what functions they perform in the lubrication of various kinds of equipment. Current theories regarding the mode of action of lubricant additives are presented. The additive groups discussed include the following: (1) detergents and dispersants, (2) corrosion inhibitors, (3) antioxidants, (4) viscosity index improvers, (5) pour point depressants, and (6) antifouling agents.

  3. Photon Upconversion Through Tb(3+) -Mediated Interfacial Energy Transfer.

    PubMed

    Zhou, Bo; Yang, Weifeng; Han, Sanyang; Sun, Qiang; Liu, Xiaogang

    2015-10-28

    A strategy of interfacial energy transfer upconversion is demonstrated through the use of a terbium (Tb(3+) ) dopant as energy donor or energy migrator in core-shell-structured nanocrystals. This mechanistic investigation presents a new pathway for photon upconversion, and, more importantly, contributes to the better control of energy transfer at the nanometer length scale. PMID:26378771

  4. Photoinduced Energy Transfer in Artificial Photosynthetic Systems

    NASA Astrophysics Data System (ADS)

    Imahori, H.; Umeyama, T.

    Artificial photosynthesis is a current topic of intensive investigations, both in order to understand the reactions that play a central role in natural photosynthesis as well as to develop highly efficient solar energy conversion systems and molecular optoelectronic devices [1-34]. Artificial photosynthesis is defined as a research field that attempts to mimic the natural process of photosynthesis. Therefore, the outline of natural photosynthesis is described briefly for the better understanding of artificial photosynthesis . Natural photosynthetic system is regarded as one of the most elaborate nanobiological machines [35,36]. It converts solar energy into electrochemical potential or chemical energy, which is prerequisite for the living organisms on the earth. The core function of photosynthesis is a cascade of photoinduced energy and electron transfer between donors and acceptors in the antenna complexes and the reaction center. For instance, in purple photosynthetic bacteria (Rhodopseudomonas acidophila and Rhodopseudomonas palustris) there are two different types of antenna complexes: a core light-harvesting antenna (LH1) and peripheral light-harvesting antenna (LH2) [37-39]. LH1 surrounds the reaction center where charge separation takes place.

  5. Energy transfer in stably stratified turbulence

    NASA Astrophysics Data System (ADS)

    Kimura, Yoshifumi; Herring, Jackson

    2015-11-01

    Energy transfer in forced stable stratified turbulence is investigated using pseudo-spectral DNS of the Navier-Stokes equations under the Boussinesq approximation with 10243 grid points. Making use of the Craya-Herring decomposition, the velocity field is decomposed into vortex (Φ1) and wave (Φ2) modes. To understand the anisotropy of stably stratified turbulence, the energy flues in terms of the spherical, the horizontal and the vertical wave numbers, are investigated for the total kinetic, Φ1, Φ2 energies, respectively. Among the three fluxes, the spherical and the horizontal look similar for strong stratification, and Φ1 flux shows a wave number region of constant value, which implies Kolmogorov's inertial range. The corresponding spectral power are, however, k - 5 / 2 for the spherical and k⊥- 5 / 3 for the horizontal cases. In contrast to these, the vertical energy fluxes show completely different features. We have observed the saturation spectrum E (kz) ~ CN2kz-3 for strong stratification as before, but the mechanism to produce this spectrum seems different from the Kolmogorov picture.

  6. Enhancing radiative energy transfer through thermal extraction

    NASA Astrophysics Data System (ADS)

    Tan, Yixuan; Liu, Baoan; Shen, Sheng; Yu, Zongfu

    2016-06-01

    Thermal radiation plays an increasingly important role in many emerging energy technologies, such as thermophotovoltaics, passive radiative cooling and wearable cooling clothes [1]. One of the fundamental constraints in thermal radiation is the Stefan-Boltzmann law, which limits the maximum power of far-field radiation to P0 = σT4S, where σ is the Boltzmann constant, S and T are the area and the temperature of the emitter, respectively (Fig. 1a). In order to overcome this limit, it has been shown that near-field radiations could have an energy density that is orders of magnitude greater than the Stefan-Boltzmann law [2-7]. Unfortunately, such near-field radiation transfer is spatially confined and cannot carry radiative heat to the far field. Recently, a new concept of thermal extraction was proposed [8] to enhance far-field thermal emission, which, conceptually, operates on a principle similar to oil immersion lenses and light extraction in light-emitting diodes using solid immersion lens to increase light output [62].Thermal extraction allows a blackbody to radiate more energy to the far field than the apparent limit of the Stefan-Boltzmann law without breaking the second law of thermodynamics. Thermal extraction works by using a specially designed thermal extractor to convert and guide the near-field energy to the far field, as shown in Fig. 1b. The same blackbody as shown in Fig. 1a is placed closely below the thermal extractor with a spacing smaller than the thermal wavelength. The near-field coupling transfers radiative energy with a density greater than σT4. The thermal extractor, made from transparent and high-index or structured materials, does not emit or absorb any radiation. It transforms the near-field energy and sends it toward the far field. As a result, the total amount of far-field radiative heat dissipated by the same blackbody is greatly enhanced above SσT4, where S is the area of the emitter. This paper will review the progress in thermal

  7. Extended emission wavelength of random dye lasers by exploiting radiative and non-radiative energy transfer

    NASA Astrophysics Data System (ADS)

    Wan Ismail, Wan Zakiah; Goldys, Ewa M.; Dawes, Judith M.

    2016-02-01

    We demonstrate long-wavelength operation (>700 nm) of random dye lasers (using a methylene blue dye) with the addition of rhodamine 6G and titania, enabled by radiative and non-radiative energy transfer. The pump energy is efficiently absorbed and transferred to the acceptors, to support lasing in random dye lasers in the near infrared. The optimum random laser performance with the highest emission intensity and the lowest lasing threshold was achieved for a concentration of methylene blue as the acceptor equal to 6× the concentration of rhodamine 6G (donor). Excessive levels of methylene blue increased the lasing threshold and broadened the methylene blue emission linewidth due to dye quenching from re-absorption. This is due to competition between the donor emission and energy transfer and between absorption loss and fluorescence quenching. The radiative and non-radiative energy transfer is analyzed as a function of the acceptor concentration and pump energy density, with consideration of the spectral overlap. The dependence of the radiative and non-radiative transfer efficiency on the acceptor concentration is obtained, and the energy transfer parameters, including the radiative and non-radiative energy transfer rate constants ( K R and K NR), are investigated using Stern-Volmer analysis. The analysis indicates that radiative energy transfer is the dominant energy transfer mechanism in this system.

  8. Energy transfer in isotropic turbulence at low Reynolds numbers

    NASA Technical Reports Server (NTRS)

    Domaradzki, J. A.; Rogallo, R. S.

    1988-01-01

    Detailed measurements were made of energy transfer among the scales of motion in incompressible turbulent fields at low Reynolds numbers generated by direct numerical simulation. It was observed that although the transfer resulted from triad interactions that were non-local in k space, the energy always transferred locally. The results are consistent with the notion of non-uniform advection of small weak eddies by larger and stronger ones, similar to transfer processes in the far dissipation range at high Reynolds numbers.

  9. Infrared radiative energy transfer in gaseous systems

    NASA Technical Reports Server (NTRS)

    Tiwari, Surendra N.

    1991-01-01

    Analyses and numerical procedures are presented to investigate the radiative interactions in various energy transfer processes in gaseous systems. Both gray and non-gray radiative formulations for absorption and emission by molecular gases are presented. The gray gas formulations are based on the Planck mean absorption coefficient and the non-gray formulations are based on the wide band model correlations for molecular absorption. Various relations for the radiative flux and divergence of radiative flux are developed. These are useful for different flow conditions and physical problems. Specific plans for obtaining extensive results for different cases are presented. The procedure developed was applied to several realistic problems. Results of selected studies are presented.

  10. Anisotropic energy transfers in quasi-static magnetohydrodynamic turbulence

    SciTech Connect

    Reddy, K. Sandeep; Kumar, Raghwendra; Verma, Mahendra K.

    2014-10-15

    We perform direct numerical simulations of quasi-static magnetohydrodynamic turbulence and compute various energy transfers including the ring-to-ring and conical energy transfers, and the energy fluxes of the perpendicular and parallel components of the velocity field. We show that the rings with higher polar angles transfer energy to ones with lower polar angles. For large interaction parameters, the dominant energy transfer takes place near the equator (polar angle θ≈(π)/2 ). The energy transfers are local both in wavenumbers and angles. The energy flux of the perpendicular component is predominantly from higher to lower wavenumbers (inverse cascade of energy), while that of the parallel component is from lower to higher wavenumbers (forward cascade of energy). Our results are consistent with earlier results, which indicate quasi two-dimensionalization of quasi-static magnetohydrodynamic flows at high interaction parameters.

  11. Femtosecond Carotenoid to Retinal Energy Transfer in Xanthorhodopsin

    PubMed Central

    Polívka, Tomáš; Balashov, Sergei P.; Chábera, Pavel; Imasheva, Eleonora S.; Yartsev, Arkady; Sundström, Villy; Lanyi, Janos K.

    2009-01-01

    Xanthorhodopsin of the extremely halophilic bacterium Salinibacter ruber represents a novel antenna system. It consists of a carbonyl carotenoid, salinixanthin, bound to a retinal protein that serves as a light-driven transmembrane proton pump similar to bacteriorhodopsin of archaea. Here we apply the femtosecond transient absorption technique to reveal the excited-state dynamics of salinixanthin both in solution and in xanthorhodopsin. The results not only disclose extremely fast energy transfer rates and pathways, they also reveal effects of the binding site on the excited-state properties of the carotenoid. We compared the excited-state dynamics of salinixanthin in xanthorhodopsin and in NaBH4-treated xanthorhodopsin. The NaBH4 treatment prevents energy transfer without perturbing the carotenoid binding site, and allows observation of changes in salinixanthin excited-state dynamics related to specific binding. The S1 lifetimes of salinixanthin in untreated and NaBH4-treated xanthorhodopsin were identical (3 ps), confirming the absence of the S1-mediated energy transfer. The kinetics of salinixanthin S2 decay probed in the near-infrared region demonstrated a change of the S2 lifetime from 66 fs in untreated xanthorhodopsin to 110 fs in the NaBH4-treated protein. This corresponds to a salinixanthin-retinal energy transfer time of 165 fs and an efficiency of 40%. In addition, binding of salinixanthin to xanthorhodopsin increases the population of the S∗ state that decays in 6 ps predominantly to the ground state, but a small fraction (<10%) of the S∗ state generates a triplet state. PMID:19289053

  12. Nonlinear energy transfer in classical and quantum systems.

    PubMed

    Manevitch, Leonid; Kovaleva, Agnessa

    2013-02-01

    In this paper we investigate the effect of slowly-varying parameters on the energy transfer in a weakly coupled system. For definiteness, we consider a system of two nonlinear oscillators, in which the directly excited first oscillator with constant parameter is attached to the oscillator with slowly time-varying frequency. It is proved that the equations of the slow passage through resonance in this system are identical to the equations of nonlinear Landau-Zener (LZ) tunneling. Three types of dynamical behavior are distinguished, namely, quasilinear, moderately nonlinear, and strongly nonlinear ones. Quasilinear systems exhibit a gradual energy transfer from the excited to the attached oscillator, while moderately nonlinear systems are characterized by an abrupt transition from the energy localization on the excited oscillator to the localization on the attached oscillator. In strongly nonlinear systems, the transition from the energy localization to strong energy exchange between the oscillators is revealed. Explicit approximate solutions describing the transient processes in moderately and strongly nonlinear systems are suggested. Correctness of the constructed approximations is confirmed by numerical results. The results presented in this paper, in addition to providing an analytical framework for understanding the transient dynamics, suggest an approximate procedure for solving the nonlinear LZ problem with arbitrary initial conditions over a finite time-interval. PMID:23496588

  13. Local energy transfer and nonlocal interactions in homogeneous, isotropic turbulence

    NASA Technical Reports Server (NTRS)

    Domaradzki, J. Andrzej; Rogallo, Robert S.

    1990-01-01

    Detailed computations were made of energy transfer among the scales of motion in incompressible turbulent fields at low Reynolds numbers, generated by direct numerical simulations. It was observed that, although the transfer resulted from triad interactions that were nonlocal in k space, the energy always transferred locally. The energy transfer calculated from the eddy-damped quasi-normal Markovian (EDQNM) theory of turbulence at low Reynolds numbers is in excellent agreement with the results of the numerical simulations. At high Reynolds numbers, the EDQNM theory predicts the same transfer mechanism in the inertial range that is observed at low Reynolds numbers.

  14. Incrementality and additionality: A new dimension to North-South resource transfers

    SciTech Connect

    Jordan, A. . School of Environmental Sciences); Werksman, J. . Foundation for International Environmental Law and Development)

    1994-06-01

    In the last four years, incrementality'' and additionality'' have emerged as new terms in the evolving lexicon of international environmental diplomacy. As Parties to the Conventions on Climate Change, Biodiversity and the Ozone Layer, industrialized states undertake to provide sufficient additional resources (the principle of additionality) to meet the incremental cost (the concept of incrementality) of measures undertaken by the developing countries to tackle global environmental problems. Issues of incrementality and additionality go to the heart of a much deeper and highly contentious debate on who should pay the costs of responding to global environmental problems; on how the payment should be made; on which agency or agencies should manage the transfers; and upon which parties should be compensated. Every sign is that if the overall North to South transfer breaks down or is retarded, then the process of implementing the aforementioned agreements may be jeopardized. This paper reviews the emergency of the two terms in international environmental politics; it pinpoints the theoretical and practical difficulties of defining and implementing them; and it assesses whether these difficulties and conflicts of opinion may, in some manner, be resolved.

  15. Excited-State-Proton-Transfer-Triggered Fluorescence Resonance Energy Transfer: from 2-Naphthylamine to Phenosafranin

    NASA Astrophysics Data System (ADS)

    Ghosh, Debanjana; Bose, Debosreeta; Sarkar, Deboleena; Chattopadhyay, Nitin

    2009-09-01

    Excited-state proton transfer (ESPT) and fluorescence resonance energy transfer (FRET) have been linearly coupled leading to an efficient pH-sensitive energy transfer from 2-naphthylamine (2NA) to a potentially bioactive cationic phenazinium dye, phenosafranin (PSF). The prototropic product produced exclusively from the photoexcited 2NA in the presence of added alkali serves as the donor for the energy transfer process. The energy transfer process is turned on at pH ≥ 12, whereas the process is turned off at a pH lower than that. Within the range of pH 12 to 13, the energy transfer efficiency (E) has been shown to follow a linear relation with the solution pH establishing the governing role of pH of the solution on the energy transfer process. The energy transfer follows a long-range dipole-dipole interaction mechanism. The critical energy transfer distance (R0) and the distance between the acceptor and the donor (r) have been determined for the ESPT-promoted FRET process at an optimum pH of 13. The present study involving the coupled processes is simple but has its implication due to its potential to be exploited for designing a pH-sensitive molecular switch.

  16. Heat transfer and material flow during laser assisted multi-layer additive manufacturing

    SciTech Connect

    Manvatkar, V.; De, A.; DebRoy, T.

    2014-09-28

    A three-dimensional, transient, heat transfer, and fluid flow model is developed for the laser assisted multilayer additive manufacturing process with coaxially fed austenitic stainless steel powder. Heat transfer between the laser beam and the powder particles is considered both during their flight between the nozzle and the growth surface and after they deposit on the surface. The geometry of the build layer obtained from independent experiments is compared with that obtained from the model. The spatial variation of melt geometry, cooling rate, and peak temperatures is examined in various layers. The computed cooling rates and solidification parameters are used to estimate the cell spacings and hardness in various layers of the structure. Good agreement is achieved between the computed geometry, cell spacings, and hardness with the corresponding independent experimental results.

  17. Heat transfer and material flow during laser assisted multi-layer additive manufacturing

    NASA Astrophysics Data System (ADS)

    Manvatkar, V.; De, A.; DebRoy, T.

    2014-09-01

    A three-dimensional, transient, heat transfer, and fluid flow model is developed for the laser assisted multilayer additive manufacturing process with coaxially fed austenitic stainless steel powder. Heat transfer between the laser beam and the powder particles is considered both during their flight between the nozzle and the growth surface and after they deposit on the surface. The geometry of the build layer obtained from independent experiments is compared with that obtained from the model. The spatial variation of melt geometry, cooling rate, and peak temperatures is examined in various layers. The computed cooling rates and solidification parameters are used to estimate the cell spacings and hardness in various layers of the structure. Good agreement is achieved between the computed geometry, cell spacings, and hardness with the corresponding independent experimental results.

  18. Transition-density-fragment interaction combined with transfer integral approach for excitation-energy transfer via charge-transfer states

    NASA Astrophysics Data System (ADS)

    Fujimoto, Kazuhiro J.

    2012-07-01

    A transition-density-fragment interaction (TDFI) combined with a transfer integral (TI) method is proposed. The TDFI method was previously developed for describing electronic Coulomb interaction, which was applied to excitation-energy transfer (EET) [K. J. Fujimoto and S. Hayashi, J. Am. Chem. Soc. 131, 14152 (2009)] and exciton-coupled circular dichroism spectra [K. J. Fujimoto, J. Chem. Phys. 133, 124101 (2010)]. In the present study, the TDFI method is extended to the exchange interaction, and hence it is combined with the TI method for applying to the EET via charge-transfer (CT) states. In this scheme, the overlap correction is also taken into account. To check the TDFI-TI accuracy, several test calculations are performed to an ethylene dimer. As a result, the TDFI-TI method gives a much improved description of the electronic coupling, compared with the previous TDFI method. Based on the successful description of the electronic coupling, the decomposition analysis is also performed with the TDFI-TI method. The present analysis clearly shows a large contribution from the Coulomb interaction in most of the cases, and a significant influence of the CT states at the small separation. In addition, the exchange interaction is found to be small in this system. The present approach is useful for analyzing and understanding the mechanism of EET.

  19. Transferability of regional permafrost disturbance susceptibility modelling using generalized linear and generalized additive models

    NASA Astrophysics Data System (ADS)

    Rudy, Ashley C. A.; Lamoureux, Scott F.; Treitz, Paul; van Ewijk, Karin Y.

    2016-07-01

    To effectively assess and mitigate risk of permafrost disturbance, disturbance-prone areas can be predicted through the application of susceptibility models. In this study we developed regional susceptibility models for permafrost disturbances using a field disturbance inventory to test the transferability of the model to a broader region in the Canadian High Arctic. Resulting maps of susceptibility were then used to explore the effect of terrain variables on the occurrence of disturbances within this region. To account for a large range of landscape characteristics, the model was calibrated using two locations: Sabine Peninsula, Melville Island, NU, and Fosheim Peninsula, Ellesmere Island, NU. Spatial patterns of disturbance were predicted with a generalized linear model (GLM) and generalized additive model (GAM), each calibrated using disturbed and randomized undisturbed locations from both locations and GIS-derived terrain predictor variables including slope, potential incoming solar radiation, wetness index, topographic position index, elevation, and distance to water. Each model was validated for the Sabine and Fosheim Peninsulas using independent data sets while the transferability of the model to an independent site was assessed at Cape Bounty, Melville Island, NU. The regional GLM and GAM validated well for both calibration sites (Sabine and Fosheim) with the area under the receiver operating curves (AUROC) > 0.79. Both models were applied directly to Cape Bounty without calibration and validated equally with AUROC's of 0.76; however, each model predicted disturbed and undisturbed samples differently. Additionally, the sensitivity of the transferred model was assessed using data sets with different sample sizes. Results indicated that models based on larger sample sizes transferred more consistently and captured the variability within the terrain attributes in the respective study areas. Terrain attributes associated with the initiation of disturbances were

  20. Luminescence energy transfer using a terbium chelate: improvements on fluorescence energy transfer.

    PubMed Central

    Selvin, P R; Hearst, J E

    1994-01-01

    We extend the technique of fluorescence resonance energy transfer (FRET) by introducing a luminescent terbium chelate as a donor and an organic dye, tetramethylrhodamine, as an acceptor. The results are consistent with a Förster theory of energy transfer, provided the appropriate parameters are used. The use of lanthanide donors, in general, and this pair, in particular, has many advantages over more conventional FRET pairs, which rely solely on organic dyes. The distance at which 50% energy transfer occurs is large, 65 A; the donor lifetime is a single exponential and long (millisecond), making lifetime measurements facile and accurate. Uncertainty in the orientation factor, which creates uncertainty in measured distances, is minimized by the donor's multiple electronic transitions and long lifetime. The sensitized emission of the acceptor can be measured with little or no interfering background, yielding a > 25-fold improvements in the signal-to-background ratio over standard donor-acceptor pairs. These improvements are expected to make distances > 100 A measurable via FRET. We also report measurement of the sensitized emission lifetime, a measurement that is completely insensitive to total concentration and incomplete labeling. PMID:7937831

  1. [INVITED] Laser-induced forward transfer: A high resolution additive manufacturing technology

    NASA Astrophysics Data System (ADS)

    Delaporte, Philippe; Alloncle, Anne-Patricia

    2016-04-01

    Among the additive manufacturing techniques, laser-induced forward transfer addresses the challenges of printing thin films in solid phase or small volume droplets in liquid phase with very high resolution. This paper reviews the physics of this process and explores the pros and cons of this technology versus other digital printing technologies. The main field of applications are printed electronics, organic electronics and tissue engineering, and the most promising short terms ones concern digital laser printing of sensors and conductive tracks. Future directions and emerging areas of interest are discussed such as printing solid from a liquid phase and 3D digital nanomanufacturing.

  2. Targeting Low-Energy Transfers to Low Lunar Orbit

    NASA Technical Reports Server (NTRS)

    Parker, Jeffrey S.; Anderson, Rodney L.

    2011-01-01

    A targeting scheme is presented to build trajectories from a specified Earth parking orbit to a specified low lunar orbit via a low-energy transfer and up to two maneuvers. The total transfer delta V (velocity) is characterized as a function of the Earth parking orbit inclination and the departure date for transfers to each given low lunar orbit. The transfer delta V (velocity) cost is characterized for transfers constructed to low lunar polar orbits with any longitude of ascending node and for transfers that arrive at the Moon at any given time during a month.

  3. Role of diffusion in excitation energy transfer and migration

    NASA Astrophysics Data System (ADS)

    Misra, V.; Mishra, H.

    2007-09-01

    Effect of diffusion on excitation energy transfer and migration in a dye pair sodium fluorescein (donor) and Rhodamine-6G (acceptor) has been studied for different viscosities by both steady state and time domain fluorescence spectroscopic measurements. The donor-donor interaction appears to be weaker as compared to donor-acceptor interaction and thus favors direct Förster-type energy transfer. Interestingly, at low viscosity (water in this case) transfer appears to be controlled by material diffusion/energy migration. Further, acceptor dynamics reveals the fact that direct Förster transfer dominates in viscous media.

  4. Ion momentum and energy transfer rates for charge exchange collisions

    NASA Technical Reports Server (NTRS)

    Horwitz, J.; Banks, P. M.

    1973-01-01

    The rates of momentum and energy transfer have been obtained for charge exchange collisions between ion and neutral gases having arbitrary Maxwellian temperatures and bulk transport velocities. The results are directly applicable to the F-region of the ionosphere where 0+ - 0 charge is the dominant mechanism affecting ion momentum and energy transfer.

  5. Detecting Plasmon Resonance Energy Transfer with Differential Interference Contrast Microscopy

    SciTech Connect

    Augspurger, Ashley E.; Stender, Anthony S.; Han, Rui; Fang, Ning

    2013-12-30

    Gold nanoparticles are ideal probes for studying intracellular environments and energy transfer mechanisms due to their plasmonic properties. Plasmon resonance energy transfer (PRET) relies on a plasmonic nanoparticle to donate energy to a nearby resonant acceptor molecule, a process which can be observed due to the plasmonic quenching of the donor nanoparticle. In this study, a gold nanosphere was used as the plasmonic donor, while the metalloprotein cytochrome c was used as the acceptor molecule. Differential interference contrast (DIC) microscopy allows for simultaneous monitoring of complex environments and noble metal nanoparticles in real time. Using DIC and specially designed microfluidic channels, we were able to monitor PRET at the single gold particle level and observe the reversibility of PRET upon the introduction of phosphate-buffered saline to the channel. In an additional experiment, single gold particles were internalized by HeLa cells and were subsequently observed undergoing PRET as the cell hosts underwent morphological changes brought about by ethanol-induced apoptosis.

  6. Energy efficiency standards for residential and commercial equipment: Additional opportunities

    SciTech Connect

    Rosenquist, Greg; McNeil, Michael; Iyer, Maithili; Meyers, Steve; McMahon, Jim

    2004-08-02

    Energy efficiency standards set minimum levels of energy efficiency that must be met by new products. Depending on the dynamics of the market and the level of the standard, the effect on the market for a given product may be small, moderate, or large. Energy efficiency standards address a number of market failures that exist in the buildings sector. Decisions about efficiency levels often are made by people who will not be responsible for the energy bill, such as landlords or developers of commercial buildings. Many buildings are occupied for their entire lives by very temporary owners or renters, each unwilling to make long-term investments that would mostly reward subsequent users. And sometimes what looks like apathy about efficiency merely reflects inadequate information or time invested to evaluate it. In addition to these sector-specific market failures, energy efficiency standards address the endemic failure of energy prices to incorporate externalities. In the U.S., energy efficiency standards for consumer products were first implemented in California in 1977. National standards became effective starting in 1988. By the end of 2001, national standards were in effect for over a dozen residential appliances, as well as for a number of commercial sector products. Updated standards will take effect in the next few years for several products. Outside the U.S., over 30 countries have adopted minimum energy performance standards. Technologies and markets are dynamic, and additional opportunities to improve energy efficiency exist. There are two main avenues for extending energy efficiency standards. One is upgrading standards that already exist for specific products. The other is adopting standards for products that are not covered by existing standards. In the absence of new and upgraded energy efficiency standards, it is likely that many new products will enter the stock with lower levels of energy efficiency than would otherwise be the case. Once in the stock

  7. Vibrational Energy Transfer Across a Reverse Micelle Surfactant Layer

    NASA Astrophysics Data System (ADS)

    Deàk, John C.; Pang, Yoonsoo; Sechler, Timothy D.; Wang, Zhaohui; Dlott, Dana D.

    2004-10-01

    In a suspension of reverse micelles, in which the surfactant sodium dioctyl sulfosuccinate (AOT) separates a water nanodroplet from a bulk nonpolar CCl4 phase, ultrafast vibrational spectroscopy was used to study vibrational energy transfer from the nanodroplet through the AOT interfacial monolayer to the surrounding CCl4. Most of the vibrational energy from the nanodroplet was transferred to the polar AOT head group within 1.8 picoseconds and then out to the CCl4 within 10 picoseconds. Vibrational energy pumped directly into the AOT tail resulted in a slower 20- to 40-picosecond transfer of energy to the CCl4.

  8. Vibrational energy transfer across a reverse micelle surfactant layer.

    PubMed

    Deàk, John C; Pang, Yoonsoo; Sechler, Timothy D; Wang, Zhaohui; Dlott, Dana D

    2004-10-15

    In a suspension of reverse micelles, in which the surfactant sodium dioctyl sulfosuccinate (AOT) separates a water nanodroplet from a bulk nonpolar CCl4 phase, ultrafast vibrational spectroscopy was used to study vibrational energy transfer from the nanodroplet through the AOT interfacial monolayer to the surrounding CCl4. Most of the vibrational energy from the nanodroplet was transferred to the polar AOT head group within 1.8 picoseconds and then out to the CCl4 within 10 picoseconds. Vibrational energy pumped directly into the AOT tail resulted in a slower 20- to 40-picosecond transfer of energy to the CCl4. PMID:15388896

  9. [Preparation of epitope imprinted particles for transferrin recognition by reversible addition fragmentation chain transfer strategy].

    PubMed

    Li, Qinran; Yang, Kaiguang; Li, Senwu; Liu, Jianxi; Zhang, Lihua; Liang, Zhen; Zhang, Yukui

    2014-10-01

    A kind of novel epitope surface imprinted particles was prepared by the reversible addition fragmentation chain transfer (RAFT) strategy. The epitope of transferrin, N-terminal peptide of the protein with nine amino acid residues, was chosen as the template and immobi- lized with covalent interaction on the surface of silica particles through the truss arm glutaraldehyde. The living/controlled polymerization was initialed by 2,2'-azobisisobutyronitrile (AIBN) at 70 °C in the solution of N,N-dimethylformamide, with the regulation by triothioester agent 2-(dodecylthiocarbonothioylthio)-2-methylpropanoic acid. Methacrylic acid and 2-hydroxyethyl methacrylate were chosen as the functional monomers and N, N-methylenebisacrylamide was chosen as the cross-linker in this polymerization. For this material, the binding capacity of the nine residue peptide could reach 2.36 mg/g with the imprinting factor (IF) of 1.89, while that for transferrin could reach 4.98 mg/g with IF of 1.61. The equilibrium could be achieved in 120 min for the transferrin recognition. In multi-protein competitive recognition, the imprinted factor of transferrin was the highest in the mixture of transferrin and other competitive proteins, such as cytochrome C and β-lactoglobulin. The results indicated that these epitope surface imprinted particles with RAFT strategy could recognize not only the nine residue peptide but also the transferrin with good selectivity, high binding capacity and fast mass transfer. PMID:25739262

  10. Geo energy research and development: technology transfer update

    SciTech Connect

    Traeger, R.K.; Dugan, V.L.

    1983-01-01

    Sandia Geo Energy Programs in geothermal, coal, oil and gas, and synfuel technologies have been effective in transferring research concepts to applications in private industry. This report updates the previous summary (SAND82-0211, March 1982) to include recent technology transfers and to reflect recent changes in philosophy on technology transfer. Over 40 items transferred to industry have been identified in the areas of Hardware, Risk Removal and Understanding. Successful transfer is due largely to personal interactions between Sandia engineers and the technical staffs of private industry.

  11. Plasmon-Induced Resonant Energy Transfer: a coherent dipole-dipole coupling mechanism

    NASA Astrophysics Data System (ADS)

    Bristow, Alan D.; Cushing, Scott K.; Li, Jiangtian; Wu, Nianqiang

    Metal-insulator-semiconductor core-shell nanoparticles have been used to demonstrate a dipole-dipole coupling mechanism that is entirely dependent on the dephasing time of the localized plasmonic resonance. Consequently, the short-time scale of the plasmons leads to broad energy uncertainty that allows for excitation of charge carriers in the semiconductor via stimulation of photons with energies below the energy band gap. In addition, this coherent energy transfer process overcomes interfacial losses often associated with direct charge transfer. This work explores the efficiency of the energy transfer process, the dipole-dipole coupling strength with dipole separation, shell thickness and plasmonic resonance overlap. We demonstrate limits where the coherent nature of the coupling is switched off and charge transfer processes can dominate. Experiments are performed using transient absorption spectroscopy. Results are compared to calculations using a quantum master equation. These nanostructures show strong potential for improving solar light-harvesting for power and fuel generation.

  12. An ultra-efficient energy transfer beyond plasmonic light scattering

    SciTech Connect

    Fu, Sze-Ming; Zhong, Yan-Kai; Lin, Albert

    2014-11-14

    The energy transfer between nano-particles is of great importance for, solar cells, light-emitting diodes, nano-particle waveguides, and other photonic devices. This study shows through novel design and algorithm optimization, the energy transfer efficiency between plasmonic and dielectric nano-particles can be greatly improved. Using versatile designs including core-shell wrapping, supercells and dielectric mediated plasmonic scattering, 0.05 dB/μm attenuation can be achieved, which is 20-fold reduction over the baseline plasmonic nano-particle chain, and 8-fold reduction over the baseline dielectric nano-particle chain. In addition, it is also found that the dielectric nano-particle chains can actually be more efficient than the plasmonic ones, at their respective optimized geometry. The underlying physics is that although plasmonic nano-particles provide stronger coupling and field emission, the effect of plasmonic absorption loss is actually more dominant resulting in high attenuation. Finally, the group velocity for all design schemes proposed in this work is shown to be maintained above 0.4c, and it is found that the geometry optimization for transmission also boosts the group velocity.

  13. Near-infrared-induced electron transfer of an uranyl macrocyclic complex without energy transfer to dioxygen.

    PubMed

    Davis, Christina M; Ohkubo, Kei; Ho, I-Ting; Zhang, Zhan; Ishida, Masatoshi; Fang, Yuanyuan; Lynch, Vincent M; Kadish, Karl M; Sessler, Jonathan L; Fukuzumi, Shunichi

    2015-04-21

    Photoexcitation of dichloromethane solutions of an uranyl macrocyclic complex with cyclo[1]furan[1]pyridine[4]-pyrrole () at the near-infrared (NIR) band (1177 nm) in the presence of electron donors and acceptors resulted in NIR-induced electron transfer without producing singlet oxygen via energy transfer. PMID:25791126

  14. A planning framework for transferring building energy technologies: Executive Summary

    SciTech Connect

    Farhar, B C; Brown, M A; Mohler, B L; Wilde, M; Abel, F H

    1990-08-01

    Accelerating the adoption of new and existing cost-effective technologies has significant potential to reduce the energy consumed in US buildings. This report summarizes some of the key results of an interlaboratory technology transfer planning effort in support of the US Department of Energy's Office of Building Technologies (the full report is published under SERI number TP-260-3729). A guiding assumption for planning was that OBT's R D program should forge linkages with existing programs whose goals involved enhancing energy efficiency in buildings. An ad hoc Technology Transfer Advisory Group reviewed the existing analysis and technology transfer program, brainstormed technology transfer approaches, interviewed DOE program managers, identified applicable research results, and developed a framework that management could use in deciding on the best investments of technology transfer resources. Representatives of 22 organizations were interviewed on their views of the potential for transferring energy efficiency technologies through active linking with OBT. The report describes in summary these programs and interview results; outlines OBT tools, technologies, and practices to be transferred; defines OBT audiences; identifies technology transfer functions and presents a framework devised using functions and audiences; presents some example technology transfer activities; and summarizes the Advisory Group's recommendations.

  15. A planning framework for transferring building energy technologies

    SciTech Connect

    Farhar, B C; Brown, M A; Mohler, B L; Wilde, M; Abel, F H

    1990-07-01

    Accelerating the adoption of new and existing cost-effective technologies has significant potential to reduce the energy consumed in US buildings. This report presents key results of an interlaboratory technology transfer planning effort in support of the US Department of Energy's Office of Building Technologies (OBT). A guiding assumption for planning was that OBT's R D program should forge linkages with existing programs whose goals involved enhancing energy efficiency in buildings. An ad hoc Technology Transfer Advisory Group reviewed the existing analysis and technology transfer program, brainstormed technology transfer approaches, interviewed DOE program managers, identified applicable research results, and developed a framework that management could use in deciding on the best investments of technology transfer resources. Representatives of 22 organizations were interviewed on their views of the potential for transferring energy efficiency technologies through active linking with OBT. The report describes these programs and interview results; outlines OBT tools, technologies, and practices to be transferred; defines OBT audiences; identifies technology transfer functions and presents a framework devised using functions and audiences; presents some 60 example technology transfer activities; and documents the Advisory Group's recommendations. 37 refs., 3 figs., 12 tabs.

  16. Investigation of energy transfer in terbium doped Y 2SiO5 phosphor particles

    NASA Astrophysics Data System (ADS)

    Salis, M.; Carbonaro, C. M.; Corpino, R.; Anedda, A.; Ricci, P. C.

    2012-07-01

    The kinetics of luminescence of sol-gel synthesized terbium doped Y 2SiO5 (YSO) phosphor particles is investigated in detail with reference to Tb concentration in the 0.001%-10% range. By increasing the dopant concentration, the luminescence profile changes from a blue to a green peaked emission spectrum because of the energy transfer among centers. The inter-center energy transfer mechanism is well accounted for by the Inokuti-Hirayama (IH) kinetic model which is based on a statistical average of inter-center distance dependent decay modes of the donor luminescence. The distribution of the decay modes is implemented from the Förster-Dexter resonance theory of energy transfer by assuming a rate constant for the energy transfer by multipolar interactions between donors and acceptors. However, the experimental results recorded in the low concentration limit show the presence of green emission contributions in the luminescence spectrum which cannot be related to the Tb concentration; for this reason an additional internal energy transfer mechanism, occurring among levels of the same center, is proposed to account for the recorded emission properties. Thus, a new and more exhaustive model which includes both the internal and external energy transfer processes is considered; the proposed model allows a better explanation of the spectroscopic features of Tb related centers in YSO crystals and discloses the critical concentration and the quantum yields of the different energy transfer mechanisms.

  17. Energy transfer in silver-doped rare gas matrices

    NASA Astrophysics Data System (ADS)

    Hebert, T.; Wiggenhauser, H.; Kolb, D. M.

    1989-08-01

    The energy transfer between Ag atoms and dimers isolated in rare gas matrices has been studied by time-resolved fluorescence spectroscopy. In the presence of dimers, excitation of the atomic 5s→5p transitions produces not only the emission bands of the Ag atom, but also those of the Ag dimer. This process has been investigated and the mechanism identified as a Förster-Dexter-type energy transfer from silver atoms (donor) to dimers (acceptor). Rise and decay curves of the emissions from atoms and dimers have been analyzed in a concentration dependence study and a critical radius for the energy transfer of 39±5 Å was derived.

  18. Resonant energy transfer assisted by off-diagonal coupling.

    PubMed

    Wu, Ning; Sun, Ke-Wei; Chang, Zhe; Zhao, Yang

    2012-03-28

    Dynamics of resonant energy transfer of a single excitation in a molecular dimer system are studied in the simultaneous presence of diagonal and off-diagonal exciton-phonon coupling. It is found that, at given temperatures, the off-diagonal coupling can enhance both the coherence of the resonant energy transfer and the net quantity of energy transferred from an initially excited monomer to the other. Also studied is the dynamics of entanglement between the dimer system and the phonon bath as measured by the von Neumann entanglement entropy, and the inter-monomer entanglement dynamics for the excitonic system. PMID:22462880

  19. Energy transfer between a biological labelling dye and gold nanorods

    NASA Astrophysics Data System (ADS)

    Racknor, Chris; Singh, Mahi R.; Zhang, Yinan; Birch, David J. S.; Chen, Yu

    2014-03-01

    We have demonstrated energy transfer between a biological labelling dye (Alexa Fluor 405) and gold nanorods experimentally and theoretically. The fluorescence lifetime imaging microscopy and density matrix method are used to study a hybrid system of dye and nanorods under one- and two-photon excitations. Energy transfer between dye and nanorods via the dipole-dipole interaction is found to cause a decrease in the fluorescence lifetime change. Enhanced energy transfer from dye to nanorods is measured in the presence of an increased density of nanorods. This study has potential applications in fluorescence lifetime-based intra-cellular sensing of bio-analytes as well as nuclear targeting cancer therapy.

  20. A quantum model of almost perfect energy transfer

    NASA Astrophysics Data System (ADS)

    Alicki, Robert; Giraldi, Filippo

    2011-08-01

    The Wigner-Weisskopf-type model describing the energy transfer between two centres mediated by a continuum of energy levels is studied. This work is motivated by the recent interest in transport phenomena at nanoscale in biology and quantum engineering. The analytical estimation for the energy transfer efficiency is derived in the weak coupling regime and the conditions for the almost perfect transfer are discussed. The embedding of the standard tight-binding model into the Wigner-Weisskopf one which includes the environmental noise is presented.

  1. Energy Transfer and Triadic Interactions in Compressible Turbulence

    NASA Technical Reports Server (NTRS)

    Bataille, F.; Zhou, Ye; Bertoglio, Jean-Pierre

    1997-01-01

    Using a two-point closure theory, the Eddy-Damped-Quasi-Normal-Markovian (EDQNM) approximation, we have investigated the energy transfer process and triadic interactions of compressible turbulence. In order to analyze the compressible mode directly, the Helmholtz decomposition is used. The following issues were addressed: (1) What is the mechanism of energy exchange between the solenoidal and compressible modes, and (2) Is there an energy cascade in the compressible energy transfer process? It is concluded that the compressible energy is transferred locally from the solenoidal part to the compressible part. It is also found that there is an energy cascade of the compressible mode for high turbulent Mach number (M(sub t) greater than or equal to 0.5). Since we assume that the compressibility is weak, the magnitude of the compressible (radiative or cascade) transfer is much smaller than that of solenoidal cascade. These results are further confirmed by studying the triadic energy transfer function, the most fundamental building block of the energy transfer.

  2. Electronic excitation energy transfer between nucleobases of natural DNA.

    PubMed

    Vayá, Ignacio; Gustavsson, Thomas; Douki, Thierry; Berlin, Yuri; Markovitsi, Dimitra

    2012-07-18

    Transfer of the electronic excitation energy in calf thymus DNA is studied by time-resolved fluorescence spectroscopy. The fluorescence anisotropy, after an initial decay starting on the femtosecond time scale, dwindles down to ca. 0.1. The in-plane depolarized fluorescence decays are described by a stretched exponential law. Our observations are consistent with one-dimensional transfer mediated by charge-transfer excited states. PMID:22765050

  3. Spectral Energy Transfer and Dissipation of Magnetic Energy from Fluid to Kinetic Scales

    SciTech Connect

    Bowers, K.; Li, H.

    2007-01-19

    We investigate the magnetic energy transfer from the fluid to kinetic scales and dissipation processes using three-dimensional fully kinetic particle-in-cell plasma simulations. The nonlinear evolution of a sheet pinch is studied where we show that it exhibits both fluid scale global relaxation and kinetic scale collisionless reconnection at multiple resonant surfaces. The interactions among collisionless tearing modes destroy the original flux surfaces and produce stochastic fields, along with generating sheets and filaments of intensified currents. In addition, the magnetic energy is transferred from the original shear length scale both to the large scales due to the global relaxation and to the smaller, kinetic scales for dissipation. The dissipation is dominated by the thermal or pressure effect in the generalized Ohm's law, and electrons are preferentially accelerated.

  4. Spectral energy transfer and dissipation of magnetic energy from fluid to kinetic scales.

    PubMed

    Bowers, K; Li, H

    2007-01-19

    We investigate the magnetic energy transfer from the fluid to kinetic scales and dissipation processes using three-dimensional fully kinetic particle-in-cell plasma simulations. The nonlinear evolution of a sheet pinch is studied where we show that it exhibits both fluid scale global relaxation and kinetic scale collisionless reconnection at multiple resonant surfaces. The interactions among collisionless tearing modes destroy the original flux surfaces and produce stochastic fields, along with generating sheets and filaments of intensified currents. In addition, the magnetic energy is transferred from the original shear length scale both to the large scales due to the global relaxation and to the smaller, kinetic scales for dissipation. The dissipation is dominated by the thermal or pressure effect in the generalized Ohm's law, and electrons are preferentially accelerated. PMID:17358690

  5. Energy transfer between thulium and praseodymium ions in solids

    SciTech Connect

    Cockroft, N.J.; Murdoch, K.M.

    1993-09-01

    New thulium-to-praseodymium upconversion and cross-relaxation energy transfer mechanisms are observed. YLiF{sub 4} has several subsets of dopant ions, which exhibit a variety of transfer efficiencies. Dual-pulse laser excitation of dimers in CsCdBr{sub 3} is used to demonstrate a probable upconversion pathway.

  6. INTRAMOLECULAR CHARGE AND ENERGY TRANSFER IN MULTICHROMOPHORIC AROMATIC SYSTEMS

    SciTech Connect

    Edward C. Lim

    2008-09-09

    A concerted experimental and computational study of energy transfer in nucleic acid bases and charge transfer in dialkylaminobenzonitriles, and related electron donor-acceptor molecules, indicate that the ultrafast photoprocesses occur through three-state conical interactions involving an intermediate state of biradical character.

  7. Energy Transfer and a Recurring Mathematical Function

    ERIC Educational Resources Information Center

    Atkin, Keith

    2013-01-01

    This paper extends the interesting work of a previous contributor concerning the analogies between physical phenomena such as mechanical collisions and the transfer of power in an electric circuit. Emphasis is placed on a mathematical function linking these different areas of physics. This unifying principle is seen as an exciting opportunity to…

  8. Third-order nonlinear optical response of energy transfer systems

    NASA Astrophysics Data System (ADS)

    Yang, Mino; Fleming, Graham R.

    1999-07-01

    The third-order nonlinear optical response of energy transfer systems is theoretically investigated. A system composed of two chromophores having the same electronic transition energies is considered. The dynamics of energy transfer between the two chromophores is assumed to occur via a hopping (incoherent) mechanism. We introduce new types of pathways incorporating the hopping processes occurring while the system is in population states and reconstruct a third-order response function which is computationally viable. The nuclear propagators in the electronic population states are written as convolution integrals between those of the nonreactive two-state system weighted by some factors for the energy transfer. The response function is given by multitime correlation functions and these are analyzed by the cumulant expansion method. Based on this approach, the three-pulse photon echo peak shift for several models of energy transfer systems is discussed. It is shown that the rephasing capability of the induced signal is reduced by the memory loss due to resonant energy transfer. A previous model which incorporates resonant energy transfers in an intuitive way is reviewed and modified to supplement the loss of dynamic correlation of nuclear motion within the framework of the theory. The response function obtained by our new approach gives a more accurate description than the existing theory and a comparative discussion is given. The effect of inhomogeneity in rate constants on the third-order signal is discussed and the temperature dependence of the echo signal is examined.

  9. Energy efficient building design. A transfer guide for local governments

    SciTech Connect

    Not Available

    1992-03-01

    The fundamental concepts of the building design process, energy codes and standards, and energy budgets are introduced. These tools were combined into Energy Design Guidelines and design contract requirements. The Guidelines were repackaged for a national audience and a videotape for selling the concept to government executives. An effort to test transfer of the Guidelines to outside agencies is described.

  10. Collisional energy transfer and quenching of electronic excitation

    PubMed Central

    Lin, S. H.; Eyring, H.

    1975-01-01

    The purpose of this paper has been to explore in a preliminary way the nature and mechanism of collisional energy transfer and quenching of electronic excitation. For this purpose, the Born approximation has been used, and the triplet-triplet and singlet-singlet transfer, and the triplet-triplet and singlet-singlet quenching have been studied. It has been shown theoretically that (i) the singlet-singlet transfer constants (or cross sections) are always larger than the triplet-triplet transfer constants (or cross sections) for the same system of donor and acceptor; (ii) for the singlet-singlet transfer, the observed cross section varies linearly with respect to the spectral overlap between the donor emission and the acceptor absorption; (iii) the reason that the quenching constants (or cross sections) are always smaller than the energy transfer constants (or cross sections) is due to the fact that for the quenching the vibration of the acceptor hardly participates in accepting the electronic excitation and for the energy transfer only part of the excited electron energy of the donor is converted into the energy of nuclear motion; and (iv) the polar acceptor molecules are better quenchers than nonpolar acceptor molecules. PMID:16592281

  11. Redefining RECs: Additionality in the voluntary Renewable Energy Certificate market

    NASA Astrophysics Data System (ADS)

    Gillenwater, Michael Wayne

    In the United States, electricity consumers are told that they can "buy" electricity from renewable energy projects, versus fossil fuel-fired facilities, through participation in a voluntary green power program. The marketing messages communicate to consumers that their participation and premium payments for a green label will cause additional renewable energy generation and thereby allow them to claim they consume electricity that is absent pollution as well as reduce pollutant emissions. Renewable Energy Certificates (RECs) and wind energy are the basis for the majority of the voluntary green power market in the United States. This dissertation addresses the question: Do project developers respond to the voluntary REC market in the United States by altering their decisions to invest in wind turbines? This question is investigated by modeling and probabilistically quantifying the effect of the voluntary REC market on a representative wind power investor in the United States using data from formal expert elicitations of active participants in the industry. It is further explored by comparing the distribution of a sample of wind power projects supplying the voluntary green power market in the United States against an economic viability model that incorporates geographic factors. This dissertation contributes the first quantitative analysis of the effect of the voluntary REC market on project investment. It is found that 1) RECs should be not treated as equivalent to emission offset credits, 2) there is no clearly credible role for voluntary market RECs in emissions trading markets without dramatic restructuring of one or both markets and the environmental commodities they trade, and 3) the use of RECs in entity-level GHG emissions accounting (i.e., "carbon footprinting") leads to double counting of emissions and therefore is not justified. The impotence of the voluntary REC market was, at least in part, due to the small magnitude of the REC price signal and lack of

  12. Shishiodoshi unidirectional energy transfer mechanism in phenylene ethynylene dendrimers

    NASA Astrophysics Data System (ADS)

    Fernandez-Alberti, S.; Roitberg, Adrian E.; Kleiman, Valeria D.; Nelson, T.; Tretiak, S.

    2012-12-01

    Non-adiabatic excited-state molecular dynamics is used to study the ultrafast intramolecular energy transfer between two-, three-, and four-ring linear polyphenylene ethynylene chromophore units linked through meta-substitutions. Twenty excited-state electronic energies, with their corresponding gradients and nonadiabatic coupling vectors were included in the simulations. The initial laser excitation creates an exciton delocalized between the different absorbing two-ring linear PPE units. Thereafter, we observe an ultrafast directional change in the spatial localization of the transient electronic transition density. The analysis of the intramolecular flux of the transition density shows a sequential through-bond two-ring→three-ring→four-ring transfer as well as an effective through-space direct two-to-four ring transfer. The vibrational excitations of C≡C stretching motions change according to that. Finally, a mechanism of unidirectional energy transfer is presented based on the variation of the energy gaps between consecutive electronic excited states in response to the intramolecular flux of the transition density. The mechanism resembles a Shishiodoshi Japanese bamboo water fountain where, once the electronic population has been transferred to the state directly below in energy, the two states decouple thereby preventing energy transfer in the opposite direction.

  13. Synthesis of carboxylic block copolymers via reversible addition fragmentation transfer polymerization for tooth erosion prevention.

    PubMed

    Lei, Y; Wang, T; Mitchell, J W; Qiu, J; Kilpatrick-Liverman, L

    2014-12-01

    Dental professionals are seeing a growing population of patients with visible signs of dental erosion. The approach currently being used to address the problem typically leverages the enamel protection benefits of fluoride. In this report, an alternative new block copolymer with a hydrophilic polyacrylic acid (PAA) block and a hydrophobic poly(methyl methacrylate) (PMMA) block was developed to similarly reduce the mineral loss from enamel under acidic conditions. This series of PMMA-b-PAA block copolymers was synthesized by reversible addition fragmentation transfer (RAFT) polymerization. Their structures were characterized by gel permeation chromatography (GPC) and (1)H nuclear magnetic resonance (NMR) spectra. The molar fractions of acrylic acid (AA) in the final block copolymer were finely controlled from 0.25 to 0.94, and the molecular weight (Mn) of PMMA-b-PAA was controlled from 10 kDa to 90 kDa. The binding capability of the block copolymer with hydroxyapatite (HAP) was investigated by ultraviolet-visible spectroscopy (UV-Vis) and Fourier transform infrared (FTIR) spectroscopy. FTIR spectra confirmed that the PMMA-b-PAA block copolymer could bind to HAP via bridging bidentate bonds. Both UV-Vis and FTIR spectra additionally indicated that a high polymer concentration and low solution pH favored the polymer binding to HAP. The erosion-preventing efficacy of the PMMA-b-PAA block copolymer in inhibiting HAP mineral loss was quantitatively evaluated by atomic absorption spectroscopy (AAS). Based on the results, polymer treatment reduced the amount of calcium released by 27% to 30% in comparison with the unprotected samples. Scanning electron microscope (SEM) observations indicated that PMMA-b-PAA polymer treatment protected enamel from acid erosion. This new amphiphilic block copolymer has significant potential to be integrated into dentifrices or mouthrinses as an alternative non-fluoride ingredient to reduce tooth erosion. PMID:25248611

  14. Synthesis of Carboxylic Block Copolymers via Reversible Addition Fragmentation Transfer Polymerization for Tooth Erosion Prevention

    PubMed Central

    Lei, Y.; Wang, T.; Mitchell, J.W.; Qiu, J.; Kilpatrick-Liverman, L.

    2014-01-01

    Dental professionals are seeing a growing population of patients with visible signs of dental erosion. The approach currently being used to address the problem typically leverages the enamel protection benefits of fluoride. In this report, an alternative new block copolymer with a hydrophilic polyacrylic acid (PAA) block and a hydrophobic poly(methyl methacrylate) (PMMA) block was developed to similarly reduce the mineral loss from enamel under acidic conditions. This series of PMMA-b-PAA block copolymers was synthesized by reversible addition fragmentation transfer (RAFT) polymerization. Their structures were characterized by gel permeation chromatography (GPC) and 1H nuclear magnetic resonance (NMR) spectra. The molar fractions of acrylic acid (AA) in the final block copolymer were finely controlled from 0.25 to 0.94, and the molecular weight (Mn) of PMMA-b-PAA was controlled from 10 kDa to 90 kDa. The binding capability of the block copolymer with hydroxyapatite (HAP) was investigated by ultraviolet–visible spectroscopy (UV-Vis) and Fourier transform infrared (FTIR) spectroscopy. FTIR spectra confirmed that the PMMA-b-PAA block copolymer could bind to HAP via bridging bidentate bonds. Both UV-Vis and FTIR spectra additionally indicated that a high polymer concentration and low solution pH favored the polymer binding to HAP. The erosion-preventing efficacy of the PMMA-b-PAA block copolymer in inhibiting HAP mineral loss was quantitatively evaluated by atomic absorption spectroscopy (AAS). Based on the results, polymer treatment reduced the amount of calcium released by 27% to 30% in comparison with the unprotected samples. Scanning electron microscope (SEM) observations indicated that PMMA-b-PAA polymer treatment protected enamel from acid erosion. This new amphiphilic block copolymer has significant potential to be integrated into dentifrices or mouthrinses as an alternative non-fluoride ingredient to reduce tooth erosion. PMID:25248611

  15. Addition of alcohols and hydrocarbons to fullerenes by photosensitized electron transfer

    SciTech Connect

    Lem, G.; Schuster, D.I.; Courtney, S.H.; Lu, Q.; Wilson, S.R. )

    1995-01-11

    We report the formation of C[sub 60] radical cations by photosensitized electron transfer and the capture of the cation by nucleophiles such as alcohols to yield alkoxy-substituted fullerenes. In addition, we report selective trapping of the radical cation by reactive hydrogen donors to produce alkyl-substituted fullerenes. The finding that fullerene radical cations in the vapor phase are unreactive toward alcohols was rationalized in terms of resistance to formation of product in which the previously highly delocalized positive charge becomes strongly localized upon the oxygen atom of the nucleophile. This inhibition is not the case in solution, probably because of solvation effects. We expect to utilize these novel reactions of fullerenes to add other types of nucleophiles (such as cyanide) and hydrogen donors (such as thiols) to C[sub 60], thus opening a wider window for functionalization of fullerenes for synthetic purposes. These studies once again demonstrate the value of using the crown ether-methanofullerene (1) to conveniently follow the progress of new chemical reactions of C[sub 60] in solution by ESI-MS. 17 refs., 2 figs.

  16. Energy transfer simulation for radiantly heated and cooled enclosures

    SciTech Connect

    Chapman, K.S.; Zhang, P.

    1996-11-01

    This paper presents the development of a three-dimensional mathematical model to compute heat transfer within a radiantly heated or cooled room, which then calculates the mass-averaged room air temperature and the wall surface temperature distributions. The radiation formulation used in the model accommodates arbitrary placement of walls and objects within the room. The convection model utilizes Nusselt number correlations published in the open literature. The complete energy transfer model is validated by comparing calculated room temperatures to temperatures measured in a radiantly heated room. This three-dimensional model may be applied to a building to assist the heating/cooling system design engineer in sizing a radiant heating/cooling system. By coupling this model with a thermal comfort model, the comfort levels throughout the room can be easily and efficiently mapped for a given radiant heater/cooler location. In addition, obstacles such as airplanes, trucks, furniture, and partitions can be easily incorporated to determine their effect on the radiant heating system performance.

  17. Proton-Coupled Electron Transfer Reactions with Photometric Bases Reveal Free Energy Relationships for Proton Transfer.

    PubMed

    Eisenhart, Thomas T; Howland, William C; Dempsey, Jillian L

    2016-08-18

    The proton-coupled electron transfer (PCET) oxidation of p-aminophenol in acetonitrile was initiated via stopped-flow rapid-mixing and spectroscopically monitored. For oxidation by ferrocenium in the presence of 7-(dimethylamino)quinoline proton acceptors, both the electron transfer and proton transfer components could be optically monitored in the visible region; the decay of the ferrocenium absorbance is readily monitored (λmax = 620 nm), and the absorbance of the 2,4-substituted 7-(dimethylamino)quinoline derivatives (λmax = 370-392 nm) red-shifts substantially (ca. 70 nm) upon protonation. Spectral analysis revealed the reaction proceeds via a stepwise electron transfer-proton transfer process, and modeling of the kinetics traces monitoring the ferrocenium and quinolinium signals provided rate constants for elementary proton and electron transfer steps. As the pKa values of the conjugate acids of the 2,4-R-7-(dimethylamino)quinoline derivatives employed were readily tuned by varying the substituents at the 2- and 4-positions of the quinoline backbone, the driving force for proton transfer was systematically varied. Proton transfer rate constants (kPT,2 = (1.5-7.5) × 10(8) M(-1) s(-1), kPT,4 = (0.55-3.0) × 10(7) M(-1) s(-1)) were found to correlate with the pKa of the conjugate acid of the proton acceptor, in agreement with anticipated free energy relationships for proton transfer processes in PCET reactions. PMID:27500804

  18. The measurement of bicycle exercising energy transfer

    NASA Astrophysics Data System (ADS)

    Cho, Hung-Pin; Jian, Zi-Jie; Jwo, Ching-Song; Wang, Jiun-Yau; Chen, Sih-Li

    2010-08-01

    The main study purpose is to develop a device capable of translating exercise energy into hot or icy drinkable water. This device can accurately measure energy consumption during exercise, transform it, and apply it to a heating and refrigerating system. Traditional energy measurements were based on the amount of exercise load from the human body. The research tapped into this non-electric form of energy transmission to run a heating and refrigerating system. The energy requirement was 50.6 kcal. When compared to 57.9 kcal, which the body consumes based actual calorie test, the difference was within a 15% striking range. In terms of energy comparisons, this study demonstrates potential R & D value with this innovative design. It complied with carbon emission requirements by producing 2,000 cc of energy at 47°C of hot water and 1,300 cc of energy at 6.6°C of ice water, all without the use of conventional energy sources. As the paper shows, this device is an innovative and environmentally conscious design. In an upcoming low-carbon emissions future, its research potential is definitely worth evaluating.

  19. Universal distance-scaling of nonradiative energy transfer to graphene.

    PubMed

    Gaudreau, L; Tielrooij, K J; Prawiroatmodjo, G E D K; Osmond, J; García de Abajo, F J; Koppens, F H L

    2013-05-01

    The near-field interaction between fluorescent emitters and graphene exhibits rich physics associated with local dipole-induced electromagnetic fields that are strongly enhanced due to the unique properties of graphene. Here, we measure emitter lifetimes as a function of emitter-graphene distance d, and find agreement with a universal scaling law, governed by the fine-structure constant. The observed energy transfer rate is in agreement with a 1/d(4) dependence that is characteristic of two-dimensional lossy media. The emitter decay rate is enhanced 90 times (energy transfer efficiency of ~99%) with respect to the decay in vacuum at distances d ≈ 5 nm. This high energy transfer rate is mainly due to the two-dimensionality and gapless character of the monatomic carbon layer. Graphene is thus shown to be an extraordinary energy sink, holding great potential for photodetection, energy harvesting, and nanophotonics. PMID:23488979

  20. Energy transfer and energy absorption in photon interactions with matter revisited: A step-by-step illustrated approach

    NASA Astrophysics Data System (ADS)

    Abdel-Rahman, W.; Podgorsak, E. B.

    2010-05-01

    A clear understanding of energy transfer and energy absorption in photon interactions with matter is essential for the understanding of radiation dosimetry and development of new dosimetry techniques. The concepts behind the two quantities have been enunciated many years ago and described in many scientific papers, review articles, and textbooks. Data dealing with energy transfer and energy absorption as well as the associated mass energy transfer coefficient and the mass energy absorption coefficient are readily available in web-based tabular forms. However, tables, even when available in detailed and easy to access form, do not lend themselves to serve as visual aid to promote better understanding of the dosimetric quantities related to energy transfer and energy absorption as well as their relationship to the photon energy and absorber atomic number. This paper uses graphs and illustrations, in addition to well-known mathematical relationships, to guide the reader in a systematic manner through the various stages involved in the derivation of energy absorbed in medium and its associated quantity, the mass energy absorption coefficient, from the mass attenuation coefficient.

  1. Hole-transfer induced energy transfer in perylene diimide dyads with a donor-spacer-acceptor motif.

    PubMed

    Kölle, Patrick; Pugliesi, Igor; Langhals, Heinz; Wilcken, Roland; Esterbauer, Andreas J; de Vivie-Riedle, Regina; Riedle, Eberhard

    2015-10-14

    We investigate the photoinduced dynamics of perylene diimide dyads based on a donor-spacer-acceptor motif with polyyne spacers of varying length by pump-probe spectroscopy, time resolved fluorescence, chemical variation and quantum chemistry. While the dyads with pyridine based polyyne spacers undergo energy transfer with near-unity quantum efficiency, in the dyads with phenyl based polyyne spacers the energy transfer efficiency drops below 50%. This suggests the presence of a competing electron transfer process from the spacer to the energy donor as the excitation sink. Transient absorption spectra, however, reveal that the spacer actually mediates the energy transfer dynamics. The ground state bleach features of the polyyne spacers appear due to the electron transfer decay with the same time constant present in the rise of the ground state bleach and stimulated emission of the perylene energy acceptor. Although the electron transfer process initially quenches the fluorescence of the donor it does not inhibit energy transfer to the perylene energy acceptor. The transient signatures reveal that electron and energy transfer processes are sequential and indicate that the donor-spacer electron transfer state itself is responsible for the energy transfer. Through the introduction of a Dexter blocker unit into the spacer we can clearly exclude any through bond Dexter-type energy transfer. Ab initio calculations on the donor-spacer and the donor-spacer-acceptor systems reveal the existence of a bright charge transfer state that is close in energy to the locally excited state of the acceptor. Multipole-multipole interactions between the bright charge transfer state and the acceptor state enable the energy transfer. We term this mechanism coupled hole-transfer FRET. These dyads represent a first example that shows how electron transfer can be connected to energy transfer for use in novel photovoltaic and optoelectronic devices. PMID:26347443

  2. Radiative energy transfer in disordered photonic crystals.

    PubMed

    Erementchouk, M V; Deych, L I; Noh, H; Cao, H; Lisyansky, A A

    2009-04-29

    The difficulty of description of the radiative transfer in disordered photonic crystals arises from the necessity to consider on an equal footing the wave scattering by periodic modulations of the dielectric function and by its random inhomogeneities. We resolve this difficulty by approaching this problem from the standpoint of the general multiple scattering theory in media with an arbitrary regular profile of the dielectric function. We use the general asymptotic solution of the Bethe-Salpeter equation in order to show that for a sufficiently weak disorder the diffusion limit in disordered photonic crystals is presented by incoherent superpositions of the modes of the ideal structure with weights inversely proportional to the respective group velocities. The radiative transfer and the diffusion equations are derived as a relaxation of long scale deviations from this limiting distribution. In particular, it is shown that in general the diffusion is anisotropic unless the crystal has sufficiently rich symmetry, say, the square lattice in 2D or the cubic lattice in 3D. In this case, the diffusion is isotropic and only in this case can the effect of the disorder be characterized by a single mean free path depending on frequency. PMID:21825416

  3. Substorms and magnetospheric energy transfer processes

    NASA Technical Reports Server (NTRS)

    Swift, D. W.

    1980-01-01

    Evidence is presented which suggests a direct process for the conversion of solar wind energy into the various manifestations of the auroral substorm. This is in contrast to the widely accepted premise that solar wind energy is accumulated in the magnetosphere and then released by an instability process occurring in the magnetotail. It is shown that much of the plasma sheet behavior associated with auroral substorms can be interpreted in terms of single-particle models and simple variations of the cross-tail electric field intensity which does not invoke release of stored magnetic energy. It is also pointed out that the major entry of substorm energy into the magnetosphere occurs through the boundaries of the lobes of the magnetotail. This paper is not intended to be a complete theory of the magnetospheric substorm - rather the intention of this paper is to point out directions of research deserving of more attention.

  4. On Kinetics Modeling of Vibrational Energy Transfer

    NASA Technical Reports Server (NTRS)

    Gilmore, John O.; Sharma, Surendra P.; Cavolowsky, John A. (Technical Monitor)

    1996-01-01

    Two models of vibrational energy exchange are compared at equilibrium to the elementary vibrational exchange reaction for a binary mixture. The first model, non-linear in the species vibrational energies, was derived by Schwartz, Slawsky, and Herzfeld (SSH) by considering the detailed kinetics of vibrational energy levels. This model recovers the result demanded at equilibrium by the elementary reaction. The second model is more recent, and is gaining use in certain areas of computational fluid dynamics. This model, linear in the species vibrational energies, is shown not to recover the required equilibrium result. Further, this more recent model is inconsistent with its suggested rate constants in that those rate constants were inferred from measurements by using the SSH model to reduce the data. The non-linear versus linear nature of these two models can lead to significant differences in vibrational energy coupling. Use of the contemporary model may lead to significant misconceptions, especially when integrated in computer codes considering multiple energy coupling mechanisms.

  5. Enhancing Förster nonradiative energy transfer via plasmon interaction

    NASA Astrophysics Data System (ADS)

    Higgins, L. J.; Zhang, X.; Marocico, C. A.; Murphy, G. P.; Karanikolas, V. K.; Gun'ko, Y. K.; Lesnyak, V.; Gaponik, N.; Susha, A. S.; Rogach, A. L.; Parbrook, P. J.; Bradley, A. L.

    2016-04-01

    Plasmon-enhanced nonradiative energy transfer is demonstrated in two inorganic semiconductor systems. The first is comprised of colloidal nanocrystal CdTe donor and acceptor quantum dots, while the second is a hybrid InGaN quantum well-CdSe/ZnS quantum dot donor-acceptor system. Both structures are in a planar geometry. In the first case a monolayer of Au nanospheres is sandwiched between donor and acceptor quantum dot monolayers. The largest energy transfer efficiency is seen when the donor is ~3 nm from the Au nanopshere. A plasmon-enhanced energy transfer efficiency of ~ 40% has been achieved for a separation of 3 nm between the Au nanopshere monolayer and the acceptor monolayer. Despite the increased energy transfer efficiency these conditions result in strong quenching of the acceptor QD emission. By tuning the Au nanosphere concentration and Au nanosphere-acceptor QD separation the acceptor QD emission can be increased by a factor of ~2.8. The plasmon-enhanced nonradiative energy transfer is observed to extend over larger distances than conventional Forster resonance energy transfer. Under the experimental conditions reported herein, it can be described by the same d-4 dependence but with a larger characteristic distance. Using a Ag nanobox array plasmonic component plasmon-enhanced nonradiative energy transfer has also demonstrated from an InGaN quantum well to a ~80 nm thick layer of CdSe/ZnS colloidal quantum dots. An efficiency of ~27% is achieved, with an overall increase in the QD emission by ~70%.

  6. Triangulating Nucleic Acid Conformations Using Multicolor Surface Energy Transfer.

    PubMed

    Riskowski, Ryan A; Armstrong, Rachel E; Greenbaum, Nancy L; Strouse, Geoffrey F

    2016-02-23

    Optical ruler methods employing multiple fluorescent labels offer great potential for correlating distances among several sites, but are generally limited to interlabel distances under 10 nm and suffer from complications due to spectral overlap. Here we demonstrate a multicolor surface energy transfer (McSET) technique able to triangulate multiple points on a biopolymer, allowing for analysis of global structure in complex biomolecules. McSET couples the competitive energy transfer pathways of Förster Resonance Energy Transfer (FRET) with gold-nanoparticle mediated Surface Energy Transfer (SET) in order to correlate systematically labeled points on the structure at distances greater than 10 nm and with reduced spectral overlap. To demonstrate the McSET method, the structures of a linear B-DNA and a more complex folded RNA ribozyme were analyzed within the McSET mathematical framework. The improved multicolor optical ruler method takes advantage of the broad spectral range and distances achievable when using a gold nanoparticle as the lowest energy acceptor. The ability to report distance information simultaneously across multiple length scales, short-range (10-50 Å), mid-range (50-150 Å), and long-range (150-350 Å), distinguishes this approach from other multicolor energy transfer methods. PMID:26795549

  7. The feasibility of coherent energy transfer in microtubules

    PubMed Central

    Craddock, Travis John Adrian; Friesen, Douglas; Mane, Jonathan; Hameroff, Stuart; Tuszynski, Jack A.

    2014-01-01

    It was once purported that biological systems were far too ‘warm and wet’ to support quantum phenomena mainly owing to thermal effects disrupting quantum coherence. However, recent experimental results and theoretical analyses have shown that thermal energy may assist, rather than disrupt, quantum coherent transport, especially in the ‘dry’ hydrophobic interiors of biomolecules. Specifically, evidence has been accumulating for the necessary involvement of quantum coherent energy transfer between uniquely arranged chromophores in light harvesting photosynthetic complexes. The ‘tubulin’ subunit proteins, which comprise microtubules, also possess a distinct architecture of chromophores, namely aromatic amino acids, including tryptophan. The geometry and dipolar properties of these aromatics are similar to those found in photosynthetic units indicating that tubulin may support coherent energy transfer. Tubulin aggregated into microtubule geometric lattices may support such energy transfer, which could be important for biological signalling and communication essential to living processes. Here, we perform a computational investigation of energy transfer between chromophoric amino acids in tubulin via dipole excitations coupled to the surrounding thermal environment. We present the spatial structure and energetic properties of the tryptophan residues in the microtubule constituent protein tubulin. Plausibility arguments for the conditions favouring a quantum mechanism of signal propagation along a microtubule are provided. Overall, we find that coherent energy transfer in tubulin and microtubules is biologically feasible. PMID:25232047

  8. Corrosion and Heat Transfer Characteristics of Water Dispersed with Carboxylate Additives and Multi Walled Carbon Nano Tubes

    NASA Astrophysics Data System (ADS)

    Moorthy, Chellapilla V. K. N. S. N.; Srinivas, Vadapalli

    2016-02-01

    This paper summarizes a recent work on anti-corrosive properties and enhanced heat transfer properties of carboxylated water based nanofluids. Water mixed with sebacic acid as carboxylate additive found to be resistant to corrosion and suitable for automotive environment. The carboxylated water is dispersed with very low mass concentration of carbon nano tubes at 0.025, 0.05 and 0.1 %. The stability of nanofluids in terms of zeta potential is found to be good with carboxylated water compared to normal water. The heat transfer performance of nanofluids is carried out on an air cooled heat exchanger similar to an automotive radiator with incoming air velocities across radiator at 5, 10 and 15 m/s. The flow Reynolds number of water is in the range of 2500-6000 indicating developing flow regime. The corrosion resistance of nanofluids is found to be good indicating its suitability to automotive environment. There is a slight increase in viscosity and marginal decrease in the specific heat of nanofluids with addition of carboxylate as well as CNTs. Significant improvement is observed in the thermal conductivity of nanofluids dispersed with CNTs. During heat transfer experimentation, the inside heat transfer coefficient and overall heat transfer coefficient has also improved markedly. It is also found that the velocity of air and flow rate of coolant plays an important role in enhancement of the heat transfer coefficient and overall heat transfer coefficient.

  9. Early Career: Templating of Liquid Crystal Microstructures by Reversible Addition-Fragmentation Chain Transfer Polymerization

    SciTech Connect

    Heinen, Jennifer M

    2014-12-31

    This research has shown that the microstructure of self-assembled copolymers can be decoupled from the polymer chemistry. The simplest polymer architecture, linear block copolymers, is valuable for a broad range of applications, including adhesives and coatings, medical devices, electronics and energy storage, because these block copolymers reproducibly self-assemble into microphase separated nanoscale domains. Unfortunately, the self-assembled microstructure is tuned by polymer composition, thus limiting the potential to simultaneously optimize chemical, mechanical, and transport properties for desired applications. To this end, much work was been put into manipulating block copolymer self-assembly independently of polymer composition. These efforts have included the use of additives or solvents to alter polymer chain conformation, the addition of a third monomer to produce ABC triblock terpolymers, architectures with mixed blocks, such as tapered/gradient polymers, and the synthesis of other nonlinear molecular architectures. This work has shown that the microstructures formed by linear ABC terpolymers can be altered by controlling the architecture of the polymer molecules at a constant monomer composition, so that the microstructure is tuned independently from the chemical properties.

  10. Photoinduced charge and energy transfer in molecular wires.

    PubMed

    Gilbert, Mélina; Albinsson, Bo

    2015-02-21

    Exploring charge and energy transport in donor-bridge-acceptor systems is an important research field which is essential for the fundamental knowledge necessary to develop future applications. These studies help creating valuable knowledge to respond to today's challenges to develop functionalized molecular systems for artificial photosynthesis, photovoltaics or molecular scale electronics. This tutorial review focuses on photo-induced charge/energy transfer in covalently linked donor-bridge-acceptor (D-B-A) systems. Of utmost importance in such systems is to understand how to control signal transmission, i.e. how fast electrons or excitation energy could be transferred between the donor and acceptor and the role played by the bridge (the "molecular wire"). After a brief description of the electron and energy transfer theory, we aim to give a simple yet accurate picture of the complex role played by the bridge to sustain donor-acceptor electronic communication. Special emphasis is put on understanding bridge energetics and conformational dynamics effects on the distance dependence of the donor-acceptor electronic coupling and transfer rates. Several examples of donor-bridge-acceptor systems from the literature are described as a support to the discussion. Finally, porphyrin-based molecular wires are introduced, and the relationship between their electronic structure and photophysical properties is outlined. In strongly conjugated porphyrin systems, limitations of the existing electron transfer theory to interpret the distance dependence of the transfer rates are also discussed. PMID:25212903

  11. A molecularly based theory for electron transfer reorganization energy

    NASA Astrophysics Data System (ADS)

    Zhuang, Bilin; Wang, Zhen-Gang

    2015-12-01

    Using field-theoretic techniques, we develop a molecularly based dipolar self-consistent-field theory (DSCFT) for charge solvation in pure solvents under equilibrium and nonequilibrium conditions and apply it to the reorganization energy of electron transfer reactions. The DSCFT uses a set of molecular parameters, such as the solvent molecule's permanent dipole moment and polarizability, thus avoiding approximations that are inherent in treating the solvent as a linear dielectric medium. A simple, analytical expression for the free energy is obtained in terms of the equilibrium and nonequilibrium electrostatic potential profiles and electric susceptibilities, which are obtained by solving a set of self-consistent equations. With no adjustable parameters, the DSCFT predicts activation energies and reorganization energies in good agreement with previous experiments and calculations for the electron transfer between metallic ions. Because the DSCFT is able to describe the properties of the solvent in the immediate vicinity of the charges, it is unnecessary to distinguish between the inner-sphere and outer-sphere solvent molecules in the calculation of the reorganization energy as in previous work. Furthermore, examining the nonequilibrium free energy surfaces of electron transfer, we find that the nonequilibrium free energy is well approximated by a double parabola for self-exchange reactions, but the curvature of the nonequilibrium free energy surface depends on the charges of the electron-transferring species, contrary to the prediction by the linear dielectric theory.

  12. A molecularly based theory for electron transfer reorganization energy

    SciTech Connect

    Zhuang, Bilin; Wang, Zhen-Gang

    2015-12-14

    Using field-theoretic techniques, we develop a molecularly based dipolar self-consistent-field theory (DSCFT) for charge solvation in pure solvents under equilibrium and nonequilibrium conditions and apply it to the reorganization energy of electron transfer reactions. The DSCFT uses a set of molecular parameters, such as the solvent molecule’s permanent dipole moment and polarizability, thus avoiding approximations that are inherent in treating the solvent as a linear dielectric medium. A simple, analytical expression for the free energy is obtained in terms of the equilibrium and nonequilibrium electrostatic potential profiles and electric susceptibilities, which are obtained by solving a set of self-consistent equations. With no adjustable parameters, the DSCFT predicts activation energies and reorganization energies in good agreement with previous experiments and calculations for the electron transfer between metallic ions. Because the DSCFT is able to describe the properties of the solvent in the immediate vicinity of the charges, it is unnecessary to distinguish between the inner-sphere and outer-sphere solvent molecules in the calculation of the reorganization energy as in previous work. Furthermore, examining the nonequilibrium free energy surfaces of electron transfer, we find that the nonequilibrium free energy is well approximated by a double parabola for self-exchange reactions, but the curvature of the nonequilibrium free energy surface depends on the charges of the electron-transferring species, contrary to the prediction by the linear dielectric theory.

  13. Efficient Radioisotope Energy Transfer by Gold Nanoclusters for Molecular Imaging.

    PubMed

    Volotskova, Olga; Sun, Conroy; Stafford, Jason H; Koh, Ai Leen; Ma, Xiaowei; Cheng, Zhen; Cui, Bianxiao; Pratx, Guillem; Xing, Lei

    2015-08-26

    Beta-emitting isotopes Fluorine-18 and Yttrium-90 are tested for their potential to stimulate gold nanoclusters conjugated with blood serum proteins (AuNCs). AuNCs excited by either medical radioisotope are found to be highly effective ionizing radiation energy transfer mediators, suitable for in vivo optical imaging. AuNCs synthesized with protein templates convert beta-decaying radioisotope energy into tissue-penetrating optical signals between 620 and 800 nm. Optical signals are not detected from AuNCs incubated with Technetium-99m, a pure gamma emitter that is used as a control. Optical emission from AuNCs is not proportional to Cerenkov radiation, indicating that the energy transfer between the radionuclide and AuNC is only partially mediated by Cerenkov photons. A direct Coulombic interaction is proposed as a novel and significant mechanism of energy transfer between decaying radionuclides and AuNCs. PMID:25973916

  14. International cooperation for renewable energy transfer

    SciTech Connect

    Wolfe, M.H.

    1992-06-01

    This paper reports that in considering the potential of major renewable energy resources in relation to their remoteness from demand centers, it is necessary to take a global view of the implications of their utilization. The present concerns regarding global warming and environmental degradation from fossil fuel combustion could be given active direction if the positive benefits of renewable energy could be realized on a meaningful scale. The dire prospect of global warming looms large in the scientific consciousness, but strategies to counter the effects of increased release of carbon dioxide and other greenhouse gases are just beginning to emerge along with remedial measures to address other environmental threats. One of the ways to achieve this is to place more reliance on renewable energy. As the impact of small-scale dispersed sources of renewable energy is minimal in comparison with fossil fuel usage, a meaningful impact could only be made by drawing upon major sources of renewable energy, mainly hydropower, tidal, and solar, in large capacity installations concentrated at sites relatively far from demand centers. There are sites that warrant serious consideration in the face of the growing environmental impact of fossil fuel usage. However, to realize this objective, an environmental imperative should be adopted that would place the importance of global environmental security on a par with present concerns for national security.

  15. Volume-energy parameters for heat transfer to supercritical fluids

    NASA Technical Reports Server (NTRS)

    Kumakawa, A.; Niino, M.; Hendricks, R. C.; Giarratano, P. J.; Arp, V. D.

    1986-01-01

    Reduced Nusselt numbers of supercritical fluids from different sources were grouped by several volume-energy parameters. A modified bulk expansion parameter was introduced based on a comparative analysis of data scatter. Heat transfer experiments on liquefied methane were conducted under near-critical conditions in order to confirm the usefulness of the parameters. It was experimentally revealed that heat transfer characteristics of near-critical methane are similar to those of hydrogen. It was shown that the modified bulk expansion parameter and the Gibbs-energy parameter grouped the heat transfer data of hydrogen, oxygen and methane including the present data on near-critical methane. It was also indicated that the effects of surface roughness on heat transfer were very important in grouping the data of high Reynolds numbers.

  16. Multi-neutron transfer reactions at sub-barrier energies.

    SciTech Connect

    Rehm, K. E.

    1998-01-20

    The optimum conditions for multi-neutron transfer have been studied in the system {sup 58}Ni + {sup 124}Sn at bombarding energies at and below the Coulomb barrier. The experiments were performed in inverse kinematics with a {sup 124}Sn beam bombarding a {sup 58}Ni target. The particles were identified with respect to mass and Z in the split-pole spectrograph with a hybrid focal plane detector with mass and Z-resolutions of A/{Delta}A = 150 and Z/{Delta}Z = 70. At all energies the transfer of up to 6 neutrons was observed. The yields for these transfer reactions are found to decrease by about a factor of four for each transferred neutron.

  17. A Classroom Demonstration of Wireless Energy Transfer

    ERIC Educational Resources Information Center

    Luczak, Matthew; Baker, Blane

    2010-01-01

    Resonance is one of the recurring themes in physics and, as such, is important in research applications and in explaining many everyday phenomena. Students often encounter resonance during studies of simple harmonic motion, sound, mechanical waves and AC circuits. Alternatively, or in addition, resonance can be demonstrated in the context of…

  18. Dependence of the energy transfer to graphene on the excitation energy

    SciTech Connect

    Mackowski, Sebastian Kamińska, Izabela

    2015-07-13

    Fluorescence studies of natural photosynthetic complexes on a graphene layer demonstrate pronounced influence of the excitation wavelength on the energy transfer efficiency to graphene. Ultraviolet light yields much faster decay of fluorescence, with average efficiencies of the energy transfer equal to 87% and 65% for excitation at 405 nm and 640 nm, respectively. This implies that focused light changes locally the properties of graphene affecting the energy transfer dynamics, in an analogous way as in the case of metallic nanostructures. Demonstrating optical control of the energy transfer is important for exploiting unique properties of graphene in photonic and sensing architectures.

  19. Energy Transfer Dynamics in Metal-Organic Frameworks

    SciTech Connect

    Kent, Caleb A.; Mehl, Brian P.; Ma, Liqing; Papanikolas, John M.; Meyer, Thomas J.; Lin, Wenbin

    2010-09-22

    Isomorphous metal-organic frameworks (MOFs) based on {M[4,4'-(HO2C)2-bpy]2bpy2+ building blocks (where M = Ru or Os) were designed and synthesized to study the classic Ru to Os energy transfer process that has potential applications in light-harvesting with supramolecular assemblies. The crystalline nature of the MOFs allows precise determination of the distances between metal centers by X-ray diffraction, thereby facilitating the study of the Ru→Os energy transfer process. The mixed-metal MOFs with 0.3, 0.6, 1.4, and 2.6 mol % Os doping were also synthesized in order to study the energy transfer dynamics with a two-photon excitation at 850 nm. The Ru lifetime at 620 nm decreases from 171 ns in the pure Ru MOF to 29 ns in the sample with 2.6 mol % Os doping. In the mixed-metal samples, energy transfer was observed with an initial growth in Os emission corresponding with the rate of decay of the Ru excited state. These results demonstrate rapid, efficient energy migration and long distance transfer in isomorphous MOFs.

  20. Paths to Förster's resonance energy transfer (FRET) theory

    NASA Astrophysics Data System (ADS)

    Masters, B. R.

    2014-02-01

    Theodor Förster (1910-1974) developed a phenomenological theory of nonradiative resonance energy transfer which proved to be transformative in the fields of chemistry, biochemistry, and biology. This paper explores the experimental and the theoretical antecedents of Förster's theory of resonance energy transfer (FRET). Early studies of sensitized fluorescence, fluorescence depolarization, and photosynthesis demonstrated the phenomena of long-range energy transfer. At the same time physicists developed theoretical models which contained common physical mechanisms and parameters: oscillating dipoles as models for the atoms or molecules, dipole-dipole coupling for the interaction, and a distance R0 that is optimal for resonance energy transfer. Early theories predicted R0 that was too large as compared to experiments. Finally, in 1946 Förster developed a classical theory and in 1948 he developed a quantum mechanical theory; both theories predicted an inverse sixth power dependence of the rate of energy transfer and a R0 that agreed with experiments. This paper attempts to determine why Förster succeeded when the other theoreticians failed to develop the correct theory. The putative roles of interdisciplinary education and collaborative research are discussed. Furthermore, I explore the role of science journals and their specific audiences in the popularization of FRET to a broad interdisciplinary community.

  1. Production and Transfer of Energy and Information in Hamiltonian Systems

    PubMed Central

    Antonopoulos, Chris G.; Bianco-Martinez, Ezequiel; Baptista, Murilo S.

    2014-01-01

    We present novel results that relate energy and information transfer with sensitivity to initial conditions in chaotic multi-dimensional Hamiltonian systems. We show the relation among Kolmogorov-Sinai entropy, Lyapunov exponents, and upper bounds for the Mutual Information Rate calculated in the Hamiltonian phase space and on bi-dimensional subspaces. Our main result is that the net amount of transfer from kinetic to potential energy per unit of time is a power-law of the upper bound for the Mutual Information Rate between kinetic and potential energies, and also a power-law of the Kolmogorov-Sinai entropy. Therefore, transfer of energy is related with both transfer and production of information. However, the power-law nature of this relation means that a small increment of energy transferred leads to a relatively much larger increase of the information exchanged. Then, we propose an “experimental” implementation of a 1-dimensional communication channel based on a Hamiltonian system, and calculate the actual rate with which information is exchanged between the first and last particle of the channel. Finally, a relation between our results and important quantities of thermodynamics is presented. PMID:24586891

  2. Correlated energy transfer between two ultracold atomic species

    NASA Astrophysics Data System (ADS)

    Krönke, Sven; Knörzer, Johannes; Schmelcher, Peter

    2015-05-01

    We study a single atom as an open quantum system, which is initially prepared in a coherent state of low energy and oscillates in a one-dimensional harmonic trap through an interacting ensemble of NA bosons, held in a displaced trap [arXiv:1410.8676]. The non-equilibrium quantum dynamics of the total system is simulated by means of an ab-initio method, giving us access to all properties of the open system and its finite environment. In this talk, we focus on unraveling the interplay of energy exchange and correlations between the subsystems, which are coupled in such a spatio-temporally localized manner. We show that an inter-species interaction-induced level splitting accelerates the energy transfer between the atomic species for larger NA, which becomes less complete at the same time. System-environment correlations prove to be significant except for times when the excess energy distribution among the subsystems is highly imbalanced. These correlations result in incoherent energy transfer processes, which accelerate the early energy donation of the single atom. By analyzing correlations between intra-subsystem excitations, certain energy transfer channels are shown to be (dis-)favored depending on the instantaneous direction of transfer.

  3. Energy transfer between laser beams crossing in ignition hohlraums

    SciTech Connect

    Michel, P; Divol, L; Williams, E A; Thomas, C A; Callahan, D A; Weber, S; Haan, S W; Salmonson, J D; Dixit, S; Hinkel, D E; Edwards, M J; MacGowan, B J; Lindl, J D; Glenzer, S H; Suter, L J

    2008-10-03

    The full scale modeling of power transfer between laser beams crossing in plasmas is presented. A new model was developed, allowing calculation of the propagation and coupling of pairs of laser beams with their associated plasma wave in three dimensions. The full laser beam smoothing techniques used in ignition experiments are modeled, and their effects on crossed-beam energy transfer is investigated. A shift in wavelength between the beams can move the instability off resonance and reduce the transfer, hence preserving the symmetry of the capsule implosion.

  4. Radiative energy transfer in molecular gases

    NASA Technical Reports Server (NTRS)

    Tiwari, Surendra N.

    1992-01-01

    Basic formulations, analyses, and numerical procedures are presented to study radiative interactions in gray as well as nongray gases under different physical and flow conditions. After preliminary fluid-dynamical considerations, essential governing equations for radiative transport are presented that are applicable under local and nonlocal thermodynamic equilibrium conditions. Auxiliary relations for relaxation times and spectral absorption models are also provided. For specific applications, several simple gaseous systems are analyzed. The first system considered consists of a gas bounded by two parallel plates having the same temperature. Within the gas there is a uniform heat source per unit volume. For this system, both vibrational nonequilibrium effects and radiation conduction interactions are studied. The second system consists of fully developed laminar flow and heat transfer in a parallel plate duct under the boundary condition of a uniform surface heat flux. For this system, effects of gray surface emittance are studied. With the single exception of a circular geometry, the third system is considered identical to the second system. Here, the influence of nongray walls is also studied.

  5. Förster-Induced Energy Transfer in Functionalized Graphene.

    PubMed

    Malic, Ermin; Appel, Heiko; Hofmann, Oliver T; Rubio, Angel

    2014-05-01

    Carbon nanostructures are ideal substrates for functionalization with molecules since they consist of a single atomic layer giving rise to an extraordinary sensitivity to changes in their surrounding. The functionalization opens a new research field of hybrid nanostructures with tailored properties. Here, we present a microscopic view on the substrate-molecule interaction in the exemplary hybrid material consisting of graphene functionalized with perylene molecules. First experiments on similar systems have been recently realized illustrating an extremely efficient transfer of excitation energy from adsorbed molecules to the carbon substrate, a process with a large application potential for high-efficiency photovoltaic devices and biomedical imaging and sensing. So far, there has been no microscopically founded explanation for the observed energy transfer. Based on first-principle calculations, we have explicitly investigated the different transfer mechanisms revealing the crucial importance of Förster coupling. Due to the efficient Coulomb interaction in graphene, we obtain strong Förster rates in the range of 1/fs. We investigate its dependence on the substrate-molecule distance R and describe the impact of the momentum transfer q for an efficient energy transfer. Furthermore, we find that the Dexter transfer mechanism is negligibly small due to the vanishing overlap between the involved strongly localized orbital functions. The gained insights are applicable to a variety of carbon-based hybrid nanostructures. PMID:24808936

  6. Förster-Induced Energy Transfer in Functionalized Graphene

    PubMed Central

    2014-01-01

    Carbon nanostructures are ideal substrates for functionalization with molecules since they consist of a single atomic layer giving rise to an extraordinary sensitivity to changes in their surrounding. The functionalization opens a new research field of hybrid nanostructures with tailored properties. Here, we present a microscopic view on the substrate–molecule interaction in the exemplary hybrid material consisting of graphene functionalized with perylene molecules. First experiments on similar systems have been recently realized illustrating an extremely efficient transfer of excitation energy from adsorbed molecules to the carbon substrate, a process with a large application potential for high-efficiency photovoltaic devices and biomedical imaging and sensing. So far, there has been no microscopically founded explanation for the observed energy transfer. Based on first-principle calculations, we have explicitly investigated the different transfer mechanisms revealing the crucial importance of Förster coupling. Due to the efficient Coulomb interaction in graphene, we obtain strong Förster rates in the range of 1/fs. We investigate its dependence on the substrate–molecule distance R and describe the impact of the momentum transfer q for an efficient energy transfer. Furthermore, we find that the Dexter transfer mechanism is negligibly small due to the vanishing overlap between the involved strongly localized orbital functions. The gained insights are applicable to a variety of carbon-based hybrid nanostructures. PMID:24808936

  7. Tech Transfer Webinar: Energy Absorbing Materials

    SciTech Connect

    Duoss, Eric

    2014-06-17

    A new material has been designed and manufactured at LLNL that can absorb mechanical energy--a cushion--while also providing protection against sheering. This ordered cellular material is 3D printed using direct ink writing techniques under development at LLNL. It is expected to find utility in application spaces that currently use unordered foams, such as sporting and consumer goods as well as defense and aerospace.

  8. Tech Transfer Webinar: Energy Absorbing Materials

    ScienceCinema

    Duoss, Eric

    2014-07-15

    A new material has been designed and manufactured at LLNL that can absorb mechanical energy--a cushion--while also providing protection against sheering. This ordered cellular material is 3D printed using direct ink writing techniques under development at LLNL. It is expected to find utility in application spaces that currently use unordered foams, such as sporting and consumer goods as well as defense and aerospace.

  9. Energy transfer at gas-liquid interface: Towards energetic materials

    NASA Astrophysics Data System (ADS)

    Szabo, Tamas

    Physicochemical surface processes have great importance in the different fields of everyday life and science. Computational characterization of collisional energy transfer at a gas-liquid interface is a helpful tool to interpret recent experimental studies and to yield insight into the energy feedback mechanism of multiphase combustion problems. As a first step, a simple Lennard-Jones system was used to investigate the dependence of the collisional energy transfer and the gas atom trapping probabilities on the temperature of the bulk liquid, on the gas/liquid particle mass ratios, on the incident angle of the impinging projectile, and on the gas-liquid interaction strength. We find in accord with the experimental results that the kinematic effects dominate the energy transfer dynamics, but the importance of the role of surface roughening as the temperature of the liquid increases is also seen. The second system, nitromethane was chosen to extend the range of simulations. It is a molecular model system, representing nitramine-type energetic materials. Having had a good potential description for the nitromethane molecule including all internal degrees of freedom, we generated simplified molecular systems based on the original nitromethane model to isolate particular features of the dynamics. We have investigated the effect of the initial incident energy, of the inclusion of the internal degrees of freedom, of the initial incident kinetic energy and of the gas-surface interaction strength. The incorporation of internal degrees of freedom enhanced the collisional energy transfer. These calculations also point to the importance of simple kinematics as it predicts the increase of the ratio of energy transferred with increased initial incident energy of the gas particle.

  10. Energy-transfer mechanisms in the CH3F-SF6 optically pumped laser

    NASA Technical Reports Server (NTRS)

    Lawandy, N. M.; Koepf, G. A.

    1980-01-01

    The power of an optically pumped CH3F laser operating on the 496-micron line has been doubled with the addition of SF6 without any corresponding increase in pump absorption. It is suggested that a near-resonant energy transfer between CH3F and SF6 followed by SF6 deactivation is the mechanism responsible for the enhancement.

  11. Collisionless inter-species energy transfer and turbulent heating in drift wave turbulence

    SciTech Connect

    Zhao, L.; Diamond, P. H.

    2012-08-15

    We reconsider the classic problems of calculating 'turbulent heating' and collisionless inter-species transfer of energy in drift wave turbulence. These issues are of interest for low collisionality, electron heated plasmas, such as ITER, where collisionless energy transfer from electrons to ions is likely to be significant. From the wave Poynting theorem at steady state, a volume integral over an annulus r{sub 1}=-S{sub r}|{sub r{sub 1}{sup r{sub 2}}}{ne}0. Here S{sub r} is the wave energy density flux in the radial direction. Thus, a wave energy flux differential across an annular region indeed gives rise to a net heating, in contrast to previous predictions. This heating is related to the Reynolds work by the zonal flow, since S{sub r} is directly linked to the zonal flow drive. In addition to net heating, there is inter-species heat transfer. For collisionless electron drift waves, the total turbulent energy source for collisionless heat transfer is due to quasilinear electron cooling. Subsequent quasilinear ion heating occurs through linear ion Landau damping. In addition, perpendicular heating via ion polarization currents contributes to ion heating. Since at steady state, Reynolds work of the turbulence on the zonal flow must balance zonal flow frictional damping ({approx}{nu}{sub ii}{sup 2}{approx}|(e{phi}(tilde sign)/T)|{sup 4}), it is no surprise that zonal flow friction appears as an important channel for ion heating. This process of energy transfer via zonal flow has not previously been accounted for in analyses of energy transfer. As an application, we compare the rate of turbulent energy transfer in a low collisionality plasma with the rate of the energy transfer by collisions. The result shows that the collisionless turbulent energy transfer is a significant energy coupling process for ITER plasma.

  12. Energy transfer in a molecular motor in the Kramers regime.

    PubMed

    Challis, K J; Jack, Michael W

    2013-10-01

    We present a theoretical treatment of energy transfer in a molecular motor described in terms of overdamped Brownian motion on a multidimensional tilted periodic potential. The tilt represents a thermodynamic force driving the system out of equilibrium and, for nonseparable potentials, energy transfer occurs between degrees of freedom. For deep potential wells, the continuous theory transforms to a discrete master equation that is tractable analytically. We use this master equation to derive formal expressions for the hopping rates, drift and diffusion, and the efficiency and rate of energy transfer in terms of the thermodynamic force. These results span both strong and weak coupling between degrees of freedom, describe the near and far from equilibrium regimes, and are consistent with generalized detailed balance and the Onsager relations. We thereby derive a number of diverse results for molecular motors within a single theoretical framework. PMID:24229123

  13. Forster energy transfer in chlorosomes of green photosynthetic bacteria

    NASA Technical Reports Server (NTRS)

    Causgrove, T. P.; Brune, D. C.; Blankenship, R. E.

    1992-01-01

    Energy transfer properties of whole cells and chlorosome antenna complexes isolated from the green sulfur bacteria Chlorobium limicola (containing bacteriochlorophyll c), Chlorobium vibrioforme (containing bacteriochlorophyll d) and Pelodictyon phaeoclathratiforme (containing bacteriochlorophyll e) were measured. The spectral overlap of the major chlorosome pigment (bacteriochlorophyll c, d or, e) with the bacteriochlorophyll a B795 chlorosome baseplate pigment is greatest for bacteriochlorophyll c and smallest for bacteriochlorophyll e. The absorbance and fluorescence spectra of isolated chlorosomes were measured, fitted to gaussian curves and the overlap factors with B795 calculated. Energy transfer times from the bacteriochlorophyll c, d or e to B795 were measured in whole cells and the results interpreted in terms of the Forster theory of energy transfer.

  14. Mapping energy transfer channels in fucoxanthin-chlorophyll protein complex.

    PubMed

    Gelzinis, Andrius; Butkus, Vytautas; Songaila, Egidijus; Augulis, Ramūnas; Gall, Andrew; Büchel, Claudia; Robert, Bruno; Abramavicius, Darius; Zigmantas, Donatas; Valkunas, Leonas

    2015-02-01

    Fucoxanthin-chlorophyll protein (FCP) is the key molecular complex performing the light-harvesting function in diatoms, which, being a major group of algae, are responsible for up to one quarter of the total primary production on Earth. These photosynthetic organisms contain an unusually large amount of the carotenoid fucoxanthin, which absorbs the light in the blue-green spectral region and transfers the captured excitation energy to the FCP-bound chlorophylls. Due to the large number of fucoxanthins, the excitation energy transfer cascades in these complexes are particularly tangled. In this work we present the two-color two-dimensional electronic spectroscopy experiments on FCP. Analysis of the data using the modified decay associated spectra permits a detailed mapping of the excitation frequency dependent energy transfer flow with a femtosecond time resolution. PMID:25445318

  15. Electronic coherence in electronic energy transfer despite fast dephasing

    NASA Astrophysics Data System (ADS)

    Scholes, Gregory

    2009-03-01

    F"orster resonance energy transfer (FRET) is a common and fundamental photophysical process in life and materials sciences. FRET is an interchromophore relaxation process that transmits the electronic excitation from an initially excited donor to a ground state acceptor chromophore (light-absorbing moleule). FRET is used, for example, to harvest light in photosynthesis, measure distances in proteins, and it accelerates the photodegradation of polymers. In recent years attention has turned to the study of FRET in complex assemblies of molecules. While F"orster theory has enabled the efficiency of FRET to be predicted and analyzed in numerous and diverse areas of study, recent work has aimed to discover ways beyond the F"oster mechanism by which electronic energy can be transferred. The talk will compare and contrast theoretical and experimental studies of excitation relaxation in photosynthetic antenna systems with the conjugated polymer poly[2-methoxy,5-(2'-ethyl-hexoxy)-1,4-phenylenevinylene] (MEH-PPV). I will report new work where we have used a new anisotropy experiment to examine coherent energy transfer and a complementary technique using two-dimensional electronic spectroscopy expose the role of coherence transfer in the fastest time dynamics. We find that coherent energy transfer occurs for many tens of femtoseconds, even at room temperature. That leads us to examine the nature and implications of the so-called intermediate coupling regime for EET.

  16. A new energy transfer model for turbulent free shear flow

    NASA Technical Reports Server (NTRS)

    Liou, William W.-W.

    1992-01-01

    A new model for the energy transfer mechanism in the large-scale turbulent kinetic energy equation is proposed. An estimate of the characteristic length scale of the energy containing large structures is obtained from the wavelength associated with the structures predicted by a weakly nonlinear analysis for turbulent free shear flows. With the inclusion of the proposed energy transfer model, the weakly nonlinear wave models for the turbulent large-scale structures are self-contained and are likely to be independent flow geometries. The model is tested against a plane mixing layer. Reasonably good agreement is achieved. Finally, it is shown by using the Liapunov function method, the balance between the production and the drainage of the kinetic energy of the turbulent large-scale structures is asymptotically stable as their amplitude saturates. The saturation of the wave amplitude provides an alternative indicator for flow self-similarity.

  17. The Synergism Between Heat and Mass Transfer Additive and Advanced Surfaces in Aqueous LiBr Horizontal Tube Absorbers

    SciTech Connect

    Miller, W.A.

    1999-03-24

    Experiments were conducted in a laboratory to investigate the absorption of water vapor into a falling-film of aqueous lithium bromide (LiBr). A mini-absorber test stand was used to test smooth tubes and a variety of advanced tube surfaces placed horizontally in a single-row bundle. The bundle had six copper tubes; each tube had an outside diameter of 15.9-mm and a length of 0.32-m. A unique feature of the stand is its ability to operate continuously and support testing of LiBr brine at mass fractions {ge} 0.62. The test stand can also support testing to study the effect of the failing film mass flow rate, the coolant mass flow rate, the coolant temperature, the absorber pressure and the tube spacing. Manufacturers of absorption chillers add small quantities of a heat and mass transfer additive to improve the performance of the absorbers. The additive causes surface stirring which enhances the transport of absorbate into the bulk of the film. Absorption may also be enhanced with advanced tube surfaces that mechanically induce secondary flows in the falling film without increasing the thickness of the film. Several tube geometry's were identified and tested with the intent of mixing the film and renewing the interface with fresh solution from the tube wall. Testing was completed on a smooth tube and several different externally enhanced tube surfaces. Experiments were conducted over the operating conditions of 6.5 mm Hg absorber pressure, coolant temperatures ranging from 20 to 35 C and LiBr mass fractions ranging from 0.60 through 0.62. Initially the effect of tube spacing was investigated for the smooth tube surface, tested with no heat and mass transfer additive. Test results showed the absorber load and the mass absorbed increased as the tube spacing increased because of the improved wetting of the tube bundle. However, tube spacing was not a critical factor if heat and mass transfer additive was active in the mini-absorber. The additive dramatically affected

  18. Spectrum and energy transfer in steady Burgers turbulence

    NASA Technical Reports Server (NTRS)

    Girimaji, Sharath S.; Zhou, YE

    1995-01-01

    The spectrum, energy transfer, and spectral interactions in steady Burgers turbulence are studied using numerically generated data. The velocity field is initially random and the turbulence is maintained steady by forcing the amplitude of a band of low wavenumbers to be invariant in time, while permitting the phase to change as dictated by the equation. The spectrum, as expected, is very different from that of Navier-Stokes turbulence. It is demonstrated that the far range of the spectrum scales as predicted by Burgers. Despite the difference in their spectra, in matters of the spectral energy transfer and triadic interactions Burgers turbulence is similar to Navier-Stokes turbulence.

  19. Determination of stepsize parameters for intermolecular vibrational energy transfer

    SciTech Connect

    Tardy, D.C.

    1992-03-01

    Intermolecular energy transfer of highly excited polyatomic molecules plays an important role in many complex chemical systems: combustion, high temperature and atmospheric chemistry. By monitoring the relaxation of internal energy we have observed trends in the collisional efficiency ({beta}) for energy transfer as a function of the substrate's excitation energy and the complexities of substrate and deactivator. For a given substrate {beta} increases as the deactivator's mass increase to {approximately}30 amu and then exhibits a nearly constant value; this is due to a mass mismatch between the atoms of the colliders. In a homologous series of substrate molecules (C{sub 3}{minus}C{sub 8}) {beta} decreases as the number of atoms in the substrate increases; replacing F with H increases {beta}. All substrates, except for CF{sub 2}Cl{sub 2} and CF{sub 2}HCl below 10,000 cm{sup {minus}1}, exhibited that {beta} is independent of energy, i.e. <{Delta}E>{sub all} is linear with energy. The results are interpreted with a simple model which considers that {beta} is a function of the ocillators energy and its vibrational frequency. Limitations of current approximations used in high temperature unimolecular reactions were evaluated and better approximations were developed. The importance of energy transfer in product yields was observed for the photoactivation of perfluorocyclopropene and the photoproduction of difluoroethyne. 3 refs., 18 figs., 4 tabs.

  20. Excitation energy transfer in the green photosynthetic bacterium Chloroflexus aurantiacus: A specific effect of 1-hexanol on the optical properties of baseplate and energy transfer processes.

    PubMed

    Mimuro, M; Nishimura, Y; Yamazaki, I; Kobayashi, M; Wang, Z Y; Nozawa, T; Shimada, K; Matsuura, K

    1996-05-01

    The effect of 1-hexanol on spectral properties and the processes of energy transfer of the green gliding photosynthetic bacterium Chloroflexus aurantiacus was investigated with reference to the baseplate region. On addition of 1-hexanol to a cell suspension in a concentration of one-fourth saturation, a specific change in the baseplate region was induced: that is, a bleach of the 793-nm component, and an increase in absorption of the 813-nm component. This result was also confirmed by fluorescence spectra of whole cells and isolated chlorosomes. The processes of energy transfer were affected in the overall transfer efficiency but not kinetically, indicating that 1-hexanol suppressed the flux of energy flow from the baseplate to the B806-866 complexes in the cytoplasmic membranes. The fluorescence excitation spectrum suggests a specific site of interaction between bacteriochlorophyll (BChl) c with a maximum at 771 nm in the rod elements and BChl a with a maximum at 793 nm in the baseplate, which is a funnel for a fast transfer of energy to the B806-866 complexes in the membranes. The absorption spectrum of chlorosomes was resolved to components consistently on the basis, including circular dichroism and magnetic circular dichroism spectra; besides two major BChl c forms, bands corresponding to tetramer, dimer, and monomer were also discernible, which are supposed to be intermediary components for a higher order structure. A tentative model for the antenna system of C. aurantiacus is proposed. PMID:24271307

  1. Technology transfer for the US Department of Energy's Energy Storage Program: Volume 1, Recommendations

    SciTech Connect

    Bruneau, C.L.; Fassbender, L.L.

    1988-10-01

    Technologies developed by the US Department of Energy's (DOE) Energy Storage (STOR) Program must be converted into products, processes, or services that benefit the private sector. The process of technology transfer is the primary means of accomplishing this. The purpose of this report is to examine the technology transfer activities of the STOR Program and suggest mechanisms that might make the transfer of technologies from national laboratories and universities to the private sector more effective. A brief summary of recommendations that would improve the effectiveness of the transfer of energy storage technologies from the national laboratories to the private sector is discussed. 33 refs., 2 figs.

  2. Interacting scales and energy transfer in isotropic turbulence

    NASA Technical Reports Server (NTRS)

    Zhou, YE

    1993-01-01

    The dependence of the energy transfer process on the disparity of the interacting scales is investigated in the inertial and far-dissipation ranges of isotropic turbulence. The strategy for generating the simulated flow fields and the choice of a disparity parameter to characterize the scaling of the interactions is discussed. The inertial range is found to be dominated by relatively local interactions, in agreement with the Kolmogorov assumption. The far-dissipation is found to be dominated by relatively non-local interactions, supporting the classical notion that the far-dissipation range is slaved to the Kolmogorov scales. The measured energy transfer is compared with the classical models of Heisenberg, Obukhov, and the more detailed analysis of Tennekes and Lumley. The energy transfer statistics measured in the numerically simulated flows are found to be nearly self-similar for wave numbers in the inertial range. Using the self-similar form measured within the limited scale range of the simulation, an 'ideal' energy transfer function and the corresponding energy flux rate for an inertial range of infinite extent are constructed. From this flux rate, the Kolmogorov constant is calculated to be 1.5, in excellent agreement with experiments.

  3. Optimal Energy Transfer in Light-Harvesting Systems.

    PubMed

    Chen, Lipeng; Shenai, Prathamesh; Zheng, Fulu; Somoza, Alejandro; Zhao, Yang

    2015-01-01

    Photosynthesis is one of the most essential biological processes in which specialized pigment-protein complexes absorb solar photons, and with a remarkably high efficiency, guide the photo-induced excitation energy toward the reaction center to subsequently trigger its conversion to chemical energy. In this work, we review the principles of optimal energy transfer in various natural and artificial light harvesting systems. We begin by presenting the guiding principles for optimizing the energy transfer efficiency in systems connected to dissipative environments, with particular attention paid to the potential role of quantum coherence in light harvesting systems. We will comment briefly on photo-protective mechanisms in natural systems that ensure optimal functionality under varying ambient conditions. For completeness, we will also present an overview of the charge separation and electron transfer pathways in reaction centers. Finally, recent theoretical and experimental progress on excitation energy transfer, charge separation, and charge transport in artificial light harvesting systems is delineated, with organic solar cells taken as prime examples. PMID:26307957

  4. Targeted energy transfer using nonlinear energy sinks for the attenuation of transient loads on building structures

    NASA Astrophysics Data System (ADS)

    Wierschem, Nicholas Edward

    Nonlinear energy sinks (NESs) have been proposed as a practical and robust means of passively protecting buildings structures subjected to extreme transient loads. NESs are a type of passive attachment that differentiate themselves from tradition linear attachments through the exploitation of essentially nonlinear stiffness elements. The essentially nonlinear restoring force provided by these elements allows the NES to interact with any mode of the primary structure to which the NES is attached and participate in targeted energy transfer (TET), the broadband transfer of energy from the primary structure to the NES where it can be rapidly dissipated. Additionally, this nonlinear restoring force allows the linear modes of the primary structure to become coupled and energy to be transferred from the lower modes of vibration to the higher modes where it is dissipated at a faster rate. Previous experimental investigations of the effectiveness of NESs have used table-top sized specimens; however, little, if any, work has been done using larger-scale models that allow practical implementation issues to be considered. In addition, the existing body of work with NESs is far from complete, with limited work presented on the use of systems of multiple NESs, the experimental realization of several different NES types, or their response to realistic loads. The primary objective of this dissertation is to explore the potential for nonlinear energy sinks to be a practical and robust means of passively protecting buildings structures subjected to extreme transient loads. In this dissertation, experimental testing and numerical simulations will be used to perform this investigation. The two types of transient loads focused on are impulsive loads, such as blasts, and broadband random loads, such as seismic ground motions. As a part of this investigation, small-, medium-, and large-scale primary structures and several types of NESs were designed and fabricated. With these structures

  5. 10 CFR 37.71 - Additional requirements for transfer of category 1 and category 2 quantities of radioactive...

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... category 2 quantities of radioactive material. 37.71 Section 37.71 Energy NUCLEAR REGULATORY COMMISSION PHYSICAL PROTECTION OF CATEGORY 1 AND CATEGORY 2 QUANTITIES OF RADIOACTIVE MATERIAL Physical Protection in... radioactive material. A licensee transferring a category 1 or category 2 quantity of radioactive material to...

  6. Encapsulated Energy Transfer Cassettes with Extremely Well Resolved Fluorescent Outputs

    PubMed Central

    Ueno, Yuichiro; Jose, Jiney; Loudet, Aurore; Pérez-Bolívar, César; Anzenbacher, Pavel; Burgess, Kevin

    2010-01-01

    This paper concerns the development of water-compatible fluorescent imaging-probes with tunable photonic properties that can be excited at a single wavelength. Bichromophoric cassettes 1a – 1c consisting of a BODIPY donor and a cyanine acceptor were prepared using a simple synthetic route, and their photophysical properties were investigated. Upon excitation of the BODIPY moiety at 488 nm the excitation energy is transferred through an acetylene bridge to the cyanine dye acceptor, which emits light at approximately 600, 700, and 800 nm, ie with remarkable dispersions. This effect is facilitated by efficient energy transfer that gives a ‘quasi-Stokes’ shift of between 86 – 290 nm opening a huge spectral window for imaging. The emissive properties of the cassettes depend on the energy transfer (ET) mechanism: the faster the transfer, the more efficient it is. Measurements of rates of energy transfer indicate that a through-bond energy transfer takes place in the cassettes 1a and 1b that is two orders of magnitude faster than the classical through-space, Förster, energy transfer (in the case of cassette 1c, however, both mechanisms are possible, and the rate measurements do not allow us to discern between them). Thus the cassettes 1a – 1c are well suited for multiplexing experiments in biotechnological methods that involve a single laser-excitation source. However, for widespread application of these probes their solubility in aqueous media must be improved. Consequently, the probes were encapsulated in calcium phosphate/silicate nanoparticles (diameter ca 22 nm) that are freely dispersible in water. This encapsulation process resulted in only minor changes in the photophysical properties of the cassettes. The system based on cassette 1a was chosen to probe how effectively these nanoparticles could be used to deliver the dyes into cells. Encapsulated cassette 1a permeated Clone 9 rat liver cells where it localized in the mitochondria and fluoresced through

  7. Technology transfer for the US Department of Energy's Energy Storage Program: Volume 2, Appendices

    SciTech Connect

    Bruneau, C.L.; Fassbender, L.L.

    1988-10-01

    This document contains the appendices to Technology Transfer Recommendations for the US Department of Energy's Storage Program (PNL-6484, Vol. 1). These appendices are a list of projects, publications, and presentations connected with the Energy Storage (STOR) program. In Volume 1, the technology transfer activities of the STOR program are examined and mechanisms for increasing the effectiveness of those activities are recommended.

  8. Utilizing Energy Transfer in Binary and Ternary Bulk Heterojunction Organic Solar Cells.

    PubMed

    Feron, Krishna; Cave, James M; Thameel, Mahir N; O'Sullivan, Connor; Kroon, Renee; Andersson, Mats R; Zhou, Xiaojing; Fell, Christopher J; Belcher, Warwick J; Walker, Alison B; Dastoor, Paul C

    2016-08-17

    Energy transfer has been identified as an important process in ternary organic solar cells. Here, we develop kinetic Monte Carlo (KMC) models to assess the impact of energy transfer in ternary and binary bulk heterojunction systems. We used fluorescence and absorption spectroscopy to determine the energy disorder and Förster radii for poly(3-hexylthiophene-2,5-diyl), [6,6]-phenyl-C61-butyric acid methyl ester, 4-bis[4-(N,N-diisobutylamino)-2,6-dihydroxyphenyl]squaraine (DIBSq), and poly(2,5-thiophene-alt-4,9-bis(2-hexyldecyl)-4,9-dihydrodithieno[3,2-c:3',2'-h][1,5]naphthyridine-5,10-dione). Heterogeneous energy transfer is found to be crucial in the exciton dissociation process of both binary and ternary organic semiconductor systems. Circumstances favoring energy transfer across interfaces allow relaxation of the electronic energy level requirements, meaning that a cascade structure is not required for efficient ternary organic solar cells. We explain how energy transfer can be exploited to eliminate additional energy losses in ternary bulk heterojunction solar cells, thus increasing their open-circuit voltage without loss in short-circuit current. In particular, we show that it is important that the DIBSq is located at the electron donor-acceptor interface; otherwise charge carriers will be trapped in the DIBSq domain or excitons in the DIBSq domains will not be able to dissociate efficiently at an interface. KMC modeling shows that only small amounts of DIBSq (<5% by weight) are needed to achieve substantial performance improvements due to long-range energy transfer. PMID:27456294

  9. Additive Manufacturing/Diagnostics via the High Frequency Induction Heating of Metal Powders: The Determination of the Power Transfer Factor for Fine Metallic Spheres

    SciTech Connect

    Rios, Orlando; Radhakrishnan, Balasubramaniam; Caravias, George; Holcomb, Matthew

    2015-03-11

    Grid Logic Inc. is developing a method for sintering and melting fine metallic powders for additive manufacturing using spatially-compact, high-frequency magnetic fields called Micro-Induction Sintering (MIS). One of the challenges in advancing MIS technology for additive manufacturing is in understanding the power transfer to the particles in a powder bed. This knowledge is important to achieving efficient power transfer, control, and selective particle heating during the MIS process needed for commercialization of the technology. The project s work provided a rigorous physics-based model for induction heating of fine spherical particles as a function of frequency and particle size. This simulation improved upon Grid Logic s earlier models and provides guidance that will make the MIS technology more effective. The project model will be incorporated into Grid Logic s power control circuit of the MIS 3D printer product and its diagnostics technology to optimize the sintering process for part quality and energy efficiency.

  10. Heavy ion mutagenesis: linear energy transfer effects and genetic linkage

    NASA Technical Reports Server (NTRS)

    Kronenberg, A.; Gauny, S.; Criddle, K.; Vannais, D.; Ueno, A.; Kraemer, S.; Waldren, C. A.; Chatterjee, A. (Principal Investigator)

    1995-01-01

    We have characterized a series of 69 independent mutants at the endogenous hprt locus of human TK6 lymphoblasts and over 200 independent S1-deficient mutants of the human x hamster hybrid cell line AL arising spontaneously or following low-fluence exposures to densely ionizing Fe ions (600 MeV/amu, linear energy transfer = 190 keV/microns). We find that large deletions are common. The entire hprt gene (> 44 kb) was missing in 19/39 Fe-induced mutants, while only 2/30 spontaneous mutants lost the entire hprt coding sequence. When the gene of interest (S1 locus = M1C1 gene) is located on a nonessential human chromosome 11, multilocus deletions of several million base pairs are observed frequently. The S1 mutation frequency is more than 50-fold greater than the frequency of hprt mutants in the same cells. Taken together, these results suggest that low-fluence exposures to Fe ions are often cytotoxic due to their ability to create multilocus deletions that may often include the loss of essential genes. In addition, the tumorigenic potential of these HZE heavy ions may be due to the high potential for loss of tumor suppressor genes. The relative insensitivity of the hprt locus to mutation is likely due to tight linkage to a gene that is required for viability.

  11. Eu2+-->Mn2+ energy transfer in NaCl

    NASA Astrophysics Data System (ADS)

    Rubio O., J.; Murrieta S., H.; Powell, R. C.; Sibley, W. A.

    1985-01-01

    Crystals of NaCl containing different concentrations of Eu2+ and Mn2+ ions (the Eu concentration always being less than that of Mn) were investigated by optical and EPR spectroscopy. The results show that Eu2+-Mn2+ pairs form preferentially in this material and that highly efficient energy transfer occurs from the Eu2+ ions to the near-neighbor Mn2+ ions. Over 99% of the Eu2+ ions are paired, and these pairs are not significantly affected by the state of aggregation of the Mn ions, although in the various samples evidence for manganese ions in their dipolar state, as well as precipitated into the Suzuki phase, exists. The excitation spectra of the orange manganese emission show, in addition to the Eu2+ 4f7-->4f65d transitions, Mn2+ transitions associated with the Suzuki phase and with Mn2+-cation vacancy dipoles. The peak positions of these Mn2+-crystal-field-sensitive transitions were fitted theoretically with expressions including Racah-Tress and seniority corrections. This procedure allowed the determination of the relevant crystal-field parameters.

  12. Excitation Energy-Transfer Dynamics of Brown Algal Photosynthetic Antennas.

    PubMed

    Kosumi, D; Kita, M; Fujii, R; Sugisaki, M; Oka, N; Takaesu, Y; Taira, T; Iha, M; Hashimoto, H

    2012-09-20

    Fucoxanthin-chlorophyll-a/c protein (FCP) complexes from brown algae Cladosiphon okamuranus TOKIDA (Okinawa Mozuku in Japanese) contain the only species of carbonyl carotenoid, fucoxanthin, which exhibits spectral characteristics attributed to an intramolecular charge-transfer (ICT) property that arises in polar environments due to the presence of the carbonyl group in its polyene backbone. Here, we investigated the role of the ICT property of fucoxanthin in ultrafast energy transfer to chlorophyll-a/c in brown algal photosynthesis using femtosecond pump-probe spectroscopic measurements. The observed excited-state dynamics show that the ICT character of fucoxanthin in FCP extends its absorption band to longer wavelengths and enhances its electronic interaction with chlorophyll-a molecules, leading to efficient energy transfer from fucoxanthin to chlorophyll-a. PMID:26295888

  13. Surface phonon polaritons mediated energy transfer between nanoscale gaps.

    PubMed

    Shen, Sheng; Narayanaswamy, Arvind; Chen, Gang

    2009-08-01

    Surface phonon polaritons are electromagnetic waves that propagate along the interfaces of polar dielectrics and exhibit a large local-field enhancement near the interfaces at infrared frequencies. Theoretical calculations show that such surface waves can lead to breakdown of the Planck's blackbody radiation law in the near field. Here, we experimentally demonstrate that surface phonon polaritons dramatically enhance energy transfer between two surfaces at small gaps by measuring radiation heat transfer between a microsphere and a flat surface down to 30 nm separation. The corresponding heat transfer coefficients at nanoscale gaps are 3 orders of magnitude larger than that of the blackbody radiation limit. The high energy flux can be exploited to develop new radiative cooling and thermophotovoltaic technologies. PMID:19719110

  14. Density functional theory for protein transfer free energy.

    PubMed

    Mills, Eric A; Plotkin, Steven S

    2013-10-24

    We cast the problem of protein transfer free energy within the formalism of density functional theory (DFT), treating the protein as a source of external potential that acts upon the solvent. Solvent excluded volume, solvent-accessible surface area, and temperature dependence of the transfer free energy all emerge naturally within this formalism, and may be compared with simplified "back of the envelope" models, which are also developed here. Depletion contributions to osmolyte induced stability range from 5 to 10 kBT for typical protein lengths. The general DFT transfer theory developed here may be simplified to reproduce a Langmuir isotherm condensation mechanism on the protein surface in the limits of short-ranged interactions, and dilute solute. Extending the equation of state to higher solute densities results in non-monotonic behavior of the free energy driving protein or polymer collapse. Effective interaction potentials between protein backbone or side chains and TMAO are obtained, assuming a simple backbone/side chain two-bead model for the protein with an effective 6-12 potential with the osmolyte. The transfer free energy δg shows significant entropy: d(δg)/dT ≈ 20 kB for a 100-residue protein. The application of DFT to effective solvent forces for use in implicit-solvent molecular dynamics is also developed. The simplest DFT expressions for implicit-solvent forces contain both depletion interactions and an "impeded-solvation" repulsive force at larger distances. PMID:23944753

  15. Plasmon resonance energy transfer and plexcitonic solar cell.

    PubMed

    Nan, Fan; Ding, Si-Jing; Ma, Liang; Cheng, Zi-Qiang; Zhong, Yu-Ting; Zhang, Ya-Fang; Qiu, Yun-Hang; Li, Xiaoguang; Zhou, Li; Wang, Qu-Quan

    2016-08-11

    Plasmon-mediated energy transfer is highly desirable in photo-electronic nanodevices, but the direct injection efficiency of "hot electrons" in plasmonic photo-detectors and plasmon-sensitized solar cells (plasmon-SSCs) is poor. On another front, Fano resonance induced by strong plasmon-exciton coupling provides an efficient channel of coherent energy transfer from metallic plasmons to molecular excitons, and organic dye molecules have a much better injection efficiency in exciton-SSCs than "hot electrons". Here, we investigate enhanced light-harvesting of chlorophyll-a molecules strongly coupled to Au nanostructured films via Fano resonance. The enhanced local field and plasmon resonance energy transfer are experimentally revealed by monitoring the ultrafast dynamical processes of the plexcitons and the photocurrent flows of the assembled plexciton-SSCs. By tuning the Fano factor and anti-resonance wavelengths, we find that the local field is largely enhanced and the efficiency of plexciton-SSCs consisting of ultrathin TiO2 films is significantly improved. Most strikingly, the output power of the plexciton-SSCs is much larger than the sum of those of the individual plasmon- and exciton-SSCs. Our observations provide a practical approach to monitor energy and electron transfer in plasmon-exciton hybrids at a strong coupling regime and also offer a new strategy to design photovoltaic nanodevices. PMID:27481652

  16. Resonance energy transfer in DNA duplexes labeled with localized dyes.

    PubMed

    Cunningham, Paul D; Khachatrian, Ani; Buckhout-White, Susan; Deschamps, Jeffrey R; Goldman, Ellen R; Medintz, Igor L; Melinger, Joseph S

    2014-12-18

    The growing maturity of DNA-based architectures has raised considerable interest in applying them to create photoactive light harvesting and sensing devices. Toward optimizing efficiency in such structures, resonant energy transfer was systematically examined in a series of dye-labeled DNA duplexes where donor-acceptor separation was incrementally changed from 0 to 16 base pairs. Cyanine dyes were localized on the DNA using double phosphoramidite attachment chemistry. Steady state spectroscopy, single-pair fluorescence, time-resolved fluorescence, and ultrafast two-color pump-probe methods were utilized to examine the energy transfer processes. Energy transfer rates were found to be more sensitive to the distance between the Cy3 donor and Cy5 acceptor dye molecules than efficiency measurements. Picosecond energy transfer and near-unity efficiencies were observed for the closest separations. Comparison between our measurements and the predictions of Förster theory based on structural modeling of the dye-labeled DNA duplex suggest that the double phosphoramidite linkage leads to a distribution of intercalated and nonintercalated dye orientations. Deviations from the predictions of Förster theory point to a failure of the point dipole approximation for separations of less than 10 base pairs. Interactions between the dyes that alter their optical properties and violate the weak-coupling assumption of Förster theory were observed for separations of less than four base pairs, suggesting the removal of nucleobases causes DNA deformation and leads to enhanced dye-dye interaction. PMID:25397906

  17. Photoexcited energy transfer in a weakly coupled dimer

    DOE PAGESBeta

    Hernandez, Laura Alfonso; Nelson, Tammie; Tretiak, Sergei; Fernandez-Alberti, Sebastian

    2015-01-08

    Nonadiabatic excited-state molecular dynamics (NA-ESMD) simulations have been performed in order to study the time-dependent exciton localization during energy transfer between two chromophore units of the weakly coupled anthracene dimer dithia-anthracenophane (DTA). Simulations are done at both low temperature (10 K) and room temperature (300 K). The initial photoexcitation creates an exciton which is primarily localized on a single monomer unit. Subsequently, the exciton experiences an ultrafast energy transfer becoming localized on either one monomer unit or the other, whereas delocalization between both monomers never occurs. In half of the trajectories, the electronic transition density becomes completely localized on themore » same monomer as the initial excitation, while in the other half, it becomes completely localized on the opposite monomer. In this article, we present an analysis of the energy transfer dynamics and the effect of thermally induced geometry distortions on the exciton localization. Finally, simulated fluorescence anisotropy decay curves for both DTA and the monomer unit dimethyl anthracene (DMA) are compared. As a result, our analysis reveals that changes in the transition density localization caused by energy transfer between two monomers in DTA is not the only source of depolarization and exciton relaxation within a single DTA monomer unit can also cause reorientation of the transition dipole.« less

  18. Photoexcited energy transfer in a weakly coupled dimer

    SciTech Connect

    Hernandez, Laura Alfonso; Nelson, Tammie; Tretiak, Sergei; Fernandez-Alberti, Sebastian

    2015-01-08

    Nonadiabatic excited-state molecular dynamics (NA-ESMD) simulations have been performed in order to study the time-dependent exciton localization during energy transfer between two chromophore units of the weakly coupled anthracene dimer dithia-anthracenophane (DTA). Simulations are done at both low temperature (10 K) and room temperature (300 K). The initial photoexcitation creates an exciton which is primarily localized on a single monomer unit. Subsequently, the exciton experiences an ultrafast energy transfer becoming localized on either one monomer unit or the other, whereas delocalization between both monomers never occurs. In half of the trajectories, the electronic transition density becomes completely localized on the same monomer as the initial excitation, while in the other half, it becomes completely localized on the opposite monomer. In this article, we present an analysis of the energy transfer dynamics and the effect of thermally induced geometry distortions on the exciton localization. Finally, simulated fluorescence anisotropy decay curves for both DTA and the monomer unit dimethyl anthracene (DMA) are compared. As a result, our analysis reveals that changes in the transition density localization caused by energy transfer between two monomers in DTA is not the only source of depolarization and exciton relaxation within a single DTA monomer unit can also cause reorientation of the transition dipole.

  19. Unprecedented laser action from energy transfer in multichromophoric BODIPY cassettes.

    PubMed

    Xiao, Yi; Zhang, Dakui; Qian, Xuhong; Costela, Angel; Garcia-Moreno, Inmaculada; Martin, Virginia; Perez-Ojeda, M Eugenia; Bañuelos, Jorge; Gartzia, Leire; Arbeloa, Iñigo López

    2011-11-01

    A cassette molecule, featuring direct integration of two donor BODIPY units to one acceptor BODIPY unit, was conveniently developed as the first highly "through-bond energy transfer" (TBET) laser dye. This multicolor absorbing dye exhibited highly efficient and photostable laser action under drastic pumping conditions. PMID:21935560

  20. Mechanical energy generation and transfer in the racket arm during table tennis topspin backhands.

    PubMed

    Iino, Yoichi; Kojima, Takeji

    2016-06-01

    The ability to generate a high racket speed and a large amount of racket kinetic energy on impact is important for table tennis players. The purpose of this study was to understand how mechanical energy is generated and transferred in the racket arm during table tennis backhands. Ten male advanced right-handed table tennis players hit topspin backhands against pre-impact topspin and backspin balls. The joint kinetics at the shoulder, elbow and wrist of the racket arm was determined using inverse dynamics. A majority of the mechanical energy of the racket arm acquired during forward swing (65 and 77% against topspin and backspin, respectively) was due to energy transfer from the trunk. Energy transfer by the shoulder joint force in the vertical direction was the largest contributor to the mechanical energy of the racket arm against both spins and was greater against backspin than against topspin (34 and 28%, respectively). The shoulder joint force directed to the right, which peaked just before impact, transferred additional energy to the racket. Our results suggest that the upward thrust of the shoulder and the late timing of the axial rotation of the upper trunk are important for an effective topspin backhand. PMID:27111711

  1. Direct observation of energy transfer in a photosynthetic membrane: Chlorophyll b to chlorophyll a transfer in LHC

    SciTech Connect

    Eads, D.D.; Castner, E.W. Jr.; Alberte, R.S.; Mets, L.; Fleming, G.R. )

    1989-12-28

    Subpicosecond fluorescence upconversion has been used to measure the rate of chlorophyll b to chlorophyll a electronic energy transfer in situ within the LHC pigment proteins of Chlamydomonas reinhardtii mutant C2. The time scale of energy transfer is 0.5 {plus minus} 0.2 ps as determined from the rise time of chlorophyll a fluorescence following chlorophyll b excitation. Estimates of the energy-transfer rate based on Foerster weak coupling theory are discussed.

  2. Removing energy from a beverage influences later food intake more than the same energy addition.

    PubMed

    McCrickerd, K; Salleh, N B; Forde, C G

    2016-10-01

    Designing reduced-calorie foods and beverages without compromising their satiating effect could benefit weight management, assuming that consumers do not compensate for the missing calories at other meals. Though research has demonstrated that compensation for overfeeding is relatively limited, the extent to which energy reductions trigger adjustments in later food intake is less clear. The current study tested satiety responses (characterised by changes in appetite and later food intake) to both a covert 200 kcal reduction and an addition of maltodextrin to a soymilk test beverage. Twenty-nine healthy male participants were recruited to consume three sensory-matched soymilk beverages across four non-consecutive study days: a medium energy control (ME: 300 kcal) and a lower energy (LE: 100 kcal) and higher energy (HE: 500 kcal) version. The ME control was consumed twice to assess individual consistency in responses to this beverage. Participants were unaware of the energy differences across the soymilks. Lunch intake 60 min later increased in response to the LE soymilk, but was unchanged after consuming the HE version. These adjustments accounted for 40% of the energy removed from the soymilk and 13% of the energy added in. Rated appetite was relatively unaffected by the soymilk energy content. No further adjustments were noted for the rest of the day. These data suggest that adult men tested were more sensitive to calorie dilution than calorie addition to a familiar beverage. PMID:27356202

  3. Effects of nitrate addition and iron speciation on trace element transfer in coastal food webs under phosphate and iron enrichment.

    PubMed

    Li, Shun-Xing; Liu, Feng-Jiao; Zheng, Feng-Ying; Zuo, Yue-Gang; Huang, Xu-Guang

    2013-06-01

    Coastal organisms are often exposed to both iron enrichment and eutrophication. Trace elements transfer in coastal food webs are critical for marine life and therefore influence coastal ecosystem function and the global carbon cycle. However, how these exposures affect algal element uptake and the subsequent element transfer to marine copepods (Tigriopus japonicus) is unknown. Here we investigated the effects of nitrate addition and iron speciation (Fe (OH)3 or EDTA-Fe) on the biological uptake of Cu, Zn, and Se under phosphate and iron enrichment, using Thalassiosira weissflogii, Skeletonema costatum, and Chlorella vulgaris as model marine algae. Algal element adsorption/absorption generally increased with increasing macronutrient concentrations. Algal element assimilation efficiencies depended on iron speciation and marine algae species. Element assimilation efficiencies of copepods were significantly correlated to the intracellular element concentrations in algal cells. Element uptake and transfer were controlled by eutrophication, iron speciation, and algal species in coastal food webs. PMID:23332676

  4. Electronic energy transfer and electron transfer in flexible bichromophoric molecules studied in a supersonic jet

    NASA Astrophysics Data System (ADS)

    Wang, Xin

    1999-08-01

    The objective of this dissertation is to use laser spectroscopy in supersonic jets to investigate the dynamics and mechanism of Electronic Energy Transfer (EET) and Photon-induced Electron Transfer (PET) in bichromophoric molecules with flexible bridges. Molecular geometry computations using molecular mechanism methods have been applied to the interpretations of experimental results. In the investigations of a series of molecules: (1- naphthalene) -(CH 2)n- (9-anthracene) (n = 1, 3 and 6), EET rate from the naphthalene moiety to the anthracene moiety has been found to be much faster than the naphthalene fluorescence lifetime. The importance of exchange mechanism has been demonstrated in the n = 3 and 6 molecules, which is explained by the formation of face-to-face inter- chromophore configurations. In the investigation of a methyldisilane-linked bichromophoric molecule containing anthracene and dimethyl-aniline, it has been found that this molecule can be directly excited to the Charge Transfer state without being excited to the Locally Excited state first. The unusually low-lying Charge Transfer state indicates a significant contribution to the electron transfer mechanism from the through Si-Si bond coupling. The silicon molecular wire is therefore shown to be a better electron conductor than the carbon molecular wire.

  5. 2013 MOLECULAR ENERGY TRANSFER GORDON RESEARCH CONFERENCE (JANUARY 13-18, 2013 - VENTURA BEACH MARRIOTT, VENTURA CA

    SciTech Connect

    Reid, Scott A.

    2012-10-18

    Sessions covered all areas of molecular energy transfer, with 10 sessions of talks and poster sessions covering the areas of :  Energy Transfer in Inelastic and Reactive Scattering  Energy Transfer in Photoinitiated and Unimolecular Reactions  Non-adiabatic Effects in Energy TransferEnergy Transfer at Surfaces and Interfaces  Energy Transfer in Clusters, Droplets, and Aerosols  Energy Transfer in Solution and Solid  Energy Transfer in Complex Systems  Energy Transfer: New vistas and horizons  Molecular Energy Transfer: Where Have We Been and Where are We Going?

  6. Direct observation of triplet energy transfer from semiconductor nanocrystals.

    PubMed

    Mongin, Cédric; Garakyaraghi, Sofia; Razgoniaeva, Natalia; Zamkov, Mikhail; Castellano, Felix N

    2016-01-22

    Triplet excitons are pervasive in both organic and inorganic semiconductors but generally remain confined to the material in which they originate. We demonstrated by transient absorption spectroscopy that cadmium selenide semiconductor nanoparticles, selectively excited by green light, engage in interfacial Dexter-like triplet-triplet energy transfer with surface-anchored polyaromatic carboxylic acid acceptors, extending the excited-state lifetime by six orders of magnitude. Net triplet energy transfer also occurs from surface acceptors to freely diffusing molecular solutes, further extending the lifetime while sensitizing singlet oxygen in an aerated solution. The successful translation of triplet excitons from semiconductor nanoparticles to the bulk solution implies that such materials are generally effective surrogates for molecular triplets. The nanoparticles could thereby potentially sensitize a range of chemical transformations that are relevant for fields as diverse as optoelectronics, solar energy conversion, and photobiology. PMID:26798011

  7. Long range energy transfer in graphene hybrid structures

    NASA Astrophysics Data System (ADS)

    Gonçalves, Hugo; Bernardo, César; Moura, Cacilda; Ferreira, R. A. S.; André, P. S.; Stauber, Tobias; Belsley, Michael; Schellenberg, Peter

    2016-08-01

    In this work we quantify the distance dependence for the extraction of energy from excited chromophores by a single layer graphene flake over a large separation range. To this end hybrid structures were prepared, consisting of a thin (2 nm) layer of a polymer matrix doped with a well chosen strongly fluorescent organic molecule, followed by an un-doped spacer layer of well-defined thicknesses made of the same polymer material and an underlying single layer of pristine, undoped graphene. The coupling strength is assessed through the variation of the fluorescence decay kinetics as a function of distance between the graphene and the excited chromophore molecules. Non-radiative energy transfer to the graphene was observed at distances of up to 60 nm a range much greater than typical energy transfer distances observed in molecular systems.

  8. Modeling crossed-beam energy transfer for inertial confinement fusion

    NASA Astrophysics Data System (ADS)

    Marion, D. J. Y.; Debayle, A.; Masson-Laborde, P.-E.; Loiseau, P.; Casanova, M.

    2016-05-01

    We developed a numerical code that describes both the energy transfer occurring when two or more laser beams overlap in a weakly non-homogeneous plasma, and the beam energy losses associated with the electron-ion collisions. The numerical solutions are validated with both the exact analytical solutions in homogeneous plasmas, and with new approximate analytical solutions in non-homogeneous plasmas that include the aforementioned inverse bremsstrahlung effect. Comparisons with kinetic particle-in-cell simulations are satisfactory, provided the acoustic wave-breaking limit and the self-focusing regime are not reached. An application of the Cross-Beam Energy Transfer model is shown for a typical case of indirect-drive implosion in a gold hohlraum.

  9. Wireless energy transfer platform for medical sensors and implantable devices.

    PubMed

    Zhang, Fei; Hackworth, Steven A; Liu, Xiaoyu; Chen, Haiyan; Sclabassi, Robert J; Sun, Mingui

    2009-01-01

    Witricity is a newly developed technique for wireless energy transfer. This paper presents a frequency adjustable witricity system to power medical sensors and implantable devices. New witricity resonators are designed for both energy transmission and reception. A prototype platform is described, including an RF power source, two resonators with new structures, and inductively coupled input and output stages. In vitro experiments, both in open air and using a human head phantom consisting of simulated tissues, are employed to verify the feasibility of this platform. An animal model is utilized to evaluate in vivo energy transfer within the body of a laboratory pig. Our experiments indicate that witricity is an effective new tool for providing a variety of medical sensors and devices with power. PMID:19964948

  10. Rotational Energy Transfer of N2 Gas Determined Using a New Ab Initio Potential Energy Surface

    NASA Technical Reports Server (NTRS)

    Huo, Winifred M.; Stallcop, James R.; Partridge, Harry; Langhoff, Stephen R. (Technical Monitor)

    1997-01-01

    Rotational energy transfer between two N2 molecules is a fundamental process of some importance. Exchange is expected to play a role, but its importance is somewhat uncertain. Rotational energy transfer cross sections of N2 also have applications in many other fields including modeling of aerodynamic flows, laser operations, and linewidth analysis in nonintrusive laser diagnostics. A number of N2-N2 rigid rotor potential energy surface (PES) has been reported in the literature.

  11. Electronic Energy transfer in light-harvesting antenna complexes

    NASA Astrophysics Data System (ADS)

    Hossein-Nejad, Hoda

    The studies presented in this thesis explore electronic energy transfer (EET) in light-harvesting antenna complexes and investigate the role of quantum coherence in EET. The dynamics of energy transfer are investigated in three distinct length scales and a different formulation of the exciton transport problem is applied at each scale. These scales include: the scale of a molecular dimer, the scale of a single protein and the scale of a molecular aggregate. The antenna protein phycoerythrin 545 (PE545) isolated from the photosynthetic cryptophyte algae Rhodomonas CS4 is specifically studied in two chapters of this thesis. It is found that formation of small aggregates delocalizes the excitation across chromophores of adjacent proteins, and that this delocalization has a dramatic effect in enhancing the rate of energy transfer between pigments. Furthermore, we investigate EET from a donor to an acceptor via an intermediate site and observe that interference of coherent pathways gives a finite correction to the transfer rate that is sensitively dependent on the nature of the vibrational interactions in the system. The statistical fluctuations of a system exhibiting EET are investigated in the final chapter. The techniques of non-equilibrium statistical mechanics are applied to investigate the steady-state of a typical system exhibiting EET that is perturbed out of equilibrium due to its interaction with a fluctuating bath.

  12. Energy transfer and excitation migration in organic semiconductors

    NASA Astrophysics Data System (ADS)

    Lane, Paul A.; Wolak, Mason A.; Cunningham, Paul D.; Melinger, Joseph S.

    2012-09-01

    Energy transfer plays a key role in various applications of organic semiconductors such as electroluminescence, photovoltaics, and sensors. We have carried out a study combining transient and continuous wave (CW) optical spectroscopy with modeling. The fluorescence spectra and dynamics of a functionalized pentacene doped into a fluorescent host (Alq3) were measured and simulated by a Monte Carlo model incorporating distributed dopants and exciton migration. For nonluminescent materials, transient absorption spectroscopy provides insight into excitation migration. Singlet diffusion rates in C60 were determined by probing delayed charge transfer to ZnPc in films with a layered nanostructure.

  13. Nonradiative exciton energy transfer in hybrid organic-inorganic heterostructures

    NASA Astrophysics Data System (ADS)

    Chanyawadee, S.; Lagoudakis, P. G.; Harley, R. T.; Lidzey, D. G.; Henini, M.

    2008-05-01

    Nonradiative energy transfer from a GaAs quantum well to a thin overlayer of an infrared organic semiconductor dye is unambiguously demonstrated. The dynamics of exciton transfer are studied in the time domain by using pump-probe spectroscopy at the donor site and fluorescence spectroscopy at the acceptor site. The effect is observed as simultaneous increase in the population decay rate at the donor and of the rise time of optical emission at the acceptor sites. The hybrid configuration under investigation provides an alternative nonradiative, noncontact pumping route to electrical carrier injection that overcomes the losses imposed by the associated low carrier mobility of organic emitters.

  14. Electro-mechanical energy conversion system having a permanent magnet machine with stator, resonant transfer link and energy converter controls

    DOEpatents

    Skeist, S. Merrill; Baker, Richard H.

    2006-01-10

    An electro-mechanical energy conversion system coupled between an energy source and an energy load comprising an energy converter device including a permanent magnet induction machine coupled between the energy source and the energy load to convert the energy from the energy source and to transfer the converted energy to the energy load and an energy transfer multiplexer to control the flow of power or energy through the permanent magnetic induction machine.

  15. Nonphotochemical Hole-Burning Studies of Energy Transfer Dynamics in Antenna Complexes of Photosynthetic Bacteria

    SciTech Connect

    Satoshi Matsuzaki

    2002-08-01

    This thesis contains the candidate's original work on excitonic structure and energy transfer dynamics of two bacterial antenna complexes as studied using spectral hole-burning spectroscopy. The general introduction is divided into two chapters (1 and 2). Chapter 1 provides background material on photosynthesis and bacterial antenna complexes with emphasis on the two bacterial antenna systems related to the thesis research. Chapter 2 reviews the underlying principles and mechanism of persistent nonphotochemical hole-burning (NPHB) spectroscopy. Relevant energy transfer theories are also discussed. Chapters 3 and 4 are papers by the candidate that have been published. Chapter 3 describes the application of NPHB spectroscopy to the Fenna-Matthews-Olson (FMO) complex from the green sulfur bacterium Prosthecochloris aestuarii; emphasis is on determination of the low energy vibrational structure that is important for understanding the energy transfer process associated within three lowest energy Qy-states of the complex. The results are compared with those obtained earlier on the FMO complex from Chlorobium tepidum. In Chapter 4, the energy transfer dynamics of the B800 molecules of intact LH2 and B800-deficient LH2 complexes of the purple bacterium Rhodopseudomonas acidophila are compared. New insights on the additional decay channel of the B800 ring of bacteriochlorophyll a (BChl a) molecules are provided. General conclusions are given in Chapter 5.

  16. Coherent or hopping like energy transfer in the chlorosome ?

    SciTech Connect

    Nalbach, Peter

    2014-08-20

    Chlorosomes, as part of the light-harvesting system of green bacteria, are the largest and most efficient antennae systems in nature. We have studied energy transfer dynamics in the chlorosome in a simplified toy model employing a master equation. Dephasing and relaxation due to environmental fluctuations are included by Lindblad dephasing and Redfield thermalization rates. We find at room temperature three separate time scales, i.e. 25 fs, 250 fs and 2.5 ps and determine the according energy pathways through the hierarchical structure in the chlorosome. Quantum coherence lives up to 150 fs at which time the energy is spread over roughly 12 pigments in our model.

  17. Coherent or hopping like energy transfer in the chlorosome ?

    NASA Astrophysics Data System (ADS)

    Nalbach, Peter

    2014-08-01

    Chlorosomes, as part of the light-harvesting system of green bacteria, are the largest and most efficient antennae systems in nature. We have studied energy transfer dynamics in the chlorosome in a simplified toy model employing a master equation. Dephasing and relaxation due to environmental fluctuations are included by Lindblad dephasing and Redfield thermalization rates. We find at room temperature three separate time scales, i.e. 25 fs, 250 fs and 2.5 ps and determine the according energy pathways through the hierarchical structure in the chlorosome. Quantum coherence lives up to 150 fs at which time the energy is spread over roughly 12 pigments in our model.

  18. K/S Lambert problem. [energy requirements for transfer orbits

    NASA Technical Reports Server (NTRS)

    Jezewski, D. J.

    1975-01-01

    The Lambert problem in orbital mechanics is formulated in Kustaanheimo/Stiefel variables. The problem is to determine the required energy and the value of the generalized eccentric anomaly such that a particle at the initial position vector will transfer to the final position vector in a physical time interval. The fictitious time solution results in two nonlinear equations in the two unknowns, energy and fictitious time. The generalized eccentric anomaly solution, however, results in only one nonlinear equation in the one unknown, the eccentric anomaly. This simplification is possible because the energy equation is separable in the eccentric anomaly formulation.

  19. Ultrafast resonance energy transfer in the umbelliferone-alizarin bichromophore.

    PubMed

    Lapini, Andrea; Fabbrizzi, Pierangelo; Piccardo, Matteo; di Donato, Mariangela; Lascialfari, Luisa; Foggi, Paolo; Cicchi, Stefano; Biczysko, Malgorzata; Carnimeo, Ivan; Santoro, Fabrizio; Cappelli, Chiara; Righini, Roberto

    2014-06-01

    In this work we present the synthesis, time-resolved spectroscopic characterization and computational analysis of a bichromophore composed of two very well-known naturally occurring dyes: 7-hydroxycoumarin (umbelliferone) and 1,2-dihydroxyanthraquinone (alizarin). The umbelliferone donor (Dn) and alizarin acceptor (Ac) moieties are linked to a triazole ring viaσ bonds, providing a flexible structure. By measuring the fluorescence quantum yields and the ultrafast transient absorption spectra we demonstrate the high efficiency (∼85%) and the fast nature (∼1.5 ps) of the energy transfer in this compound. Quantum chemical calculations, within the density functional theory (DFT) approach, are used to characterize the electronic structure of the bichromophore (Bi) in the ground and excited states. We simulate the absorption and fluorescence spectra using the TD-DFT methods and the vertical gradient approach (VG), and include the solvent effects by adopting the conductor-like polarizable continuum model (CPCM). The calculated electronic structure suggests the occurrence of weak interactions between the electron densities of Dn and Ac in the excited state, indicating that the Förster-type transfer is the appropriate model for describing the energy transfer in this system. The average distance between Dn and Ac moieties calculated from the conformational analysis (12 Å) is in very good agreement with the value estimated from the Förster equation (∼11 Å). At the same time, the calculated rate constant for energy transfer, averaged over multiple conformations of the system (3.6 ps), is in reasonable agreement with the experimental value (1.6 ps) estimated by transient absorption spectroscopy. The agreement between experimental results and computational data leads us to conclude that the energy transfer in Bi is well described by the Förster mechanism. PMID:24513677

  20. Molding resonant energy transfer by colloidal crystal: Dexter transfer and electroluminescence

    NASA Astrophysics Data System (ADS)

    González-Urbina, Luis; Kolaric, Branko; Libaers, Wim; Clays, Koen

    2010-05-01

    Building photonic crystals by combination of colloidal ordering and metal sputtering we were able to construct a system sensitive to an electrical field. In corresponding crystals we embedded the Dexter pair (Ir(ppy3) and BAlq) and investigated the influence of the band gap on the resonant energy transfer when the system is excited by light and by an electric field respectively. Our investigations extend applications of photonic crystals into the field of electroluminescence and LED technologies.

  1. Regulation control and energy management scheme for wireless power transfer

    DOEpatents

    Miller, John M.

    2015-12-29

    Power transfer rate at a charging facility can be maximized by employing a feedback scheme. The state of charge (SOC) and temperature of the regenerative energy storage system (RESS) pack of a vehicle is monitored to determine the load due to the RESS pack. An optimal frequency that cancels the imaginary component of the input impedance for the output signal from a grid converter is calculated from the load of the RESS pack, and a frequency offset f* is made to the nominal frequency f.sub.0 of the grid converter output based on the resonance frequency of a magnetically coupled circuit. The optimal frequency can maximize the efficiency of the power transfer. Further, an optimal grid converter duty ratio d* can be derived from the charge rate of the RESS pack. The grid converter duty ratio d* regulates wireless power transfer (WPT) power level.

  2. Energy Characterization of Short-Circuiting Transfer of Metal Droplet in Gas Metal Arc Welding

    NASA Astrophysics Data System (ADS)

    Yi, Luo; Yang, Zhu; Xiaojian, Xie; Rui, Wan

    2015-08-01

    The structure-borne acoustic emission (AE) signals were detected in real time in gas metal arc (GMA) welding and pulse GMA (P-GMA) welding. According to the AE signals, the mode of short-circuiting transfer was analyzed, and the energy gradient and total energy were calculated. The calculation to the AE signals of one metal droplet transfer (MDT) showed that the energy gradient increased with increasing welding heat input not only in GMA welding but also in P-GMA welding. The energy gradient of one MDT in P-GMA welding was higher than that in GMA welding, which indicated that a high energy gradient was the basic reason for the additional vibration energy provided by pulse effect in P-GMA welding. The total energy of AE signals increased with increasing welding heat input not only in GMA welding but also in P-GMA welding. The total energy of AE signals in P-GMA welding was higher than that in GMA welding, which indicated that the additional vibration energy provided by welding pulses was the main cause of the grain structure refining in P-GMA welding. So, the results provided another means to predict the weld grain size and optimize the welding process by AE signals detected in welding.

  3. Nonlinear mode coupling and vibrational energy transfer in Yukawa clusters

    NASA Astrophysics Data System (ADS)

    Qiao, Ke; Kong, Jie; Matthews, Lorin; Hyde, Truell

    2015-11-01

    Nonlinear mode coupling and the subsequent vibrational energy transfer that results is an important topic in chemical physics research, ranging from small molecules consisting of several atoms to macromolecules such as those found in proteins and DNA. Nonlinear mode coupling is recognized as the mechanism leading to ergodicity, which is a foundational tenet of statistical mechanics. Over the past two decades, Yukawa systems of particles such as those found in complex plasma, have been shown to be an effective model across a large number of physical systems. In this research, nonlinear mode coupling in Yukawa clusters consisting of 3-10 particles is examined via numerical simulation of the vibrational energy transfer between modes starting from an initial excited state. The relationship between the energy transfer process and the internal resonance between modes having a specified frequency ratio and the temporal evolution of the system to a state of equal energy across all modes, i.e., the state of ergodicity, will be discussed. Support from the NSF and the DOE (award numbers PHY-1262031 and PHY-1414523) is gratefully acknowledged.

  4. Laser induced vibrational energy transfer in iron pentacarbonyl

    NASA Astrophysics Data System (ADS)

    Langsam, Yedidyah; Ronn, A. M.

    1984-01-01

    The internal kinetics of Fe(CO)5 as well as the kinetics between Fe(CO)5 and other nonreactive species were studied using the technique of laser induced fluorescence. The energy transfer behavior of this large polyatomic is discussed in terms of existing V-V and V-T/R theories and collisional energy transfer. Iron pentacarbonyl's vibrational energy structure is treated by means of a simple three and four level energy transfer scheme. Subsequent to excitation of the 10 μ region by a CO2 laser, infrared fluorescence has been detected from the ˜16, ˜5, and ˜4 μ regions of Fe(CO)5. A single exponential decay rate of 13.6 ms-1 Torr-1 is observed from the ˜5 μ region, in good agreement with other decay rates established for smaller polyatomics possessing similar vibrational level structure. Under conditions of low fluence (˜30 mJ/cm2), this region is activated at a rate of 474 ms-1 Torr-1 suggesting a rapid near resonant collisional energy transfer. Under conditions of high fluence (˜5 J/cm2), the activation of the ˜5 μ region proceeds at a rate of 1250 ms-1 Torr-1 suggesting a different pathway for the determining step of the excitation process. The rare gas deactivation rates as well as those with Ni(CO)4, CO(CO)3No, and CO (as well as the reverse rate) and the crossover rate from excited Fe(CO)5 to CO in high rare gas dilution have also been determined.

  5. Effect of ferrite addition above the base ferrite on the coupling factor of wireless power transfer for vehicle applications

    NASA Astrophysics Data System (ADS)

    Batra, T.; Schaltz, E.; Ahn, S.

    2015-05-01

    Power transfer capability of wireless power transfer systems is highly dependent on the magnetic design of the primary and secondary inductors and is measured quantitatively by the coupling factor. The inductors are designed by placing the coil over a ferrite base to increase the coupling factor and reduce magnetic emissions to the surroundings. Effect of adding extra ferrite above the base ferrite at different physical locations on the self-inductance, mutual inductance, and coupling factor is under investigation in this paper. The addition can increase or decrease the mutual inductance depending on the placement of ferrite. Also, the addition of ferrite increases the self-inductance of the coils, and there is a probability for an overall decrease in the coupling factor. Correct placement of ferrite, on the other hand, can increase the coupling factor relatively higher than the base ferrite as it is closer to the other inductor. Ferrite being a heavy compound of iron increases the inductor weight significantly and needs to be added judiciously. Four zones have been identified in the paper, which shows different sensitivity to addition of ferrite in terms of the two inductances and coupling factor. Simulation and measurement results are presented for different air gaps between the coils and at different gap distances between the ferrite base and added ferrite. This paper is beneficial in improving the coupling factor while adding minimum weight to wireless power transfer system.

  6. Intramolecular electronic energy transfer in bichromophoric molecular macrocyclic systems

    NASA Astrophysics Data System (ADS)

    Speiser, Shammai

    1993-01-01

    The structures and spectral properties of several bichromophoric molecules, suitable for optical data processing, are presented. The bichromophoric molecules are composed of an aromatic ring connected by two methylene chains to an (alpha) -diketone moiety. Both the absorption and emission spectra of these compounds can be attributed to a superposition of the individual spectra of the separate chromophores. The critical transfer radia for electronic energy transfer from the aromatic (donor) chromophore to the (alpha) -diketone (acceptor) chromophore was calculated from the spectral overlap between the fluorescence spectrum of the aromatic ring with the absorption spectrum of the (alpha) -diketone chromophore. The results show that this series of molecules is well suited for a mechanistic study of short-range intramolecular electronic energy transfer (intra-EET). The temperature and the molecular structure dependence of the intra-EET efficiency in this series was measured and analyzed for both singlet-singlet and triplet-triplet routes. The results show that the transfer efficiency is strongly temperature and structure dependent, indicating that exchange interaction is responsible for intra-EET between close chromophores in a bichromophoric molecule. The relative contributions of interchromophoric distance and that of the relative orientation of the two chromophores to exchange interaction are discussed.

  7. Structure and energy transfer in photosystems of oxygenic photosynthesis.

    PubMed

    Nelson, Nathan; Junge, Wolfgang

    2015-01-01

    Oxygenic photosynthesis is the principal converter of sunlight into chemical energy on Earth. Cyanobacteria and plants provide the oxygen, food, fuel, fibers, and platform chemicals for life on Earth. The conversion of solar energy into chemical energy is catalyzed by two multisubunit membrane protein complexes, photosystem I (PSI) and photosystem II (PSII). Light is absorbed by the pigment cofactors, and excitation energy is transferred among the antennae pigments and converted into chemical energy at very high efficiency. Oxygenic photosynthesis has existed for more than three billion years, during which its molecular machinery was perfected to minimize wasteful reactions. Light excitation transfer and singlet trapping won over fluorescence, radiation-less decay, and triplet formation. Photosynthetic reaction centers operate in organisms ranging from bacteria to higher plants. They are all evolutionarily linked. The crystal structure determination of photosynthetic protein complexes sheds light on the various partial reactions and explains how they are protected against wasteful pathways and why their function is robust. This review discusses the efficiency of photosynthetic solar energy conversion. PMID:25747397

  8. Modelling excitonic-energy transfer in light-harvesting complexes

    SciTech Connect

    Kramer, Tobias; Kreisbeck, Christoph

    2014-01-08

    The theoretical and experimental study of energy transfer in photosynthesis has revealed an interesting transport regime, which lies at the borderline between classical transport dynamics and quantum-mechanical interference effects. Dissipation is caused by the coupling of electronic degrees of freedom to vibrational modes and leads to a directional energy transfer from the antenna complex to the target reaction-center. The dissipative driving is robust and does not rely on fine-tuning of specific vibrational modes. For the parameter regime encountered in the biological systems new theoretical tools are required to directly compare theoretical results with experimental spectroscopy data. The calculations require to utilize massively parallel graphics processor units (GPUs) for efficient and exact computations.

  9. Intermolecular nonradiative energy transfer in clusters with plasmonic nanoparticles

    NASA Astrophysics Data System (ADS)

    Kucherenko, M. G.; Stepanov, V. N.; Kruchinin, N. Yu.

    2015-01-01

    The influence of carbon (fullerenes, nanotubes) and metal (Ni, Co, Cu, Ag) nanoparticles on the nonradiative electronic excitation energy transfer between the molecules of organic dyes (acrylic orange as a donor and Nile blue as an acceptor) in alcohol solutions of polyvinylbutyral is studied. It is found that, at particular concentrations of the mixture components, plasmonic nanoparticles affect the nonradiative electronic excitation energy transfer, which is manifested in an increase in the intensity of sensitized fluorescence of acceptors with simultaneous quenching of the fluorescence of donors. A very simple model is proposed to illustrate the observed redistribution of luminescence intensity between the spectral bands of the general spectrum. Molecular-dynamic calculations of the structure of nanocomposites performed for the same purpose confirmed the formation of associated molecular plasmonic complexes fixed by macrochain links.

  10. Additive Fabrication of Conductive Patterns by a Template Transfer Process Based on Benzotriazole Adsorption As a Separation Layer.

    PubMed

    Chang, Yu; Yang, Zhen-Guo

    2016-06-01

    The traditional subtractive process to fabricate conductive patterns is environmentally harmful, wasteful, and limited in line width. The additive process, including direct printing of conductive paste or ink, direct printing of catalytic ink, laser-induced forward transfer, etc., can solve these problems. However, the current additive process also faces many difficulties such as low electrical and adhesion properties, low pattern thickness, high cost, etc. Benzotriazole (BTA), as widely used corrosion inhibitor, can be adsorbed onto a copper surface. The electroplated copper film on BTA-adsorbed copper foil shows poor adhesion. On the basis of this phenomenon, a novel template transfer process to additively fabricate conductive patterns has been developed. A permeant antiadhesive mask is printed on carrier copper foil, and then, BTA is adsorbed onto the exposed area of the carrier foil, thus forming the template. The template is electroplated to grow conductive patterns in the exposed parts, and then can be adhered to the flexible substrate. The substrate is peeled off, with the transfer of the conductive patterns to the substrate, to form the designed conductive patterns on PET. By reimmersing the template into BTA solution, the template can be used again. The mechanism of BTA adsorption and the reason for the low peeling strength are researched using Raman spectra, XPS and electrochemical impedance spectroscopy. Copper patterns more than 20 μm in thickness can be prepared on PET, the resistivity of the prepared copper patterns is 2.01 μΩ cm, which is about the same as bulk copper, and the peeling strength of the pattern on PET is measured to be 6.97 N/cm. This template transfer process, with no waste, low pollution, high electrical and adhesion properties, and low cost, shows high potential in the large scale manufacturing of electronic devices, such as RFID circuitry, FPCs, etc. PMID:27171553

  11. Energy transfer processes in solar energy conversion. Final report

    SciTech Connect

    Fayer, M.D.

    1984-01-01

    The following were studied experimentally and/or theoretically: dynamics of energy transport and trapping in two-component systems (using rhodamine 6G and malachite green as traps), electronic excited state transport among molecules randomly distributed in a finite volume, electronic excitation transport in polymer systems, and excitation transport in synthetic Zn-chlorophyllide substituted hemoglobin. (DLC)

  12. Response of silicon-Based Linear Energy Transfer Spectrometers

    NASA Technical Reports Server (NTRS)

    Aman, A.; Bman, B.; Badhwar, G. D.; ONeill, P. M. O.

    2000-01-01

    Silicon-based linear energy transfer (LET) telescope,(e. g., DOSTEL and RRMD) have recently been flown in space. LET spectra measured using tissue equivalent proportional counters show differences that need to be fully understood. A Monte Carlo technique based on: 1. radiation transport cluster intra-cascade model. 2. Landau-Vavilov distribution, 3. telescope geometry and detector coincidence & discriminator settings, 4. spacecraft shielding geometry, and 5. the external free space radiation environment, including recent albedo measurements, was developed.

  13. Carotenoid charge transfer states and their role in energy transfer processes in LH1-RC complexes from aerobic anoxygenic phototrophs.

    PubMed

    Šlouf, Václav; Fuciman, Marcel; Dulebo, Alexander; Kaftan, David; Koblížek, Michal; Frank, Harry A; Polívka, Tomáš

    2013-09-26

    Light-harvesting complexes ensure necessary flow of excitation energy into photosynthetic reaction centers. In the present work, transient absorption measurements were performed on LH1-RC complexes isolated from two aerobic anoxygenic phototrophs (AAPs), Roseobacter sp. COL2P containing the carotenoid spheroidenone, and Erythrobacter sp. NAP1 which contains the carotenoids zeaxanthin and bacteriorubixanthinal. We show that the spectroscopic data from the LH1-RC complex of Roseobacter sp. COL2P are very similar to those previously reported for Rhodobacter sphaeroides, including the transient absorption spectrum originating from the intramolecular charge-transfer (ICT) state of spheroidenone. Although the ICT state is also populated in LH1-RC complexes of Erythrobacter sp. NAP1, its appearance is probably related to the polarity of the bacteriorubixanthinal environment rather than to the specific configuration of the carotenoid, which we hypothesize is responsible for populating the ICT state of spheroidenone in LH1-RC of Roseobacter sp. COL2P. The population of the ICT state enables efficient S1/ICT-to-bacteriochlorophyll (BChl) energy transfer which would otherwise be largely inhibited for spheroidenone and bacteriorubixanthinal due to their low energy S1 states. In addition, the triplet states of these carotenoids appear well-tuned for efficient quenching of singlet oxygen or BChl-a triplets, which is of vital importance for oxygen-dependent organisms such as AAPs. PMID:23130956

  14. Disk-to-disk transfer as the rate-limiting step for energy flow in phycobilisomes

    SciTech Connect

    Glazer, A.N.; Yeh, S.W.; Webb, S.P.; Clark, J.H.

    1985-01-25

    A broadly tunable picosecond laser source and an ultrafast streak camera were used to measure temporally and spectrally resolved emission from intact phycobilisomes and from individual phycobiliproteins as a function of excitation wavelength. Both wild-type and mutant phycobilisomes of the unicellular cyanobacterium Synechocystis 6701 were examined, as well as two biliproteins, R-phycoerythrin (240 kilodaltons, 34 bilins) and allophycocyanin (100 kilodaltons, 6 bilins). Measurements of intact phycobilisomes with known structural differences showed that the addition of an average of 1.6 phycoerythrin disks in the phycobilisome rod increased the overall energy transfer time by 30 +/- 5 picoseconds. In the isolated phycobiliproteins the onset of emission was as prompt as that of a solution of rhodamine B laser dye and was independent of excitation wavelength. This imposes an upper limit of 8 picoseconds (instrument-limited) on the transfer time from sensitizing to fluorescing chromophores in these biliproteins. These results indicate that disk-to-disk transfer is the slowest energy transfer process in phycobilisomes and, in combination with previous structural analyses, show that with respect to energy transfer the lattice of approximately 625 light-harvesting chromophores in the Synechocystis 6701 wild-type phycobilisome functions as a linear five-point array.

  15. Modeling coherent excitation energy transfer in photosynthetic light harvesting systems

    NASA Astrophysics Data System (ADS)

    Huo, Pengfei

    2011-12-01

    Recent non-linear spectroscopy experiments suggest the excitation energy transfer in some biological light harvesting systems initially occurs coherently. Treating such processes brings significant challenge for conventional theoretical tools that usually involve different approximations. In this dissertation, the recently developed Iterative Linearized Density Matrix (ILDM) propagation scheme, which is non-perturbative and non-Markovian is extended to study coherent excitation energy transfer in various light harvesting complexes. It is demonstrated that the ILDM approach can successfully describe the coherent beating of the site populations on model systems and gives quantitative agreement with both experimental results and the results of other theoretical methods have been developed recently to going beyond the usual approximations, thus providing a new reliable theoretical tool to study this phenomenon. This approach is used to investigate the excited energy transfer dynamics in various experimentally studied bacteria light harvesting complexes, such as Fenna-Matthews-Olsen (FMO) complex, Phycocyanin 645 (PC645). In these model calculations, quantitative agreement is found between computed de-coherence times and quantum beating pattens observed in the non-linear spectroscopy. As a result of these studies, it is concluded that the stochastic resonance behavior is important in determining the optimal throughput. To begin addressing possible mechanics for observed long de-coherence time, various models which include correlation between site energy fluctuations as well as correlation between site energy and inter-site coupling are developed. The influence of both types of correlation on the coherence and transfer rate is explored using with a two state system-bath hamiltonian parametrized to model the reaction center of Rhodobacter sphaeroides bacteria. To overcome the disadvantages of a fully reduced approach or a full propagation method, a brownian dynamics

  16. Energy transfer processes in semiconductor quantum dots: bacteriorhodopsin hybrid system

    NASA Astrophysics Data System (ADS)

    Rakovich, Aliaksandra; Sukhanova, Alyona; Bouchonville, Nicolas; Molinari, Michael; Troyon, Michel; Cohen, Jacques H. M.; Rakovich, Yury; Donegan, John F.; Nabiev, Igor

    2009-05-01

    The potential impact of nanoscience on energy transfer processes in biomolecules was investigated on the example of a complex between fluorescent semiconductor nanocrystals and photochromic membrane protein. The interactions between colloidal CdTe quantum dots (QDs) and bacteriorhodopsin (bR) protein were studied by a variety of spectroscopic techniques, including integrated and time-resolved fluorescence spectroscopies, zeta potential and size measurement, and fluorescence correlation spectroscopy. QDs' luminescence was found to be strongly modulated by bacteriorhodopsin, but in a controllable way. Decreasing emission lifetimes and blue shifts in QDs' emission at increasing protein concentrations suggest that quenching occurs via Förster resonance energy transfer. On the other hand, concave Stern-Volmer plots and sigmoidal photoluminescence quenching curves imply that the self-assembling of NCs and bR exists, and the number of nanocrystals (NCs) per bacteriorhodopsin contributing to energy transfer can be determined from the inflection points of sigmoidal curves. This number was found to be highly dependent not only on the spectral overlap between NC emission and bR absorption bands, but also on nanocrystal surface charge. These results demonstrate the potential of how inorganic nanoscale materials can be employed to improve the generic molecular functions of biomolecules. The observed interactions between CdTe nanocrystals and bacteriorhodopsin can provide the basis for the development of novel functional materials with unique photonic properties and applications in areas such as all-optical switching, photovoltaics and data storage.

  17. Energy and charge transfer in ionized argon coated water clusters

    SciTech Connect

    Kočišek, J. E-mail: michal.farnik@jh-inst.cas.cz Lengyel, J.; Fárník, M. E-mail: michal.farnik@jh-inst.cas.cz; Slavíček, P. E-mail: michal.farnik@jh-inst.cas.cz

    2013-12-07

    We investigate the electron ionization of clusters generated in mixed Ar-water expansions. The electron energy dependent ion yields reveal the neutral cluster composition and structure: water clusters fully covered with the Ar solvation shell are formed under certain expansion conditions. The argon atoms shield the embedded (H{sub 2}O){sub n} clusters resulting in the ionization threshold above ≈15 eV for all fragments. The argon atoms also mediate more complex reactions in the clusters: e.g., the charge transfer between Ar{sup +} and water occurs above the threshold; at higher electron energies above ∼28 eV, an excitonic transfer process between Ar{sup +}* and water opens leading to new products Ar{sub n}H{sup +} and (H{sub 2}O){sub n}H{sup +}. On the other hand, the excitonic transfer from the neutral Ar* state at lower energies is not observed although this resonant process was demonstrated previously in a photoionization experiment. Doubly charged fragments (H{sub 2}O){sub n}H{sub 2}{sup 2+} and (H{sub 2}O){sub n}{sup 2+} ions are observed and Intermolecular Coulomb decay (ICD) processes are invoked to explain their thresholds. The Coulomb explosion of the doubly charged cluster formed within the ICD process is prevented by the stabilization effect of the argon solvent.

  18. Resonant energy transfer based biosensor for detection of multivalent proteins.

    SciTech Connect

    Song, X.; Swanson, Basil I.

    2001-01-01

    We have developed a new fluorescence-based biosensor for sensitive detection of species involved in a multivslent interaction. The biosensor system utilizes specific interactions between proteins and cell surface receptors, which trigger a receptor aggregation process. Distance-dependent fluorescence self-quenching and resonant energy transfer mechanisms were coupled with a multivalent interaction to probe the receptor aggregation process, providing a sensitive and specific signal transduction method for such a binding event. The fluorescence change induced by the aggregation process can be monitored by different instrument platforms, e.g. fluorimetry and flow cytometry. In this article, a sensitive detection of pentavalent cholera toxin which recognizes ganglioside GM1 has been demonstrated through the resonant energy transfer scheme, which can achieve a double color change simultaneously. A detection sensitivity as high as 10 pM has been achieved within a few minutes (c.a. 5 minutes). The simultaneous double color change (an increase of acceptor fluorescence and a decrease of donor fluorescence intensity) of two similar fluorescent probes provides particularly high detection reliability owing to the fact that they act as each other's internal reference. Any external perturbation such as environmental temperature change causes no significant change in signal generation. Besides the application for biological sensing, the method also provides a useful tool for investigation of kinetics and thermodynamics of a multivalent interaction. Keywords: Biosensor, Fluorescence resonant energy transfer, Multivalent interaction, Cholera Toxin, Ganglioside GM1, Signal Transduction

  19. Humic substances enhance chlorothalonil phototransformation via photoreduction and energy transfer.

    PubMed

    Porras, Jazmín; Fernández, Jhon J; Torres-Palma, Ricardo A; Richard, Claire

    2014-02-18

    The photodegradation of chlorothalonil, a polychlorinated aromatic fungicide widely used in agriculture, was investigated under ultraviolet-visible irradiation in the presence and absence of different humic substances that significantly enhance the chlorothalonil phototransformation. On the basis of a kinetic model, an analytical study, the effect of scavengers, the chlorothalonil phosphorescence measurement, and varying irradiation conditions, it was possible to demonstrate that this accelerating effect is due to their capacity to reduce the chlorothalonil triplet state via H-donor reaction and to energy transfer from the triplet humic to ground state chlorothalonil. Energy transfer occurs at wavelengths below 450 nm and accounts for up to 30% of the reaction in deoxygenated medium upon irradiation with polychromatic light (300-450 nm). This process is more important with Elliott humic and fulvic acids and with humic acids extracted from natural carbonaceous material than with Nordic NOM and Pahokee peat humic acids. The obtained results are of high relevance to understanding the processes involved in chlorothalonil phototransformation and the photoreactivity of humic substances. Chlorothalonil is one of the rare molecules shown to react by energy transfer from excited humic substances. PMID:24455968

  20. Homopolar machine for reversible energy storage and transfer systems

    DOEpatents

    Stillwagon, Roy E.

    1981-01-01

    A homopolar machine designed to operate as a generator and motor in reversibly storing and transferring energy between the machine and a magnetic load coil for a thermo-nuclear reactor. The machine rotor comprises hollow thin-walled cylinders or sleeves which form the basis of the system by utilizing substantially all of the rotor mass as a conductor thus making it possible to transfer substantially all the rotor kinetic energy electrically to the load coil in a highly economical and efficient manner. The rotor is divided into multiple separate cylinders or sleeves of modular design, connected in series and arranged to rotate in opposite directions but maintain the supply of current in a single direction to the machine terminals. A stator concentrically disposed around the sleeves consists of a hollow cylinder having a number of excitation coils each located radially outward from the ends of adjacent sleeves. Current collected at an end of each sleeve by sleeve slip rings and brushes is transferred through terminals to the magnetic load coil. Thereafter, electrical energy returned from the coil then flows through the machine which causes the sleeves to motor up to the desired speed in preparation for repetition of the cycle. To eliminate drag on the rotor between current pulses, the brush rigging is designed to lift brushes from all slip rings in the machine.

  1. Homopolar machine for reversible energy storage and transfer systems

    DOEpatents

    Stillwagon, Roy E.

    1978-01-01

    A homopolar machine designed to operate as a generator and motor in reversibly storing and transferring energy between the machine and a magnetic load coil for a thermo-nuclear reactor. The machine rotor comprises hollow thin-walled cylinders or sleeves which form the basis of the system by utilizing substantially all of the rotor mass as a conductor thus making it possible to transfer substantially all the rotor kinetic energy electrically to the load coil in a highly economical and efficient manner. The rotor is divided into multiple separate cylinders or sleeves of modular design, connected in series and arranged to rotate in opposite directions but maintain the supply of current in a single direction to the machine terminals. A stator concentrically disposed around the sleeves consists of a hollow cylinder having a number of excitation coils each located radially outward from the ends of adjacent sleeves. Current collected at an end of each sleeve by sleeve slip rings and brushes is transferred through terminals to the magnetic load coil. Thereafter, electrical energy returned from the coil then flows through the machine which causes the sleeves to motor up to the desired speed in preparation for repetition of the cycle. To eliminate drag on the rotor between current pulses, the brush rigging is designed to lift brushes from all slip rings in the machine.

  2. Energy release and transfer in guide field reconnection

    NASA Astrophysics Data System (ADS)

    Birn, J.; Hesse, M.

    2010-01-01

    Properties of energy release and transfer by magnetic reconnection in the presence of a guide field are investigated on the basis of 2.5-dimensional magnetohydrodynamic (MHD) and particle-in-cell (PIC) simulations. Two initial configurations are considered: a plane current sheet with a uniform guide field of 80% of the reconnecting magnetic field component and a force-free current sheet in which the magnetic field strength is constant but the field direction rotates by 180° through the current sheet. The onset of reconnection is stimulated by localized, temporally limited compression. Both MHD and PIC simulations consistently show that the outgoing energy fluxes are dominated by (redirected) Poynting flux and enthalpy flux, whereas bulk kinetic energy flux and heat flux (in the PIC simulation) are small. The Poynting flux is mainly associated with the magnetic energy of the guide field which is carried from inflow to outflow without much alteration. The conversion of annihilated magnetic energy to enthalpy flux (that is, thermal energy) stems mainly from the fact that the outflow occurs into a closed field region governed by approximate force balance between Lorentz and pressure gradient forces. Therefore, the energy converted from magnetic to kinetic energy by Lorentz force acceleration becomes immediately transferred to thermal energy by the work done by the pressure gradient force. Strong similarities between late stages of MHD and PIC simulations result from the fact that conservation of mass and entropy content and footpoint displacement of magnetic flux tubes, imposed in MHD, are also approximately satisfied in the PIC simulations.

  3. State-to-state dynamics of molecular energy transfer

    SciTech Connect

    Gentry, W.R.; Giese, C.F.

    1993-12-01

    The goal of this research program is to elucidate the elementary dynamical mechanisms of vibrational and rotational energy transfer between molecules, at a quantum-state resolved level of detail. Molecular beam techniques are used to isolate individual molecular collisions, and to control the kinetic energy of collision. Lasers are used both to prepare specific quantum states prior to collision by stimulated-emission pumping (SEP), and to measure the distribution of quantum states in the collision products by laser-induced fluorescence (LIF). The results are interpreted in terms of dynamical models, which may be cast in a classical, semiclassical or quantum mechanical framework, as appropriate.

  4. Vibrational Energy Transfer of Diatomic Gases in Hypersonic Expanding Flows.

    NASA Astrophysics Data System (ADS)

    Ruffin, Stephen Merrick

    In high temperature flows related to vehicles at hypersonic speeds significant excitation of the vibrational energy modes of the gas can occur. Accurate predictions of the vibrational state of the gas and the rates of vibrational energy transfer are essential to achieve optimum engine performance, for design of heat shields, and for studies of ground based hypersonic test facilities. The Landau -Teller relaxation model is widely used because it has been shown to give accurate predictions in vibrationally heating flows such as behind forebody shocks. However, a number of experiments in nozzles have indicated that it fails to accurately predict the rate of energy transfer in expanding, or cooling, flow regions and fails to predict the distribution of energy in the vibrational quantum levels. The present study examines the range of applicability of the Landau -Teller model in expanding flows and develops techniques which provide accurate predictions in expanding flows. In the present study, detailed calculations of the vibrational relaxation process of N_2 and CO in cooling flows are conducted. A coupled set of vibrational transition rate equations and quasi one-dimensional fluid dynamic equations is solved. Rapid anharmonic Vibration-Translation transition rates and Vibration -Vibration exchange collisions are found to be responsible for vibrational relaxation acceleration in situations of high vibrational temperature and low translational temperature. The predictions of the detailed master equation solver are in excellent agreement with experimental results. The exact degree of acceleration is cataloged in this study for N_2 and is found to be a function of both the translational temperature (T) and the ratio of vibrational to translational temperatures (T_{vib}/T). Non-Boltzmann population distributions are observed for values of T _{vib}/T as low as 2.0. The local energy transfer rate is shown to be an order of magnitude or more faster than the Landau-Teller model

  5. Modulating the electronic structure of chromophores by chemical substituents for efficient energy transfer: application to fluorone.

    PubMed

    Sand, Andrew M; Liu, Claire; Valentine, Andrew J S; Mazziotti, David A

    2014-08-01

    Strong electron correlation within a quasi-spin model of chromophores was recently shown to enhance exciton energy transfer significantly. Here we investigate how the modulation of the electronic structure of the chromophores by chemical substitution can enhance energy-transfer efficiency. Unlike previous work that does not consider the direct effect of the electronic structure on exciton dynamics, we add chemical substituents to the fluorone dimer to study the effect of electron-donating and electron-withdrawing substituents on exciton energy transfer. The exciton dynamics are studied from the solution of a quantum Liouville equation for an open system whose model Hamiltonian is derived from excited-state electronic structure calculations. Both van der Waals energies and coupling energies, arising from the Hellmann-Feynman force generated upon transferring the dimers from infinity to a finite separation, are built into the model Hamiltonian. Though these two effects are implicitly treated in dipole-based models, their explicit and separate treatment as discussed here is critical to forging the correct connection with the electronic structure calculations. We find that the addition of electron-donating substituents to the fluorone system results in an increase in exciton-transfer rates by factors ranging from 1.3-1.9. The computed oscillator strength is consistent with the recent experimental results on a larger heterodimer system containing fluorone. The oscillator strength increases with the addition of electron-donating substituents. Our results indicate that the study of chromophore networks via electronic structure will help in the future design of efficient synthetic light-harvesting systems. PMID:25062094

  6. Rotational And Rovibrational Energy Transfer In Electron Collisions With Molecules

    NASA Technical Reports Server (NTRS)

    Thuemmel, Helmar T.; Langhoff, Stephen R. (Technical Monitor)

    1995-01-01

    Air flows around a hypervelocity reentry vehicle undergo dissociation, rovibrational excitation and ionization. More specifically the air, initially 80% N2 and 20% O2, in the shock layer consists of species such as N, O, N2, O2, NO, N+, O+, N+, O+, NO+ and 2 free electrons. It was pointed out in multi temperature models'' that the temperature of the rotational energy modes and the gas-kinetic translational temperature are quickly equilibrated by a few collisions and rise rapidly to high temperatures as 50000K before falling off to equilibrium value of 10000K. Contrary, the electronic and vibrational temperatures state energy distributions remain low (less than 15000K) because of the slow equilibration. Electron vibrational energy transfer is thought to play a crucial role in such a ionizing flow regime since chemical reaction rates and dissociation depend strongly on the vibrational temperatures. Modeling of these flowfields in principle require the rovibrational excitation and de-excitation cross section data for average electron energies from threshold up to several eV (leV=11605.4 K). In this lecture we focus on theoretical description of rotational effects i.e. energy transfer of electrons to molecules such that the molecular rotational (vojo goes to voj) or vibrational and rotational (v(sub 0)j(sub 0) goes to vj) states are changed. Excitation and de-excitation of electronic states was discussed in a previous talk at this conference.

  7. Energy transfer among isoelectronic dopants in GaP

    NASA Astrophysics Data System (ADS)

    Christian, Theresa; Alberi, Kirstin; Fluegel, Brian; Mascarenhas, Angelo

    2014-03-01

    Although GaP is an indirect-bandgap material, it can also be an efficient light-emitter at visible wavelengths when isoelectronic impurities mediate radiative recombination via states within the bandgap. Since these states also provide a medium for energy transfer via exciton hopping among localized isoelectronic trap sites, the carrier dynamics in doped GaP are strongly dependent on the distribution and density of impurity species. We present spectroscopic data demonstrating the role of energy transfer among isoelectronic states in GaP via temperature-dependent and time-resolved photoluminescence. Research was supported by the U. S. Department of Energy, Basic Energy Sciences, Materials Sciences and Engineering Division under contract DE-AC36-08GO28308 and by the Department of Energy Office of Science Graduate Fellowship Program (DOE SCGF), made possible in part by the American Recovery and Reinvestment Act of 2009, administered by ORISE-ORAU under contract no. DE-AC05-06OR23100.

  8. Preliminary investigation into the design of thermally responsive Forster resonance energy transfer colloids

    NASA Astrophysics Data System (ADS)

    Bedford, Monte Scott

    While nuclear imaging techniques (Magnetic Resonance Imaging, Computed Tomography, and Positron Emission Tomography) have proven effective for diagnosis and treatment of disease in the human body, fluorescence-enhanced optical imaging offers additional benefits. Fluorescent imaging provides high resolution with real-time response, persistent lifetime (hours to days), cell targeting, and transdermal penetration with minimal physical encumbrance. Malignant cells can be targeted by absorbance of exogenous fluorescent nanoprobe contrast agents. Imaging is improved by fluorescent enhancement, especially by energy transfer between attached dyes. Also for use against cancer are heat-active treatments, such as hyperthermal, photothermal, and chemothermal therapies. Helpful to these treatments is the thermal response from nanoprobes, within human cells, which provide real-time feedback. The present study investigates the design and feasibility of a nanoprobe molecular device, absorbable into malignant human cells, which provides real-time tracking and thermal response, as indicated by enhanced fluorescence by energy transfer. A poly(propargyl acrylate) colloidal suspension was synthesized. The particles were modified with a triblock copolymer, previously shown to be thermally responsive, and an end-attached fluorescent dye. A second dye was modeled for attachment in subsequent work. When two fluorescent dyes are brought within sufficiently close proximity, and excitation light is supplied, energy can be transferred between dyes to give enhanced fluorescence with a large Stokes shift (increase in wavelength between excitation and emission). The dye pair was modeled for overlap of emission and absorbance wavelengths, and energy transfer was demonstrated with 23% efficiency and a 209 nm Stokes shift. The quantum yield of the donor dye was determined at 70%, and the distance for 50% energy transfer was calculated at 2.9 nm, consistent with reports for similar compounds. When

  9. Targeted Energy Transfer Phenomena in Vibro-Impact Oscillators

    SciTech Connect

    Lee, Young S.; McFarland, D. Michael; Bergman, Lawrence A.; Nucera, Francesco; Vakakis, Alexander F.

    2008-07-08

    We study targeted energy transfer (TET) in a coupled oscillator, consisting of a single-degree-of-freedom primary linear oscillator coupled to a vibro-impact nonlinear energy sink (VI NES). For this purpose, we first compute the VI periodic orbits of the underlying hamiltonian VI system, and construct the corresponding frequency-energy plot (FEP). Then, considering inelastic impacts and viscous dissipation, we examine VI damped transitions on the FEP to identify a TET phenomenon by exciting a VI impulsive orbit, which is the most efficient mechanism for TET. Not only can the VI TET involve passive absorption and local dissipation of significant portions of the energy from the primary systems, but it occurs at sufficiently fast time scales. This renders VI NESs suitable for applications, like seismic mitigation, where shock elimination in the early, highly energetic regime of the motion is a critical requirement.

  10. Experimental study of low-energy charge transfer in nitrogen

    NASA Technical Reports Server (NTRS)

    Smith, A.

    1979-01-01

    Total charge transfer cross sections were obtained for the N2(+)-N2 system with relative translational ion energies between 9 and 441 eV. Data were obtained to examine the dependence of total cross section on ion energy. The effect of ion excitation on the cross sections was studied by varying the electron ionization energy in the mass spectrometer ion source over an electron energy range between 14.5 and 32.1 eV. The dependence of total cross section on the neutralization chamber gas pressure was examined by obtaining data at pressure values from 9.9 to 0.000199 torr. Cross section values obtained were compared with experimental and theoretical results of other investigations.

  11. Micro-beam friction liner and method of transferring energy

    DOEpatents

    Mentesana, Charles

    2007-07-17

    A micro-beam friction liner adapted to increase performance and efficiency and reduce wear in a piezoelectric motor or actuator or other device using a traveling or standing wave to transfer energy in the form of torque and momentum. The micro-beam friction liner comprises a dense array of micro-beam projections having first ends fixed relative to a rotor and second ends projecting substantially toward a plurality of teeth of a stator, wherein the micro-beam projections are compressed and bent during piezoelectric movement of the stator teeth, thereby storing the energy, and then react against the stator teeth to convert the stored energy stored to rotational energy in the rotor.

  12. Heat transfer and flow in solar energy and bioenergy systems

    NASA Astrophysics Data System (ADS)

    Xu, Ben

    The demand for clean and environmentally benign energy resources has been a great concern in the last two decades. To alleviate the associated environmental problems, reduction of the use of fossil fuels by developing more cost-effective renewable energy technologies becomes more and more significant. Among various types of renewable energy sources, solar energy and bioenergy take a great proportion. This dissertation focuses on the heat transfer and flow in solar energy and bioenergy systems, specifically for Thermal Energy Storage (TES) systems in Concentrated Solar Power (CSP) plants and open-channel algal culture raceways for biofuel production. The first part of this dissertation is the discussion about mathematical modeling, numerical simulation and experimental investigation of solar TES system. First of all, in order to accurately and efficiently simulate the conjugate heat transfer between Heat Transfer Fluid (HTF) and filler material in four different solid-fluid TES configurations, formulas of an e?ective heat transfer coe?cient were theoretically developed and presented by extending the validity of Lumped Capacitance Method (LCM) to large Biot number, as well as verifications/validations to this simplified model. Secondly, to provide design guidelines for TES system in CSP plant using Phase Change Materials (PCM), a general storage tank volume sizing strategy and an energy storage startup strategy were proposed using the enthalpy-based 1D transient model. Then experimental investigations were conducted to explore a novel thermal storage material. The thermal storage performances were also compared between this novel storage material and concrete at a temperature range from 400 °C to 500 °C. It is recommended to apply this novel thermal storage material to replace concrete at high operating temperatures in sensible heat TES systems. The second part of this dissertation mainly focuses on the numerical and experimental study of an open-channel algae

  13. Energy transfer and constrained simulations in isotropic turbulence

    NASA Technical Reports Server (NTRS)

    Jimenez, Javier

    1993-01-01

    The defining characteristic of turbulent flows is their ability to dissipate energy, even in the limit of zero viscosity. The Euler equations, if constrained in such a way that the velocity derivatives remain bounded, conserve energy. But when they arise as the limit of the Navier-Stokes (NS) equations, when the Reynolds number goes to infinity, there is persuasive empirical evidence that the gradients become singular as just the right function of Re for the dissipation to remain non-zero and to approach a well defined limit. It is generally believed that this limiting value of the dissipation is a property of the Euler equations themselves, independent of the particular dissipative mechanism involved, and that it can be normalized with the large scale properties of the turbulent flow (e.g. the kinetic energy per unit volume u'(exp 2)/2, and the integral scale L) without reference to the Reynolds number or to other dissipative quantities. This is usually taken to imply that the low wave number end of the energy spectrum, far from the dissipative range, is also independent of the particular mechanism chosen to dispose of the energy transfer. In the following sections, we present some numerical experiments on the effect of substituting different dissipation models into the truncated Euler equations. We will see that the effect is mainly felt in the 'near dissipation' range of the energy spectrum, but that this range can be quite wide in some cases, contaminating a substantial range of wave numbers. In the process, we will develop a 'practical' approximation to the subgrid energy transfer in isotropic turbulence, and we will gain insight into the structure of the nonlinear interactions among turbulent scales of comparable size, and into the nature of energy backscatter. Some considerations on future research directions are offered at the end.

  14. Biodegradable Multiblock Poly[N-(2-hydroxypropyl)methacrylamide] via Reversible Addition-Fragmentation Chain Transfer Polymerization and Click Chemistry

    PubMed Central

    Luo, Kui; Yang, Jiyuan; Kopečková, Pavla; Kopeček, Jindřich

    2011-01-01

    A new bifunctional chain transfer agent (CTA) containing alkyne end groups was designed, synthesized and used for direct synthesis of clickable telechelic polymers. Good control of reversible addition-fragmentation chain transfer (RAFT) polymerization of N-(2-hydroxypropyl)methacrylamide (HPMA) was achieved by using the new CTA, as indicated by a linear increase of number average molecular weight (Mn) with conversion and low polydispersity (PDI) (<1.1). In particular, enzymatically degradable multiblock HPMA polymers were readily prepared by subsequent reaction with αω, -diazido oligopeptide (GFLG) sequence via CuI catalyzed alkyne-azide cycloaddition. Upon exposure of high molecular weight fractions of multiblock polyHPMA to papain or cathepsin B, the polymer was degraded into segments of molecular weight and narrow polydispersity similar to those of the initial telechelic polyHPMA. PMID:21552355

  15. A stochastic reorganizational bath model for electronic energy transfer

    SciTech Connect

    Fujita, Takatoshi E-mail: aspuru@chemistry.harvard.edu; Huh, Joonsuk; Aspuru-Guzik, Alán E-mail: aspuru@chemistry.harvard.edu

    2014-06-28

    Environmentally induced fluctuations of the optical gap play a crucial role in electronic energy transfer dynamics. One of the simplest approaches to incorporate such fluctuations in energy transfer dynamics is the well known Haken-Strobl-Reineker (HSR) model, in which the energy-gap fluctuation is approximated as white noise. Recently, several groups have employed molecular dynamics simulations and excited-state calculations in conjunction to account for excitation energies’ thermal fluctuations. On the other hand, since the original work of HSR, many groups have employed stochastic models to simulate the same transfer dynamics. Here, we discuss a rigorous connection between the stochastic and the atomistic bath models. If the phonon bath is treated classically, time evolution of the exciton-phonon system can be described by Ehrenfest dynamics. To establish the relationship between the stochastic and atomistic bath models, we employ a projection operator technique to derive the generalized Langevin equations for the energy-gap fluctuations. The stochastic bath model can be obtained as an approximation of the atomistic Ehrenfest equations via the generalized Langevin approach. Based on this connection, we propose a novel scheme to take account of reorganization effects within the framework of stochastic models. The proposed scheme provides a better description of the population dynamics especially in the regime of strong exciton-phonon coupling. Finally, we discuss the effect of the bath reorganization in the absorption and fluorescence spectra of ideal J-aggregates in terms of the Stokes shifts. We find a simple expression that relates the reorganization contribution to the Stokes shifts – the reorganization shift – to the ideal or non-ideal exciton delocalization in a J-aggregate. The reorganization shift can be described by three parameters: the monomer reorganization energy, the relaxation time of the optical gap, and the exciton delocalization length

  16. Energy transfer in the Richtmyer-Meshkov instability.

    PubMed

    Thornber, Ben; Zhou, Ye

    2012-11-01

    The variable-density spectral kinetic energy budget for the Richtmyer-Meshkov-induced turbulent mixing layer is presented using results from a 512{3} implicit large eddy simulation. The budget is presented at several time instants and as a function of the inhomogeneous direction as the layer transitions from the initial impulse through to self-similarity. There are clear parallels in the development of the mixing layer with a previous analysis for the Rayleigh-Taylor instability. In the core of the layer, the quadratic terms are largely negative in the energy-containing scales. The transfer spectra are clearly asymmetric, where the majority of the activity occurrs on the spike side. The quadratic and pressure components are of opposite sign and almost cancel each other out in the spikes. The dilatational terms are negligible in comparison to the difference between the quadratic and pressure transfer. A notable result is that vortex rings are identified as the key source of alternating fields of negative and positive energy transfer within the mixing layer. This helps explain similar observations noted in direct numerical simulations of Rayleigh-Taylor instability. Finally, the spectral numerical dissipation for this scheme is computed for the self-similar layer. This demonstrated that the effects of numerical dissipation are small compared to the other terms at low wave numbers, whereas at higher wave numbers where modes become significantly underresolved the numerical dissipation is approximately twice the nonlinear transfer term and behaves in approximate analogy to an effective spectral eddy viscosity. PMID:23214871

  17. Investigating Protein-protein Interactions in Live Cells Using Bioluminescence Resonance Energy Transfer

    PubMed Central

    Estruch, Sara B.; Fisher, Simon E.

    2014-01-01

    Assays based on Bioluminescence Resonance Energy Transfer (BRET) provide a sensitive and reliable means to monitor protein-protein interactions in live cells. BRET is the non-radiative transfer of energy from a 'donor' luciferase enzyme to an 'acceptor' fluorescent protein. In the most common configuration of this assay, the donor is Renilla reniformis luciferase and the acceptor is Yellow Fluorescent Protein (YFP). Because the efficiency of energy transfer is strongly distance-dependent, observation of the BRET phenomenon requires that the donor and acceptor be in close proximity. To test for an interaction between two proteins of interest in cultured mammalian cells, one protein is expressed as a fusion with luciferase and the second as a fusion with YFP. An interaction between the two proteins of interest may bring the donor and acceptor sufficiently close for energy transfer to occur. Compared to other techniques for investigating protein-protein interactions, the BRET assay is sensitive, requires little hands-on time and few reagents, and is able to detect interactions which are weak, transient, or dependent on the biochemical environment found within a live cell. It is therefore an ideal approach for confirming putative interactions suggested by yeast two-hybrid or mass spectrometry proteomics studies, and in addition it is well-suited for mapping interacting regions, assessing the effect of post-translational modifications on protein-protein interactions, and evaluating the impact of mutations identified in patient DNA. PMID:24893771

  18. Ab Initio Investigation of Cation Proton Affinity and Proton Transfer Energy for Energetic Ionic Liquids.

    PubMed

    Carlin, Caleb M; Gordon, Mark S

    2016-08-01

    Protonation of the anion in an ionic liquid plays a key role in the hypergolic reaction between ionic liquids and oxidizers such as white fuming nitric acid. To investigate the influence of the cation on the protonation reaction, the deprotonation energy of a set of cations has been calculated at the MP2 level of theory. Specifically, guanidinium, dimethyltriazanium, triethylamine, N-ethyl-N-methyl-pyrrolidinium, N-ethyl-pyridinium, 1,4-dimethyl-1,2,4-triazolium, 1-ethyl-4-methyl-1,2,4-triazolium, and 1-butyl-4-methyl-1,2,4-triazolium were studied. In addition, the net proton transfer energies from the cations to a set of previously studied anions was calculated, demonstrating an inverse correlation between the net proton transfer energy and the likelihood that the cation/anion combination will react hypergolically with white fuming nitric acid. It is suggested that this correlation occurs due to a balance between the energy released by the proton transfer and the rate of proton transfer as determined by the ionicity of the ionic liquid. PMID:27397644

  19. Firefly Luciferase-Based Sequential Bioluminescence Resonance Energy Transfer (BRET)-Fluorescence Resonance Energy Transfer (FRET) Protease Assays.

    PubMed

    Branchini, Bruce

    2016-01-01

    We describe here the preparation of ratiometric luminescent probes that contain two well-separated emission peaks produced by a sequential bioluminescence resonance energy transfer (BRET)-fluorescence resonance energy transfer (FRET) process. The probes are single soluble fusion proteins consisting of a thermostable firefly luciferase variant that catalyzes yellow-green (560 nm maximum) bioluminescence and a red fluorescent protein covalently labeled with a near-Infrared fluorescent dye. The two proteins are connected by a decapeptide containing a protease recognition site specific for factor Xa, thrombin, or caspase 3. The rates of protease cleavage of the fusion protein substrates were monitored by recording emission spectra and plotting the change in peak ratios over time. Detection limits of 0.41 nM for caspase 3, 1.0 nM for thrombin, and 58 nM for factor Xa were realized with a scanning fluorometer. This method successfully employs an efficient sequential BRET-FRET energy transfer process based on firefly luciferase bioluminescence to assay physiologically important protease activities and should be generally applicable to the measurement of any endoprotease lacking accessible cysteine residues. PMID:27424898

  20. Rotational and vibrational energy transfer in vibrationally excited acetylene at energies near 6560 cm(-1).

    PubMed

    Han, Jiande; Freel, Keith; Heaven, Michael C

    2011-12-28

    Collisional energy transfer kinetics of vibrationally excited acetylene has been examined for states with internal energies near 6560 cm(-1). Total population removal rate constants were determined for selected rotational levels of the (1,0,1,0(0),0(0)) and (0,1,1,2(0),0(0)) states. Values in the range of (10-18) × 10(-10) cm(3) s(-1) were obtained. Measurements of state-to-state rotational energy transfer rate constants were also carried out for these states. The rotational energy transfer kinetics was found to be consistent with simple energy gap models for the transfer probabilities. Vibrational transfer out of the (0,1,1,2(0),0(0)) state accounted for no more than 16% of the total removal process. Transfer from (1,0,1,0(0),0(0)) to the u-symmetry (0,2,0,3(1),1(-1)), (0,1,1,2(0),0(0)), and (1,1,0,1(1),1(-1)) states was observed. Applying the principle of detailed balance to these data indicated that vibrational transfer to (1,0,1,0(0),0(0)) accounted for ~0.1% of the population loss from (0,2,0,3(1),1(-1)) or (0,1,1,2(0),0(0)), and 3% of the loss from (1,1,0,1(1),1(-1)). Relative rotational transfer probabilities were obtained for transfer to the g-symmetry (1,1,0,2(0),0(0))∕(0,0,2,0(0),0(0)) dyad. These results are related to recent studies of optically pumped acetylene lasers. PMID:22225153

  1. Optimal aeroassisted coplanar orbital transfer using an energy model

    NASA Technical Reports Server (NTRS)

    Halyo, Nesim; Taylor, Deborah B.

    1989-01-01

    The atmospheric portion of the trajectories for the aeroassisted coplanar orbit transfer was investigated. The equations of motion for the problem are expressed using reduced order model and total vehicle energy, kinetic plus potential, as the independent variable rather than time. The order reduction is achieved analytically without an approximation of the vehicle dynamics. In this model, the problem of coplanar orbit transfer is seen as one in which a given amount of energy must be transferred from the vehicle to the atmosphere during the trajectory without overheating the vehicle. An optimal control problem is posed where a linear combination of the integrated square of the heating rate and the vehicle drag is the cost function to be minimized. The necessary conditions for optimality are obtained. These result in a 4th order two-point-boundary-value problem. A parametric study of the optimal guidance trajectory in which the proportion of the heating rate term versus the drag varies is made. Simulations of the guidance trajectories are presented.

  2. Charge transfer and negative curvature energy in magnesium boride nanotubes

    NASA Astrophysics Data System (ADS)

    Tang, Hui; Ismail-Beigi, Sohrab

    2016-07-01

    Using first-principles calculations based on density functional theory, we study the energetics and charge transfer effects in MgBx nanotubes and two-dimensional (2D) sheets. The behavior of adsorbed Mg on 2D boron sheets is found to depend on the amount of electron transfer between the two subsystems. The amount is determined by both the density of adsorbed Mg as well as the atomic-scale structure of the boron subsystem. The degree of transfer can lead to repulsive or attractive Mg-Mg interactions. In both cases, model MgBx nanotubes built from 2D MgBx sheets can display negative curvature energy: a relatively unusual situation in nanosystems where the energy cost to curve the parent 2D sheet into a small-diameter nanotube is negative. Namely, the small-diameter nanotube is energetically preferred over the corresponding flat sheet. We also discuss how these findings may manifest themselves in experimentally synthesized MgBx nanotubes.

  3. Gamma-ray transfer and energy deposition in supernovae

    NASA Technical Reports Server (NTRS)

    Swartz, Douglas A.; Sutherland, Peter G.; Harkness, Robert P.

    1995-01-01

    Solutions to the energy-independent (gray) radiative transfer equations are compared to results of Monte Carlo simulations of the Ni-56 and Co-56 decay gamma-ray energy deposition in supernovae. The comparison shows that an effective, purely absorptive, gray opacity, kappa(sub gamma) approximately (0. 06 +/- 0.01)Y(sub e) sq cm/g, where Y is the total number of electrons per baryon, accurately describes the interaction of gamma-rays with the cool supernova gas and the local gamma-ray energy deposition within the gas. The nature of the gamma-ray interaction process (dominated by Compton scattering in the relativistic regime) creates a weak dependence of kappa(sub gamma) on the optical thickness of the (spherically symmetric) supernova atmosphere: The maximum value of kappa(sub gamma) applies during optically thick conditions when individual gamma-rays undergo multiple scattering encounters and the lower bound is reached at the phase characterized by a total Thomson optical depth to the center of the atmosphere tau(sub e) approximately less than 1. Gamma-ray deposition for Type Ia supernova models to within 10% for the epoch from maximum light to t = 1200 days. Our results quantitatively confirm that the quick and efficient solution to the gray transfer problem provides an accurate representation of gamma-ray energy deposition for a broad range of supernova conditions.

  4. Excitation energy transfer in vitro between phycobiliproteins and thylakoid photosystem II of higher plants

    NASA Astrophysics Data System (ADS)

    Wu, Xiaonan; Tseng, C. K.

    1992-12-01

    The excitation energy transfer from phycobiliproteins to thylakoid PSII of higher plants was investigated. When incubated with spinach thylakoids, phycobiliproteins isolated from red and blue-green algae transferred light energy absorbed to spinach PSII. The efficiency of energy transfer was dependent on the kind of phycobiliproteins used. If spinach thylakoids were replaced by the thylakoids of Brassica chinensis, R-phycoerythin or C-phycocyanin did not transfer their excitation energy to PSII of Brassica chinensis unless allophycocyanin was present.

  5. Photoinduced Charge and Energy Transfer Processes in Molecular Aggregates

    SciTech Connect

    John F. Endicott

    2009-10-20

    This project involved the experimental probing of the electronic excited states generated by photoinduced (center-to-center) electron and energy transfer processes in several classes of transition metal donor/acceptor (D/A) complexes. Some of the general properties inferred from these studies should be useful in the design of new systems for energy conversion applications. Pursuit of the project goals has involved the determination of electron transfer efficiencies and the detailed study of variations in the electronic spectra of D/A complexes. This has resulted in the study of some very fundamental issues of photoinduced charge transfer and the identification of some of the constraints on its efficiency. The experimental studies of the competition between the degradative non-radiative unimolecular relaxation of transition metal excited states and their transfer of charge from these excited states to external acceptors have involved a range of techniques such as transient decay kinetics, photoacoustic calorimetry and transient or stationary state spectroscopy. The substrates synthesized for these studies were selected to provide model systems, or series of model systems to probe the validity of models of electronic excited states and their reactivity. The work during the last few years has focused largely, but not exclusively, on the use of emission spectral band shapes to probe the properties of charge transfer (CT) excited states. Bandshape variations are one of the very few approaches for systematically probing electronic excited states and good band shape resolution is necessary in order to gain information about the structural variations that correlate with excited state reactivity. Differences in molecular structure correlate with differences in chemical reactivity, and the variations in emission bandshapes are well known to relate to variations in the molecular structural differences between the excited and ground electronic states. However, it is has been

  6. Effect of PTFE addition on the transfer film, wear and friction of PEEK-CuO composite

    SciTech Connect

    Vande Voort, J.; Bahadur, S.

    1995-12-31

    This work was done in part as a follow-up of an earlier study which had showed that CuO was effective in reducing the wear of PEEK, but the coefficient of friction of PEEK increased with the addition of CuO. In order to reduce the coefficient of friction, the organic filler PTFE was added to the CUO-PEEK composite so as to increase its appeal for practical applications. Initially, the optimum volume fraction of CuO in PEEK was determined for minimum wear by varying the proportion of the inorganic filler. With this composition as the basis for total filler content, PTFE was added to CuO-filled composites in 5 and 10 vol.% proportions. The friction and wear behaviors of these composites sliding against a tool steel surface were studied in a pin-on-disk configuration. It was determined from experiment that the optimum filler proportion of CuO in PEEK for minimum wear rate was 35 vol.%. The greater the content of CuO, the higher was the coefficient of friction. The optimum composition with PTFE and Cu additions was PEEK-30 vol.% CuO-5 vol.% PTFE. The wear rate and the coefficient of friction both of these compositions were lower than those of PEEK-35 vol.% CuO. The wear behavior has been analyzed by optical and scanning electron microscopy in terms of the ability of these composites to form transfer film on the steel counterface and the transfer film of PEEK-CuO-PTFE formulation has been investigated by XPS analysis. The XPS results revealed the presence of Cu ions and FeF{sub 2} compounds near the interface of the transfer film and the steel substrate. These observations have been used to support the hypothesis of reduced wear by the addition of inorganic and organic fillers to the polymer material.

  7. Iodinated (Perfluoro)alkyl Quinoxalines by Atom Transfer Radical Addition Using ortho-Diisocyanoarenes as Radical Acceptors.

    PubMed

    Leifert, Dirk; Studer, Armido

    2016-09-12

    A simple method for the preparation of functionalized quinoxalines is reported. Starting from readily accessible ortho-diisocyanoarenes and (perfluoro)alkyl iodides, the quinoxaline core is constructed during (perfluoro)alkylation by atom transfer radical addition (ATRA), resulting in 2-iodo-3-(perfluoro)alkylquinoxalines. The radical cascades are readily initiated either with visible light or by using α,α'-azobisisobutyronitrile (AIBN). The heteroarene products are obtained in high yields (up to 94 %), and the method can be readily scaled up. Useful follow-up chemistry documents the value of the novel radical quinoxaline synthesis. PMID:27510610

  8. Comparison of vibrational conductivity and radiative energy transfer methods

    NASA Astrophysics Data System (ADS)

    Le Bot, A.

    2005-05-01

    This paper is concerned with the comparison of two methods well suited for the prediction of the wideband response of built-up structures subjected to high-frequency vibrational excitation. The first method is sometimes called the vibrational conductivity method and the second one is rather known as the radiosity method in the field of acoustics, or the radiative energy transfer method. Both are based on quite similar physical assumptions i.e. uncorrelated sources, mean response and high-frequency excitation. Both are based on analogies with some equations encountered in the field of heat transfer. However these models do not lead to similar results. This paper compares the two methods. Some numerical simulations on a pair of plates joined along one edge are provided to illustrate the discussion.

  9. Heat transfer in vertically aligned phase change energy storage systems

    SciTech Connect

    El-Dessouky, H.T.; Bouhamra, W.S.; Ettouney, H.M.; Akbar, M.

    1999-05-01

    Convection effects on heat transfer are analyzed in low temperature and vertically aligned phase change energy storage systems. This is performed by detailed temperature measurements in the phase change material (PCM) in eighteen locations forming a grid of six radial and three axial positions. The system constitutes a double pipe configuration, where commercial grade paraffin wax is stored in the annular space between the two pipes and water flows inside the inner pipe. Vertical alignment of the system allowed for reverse of the flow direction of the heat transfer fluid (HTF), which is water. Therefore, the PCM is heated from the bottom for HTF flow from bottom to top and from the top as the HTF flow direction is reversed. For the former case, natural convection affects the melting process. Collected data are used to study variations in the transient temperature distribution at axial and radial positions as well as for the two-dimensional temperature field. The data are used to calculate the PCM heat transfer coefficient and to develop correlations for the melting Fourier number. Results indicate that the PCM heat transfer coefficient is higher for the case of PCM heating from bottom to top. Nusselt number correlations are developed as a function of Rayleigh, Stefan, and Fourier numbers for the HTF flow from bottom to top and as a function of Stefan and Fourier numbers for HTF flow from top to bottom. The enhancement ratio for heat transfer caused by natural convection increases and then levels off as the inlet temperature of the HTF is increased.

  10. Non-additive three-body interaction energies for H3 (quartet spin state)

    NASA Astrophysics Data System (ADS)

    Zhang, Z. C.; Allnatt, A. R.; Talman, James D.; Meath, William J.

    The results of an Unsold average energy calculation of the non-additive interaction energy for H3 (quartet spin state) are presented for equilateral triangular configurations. They are discussed in the context of the problems associated with the representation of non-additive energies for the interaction of closed-shell species.

  11. Prediction of Protein Solubility from Calculation of Transfer Free Energy

    PubMed Central

    Tjong, Harianto; Zhou, Huan-Xiang

    2008-01-01

    Solubility plays a major role in protein purification, and has serious implications in many diseases. We studied the effects of pH and mutations on protein solubility by calculating the transfer free energy from the condensed phase to the solution phase. The condensed phase was modeled as an implicit solvent, with a dielectric constant lower than that of water. To account for the effects of pH, the protonation states of titratable side chains were sampled by running constant-pH molecular dynamics simulations. Conformations were then selected for calculations of the electrostatic solvation energy: once for the condensed phase, and once for the solution phase. The average transfer free energy from the condensed phase to the solution phase was found to predict reasonably well the variations in solubility of ribonuclease Sa and insulin with pH. This treatment of electrostatic contributions combined with a similar approach for nonelectrostatic contributions led to a quantitative rationalization of the effects of point mutations on the solubility of ribonuclease Sa. This study provides valuable insights into the physical basis of protein solubility. PMID:18515380

  12. Energy transfer in mesoscopic vibrational systems enabled by eigenfrequency fluctuations

    NASA Astrophysics Data System (ADS)

    Atalaya, Juan

    Energy transfer between low-frequency vibrational modes can be achieved by means of nonlinear coupling if their eigenfrequencies fulfill certain nonlinear resonance conditions. Because of the discreteness of the vibrational spectrum at low frequencies, such conditions may be difficult to satisfy for most low-frequency modes in typical mesoscopic vibrational systems. Fluctuations of the vibrational eigenfrequencies can also be relatively strong in such systems. We show that energy transfer between modes can occur in the absence of nonlinear resonance if frequency fluctuations are allowed. The case of three modes with cubic nonlinear coupling and no damping is particularly interesting. It is found that the system has a non-thermal equilibrium state which depends only on the initial conditions. The rate at which the system approaches to such state is determined by the parameters such as the noise strength and correlation time, the nonlinearity strength and the detuning from exact nonlinear resonance. We also discuss the case of many weakly coupled modes. Our results shed light on the problem of energy relaxation of low-frequency vibrational modes into the continuum of high-frequency vibrational modes. The results have been obtained with Mark Dykman. Alternative email: jatalaya2012@gmail.com.

  13. Microscopic energy transfer spectroscopy to determine mitochondrial malfunction in human myotubes

    NASA Astrophysics Data System (ADS)

    Gschwend, Michael H.; Strauss, Wolfgang S. L.; Brinkmeier, H.; Ruedel, R.; Steiner, Rudolf W.; Schneckenburger, Herbert

    1996-12-01

    A microscopic equipment is reported for examination of cellular autofluorescence and determination of energy transfer in vitro, which is proposed to be an appropriate tool to investigate mitochondrial malfunction. The method includes fluorescence microscopy combined with time-gated (nanosecond) fluorescence emission spectroscopy and is presently used to study mitochondrial metabolism of human myotube primary cultures Enzyme complexes of the respiratory chain, located at the inner mitochondrial membrane, were inhibited by various drugs, and fluorescence of the mitochondrial coenzyme nicotinamide adenine dinucleotide (NADH) as well as of the mitochondrial marker rhodamine 123 (R123) was examined. After inhibition of enzyme complex I (NADH-coenzyme Q reductase) by rotenone or enzyme complex III (coenzyme QH2-cytochrome c reductase) by antimycin a similar or increased NADH fluorescence was observed. In addition, energy transfer from excited states of NADH (energy donor) to R123 (energy acceptor) was deduced from a decrease of NADH fluorescence after coincubation with these inhibitors and R123. Application of microscopic energy transfer spectroscopy for diagnosis of congenital mitochondrial deficiencies is currently in preparation.

  14. Rotational Energy Transfer and Collisional Induced Raman Linewidths in N2 Gas. 1; Energy Transfer Rates

    NASA Technical Reports Server (NTRS)

    Huo, Winifred M.; Green, Sheldon; Langhoff, Stephen R. (Technical Monitor)

    1995-01-01

    Rotationally inelastic transitions of N2 have been studied in the coupled state (CS) and infinite-order-sudden (IOS) approximations, using the N2-N2 rigidrotor potential of van der Avoird et al. For benchmarking purposes, close coupling (CC) calculations have also been carried out over a limited energy range. The CC and CS cross sections have been obtained both with and without identical molecule exchange symmetry, whereas exchange was neglected in the IOS calculations. The CS results track the CC cross sections rather well; between 113 - 219 cm(exp -1) the average deviation is 14%. Comparison between the CS and IOS cross sections at the high energy end of the CS calculation, 500 - 680 cm(exp -1), shows that IOS is sensitive to the amount of inelasticity and the results for large DELTA J transitions are subject to larger errors. It is found that the state-to-state cross sections with even and odd exchange symmetry agree to better than 2% and are well represented as a sum of direct and exchange cross sections for distinguishable molecules, an indication of the applicability of a classical treatment for this system. This result, however, does not apply to partial cross sections for given total J, but arises from a near cancellation in summing over partial waves. In order to use rigid-rotor results for the calculation of effective rotational excitation rates of N2 in the v=1 vibrational level colliding with bath N2 molecules in the v=0 level, it is assumed that exchange scattering between molecules in different vibrational levels is negligible and direct scattering is independent of Y. Good agreement with room temperature experimental data is obtained. The effective rates determined using the IOS and energy corrected sudden (ECS) approximations are also in reasonable agreement with experiment, with the ECS results being somewhat better. The problem with a degeneracy factor in earlier cross section expressions for collisions between identical molecules is pointed out

  15. Rotational-translational energy transfer in rarefied nonequilibrium flows

    NASA Technical Reports Server (NTRS)

    Boyd, Iain D.

    1990-01-01

    A new model for simulating the transfer of energy between the translational and rotational modes is derived for a homogeneous gas of diatomic molecules. The model has been developed specifically for use in discrete particle simulation methods where molecular motion and intermolecular collisions are treated at the molecular level. A temperature dependence is introduced which has been predicted by theory and observed in experiment. The new model is applied to the relaxation of rotational temperature, and is found to produce significant differences in comparison with the model normally employed at both high and low temperatures. Calculations have also been performed for a Mach 7 normal shock wave.

  16. Heat transfer research for ocean thermal energy conversion

    NASA Astrophysics Data System (ADS)

    Kreith, F.; Bharathan, D.

    1987-03-01

    In this lecture an overview of the heat- and mass-transfer phenomena of importance in ocean thermal energy conversion (OTEC) is presented with particular emphasis on open-cycle OTEC systems. Also included is a short historical review of OTEC developments in the past century and a comparison of open- and closed-cycle thermodynamics. Finally, results of system analyses, showing the effect of plant size on cost and the near-term potential of using OTEC for combined power production and desalination systems are briefly discussed.

  17. Fluorescence resonance energy transfer from allophycocyanin to malachite green

    NASA Astrophysics Data System (ADS)

    Rolinski, O. J.; Birch, D. J. S.; McCartney, L. J.; Pickup, J. C.

    1999-08-01

    The near-infrared fluorescence resonance energy transfer kinetics of the phycobiliprotein allophycocyanin (APC) to malachite green (MG) have been investigated. A model is proposed to account for the fluorescence decay whereby MG binds to APC with a donor-acceptor site distribution which can be best described by 2D quenching kinetics. The results highlight a potential fallacy when interpreting the dimensionality of complex systems or the location of binding sites from Förster decay kinetics. The use of APC in trans-dermal measurements is proposed.

  18. FY86 Technology Transfer Program Morgantown Energy Technology Center

    SciTech Connect

    Not Available

    1986-10-01

    The actual technology transfer was accomplished by several integrated activities during fiscal year (FY) 1986: R and D contracts with industry and academia, including cost-shared contracts; technical information exchange for scientist-to-scientist communication through conferences, visitors to the Center, and federal personnel visits with US industry; technical documents for information dissemination; patents to advance technology adoption and use in US industry; on-site training activities as personnel exchange; and technical assistance through the use of fossil energy technology data bases.

  19. Radiative interactions in transient energy transfer in gaseous systems

    NASA Technical Reports Server (NTRS)

    Tiwari, S. N.

    1985-01-01

    Analyses and numerical procedures are presented to investigate the radiative interactions in transient energy transfer processes in gaseous systems. The nongray radiative formulations are based on the wide-band model correlations for molecular absorption. Various relations for the radiative flux are developed; these are useful for different flow conditions and physical problems. Specific plans for obtaining extensive results for different cases are presented. The methods presented in this study can be extended easily to investigate the radiative interactions in realistic flows of hydrogen-air species in the scramjet engine.

  20. The Energy Transfer Dependence of the Quasielastic Carbon

    NASA Astrophysics Data System (ADS)

    Morrison, John Horton

    This thesis describes the measurement of coincidence electron scattering from ^{12} C at a momentum transfer of approximately 1000 MeV/c at quasielastic kinematics and below quasielastic kinematics. We detected the scattered electron and a knocked-out proton in coincidence. We measured the coincidence cross section as a function of missing energy E_{m }, at two values of the momentum transfer q and energy transfer w: below quasielastic kinematics at q = 970 MeV/c and w = 330 MeV, and at quasielastic kinematics at q = 990 MeV/c and w = 475 MeV. We produced missing energy spectra for each of the measurements. The dependence of the cross sections on w around the central values is indicated by expanding the cross sections in orthogonal polynomials in w and displaying the lowest few terms. Radiative corrections are applied to the spectra. We identify two peaks in the missing energy spectra corresponding to single-particle proton knockout from the p-shell and the s-shell. At quasielastic kinematics, we identify two continuum regions in missing energy: the near continuum where the cross section decreases with E _{m} and increases with w, and the far continuum where the cross section is constant in E_{m} and w. In contrast to quasielastic kinematics, the near continuum cross section is strongly suppressed below quasielastic kinematics, and the far continuum cross section is zero. We compared the p-shell and s-shell single-particle knockout cross section measured from the data with Distorted Wave Impulse Approximation calculations. Single-particle knockout accounted for most of the cross section below quasielastic kinematics, but only for half the cross section at quasielastic kinematics. We compared the quasielastic continuum cross section with calculations of multinucleon knockout and pion production. Pion production probably accounts for no more than half the cross section beyond pion threshold in missing energy. Neither Final State Interactions modeled as (N

  1. An enzymatically-sensitized sequential and concentric energy transfer relay self-assembled around semiconductor quantum dots

    NASA Astrophysics Data System (ADS)

    Samanta, Anirban; Walper, Scott A.; Susumu, Kimihiro; Dwyer, Chris L.; Medintz, Igor L.

    2015-04-01

    The ability to control light energy within de novo nanoscale structures and devices will greatly benefit their continuing development and ultimate application. Ideally, this control should extend from generating the light itself to its spatial propagation within the device along with providing defined emission wavelength(s), all in a stand-alone modality. Here we design and characterize macromolecular nanoassemblies consisting of semiconductor quantum dots (QDs), several differentially dye-labeled peptides and the enzyme luciferase which cumulatively demonstrate many of these capabilities by engaging in multiple-sequential energy transfer steps. To create these structures, recombinantly-expressed luciferase and the dye-labeled peptides were appended with a terminal polyhistidine sequence allowing for controlled ratiometric self-assembly around the QDs via metal-affinity coordination. The QDs serve to provide multiple roles in these structures including as central assembly platforms or nanoscaffolds along with acting as a potent energy harvesting and transfer relay. The devices are activated by addition of coelenterazine H substrate which is oxidized by luciferase producing light energy which sensitizes the central 625 nm emitting QD acceptor by bioluminescence resonance energy transfer (BRET). The sensitized QD, in turn, acts as a relay and transfers the energy to a first peptide-labeled Alexa Fluor 647 acceptor dye displayed on its surface. This dye then transfers energy to a second red-shifted peptide-labeled dye acceptor on the QD surface through a second concentric Förster resonance energy transfer (FRET) process. Alexa Fluor 700 and Cy5.5 are both tested in the role of this terminal FRET acceptor. Photophysical analysis of spectral profiles from the resulting sequential BRET-FRET-FRET processes allow us to estimate the efficiency of each of the transfer steps. Importantly, the efficiency of each step within this energy transfer cascade can be controlled to

  2. Ultrafast Energy Transfer in Ultrathin Organic Donor/Acceptor Blend

    PubMed Central

    Kandada, Ajay Ram Srimath; Grancini, Giulia; Petrozza, Annamaria; Perissinotto, Stefano; Fazzi, Daniele; Raavi, Sai Santosh Kumar; Lanzani, Guglielmo

    2013-01-01

    It is common knowledge that poly(3-hexylthiophene) (P3HT)/[6,6]-phenyl-C61-butyric acid methyl ester (PCBM) blend, a prototype system for bulk heterojunction (BHJ) solar cells, consists of a network of tens of nanometers-large donor-rich and acceptor-rich phases separated by extended finely intermixed border regions where PCBM diffuse into P3HT. Here we specifically address the photo-induced dynamics in a 10 nm thin P3HT/PCBM blend that consists of the intermixed region only. Using the multi-pass transient absorption technique (TrAMP) that enables us to perform ultra high sensitive measurements, we find that the primary process upon photoexcitation is ultrafast energy transfer from P3HT to PCBM. The expected charge separation due to hole transfer from PCBM to P3HT occurs in the 100 ps timescale. The derived picture is much different from the accepted view of ultra-fast electron transfer at the polymer/PCBM interface and provides new directions for the development of efficient devices. PMID:23797845

  3. Protein Transfer Free Energy Obeys Entropy-Enthalpy Compensation.

    PubMed

    Mills, Eric A; Plotkin, Steven S

    2015-11-01

    We have found significant entropy-enthalpy compensation for the transfer of a diverse set of two-state folding proteins from water into water containing a diverse set of cosolutes, including osmolytes, denaturants, and crowders. In extracting thermodynamic parameters from experimental data, we show the potential importance of accounting for the cosolute concentration-dependence of the heat capacity change upon unfolding, as well as the potential importance of the temperature-dependence of the heat capacity change upon unfolding. We introduce a new Monte Carlo method to estimate the experimental uncertainty in the thermodynamic data and use this to show by bootstrapping methods that entropy-enthalpy compensation is statistically significant, in spite of large, correlated scatter in the data. We show that plotting the data at the transition midpoint provides the most accurate experimental values by avoiding extrapolation errors due to uncertainty in the heat capacity, and that this representation exhibits the strongest evidence of compensation. Entropy-enthalpy compensation is still significant at lab temperature however. We also find that compensation is still significant when considering variations due to heat capacity models, as well as typical measurement discrepancies lab-to-lab when such data is available. Extracting transfer entropy and enthalpy along with their uncertainties can provide a valuable consistency check between experimental data and simulation models, which may involve tests of simulated unfolded ensembles and/or models of the transfer free energy; we include specific applications to cold shock protein and protein L. PMID:26423005

  4. Technology transfer at the Department of Energy (DOE) National Laboratories

    SciTech Connect

    Harrer, B.J.; Good, M.S.; Lemon, D.K.; Morgen, G.P.

    1996-12-31

    Over the past 15 years, efforts to move technology generated from government-funded research and development activities at the Department of Energy (DOE) laboratories into commercial application by the private sector have faced an ever-changing environment. This environment has been primarily dictated by changes in the governing political philosophies of the Congress and the Administration that fund the laboratories and direct their activities. To review the role of the DOE laboratories, the following are discussed: the past, current, and potential future legislative and political environment impacting upon technology transfer from the laboratories; mechanisms of technology transfer; and three selected projects involving transfer of nondestructive evaluation technologies to the private sector. The technologies include computer-aided fabric evaluation (CAFE), measurement of the depth to which steel parts are hardened, and compensation for wear variations in the grinding wheel during the fabrication of wood shaper tools. These respectively deal with a large partnership of companies and institutes, a single but large manufacturing company, and a small business.

  5. Förster resonance energy transfer and kinesin motor proteins.

    PubMed

    Prevo, Bram; Peterman, Erwin J G

    2014-02-21

    Förster Resonance Energy Transfer (FRET) is the phenomenon of non-radiative transfer of electronic excitations from a donor fluorophore to an acceptor, mediated by electronic dipole-dipole coupling. The transfer rate and, as a consequence, efficiency depend non-linearly on the distance between the donor and the acceptor. FRET efficiency can thus be used as an effective and accurate reporter of distance between two fluorophores and changes thereof. Over the last 50 years or so, FRET has been used as a spectroscopic ruler to measure conformations and conformational changes of biomolecules. More recently, FRET has been combined with microscopy, ultimately allowing measurement of FRET between a single donor and a single acceptor pair. In this review, we will explain the physical foundations of FRET and how FRET can be applied to biomolecules. We will highlight the power of the different FRET approaches by focusing on its application to the motor protein kinesin, which undergoes several conformational changes driven by enzymatic action, that ultimately result in unidirectional motion along microtubule filaments, driving active transport in the cell. Single-molecule and ensemble FRET studies of different aspects of kinesin have provided numerous insights into the complex chemomechanical mechanism of this fascinating protein. PMID:24071719

  6. Ultrafast Energy Transfer in Ultrathin Organic Donor/Acceptor Blend

    NASA Astrophysics Data System (ADS)

    Kandada, Ajay Ram Srimath; Grancini, Giulia; Petrozza, Annamaria; Perissinotto, Stefano; Fazzi, Daniele; Raavi, Sai Santosh Kumar; Lanzani, Guglielmo

    2013-06-01

    It is common knowledge that poly(3-hexylthiophene) (P3HT)/[6,6]-phenyl-C61-butyric acid methyl ester (PCBM) blend, a prototype system for bulk heterojunction (BHJ) solar cells, consists of a network of tens of nanometers-large donor-rich and acceptor-rich phases separated by extended finely intermixed border regions where PCBM diffuse into P3HT. Here we specifically address the photo-induced dynamics in a 10 nm thin P3HT/PCBM blend that consists of the intermixed region only. Using the multi-pass transient absorption technique (TrAMP) that enables us to perform ultra high sensitive measurements, we find that the primary process upon photoexcitation is ultrafast energy transfer from P3HT to PCBM. The expected charge separation due to hole transfer from PCBM to P3HT occurs in the 100 ps timescale. The derived picture is much different from the accepted view of ultra-fast electron transfer at the polymer/PCBM interface and provides new directions for the development of efficient devices.

  7. Detection of Medium-Sized Polycyclic Aromatic Hydrocarbons via Fluorescence Energy Transfer

    PubMed Central

    Serio, Nicole; Prignano, Lindsey; Peters, Sean; Levine, Mindy

    2015-01-01

    Reported herein is the use of proximity-induced non-covalent energy transfer for the detection of medium-sized polycyclic aromatic hydrocarbons (PAHs). This energy transfer occurs within the cavity of γ-cyclodextrin in various aqueous environments, including human plasma and coconut water. Highly efficient energy transfer was observed, and the efficiency of the energy transfer is independent of the concentration of γ-cyclodextrin used, demonstrating the importance of hydrophobic binding in facilitating such energy transfer. Low limits of detection were also observed for many of the PAHs investigated, which is promising for the development of fluorescence-based detection schemes. PMID:25821390

  8. Information systems and technology transfer programs on geothermal energy and other renewable sources of energy

    SciTech Connect

    Lippmann, Marcelo J.; Antunez, Emilio u.

    1996-01-24

    In order to remain competitive it is necessary to stay informed and use the most advanced technologies available. Recent developments in communication, like the Internet and the World Wide Web, enormously facilitate worldwide data and technology transfer. A compilation of the most important sources of data on renewable energies, especially geothermal, as well as lists of relevant technology transfer programs are presented. Information on how to gain access to, and learn more about them is also given.

  9. Vibrational coherence and energy transfer in two-dimensional spectra with the optimized mean-trajectory approximation

    SciTech Connect

    Alemi, Mallory; Loring, Roger F.

    2015-06-07

    The optimized mean-trajectory (OMT) approximation is a semiclassical method for computing vibrational response functions from action-quantized classical trajectories connected by discrete transitions that represent radiation-matter interactions. Here, we extend the OMT to include additional vibrational coherence and energy transfer processes. This generalized approximation is applied to a pair of anharmonic chromophores coupled to a bath. The resulting 2D spectra are shown to reflect coherence transfer between normal modes.

  10. Vibrational coherence and energy transfer in two-dimensional spectra with the optimized mean-trajectory approximation

    NASA Astrophysics Data System (ADS)

    Alemi, Mallory; Loring, Roger F.

    2015-06-01

    The optimized mean-trajectory (OMT) approximation is a semiclassical method for computing vibrational response functions from action-quantized classical trajectories connected by discrete transitions that represent radiation-matter interactions. Here, we extend the OMT to include additional vibrational coherence and energy transfer processes. This generalized approximation is applied to a pair of anharmonic chromophores coupled to a bath. The resulting 2D spectra are shown to reflect coherence transfer between normal modes.

  11. Vibrational coherence and energy transfer in two-dimensional spectra with the optimized mean-trajectory approximation

    PubMed Central

    Alemi, Mallory; Loring, Roger F.

    2015-01-01

    The optimized mean-trajectory (OMT) approximation is a semiclassical method for computing vibrational response functions from action-quantized classical trajectories connected by discrete transitions that represent radiation-matter interactions. Here, we extend the OMT to include additional vibrational coherence and energy transfer processes. This generalized approximation is applied to a pair of anharmonic chromophores coupled to a bath. The resulting 2D spectra are shown to reflect coherence transfer between normal modes. PMID:26049437

  12. Photoluminescence and energy transfer process in Gd2O3:Eu3+, Tb3+

    NASA Astrophysics Data System (ADS)

    Selvalakshmi, T.; Bose, A. Chandra

    2016-05-01

    Variation in photoluminescence (PL) properties of Eu3+ and Tb3+ as a function of co-dopant (Tb3+) concentration are studied for Gd2-x-yO3: Eu3+x Tb3+y (x = 0.02, y = 0.01, 0.03, 0.05). The crystal structure analysis is carried out by X-ray Diffraction (XRD). Absence of addition peaks corresponding europium or terbium phase confirms the phase purity. Diffuse reflectance spectroscopy (DRS) reveals the absorption peaks corresponding to host matrix, Eu3+ and Tb3+. The bandgap calculated from Kubelka - Munk function is also reported. PL spectra are recorded at the excitation wavelength of 307 nm and the emission peak corresponding to Eu3+ confirms the energy transfer from Tb3+ to Eu3+. The agglomeration of particles acts as quenching centres for energy transfer at higher concentrations.

  13. Efficient near-field energy transfer and relieved Casimir stiction between sub-wavelength gratings

    NASA Astrophysics Data System (ADS)

    Liu, Xianglei; Zhao, Bo; Zhang, Zhuomin

    2015-03-01

    The promising applications of near-field heat transfer in thermophotovoltaic devices, thermal imaging, thermal rectifiers, and local thermal management have motivated the search for nanostructures capable of supporting higher efficiency or greater heat flux than simple planar substances. In this work, efficient and delocalized radiative heat transfer between two aligned 1D sub-wavelength gratings is demonstrated based on the scattering theory using the rigorous coupled-wave analysis (RCWA). It is shown that the heat flux can be greatly enhanced and the accurate prediction may differ significantly from that of the geometry-based Derjaguin's proximity approximation (PA). The underlying mechanism is attributed to the excitation of hyperbolic modes that increase the energy transmission by supporting propagation of waves with large parallel wavevectors and. Besides efficient energy transport, the performance is robust, insensitive to the relative lateral shift. In addition, the Casimir stiction considering both quantum and thermal fluctuations is found to be relieved compared with bulks.

  14. Estimating three-demensional energy transfer in isotropic turbulence

    NASA Technical Reports Server (NTRS)

    Li, K. S.; Helland, K. N.; Rosenblatt, M.

    1980-01-01

    To obtain an estimate of the spectral transfer function that indicates the rate of decay of energy, an x-wire probe was set at a fixed position, and two single wire probes were set at a number of locations in the same plane perpendicular to the mean flow in the wind tunnel. The locations of the single wire probes are determined by pseudo-random numbers (Monte Carlo). Second order spectra and cross spectra are estimated. The assumption of isotropy relative to second order spectra is examined. Third order spectra are also estimated corresponding to the positions specified. A Monte Carlo Fourier transformation of the downstream bispectra corresponding to integration across the plane perpendicular to the flow is carried out assuming isotropy. Further integration is carried out over spherical energy shells.

  15. Luminescence and energy transfer in the columbite structure

    SciTech Connect

    Blasse, G.; van Leur, M.G.J.

    1985-09-01

    The luminescence properties of undoped and Eu/sup 3 +/- and Dy/sup 3 +/doped CdNb/sub 2/O/sub 6/ and CaNb/sub 2/O/sub 6/ are reported and discussed in connection with the luminescence of niobates and tungstates with wolframite and columbite structure. It is shown that these structures lead in principle to highly efficient luminescent materials. However, disorder between the metal ions reduces the efficiency considerably. In CdNb/sub 2/O/sub 6/ the niobate excitation energy is more mobile than in CaNb/sub 2/O/sub 6/. This has important consequences for the rare-earth activated materials. At 300 K the amount of rare-earth emission from the CdNb/sub 2/O/sub 6/-based samples is high. This is due to energy migration in the host lattice and efficient transfer to the activator (R /SUB c/ approx. = 7A).

  16. Crossed-beam energy transfer in direct-drive implosions

    SciTech Connect

    Seka, W; Edgell, D H; Michel, D T; Froula, D H; Goncharov, V N; Craxton, R S; Divol, L; Epstein, R; Follett, R; Kelly, J H; Kosc, T Z; Maximov, A V; McCrory, R L; Meyerhofer, D D; Michel, P; Myatt, J F; Sangster, T C; Shvydky, A; Skupsky, S; Stoeckl, C

    2012-05-22

    Direct-drive-implosion experiments on the OMEGA laser [T. R. Boehly et al., Opt. Commun. 133, 495 (1997)] have showed discrepancies between simulations of the scattered (non-absorbed) light levels and measured ones that indicate the presence of a mechanism that reduces laser coupling efficiency by 10%-20%. This appears to be due to crossed-beam energy transfer (CBET) that involves electromagnetic-seeded, low-gain stimulated Brillouin scattering. CBET scatters energy from the central portion of the incoming light beam to outgoing light, reducing the laser absorption and hydrodynamic efficiency of implosions. One-dimensional hydrodynamic simulations including CBET show good agreement with all observables in implosion experiments on OMEGA. Three strategies to mitigate CBET and improve laser coupling are considered: the use of narrow beams, multicolor lasers, and higher-Z ablators. Experiments on OMEGA using narrow beams have demonstrated improvements in implosion performance.

  17. Energy transfer in real and artificial photosynthetic systems

    SciTech Connect

    Hunt, J.E.; Katz, J.J.; Hindman, J.C.

    1984-01-01

    A comparative study of the fluorescence emitted by three photosynthetic organisms (chlorella, tribonema, and anacystis) and the fluorescence of some model systems selected for study by criteria described below are reported. Light emission has been studied as a function of excitation wavelength and of temperature. Low temperature fluorescence studies on photosynthetic organisms and chloroplast preparations provide the chief experimental support for the existence of a PSII in green plants, and fluorescence at low temperatures has been used as the principal source of information on energy flow between the photosynthetic pigments. The nature and functional aspects of PSII and the course of energy transfer in the photosynthetic apparatus are highly pertinent to the oxygen evolution in green plant photosynthesis.

  18. Enhanced luminescence excitation via efficient optical energy transfer (Presentation Recording)

    NASA Astrophysics Data System (ADS)

    Aad, Roy; Nomenyo, Komla D.; Bercu, Bogdan; Couteau, Christophe; Sallet, Vincent; Rogers, David J.; Molinari, Michael; Lérondel, Gilles

    2015-10-01

    Luminescent nanoscale materials (LNMs) have received widespread interest in sensing and lighting applications due to their enhanced emissive properties. For sensing applications, LNMs offer improved sensitivity and fast response time which allow for lower limits of detection. Meanwhile, for lighting applications, LNMs, such as quantum dots, offer an improved internal quantum efficiency and controlled color rendering which allow for better lighting performances. Nevertheless, due to their nanometric dimensions, nanoscale materials suffer from extremely weak luminescence excitation (i.e. optical absorption) limiting their luminescence intensity, which in turn results in a downgrade in the limits of detection and external quantum efficiencies. Therefore, enhancing the luminescence excitation is a major issue for sensing and lighting applications. In this work, we report on a novel photonic approach to increase the luminescence excitation of nanoscale materials. Efficient luminescence excitation increase is achieved via a gain-assisted waveguided energy transfer (G-WET). The G-WET concept consists on placing nanoscale materials atop of a waveguiding active (i.e. luminescent) layer with optical gain. Efficient energy transfer is thus achieved by exciting the nanoscale material via the tail of the waveguided mode of the active layer emission. The G-WET concept is demonstrated on both a nanothin layer of fluorescent sensitive polymer and on CdSe/ZnS quantum dots coated on ZnO thin film, experimentally proving up to an 8-fold increase in the fluorescence of the polymer and a 3-fold increase in the luminescence of the CdSe/ZnS depending of the active layer emission regime (stimulated vs spontaneous emission). Furthermore, we will discuss on the extended G-WET concept which consists on coating nanoscale materials on a nanostructured active layer. The nanostructured active layer offers the necessary photonic modulation and a high specific surface which can presumably lead to

  19. Near-field effects and energy transfer in hybrid metal-oxide nanostructures

    PubMed Central

    Kuerbanjiang, Balati; Benel, Cahit; Papageorgiou, Giorgos; Goncalves, Manuel; Boneberg, Johannes; Leiderer, Paul; Ziemann, Paul; Marek, Peter; Hahn, Horst

    2013-01-01

    Summary One of the big challenges of the 21st century is the utilization of nanotechnology for energy technology. Nanoscale structures may provide novel functionality, which has been demonstrated most convincingly by successful applications such as dye-sensitized solar cells introduced by M. Grätzel. Applications in energy technology are based on the transfer and conversion of energy. Following the example of photosynthesis, this requires a combination of light harvesting, transfer of energy to a reaction center, and conversion to other forms of energy by charge separation and transfer. This may be achieved by utilizing hybrid nanostructures, which combine metallic and nonmetallic components. Metallic nanostructures can interact strongly with light. Plasmonic excitations of such structures can cause local enhancement of the electrical field, which has been utilized in spectroscopy for many years. On the other hand, the excited states in metallic structures decay over very short lifetimes. Longer lifetimes of excited states occur in nonmetallic nanostructures, which makes them attractive for further energy transfer before recombination or relaxation sets in. Therefore, the combination of metallic nanostructures with nonmetallic materials is of great interest. We report investigations of hybrid nanostructured model systems that consist of a combination of metallic nanoantennas (fabricated by nanosphere lithography, NSL) and oxide nanoparticles. The oxide particles were doped with rare-earth (RE) ions, which show a large shift between absorption and emission wavelengths, allowing us to investigate the energy-transfer processes in detail. The main focus is on TiO2 nanoparticles doped with Eu3+, since the material is interesting for applications such as the generation of hydrogen by photocatalytic splitting of water molecules. We use high-resolution techniques such as confocal fluorescence microscopy for the investigation of energy-transfer processes. The experiments

  20. Near-field effects and energy transfer in hybrid metal-oxide nanostructures.

    PubMed

    Herr, Ulrich; Kuerbanjiang, Balati; Benel, Cahit; Papageorgiou, Giorgos; Goncalves, Manuel; Boneberg, Johannes; Leiderer, Paul; Ziemann, Paul; Marek, Peter; Hahn, Horst

    2013-01-01

    One of the big challenges of the 21st century is the utilization of nanotechnology for energy technology. Nanoscale structures may provide novel functionality, which has been demonstrated most convincingly by successful applications such as dye-sensitized solar cells introduced by M. Grätzel. Applications in energy technology are based on the transfer and conversion of energy. Following the example of photosynthesis, this requires a combination of light harvesting, transfer of energy to a reaction center, and conversion to other forms of energy by charge separation and transfer. This may be achieved by utilizing hybrid nanostructures, which combine metallic and nonmetallic components. Metallic nanostructures can interact strongly with light. Plasmonic excitations of such structures can cause local enhancement of the electrical field, which has been utilized in spectroscopy for many years. On the other hand, the excited states in metallic structures decay over very short lifetimes. Longer lifetimes of excited states occur in nonmetallic nanostructures, which makes them attractive for further energy transfer before recombination or relaxation sets in. Therefore, the combination of metallic nanostructures with nonmetallic materials is of great interest. We report investigations of hybrid nanostructured model systems that consist of a combination of metallic nanoantennas (fabricated by nanosphere lithography, NSL) and oxide nanoparticles. The oxide particles were doped with rare-earth (RE) ions, which show a large shift between absorption and emission wavelengths, allowing us to investigate the energy-transfer processes in detail. The main focus is on TiO2 nanoparticles doped with Eu(3+), since the material is interesting for applications such as the generation of hydrogen by photocatalytic splitting of water molecules. We use high-resolution techniques such as confocal fluorescence microscopy for the investigation of energy-transfer processes. The experiments are

  1. Transfer of energy between a pair of molecules near a plasmonic core-shell nanoparticle: Tunability and sensing

    NASA Astrophysics Data System (ADS)

    Daneshfar, Nader; Yavari, Asghar

    2016-05-01

    Our model is applied to the calculation of interaction energy between a pair of dipolar molecules (point dipoles) in the vicinity of a nanoshell monomer with core-shell structure, based on the dipole quasi-electrostatic theory of classical electrodynamics and using the Drude and Maxwell-Garnett model. In other words, this work discusses the intermolecular energy transfer from a donor molecule to an acceptor molecule near a spherical nanoparticle that is important for practical applications like sensing. It is shown that the proximity of plasmonic nanoparticles can have a strong effect on the energy transfer between molecules. In addition to the influence of the size, composition, embedding medium, and the filling fraction of doped particles on the interaction energy, the contribution of the dipolar, quadrupolar, octupolar, hexadecapolar, triakontadipolar, and higher order multipole interactions is presented and analyzed. Briefly, we will show that it is possible to achieve enhanced energy transfer by manipulation of different parameters as mentioned above.

  2. Elementary Energy Transfer Pathways in Allochromatium vinosum Photosynthetic Membranes.

    PubMed

    Lüer, Larry; Carey, Anne-Marie; Henry, Sarah; Maiuri, Margherita; Hacking, Kirsty; Polli, Dario; Cerullo, Giulio; Cogdell, Richard J

    2015-11-01

    Allochromatium vinosum (formerly Chromatium vinosum) purple bacteria are known to adapt their light-harvesting strategy during growth according to environmental factors such as temperature and average light intensity. Under low light illumination or low ambient temperature conditions, most of the LH2 complexes in the photosynthetic membranes form a B820 exciton with reduced spectral overlap with LH1. To elucidate the reason for this light and temperature adaptation of the LH2 electronic structure, we performed broadband femtosecond transient absorption spectroscopy as a function of excitation wavelength in A. vinosum membranes. A target analysis of the acquired data yielded individual rate constants for all relevant elementary energy transfer (ET) processes. We found that the ET dynamics in high-light-grown membranes was well described by a homogeneous model, with forward and backward rate constants independent of the pump wavelength. Thus, the overall B800→B850→B890→ Reaction Center ET cascade is well described by simple triexponential kinetics. In the low-light-grown membranes, we found that the elementary backward transfer rate constant from B890 to B820 was strongly reduced compared with the corresponding constant from B890 to B850 in high-light-grown samples. The ET dynamics of low-light-grown membranes was strongly dependent on the pump wavelength, clearly showing that the excitation memory is not lost throughout the exciton lifetime. The observed pump energy dependence of the forward and backward ET rate constants suggests exciton diffusion via B850→ B850 transfer steps, making the overall ET dynamics nonexponential. Our results show that disorder plays a crucial role in our understanding of low-light adaptation in A. vinosum. PMID:26536265

  3. Nonphotochemical Hole-Burning Studies of Energy Transfer Dynamics in Antenna Complexes of Photosynthetic Bacteria

    SciTech Connect

    Satoshi Matsuzaki

    2002-06-27

    This thesis contains the candidate's original work on excitonic structure and energy transfer dynamics of two bacterial antenna complexes as studied using spectral hole-burning spectroscopy. The general introduction is divided into two chapters (1 and 2). Chapter 1 provides background material on photosynthesis and bacterial antenna complexes with emphasis on the two bacterial antenna systems related to the thesis research. Chapter 2 reviews the underlying principles and mechanism of persistent nonphotochemical hole-burning (NPHB) spectroscopy. Relevant energy transfer theories are also discussed. Chapters 3 and 4 are papers by the candidate that have been published. Chapter 3 describes the application of NPHB spectroscopy to the Fenna-Matthews-Olson (FMO) complex from the green sulfur bacterium Prosthecochloris aestuarii; emphasis is on determination of the low energy vibrational structure that is important for understanding the energy transfer process associated within three lowest energy Q{sub y}-states of the complex. The results are compared with those obtained earlier on the FMO complex from Chlorobium tepidum. In Chapter 4, the energy transfer dynamics of the B800 molecules of intact LH2 and B800-deficient LH2 complexes of the purple bacterium Rhodopseudomonas acidophila are compared. New insights on the additional decay channel of the B800 ring of bacteriochlorophyll{sub a} (BChl{sub a}) molecules are provided. General conclusions are given in Chapter 5. A version of the hole spectrum simulation program written by the candidate for the FMO complex study (Chapter 3) is included as an appendix. The references for each chapter are given at the end of each chapter.

  4. Energy transfer in systems with random forcing and nonlinear dissipation

    NASA Astrophysics Data System (ADS)

    Pignol, Ricardo Jorge

    The purpose of this thesis is to study energy transfer in nonlinear systems. In the first part, I focus on a model of two nonlinearly coupled (complex) oscillators subject to stochastic forcing and nonlinear dissipation. This model arises from isolating an individual resonant quartet in a general dispersive system, and reducing it further by exploiting some of the system's symmetries. It turns out that the reduced model exhibits a rich and complex behavior encountered in far larger systems, with two qualitatively distinct regimes arising as one varies the system's single non-dimensional parameter: one that can be characterized as a perturbation of thermal equilibrium, and another highly constrained state, with phase and amplitude locking , and singular invariant measures. The relative simplicity of the reduced model allows a thorough numerical and theoretical treatment (including a closed expression for the system's invariant measures) that furnishes valuable insight on the energy transfer process in systems with much higher dimensionality. In the second part, the damped oscillator is replaced by an individual mode of the inviscid Burgers equation. Here, the dissipation occurs through shocks. Despite the complexity resulting from the inclusion of a nonlinear partial differential equation, I show that much of this system's behavior can be inferred precisely from a reduction to one of the cases studied in the first part.

  5. Molecular distances determined with resonant vibrational energy transfers.

    PubMed

    Chen, Hailong; Wen, Xiewen; Li, Jiebo; Zheng, Junrong

    2014-04-01

    In general, intermolecular distances in condensed phases at the angstrom scale are difficult to measure. We were able to do so by using the vibrational energy transfer method, an ultrafast vibrational analogue of Förster resonance energy transfer. The distances among SCN(-) anions in KSCN crystals and ion clusters of KSCN aqueous solutions were determined with the method. In the crystalline samples, the closest anion distance was determined to be 3.9 ± 0.3 Å, consistent with the XRD result. In the 1.8 and 1 M KSCN aqueous solutions, the anion distances in the ion clusters were determined to be 4.4 ± 0.4 Å. The clustered anion distances in aqueous solutions are very similar to the closest anion distance in the KSCN crystal but significantly shorter than the average anion distance (0.94-1.17 nm) in the aqueous solutions if ion clustering did not occur. The result suggests that ions in the strong electrolyte aqueous solutions can form clusters inside of which they have direct contact with each other. PMID:24641170

  6. Photoinduced energy transfer in transition metal complex oligomers

    SciTech Connect

    1997-06-01

    The work done over the past three years has been directed toward the preparation, characterization and photophysical examination of mono- and bimetallic diimine complexes. The work is part of a broader project directed toward the development of stable, efficient, light harvesting arrays of transition metal complex chromophores. One focus has been the synthesis of rigid bis-bidentate and bis-tridentate bridging ligands. The authors have managed to make the ligand bphb in multigram quantities from inexpensive starting materials. The synthetic approach used has allowed them to prepare a variety of other ligands which may have unique applications (vide infra). They have prepared, characterized and examined the photophysical behavior of Ru(II) and Re(I) complexes of the ligands. Energy donor/acceptor complexes of bphb have been prepared which exhibit nearly activationless energy transfer. Complexes of Ru(II) and Re(I) have also been prepared with other polyunsaturated ligands in which two different long lived (> 50 ns) excited states exist; results of luminescence and transient absorbance measurements suggest the two states are metal-to-ligand charge transfer and ligand localized {pi}{r_arrow}{pi}* triplets. Finally, the authors have developed methods to prepare polymetallic complexes which are covalently bound to various surfaces. The long term objective of this work is to make light harvesting arrays for the sensitization of large band gap semiconductors. Details of this work are provided in the body of the report.

  7. Photoinduced energy transfer in transition metal complex oligomers

    SciTech Connect

    1997-04-01

    The work we have done over the past three years has been directed toward the preparation, characterization and photophysical examination of mono- and bimetallic diimine complexes. The work is part of a broader project directed toward the development of stable, efficient, light harvesting arrays of transition metal complex chromophores. One focus has been the synthesis of rigid bis-bidentate and bis-tridentate bridging ligands. We have managed to make the ligand bphb in multigram quantities from inexpensive starting materials. The synthetic approach used has allowed us prepare a variety of other ligands which may have unique applications (vide infra). We have prepared, characterized and examined the photophysical behavior of Ru(II) and Re(I) complexes of the ligands. Energy donor/acceptor complexes of bphb have been prepared which exhibit nearly activationless energy transfer. Complexes of Ru(II) and Re(I) have also been prepared with other polyunsaturated ligands in which two different long lived ( > 50 ns) excited states exist; results of luminescence and transient absorbance measurements suggest the two states are metal-to-ligand charge transfer and ligand localized {pi}{r_arrow}{pi}* triplets. Finally, we have developed methods to prepare polymetallic complexes which are covalently bound to various surfaces. The long term objective of this work is to make light harvesting arrays for the sensitization of large band gap semiconductors. Details of this work are provided in the body of the report.

  8. Miniature fiber optic sensor based on fluorescence energy transfer

    NASA Astrophysics Data System (ADS)

    Meadows, David L.; Schultz, Jerome S.

    1992-04-01

    Optical fiber biosensors based on fluorescence assays have several distinct advantages when measuring biological analytes such as metabolites, cofactors, toxins, etc. Not only are optical signals immune to electronic interferences, but the polychromatic nature of most fluorochemical assays provides more potentially useful data about the system being studied. One of the most common difficulties normally encountered with optical biosensors is the inability to routinely recalibrate the optical and electronic components of the system throughout the life of the sensor. With this in mind, we present an optical fiber assay system for glucose based on a homogeneous singlet/singlet energy transfer assay along with the electronic instrumentation built to support the sensor system. In the sensor probe, glucose concentrations are indirectly measured from the level of fluorescence quenching caused by the homogeneous competition assay between TRITC labeled concanavalin A (receptor) and FITC labeled Dextran (ligand). The FITC signal is used to indicate glucose concentrations and the TRITC signal is used for internal calibration. Data is also presented on a protein derivatization procedure that was used to prevent aggregation of the receptor protein in solution. Also, a molecular model is described for the singlet/singlet energy transfer interactions that can occur in a model system composed of a monovalent ligand (FITC labeled papain) and a monovalent receptor (TRITC labeled concanavalin A).

  9. Ultrafast Single and Multiexciton Energy Transfer in Semiconductor Nanoplatelets

    NASA Astrophysics Data System (ADS)

    Schaller, Richard

    Photophysical processes such as fluorescence resonance energy transfer (FRET) enable optical antennas, wavelength down-conversion in light-emitting diodes (LEDs), and optical bio-sensing schemes. The rate and efficiency of this donor to acceptor transfer of excitation between chromophores dictates the utility of FRET and can unlock new device operation motifs including quantum-funnel solar cells and reduced gain thresholds. However, the fastest reported FRET time constants involving spherical quantum dots (QDs) (0.12-1 ns), do not outpace biexciton Auger recombination (0.01-0.1 ns), which impedes multiexciton-driven applications including electrically-pumped lasers and carrier-multiplication-enhanced photovoltaics. Precisely controlled, few-monolayer thick semiconductor nano-platelets with tens-of-nanometer diameters exhibit intense optical transitions and hundreds-of-picosecond Auger recombination, but heretofore lack FRET characterizations. We examine binary CdSe NPL solids and show that inter-plate FRET (~6-23 ps, presumably for co-facial arrangements) can occur 15-50 times faster than Auger recombination and demonstrate multiexcitonic FRET, making such materials ideal candidates for advanced technologies. This work was performed at the Center for Nanoscale Materials, a U.S. Department of Energy Office of Science User Facility under Contract No. DE-AC02-06CH11357.

  10. Fluorescence resonance energy transfer imaging by maximum likelihood estimation

    NASA Astrophysics Data System (ADS)

    Zhang, Yupeng; Yuan, Yumin; Holmes, Timothy J.

    2004-06-01

    Fluorescence resonance energy transfer (FRET) is a fluorescence microscope imaging process involving nonradiative energy transfer between two fluorophores (the donor and the acceptor). FRET is used to detect the chemical interactions and, in some cases, measure the distance between molecules. Existing approaches do not always well compensate for bleed-through in excitation, cross-talk in emission detection and electronic noise in image acquisition. We have developed a system to automatically search for maximum-likelihood estimates of the FRET image, donor concentration and acceptor concentration. It also produces other system parameters, such as excitation/emission filter efficiency and FRET conversion factor. The mathematical model is based upon a Poisson process since the CCD camera is a photon-counting device. The main advantage of the approach is that it automatically compensates for bleed-through and cross-talk degradations. Tests are presented with synthetic images and with real data referred to as positive and negative controls, where FRET is known to occur and to not occur, respectively. The test results verify the claimed advantages by showing consistent accuracy in detecting FRET and by showing improved accuracy in calculating FRET efficiency.

  11. Picosecond energy transfer and multiexciton transfer outpaces Auger recombination in binary CdSe nanoplatelet solids

    NASA Astrophysics Data System (ADS)

    Rowland, Clare E.; Fedin, Igor; Zhang, Hui; Gray, Stephen K.; Govorov, Alexander O.; Talapin, Dmitri V.; Schaller, Richard D.

    2015-05-01

    Fluorescence resonance energy transfer (FRET) enables photosynthetic light harvesting, wavelength downconversion in light-emitting diodes (LEDs), and optical biosensing schemes. The rate and efficiency of this donor to acceptor transfer of excitation between chromophores dictates the utility of FRET and can unlock new device operation motifs including quantum-funnel solar cells, non-contact chromophore pumping from a proximal LED, and markedly reduced gain thresholds. However, the fastest reported FRET time constants involving spherical quantum dots (0.12-1 ns; refs , , ) do not outpace biexciton Auger recombination (0.01-0.1 ns; ref. ), which impedes multiexciton-driven applications including electrically pumped lasers and carrier-multiplication-enhanced photovoltaics. Few-monolayer-thick semiconductor nanoplatelets (NPLs) with tens-of-nanometre lateral dimensions exhibit intense optical transitions and hundreds-of-picosecond Auger recombination, but heretofore lack FRET characterizations. We examine binary CdSe NPL solids and show that interplate FRET (˜6-23 ps, presumably for co-facial arrangements) can occur 15-50 times faster than Auger recombination and demonstrate multiexcitonic FRET, making such materials ideal candidates for advanced technologies.

  12. Structural and orientation effects on electronic energy transfer between silicon quantum dots with dopants and with silver adsorbates

    SciTech Connect

    Vinson, N.; Freitag, H.; Micha, D. A.

    2014-06-28

    Starting from the atomic structure of silicon quantum dots (QDs), and utilizing ab initio electronic structure calculations within the Förster resonance energy transfer (FRET) treatment, a model has been developed to characterize electronic excitation energy transfer between QDs. Electronic energy transfer rates, K{sub EET}, between selected identical pairs of crystalline silicon quantum dots systems, either bare, doped with Al or P, or adsorbed with Ag and Ag{sub 3}, have been calculated and analyzed to extend previous work on light absorption by QDs. The effects of their size and relative orientation on energy transfer rates for each system have also been considered. Using time-dependent density functional theory and the hybrid functional HSE06, the FRET treatment was employed to model electronic energy transfer rates within the dipole-dipole interaction approximation. Calculations with adsorbed Ag show that: (a) addition of Ag increases rates up to 100 times, (b) addition of Ag{sub 3} increases rates up to 1000 times, (c) collinear alignment of permanent dipoles increases transfer rates by an order of magnitude compared to parallel orientation, and (d) smaller QD-size increases transfer due to greater electronic orbitals overlap. Calculations with dopants show that: (a) p-type and n-type dopants enhance energy transfer up to two orders of magnitude, (b) surface-doping with P and center-doping with Al show the greatest rates, and (c) K{sub EET} is largest for collinear permanent dipoles when the dopant is on the outer surface and for parallel permanent dipoles when the dopant is inside the QD.

  13. Additions to compact heat exchanger technology: Jet impingement cooling & flow & heat transfer in metal foam-fins

    NASA Astrophysics Data System (ADS)

    Onstad, Andrew J.

    Compact heat exchangers have been designed following the same basic methodology for over fifty years. However, with the present emphasis on energy efficiency and light weight of prime movers there is increasing demand for completely new heat exchangers. Moreover, new materials and mesoscale fabrication technologies offer the possibility of significantly improving heat exchanger performance over conventional designs. This work involves fundamental flow and heat transfer experimentation to explore two new heat exchange systems: in Part I, large arrays of impinging jets with local extraction and in Part II, metal foams used as fins. Jet impingement cooling is widely used in applications ranging from paper manufacturing to the cooling of gas turbine blades because of the very high local heat transfer coefficients that are possible. While the use of single jet impingement results in non-uniform cooling, increased and more uniform mean heat transfer coefficients may be attained by dividing the total cooling flow among an array of smaller jets. Unfortunately, when the spent fluid from the array's central jets interact with the outer jets, the overall mean heat transfer coefficient is reduced. This problem can be alleviated by locally extracting the spent fluid before it is able to interact with the surrounding jets. An experimental investigation was carried out on a compact impingement array (Xn/Djet = 2.34) utilizing local extraction of the spent fluid (Aspent/Ajet = 2.23) from the jet exit plane. Spatially resolved measurements of the mean velocity field within the array were carried out at jet Reynolds numbers of 2300 and 5300 by magnetic resonance velocimetry, MRV. The geometry provided for a smooth transition from the jet to the target surface and out through the extraction holes without obvious flow recirculation. Mean Nusselt number measurements were also carried out for a Reynolds number range of 2000 to 10,000. The Nusselt number was found to increase with the

  14. 78 FR 13661 - Energy Transfer Fuel, LP; Notice of Petition for Rate Approval

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-02-28

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF ENERGY Federal Energy Regulatory Commission Energy Transfer Fuel, LP; Notice of Petition for Rate Approval Take notice that on February 15, 2013, Energy Transfer Fuel, LP filed for approval of rates for...

  15. Ultrafast exciton energy transfer between nanoscale coaxial cylinders: intertube transfer and luminescence quenching in double-walled carbon nanotubes.

    PubMed

    Koyama, Takeshi; Asada, Yuki; Hikosaka, Naoki; Miyata, Yasumitsu; Shinohara, Hisanori; Nakamura, Arao

    2011-07-26

    We study exciton energy transfer in double-walled carbon nanotubes using femtosecond time-resolved luminescence measurements. From direct correspondence between decay of the innertube luminescence and the rise behavior in outertube luminescence, it is found that the time constant of exciton energy transfer from the inner to the outer semiconducting tubes is ∼150 fs. This ultrafast transfer indicates that the relative intensity of steady-state luminescence from the innertubes is ∼700 times weaker than that from single-walled carbon nanotubes. PMID:21682277

  16. Size-Independent Energy Transfer in Biomimetic Nanoring Complexes.

    PubMed

    Parkinson, Patrick; Kamonsutthipaijit, Nuntaporn; Anderson, Harry L; Herz, Laura M

    2016-06-28

    Supramolecular antenna-ring complexes are of great interest due to their presence in natural light-harvesting complexes. While such systems are known to provide benefits through robust and efficient energy funneling, the relationship between molecular structure, strain (governed by nuclear coordinates and motion), and energy dynamics (arising from electronic behavior) is highly complex. We present a synthetic antenna-nanoring system based on a series of conjugated porphyrin chromophores ideally suited to explore such effects. By systematically varying the size of the acceptor nanoring, we reveal the interplay between antenna-nanoring binding, local strain, and energy dynamics on the picosecond time scale. Binding of the antenna unit creates a local strain in the nanoring, and this strain was measured as a function of the size of the nanoring, by UV-vis-NIR titration, providing information on the conformational flexibility of the system. Strikingly, the energy-transfer rate is independent of nanoring size, indicating the existence of strain-localized acceptor states, spread over about six porphyrin units, arising from the noncovalent antenna-nanoring association. PMID:27176553

  17. Size-Independent Energy Transfer in Biomimetic Nanoring Complexes

    PubMed Central

    2016-01-01

    Supramolecular antenna-ring complexes are of great interest due to their presence in natural light-harvesting complexes. While such systems are known to provide benefits through robust and efficient energy funneling, the relationship between molecular structure, strain (governed by nuclear coordinates and motion), and energy dynamics (arising from electronic behavior) is highly complex. We present a synthetic antenna-nanoring system based on a series of conjugated porphyrin chromophores ideally suited to explore such effects. By systematically varying the size of the acceptor nanoring, we reveal the interplay between antenna-nanoring binding, local strain, and energy dynamics on the picosecond time scale. Binding of the antenna unit creates a local strain in the nanoring, and this strain was measured as a function of the size of the nanoring, by UV–vis-NIR titration, providing information on the conformational flexibility of the system. Strikingly, the energy-transfer rate is independent of nanoring size, indicating the existence of strain-localized acceptor states, spread over about six porphyrin units, arising from the noncovalent antenna-nanoring association. PMID:27176553

  18. Surface-imprinted magnetic particles for highly selective sulfonamides recognition prepared by reversible addition fragmentation chain transfer polymerization.

    PubMed

    Xie, Xiaoyu; Liu, Xia; Pan, Xiaoyan; Chen, Liang; Wang, Sicen

    2016-01-01

    In this work, novel magnetic molecularly imprinted polymers (MMIPs) were prepared by reversible addition fragmentation chain transfer (RAFT) polymerization using sulfamerazine as the template. With the controlled/living property of RAFT polymerization, the resulting MMIPs showed high selectivity for sulfonamides recognition. The MMIPs were characterized by transmission electron microscopy, Fourier transform infrared, vibrating sample magnetometer, X-ray diffraction, X-ray photoelectron spectroscopy, and thermogravimetric analysis. The static and selectivity binding experiments demonstrated the desirable adsorption capacity and high selectivity of the MMIPs. The developed MMIPs were used as the solid-phase extraction sorbents to selectively extract four sulfonamides from aqueous solution. The recoveries of the spiked pond water ranged from 61.2 to 94.1% with RSD lower than 6.5%. This work demonstrated a versatile approach for the preparation of well-constructed MMIPs for application in the field of solid-phase extraction. PMID:26637219

  19. Study on the performance of polycarboxylate-based superplasticizers synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization

    NASA Astrophysics Data System (ADS)

    Yu, Binbin; Zeng, Zhong; Ren, Qinyu; Chen, Yang; Liang, Mei; Zou, Huawei

    2016-09-01

    A series of block type polycarboxylate-based superplasticizers (PCs) with different molecular architectures were synthesized with macromonomer butenyl alkylene polyoxyethylene-polyoxypropylene ether (BAPP) and acrylic acid (AA) by reversible addition-fragmentation chain transfer (RAFT) polymerization. Fourier-Transformed Infrared (FTIR) Spectroscopy and dynamic light scattering (DLS) were applied to investigate the PCs' molecular structure. The dispersion capacity of the PCs in cement were also measured, and the results showed that the polycarboxylic dispersing agents prepared by this method were suitable for portlant cement. It was found that the PCs could affect the hydration process, which was performed through retarding the generation of ettringite in the hydrated product. Our studies with X-ray diffraction (XRD), scanning electron microscopy (SEM) and compressive strength measurement of hydrated production were all supporting this conclusion.

  20. Addition of gut active carbohydrates to colostrum replacer does not improve passive transfer of immunoglobulin G in Holstein dairy calves.

    PubMed

    Villettaz Robichaud, M; Godden, S M; Haines, D M; Haley, D B; Pearl, D L

    2014-09-01

    The primary objective of this study was to investigate the effects of supplementing a commercial colostrum replacer (CR) with gut active carbohydrates (GAC) on passive transfer of IgG in commercial dairy calves. A secondary objective was to evaluate the effect of treatment on preweaning health and growth. A total of 240 newborn Holstein dairy calves on a commercial dairy farm were enrolled in this study. Newborn heifer and bull calves were weighed and then randomly assigned to either the treated group [GAC: 30g of GAC mixed into 1.5 doses (150g of IgG) of commercial colostrum replacer; n=119] or the control group [CON: 1.5 doses (150g of IgG) of CR; n=121]. The assigned CR treatment was fed within 3.5h of birth using an esophageal tube feeder. Venous blood samples were collected at 0 and 24h of age and used to measure serum IgG (mg/mL) and serum total protein (g/dL) concentrations and to estimate the apparent efficiency of absorption of IgG (%). The 129 heifers calves enrolled (CON=60; GAC=69) were also followed until weaning to assess the effect of GAC addition on preweaning health and growth. Multivariable linear regression showed that the addition of GAC to CR did not influence passive transfer of IgG, as measured by apparent efficiency of absorption at 24h of age (CON=54.0 vs. GAC=54.3%), serum IgG (CON=20.3 vs. GAC=20.2mg/mL), and serum total protein (CON=5.69 vs. GAC=5.68g/dL). Although study sample sizes were not originally derived to evaluate health outcomes, treatment had no effect on weight gain or incidence of health events (diarrhea, pneumonia, mortality) for heifer calves between birth and 7 wk of age. PMID:25022688

  1. Optimum rocket propulsion for energy-limited transfer

    NASA Technical Reports Server (NTRS)

    Zuppero, Anthony; Landis, Geoffrey A.

    1991-01-01

    In order to effect large-scale return of extraterrestrial resources to Earth orbit, it is desirable to optimize the propulsion system to maximize the mass of payload returned per unit energy expended. This optimization problem is different from the conventional rocket propulsion optimization. A rocket propulsion system consists of an energy source plus reaction mass. In a conventional chemical rocket, the energy source and the reaction mass are the same. For the transportation system required, however, the best system performance is achieved if the reaction mass used is from a locally available source. In general, the energy source and the reaction mass will be separate. One such rocket system is the nuclear thermal rocket, in which the energy source is a reactor and the reaction mass a fluid which is heated by the reactor and exhausted. Another energy-limited rocket system is the hydrogen/oxygen rocket where H2/O2 fuel is produced by electrolysis of water using a solar array or a nuclear reactor. The problem is to choose the optimum specific impulse (or equivalently exhaust velocity) to minimize the amount of energy required to produce a given mission delta-v in the payload. The somewhat surprising result is that the optimum specific impulse is not the maximum possible value, but is proportional to the mission delta-v. In general terms, at the beginning of the mission it is optimum to use a very low specific impulse and expend a lot of reaction mass, since this is the most energy efficient way to transfer momentum. However, as the mission progresses, it becomes important to minimize the amount of reaction mass expelled, since energy is wasted moving the reaction mass. Thus, the optimum specific impulse will increase with the mission delta-v. Optimum I(sub sp) is derived for maximum payload return per energy expended for both the case of fixed and variable I(sub sp) engines. Sample missions analyzed include return of water payloads from the moons of Mars and of

  2. Modeling and assessing the influence of linear energy transfer on multiple bit upset susceptibility

    NASA Astrophysics Data System (ADS)

    Geng, Chao; Liu, Jie; Xi, Kai; Zhang, Zhan-Gang; Gu, Song; Liu, Tian-Qi

    2013-10-01

    The influence of the metric of linear energy transfer (LET) on single event upset (SEU), particularly multiple bit upset (MBU) in a hypothetical 90-nm static random access memory (SRAM) is explored. To explain the odd point of higher LET incident ion but induced lower cross section in the curve of SEU cross section, MBUs induced by incident ions 132Xe and 209Bi with the same LET but different energies at oblique incidence are investigated using multi-functional package for single event effect analysis (MUFPSA). In addition, a comprehensive analytical model of the radial track structure is incorporated into MUFPSA, which is a complementation for assessing and interpreting MBU susceptibility of SRAM. The results show that (i) with the increase of incident angle, MBU multiplicity and probability each present an increasing trend; (ii) due to the higher ion relative velocity and longer range of δ electrons, higher energy ions trigger the MBU with less probability than lower energy ions.

  3. Enhancing the dynamic range of targeted energy transfer in acoustics using several nonlinear membrane absorbers

    NASA Astrophysics Data System (ADS)

    Bellet, R.; Cochelin, B.; Côte, R.; Mattei, P.-O.

    2012-12-01

    In order to enhance the robustness and the energy range of efficiency of targeted energy transfer (TET) phenomena in acoustics, we discuss in this paper about the use of multiple nonlinear membrane absorbers (called nonlinear energy sinks or NES) placed in parallel. We show this way, mainly thanks to an experimental set-up with two membranes, that the different absorbers have additional effects that extend the efficiency and the possibilities of observation of TET. More precisely, we present the different behavior of the system under sinusoidal forcing and free oscillations, characterizing the phenomena for all input energies. The frequency responses are also presented, showing successive clipping of the original resonance peak of the system, and strongly modulated regimes (SMR). A model is finally used to generalize these results to more than two NES and to simulate the case of several very similar membranes in parallel which shows how to extend the existence zone of TET.

  4. 48 CFR 204.470 - U.S.-International Atomic Energy Agency Additional Protocol.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 48 Federal Acquisition Regulations System 3 2010-10-01 2010-10-01 false U.S.-International Atomic Energy Agency Additional Protocol. 204.470 Section 204.470 Federal Acquisition Regulations System DEFENSE... Information Within Industry 204.470 U.S.-International Atomic Energy Agency Additional Protocol....

  5. 48 CFR 204.470 - U.S.-International Atomic Energy Agency Additional Protocol.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 48 Federal Acquisition Regulations System 3 2011-10-01 2011-10-01 false U.S.-International Atomic Energy Agency Additional Protocol. 204.470 Section 204.470 Federal Acquisition Regulations System DEFENSE... Information Within Industry 204.470 U.S.-International Atomic Energy Agency Additional Protocol....

  6. 48 CFR 204.470 - U.S.-International Atomic Energy Agency Additional Protocol.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 48 Federal Acquisition Regulations System 3 2012-10-01 2012-10-01 false U.S.-International Atomic Energy Agency Additional Protocol. 204.470 Section 204.470 Federal Acquisition Regulations System DEFENSE... Information Within Industry 204.470 U.S.-International Atomic Energy Agency Additional Protocol....

  7. 48 CFR 204.470 - U.S.-International Atomic Energy Agency Additional Protocol.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 48 Federal Acquisition Regulations System 3 2013-10-01 2013-10-01 false U.S.-International Atomic Energy Agency Additional Protocol. 204.470 Section 204.470 Federal Acquisition Regulations System DEFENSE... Information Within Industry 204.470 U.S.-International Atomic Energy Agency Additional Protocol....

  8. 48 CFR 204.470 - U.S.-International Atomic Energy Agency Additional Protocol.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 48 Federal Acquisition Regulations System 3 2014-10-01 2014-10-01 false U.S.-International Atomic Energy Agency Additional Protocol. 204.470 Section 204.470 Federal Acquisition Regulations System DEFENSE... Information Within Industry 204.470 U.S.-International Atomic Energy Agency Additional Protocol....

  9. Modular organization of cardiac energy metabolism: energy conversion, transfer and feedback regulation

    PubMed Central

    Guzun, R.; Kaambre, T.; Bagur, R.; Grichine, A.; Usson, Y.; Varikmaa, M.; Anmann, T.; Tepp, K.; Timohhina, N.; Shevchuk, I.; Chekulayev, V.; Boucher, F.; Santos, P. Dos; Schlattner, U.; Wallimann, T.; Kuznetsov, A. V.; Dzeja, P.; Aliev, M.; Saks, V.

    2014-01-01

    To meet high cellular demands, the energy metabolism of cardiac muscles is organized by precise and coordinated functioning of intracellular energetic units (ICEUs). ICEUs represent structural and functional modules integrating multiple fluxes at sites of ATP generation in mitochondria and ATP utilization by myofibrillar, sarcoplasmic reticulum and sarcolemma ion-pump ATPases. The role of ICEUs is to enhance the efficiency of vectorial intracellular energy transfer and fine tuning of oxidative ATP synthesis maintaining stable metabolite levels to adjust to intracellular energy needs through the dynamic system of compartmentalized phosphoryl transfer networks. One of the key elements in regulation of energy flux distribution and feedback communication is the selective permeability of mitochondrial outer membrane (MOM) which represents a bottleneck in adenine nucleotide and other energy metabolite transfer and microcompartmentalization. Based on the experimental and theoretical (mathematical modelling) arguments, we describe regulation of mitochondrial ATP synthesis within ICEUs allowing heart workload to be linearly correlated with oxygen consumption ensuring conditions of metabolic stability, signal communication and synchronization. Particular attention was paid to the structure–function relationship in the development of ICEU, and the role of mitochondria interaction with cytoskeletal proteins, like tubulin, in the regulation of MOM permeability in response to energy metabolic signals providing regulation of mitochondrial respiration. Emphasis was given to the importance of creatine metabolism for the cardiac energy homoeostasis. PMID:24666671

  10. Trajectory study of energy transfer and unimolecular dissociation of highly excited allyl with argon.

    PubMed

    Conte, Riccardo; Houston, Paul L; Bowman, Joel M

    2014-09-11

    The influence of rotational excitation on energy transfer in single collisions of allyl with argon and on allyl dissociation is investigated. About 90,000 classical scattering simulations are performed in order to determine collision-induced changes in internal energy and in allyl rotational angular momentum. Dissociation is studied by means of about 50,000 additional trajectories evolved for the isolated allyl under three different conditions: allyl with no angular momentum (J = 0); allyl with the same microcanonically sampled initial conditions used for the collisions (J*); allyl evolving from the corresponding exit conditions after the collision. The potential energy surface is the sum of an intramolecular potential and an interaction one, and it has already been used in a previous work on allyl-argon scattering (Conte, R.; Houston, P. L.; Bowman, J. M. J. Phys. Chem. A 2013, 117, 14028-14041). Energy transfer data show that increased initial rotation favors, on average, increased relaxation of the excited molecule. The availability of a high-level intramolecular potential energy surface permits us to study the dependence of energy transfer on the type of starting allyl isomer. A turning point analysis is presented, and highly efficient collisions are detected. Collision-induced variations in the allyl rotational angular momentum may be quite large and are found to be distributed according to three regimes. The roles of rotational angular momentum, collision, and type of isomer on allyl unimolecular dissociation are considered by looking at dissociations times, kinetic energies of the fragments, and branching ratios. Generally, rotational angular momentum has a strong influence on the dissociation dynamics, while the single collision and the type of starting isomer are less influential. PMID:25116695

  11. Quantitative Analysis of Energy Transfer and Origin of Quenching in Er(3+)/Ho(3+) Codoped Germanosilicate Glasses.

    PubMed

    Wei, Tao; Tian, Ying; Tian, Cong; Cai, Muzhi; Jing, Xufeng; Li, Bingpeng; Chen, Rong; Zhang, Junjie; Xu, Shiqing

    2015-07-01

    The energy transfer mechanism between Ho(3+) and Er(3+) ions has been investigated in germanosilicate glass excited by 980 nm laser diode. A rate equation model was developed to demonstrate the energy transfer from Er(3+) to Ho(3+) ions, quantitatively. Energy transfer efficiency from the Er(3+):(4)I13/2 to the Ho(3+):(5)I7 level can reach as high as 75%. Such a high efficiency was attributed to the excellent matching of the host phonon energy with the energy gap between Er(3+):(4)I13/2 and Ho(3+):(5)I7 levels. In addition, the energy transfer microparameter (CDA) from Er(3+):(4)I13/2 to Ho(3+):(5)I7 level was estimated to (4.16 ± 0.03) × 10(-40) cm(6)·s(-1) via the host-assisted spectral overlap function, coinciding with the CDA (2,88 ± 0.04) × 10(-40) cm(6)·s(-1) from decay analysis of the Er(3+):(4)I13/2 level which also indicated hopping migration-assisted energy transfer. Furthermore, the concentration quenching of Ho(3+):(5)I7 → (5)I8 transition was the dipole-dipole interaction in the diffusion-limited regime, and the quenching concentration of Ho(3+) reached 4.13 × 10(20) cm(-3). PMID:26061719

  12. Optimization of exciton trapping in energy transfer processes.

    PubMed

    Cao, Jianshu; Silbey, Robert J

    2009-12-17

    In this paper, we establish optimal conditions for maximal energy transfer efficiency using solutions for multilevel systems and interpret these analytical solutions with more intuitive kinetic networks resulting from a systematic mapping procedure. The mapping procedure defines an effective hopping rate as the leading order picture and nonlocal kinetic couplings as the quantum correction, hence leading to a rigorous separation of thermal hopping and coherent transfer useful for visualizing pathway connectivity and interference in quantum networks. As a result of these calculations, the dissipative effects of the surrounding environments can be optimized to yield the maximal efficiency, and modulation of the efficiency can be achieved using the cumulative quantum phase along any closed loops. The optimal coupling of the system and its environments is interpreted with the generic mechanisms: (i) balancing localized trapping and delocalized coherence, (ii) reducing the effective detuning via homogeneous line-broadening, (iii) suppressing the destructive interference in nonlinear network configurations, and (iv) controlling phase modulation in closed loop configurations. Though these results are obtained for simple model systems, the physics thus derived provides insights into the working of light harvesting systems, and the approaches thus developed apply to large-scale computation. PMID:19929005

  13. Electronic energy transfer: Localized operator partitioning of electronic energy in composite quantum systems

    NASA Astrophysics Data System (ADS)

    Khan, Yaser; Brumer, Paul

    2012-11-01

    A Hamiltonian based approach using spatially localized projection operators is introduced to give precise meaning to the chemically intuitive idea of the electronic energy on a quantum subsystem. This definition facilitates the study of electronic energy transfer in arbitrarily coupled quantum systems. In particular, the decomposition scheme can be applied to molecular components that are strongly interacting (with significant orbital overlap) as well as to isolated fragments. The result defines a consistent electronic energy at all internuclear distances, including the case of separated fragments, and reduces to the well-known Förster and Dexter results in their respective limits. Numerical calculations of coherent energy and charge transfer dynamics in simple model systems are presented and the effect of collisionally induced decoherence is examined.

  14. Study of Energy Transfer in Organic Dye Pairs Using Thermal Lens Technique

    NASA Astrophysics Data System (ADS)

    Kurian, Achamma; Unnikrishnan, K. P.; Gopinath, Pramod; Nampoori, V. P. N.; Vallabhan, C. P. G.

    It is demonstrated that the dual beam thermal lens technique can be very effectively used for the study of energy transfer processes in organic dye mixtures. The energy transfer rate and critical transfer radius in Rhodamine 6G - Rhodamine B are calculated using this technique. The observed results support Forster type resonance transfer due to long-range dipole-dipole interaction as reported by earlier workers using other techniques.

  15. Chlorophyll a Franck-Condon factors and excitation energy transfer

    SciTech Connect

    Pieper, J. ||; Voigt, J.; Small, G.J. |

    1999-04-01

    The Franck-Condon factors for the S{sub 1}(Q{sub y}) {leftrightarrow} S{sub 0} electronic transition of chlorophyll (Chl) molecules are important for understanding excitation energy transfer in photosynthetic complexes. Currently, there are two sets of Chl a Frank-Condon factors for over 40 modes, one determined by spectral hole burning and the other by fluorescence line narrowing. Those obtained by the latter spectroscopy are, on average, a factor of 30 times smaller than the hole burning values. Nonline-narrowed fluorescence results for the light-harvesting complex 2 of photosystem 2 at 4.2 K are presented that agree quite well with the hole burning but not the fluorescence line narrowing values.

  16. Control of particle precipitation by energy transfer from solar wind

    NASA Astrophysics Data System (ADS)

    Bremer, J.; Gernandt, H.

    1985-12-01

    The energy transfer function (epsilon), introduced by Perreault and Akasofu (1978), appears to be well suited for the description of the long-term control of the particle precipitation by interplanetary parameters. An investigation was conducted with the objective to test this control in more detail. This investigation included the calculation of hourly epsilon values on the basis of satellite-measured solar wind and IMF (interplanetary magnetic field) data. The results were compared with corresponding geomagnetic and ionospheric data. The ionospheric data had been obtained by three GDR (German Democratic Republic) teams during the 21st, 22nd, and 23rd Soviet Antarctic Expeditions in the time period from 1976 to 1979. It was found that, in high latitudes, the properties of the solar wind exercise a pronounced degree of control on the precipitation of energetic particles into the atmosphere, taking into account a time delay of about one hour due to the occurrence of magnetospheric storage processes.

  17. Resonance energy transfer: The unified theory via vector spherical harmonics.

    PubMed

    Grinter, Roger; Jones, Garth A

    2016-08-21

    In this work, we derive the well-established expression for the quantum amplitude associated with the resonance energy transfer (RET) process between a pair of molecules that are beyond wavefunction overlap. The novelty of this work is that the field of the mediating photon is described in terms of a spherical wave rather than a plane wave. The angular components of the field are constructed in terms of vector spherical harmonics while Hankel functions are used to define the radial component. This approach alleviates the problem of having to select physically correct solution from non-physical solutions, which seems to be inherent in plane wave derivations. The spherical coordinate system allows one to easily decompose the photon's fields into longitudinal and transverse components and offers a natural way to analyse near-, intermediate-, and far-zone RET within the context of the relative orientation of the transition dipole moments for the two molecules. PMID:27544087

  18. Application of fluorescence resonance energy transfer in protein studies

    PubMed Central

    Ma, Linlin; Yang, Fan; Zheng, Jie

    2014-01-01

    Since the physical process of fluorescence resonance energy transfer (FRET) was elucidated more than six decades ago, this peculiar fluorescence phenomenon has turned into a powerful tool for biomedical research due to its compatibility in scale with biological molecules as well as rapid developments in novel fluorophores and optical detection techniques. A wide variety of FRET approaches have been devised, each with its own advantages and drawbacks. Especially in the last decade or so, we are witnessing a flourish of FRET applications in biological investigations, many of which exemplify clever experimental design and rigorous analysis. Here we review the current stage of FRET methods development with the main focus on its applications in protein studies in biological systems, by summarizing the basic components of FRET techniques, most established quantification methods, as well as potential pitfalls, illustrated by example applications. PMID:25368432

  19. Calibration of fluorescence resonance energy transfer in microscopy

    DOEpatents

    Youvan, Douglas C.; Silva, Christopher M.; Bylina, Edward J.; Coleman, William J.; Dilworth, Michael R.; Yang, Mary M.

    2002-09-24

    Imaging hardware, software, calibrants, and methods are provided to visualize and quantitate the amount of Fluorescence Resonance Energy Transfer (FRET) occurring between donor and acceptor molecules in epifluorescence microscopy. The MicroFRET system compensates for overlap among donor, acceptor, and FRET spectra using well characterized fluorescent beads as standards in conjunction with radiometrically calibrated image processing techniques. The MicroFRET system also provides precisely machined epifluorescence cubes to maintain proper image registration as the sample is illuminated at the donor and acceptor excitation wavelengths. Algorithms are described that pseudocolor the image to display pixels exhibiting radiometrically-corrected fluorescence emission from the donor (blue), the acceptor (green) and FRET (red). The method is demonstrated on samples exhibiting FRET between genetically engineered derivatives of the Green Fluorescent Protein (GFP) bound to the surface of Ni chelating beads by histidine-tags.

  20. Calibration of fluorescence resonance energy transfer in microscopy

    DOEpatents

    Youvan, Dougalas C.; Silva, Christopher M.; Bylina, Edward J.; Coleman, William J.; Dilworth, Michael R.; Yang, Mary M.

    2003-12-09

    Imaging hardware, software, calibrants, and methods are provided to visualize and quantitate the amount of Fluorescence Resonance Energy Transfer (FRET) occurring between donor and acceptor molecules in epifluorescence microscopy. The MicroFRET system compensates for overlap among donor, acceptor, and FRET spectra using well characterized fluorescent beads as standards in conjunction with radiometrically calibrated image processing techniques. The MicroFRET system also provides precisely machined epifluorescence cubes to maintain proper image registration as the sample is illuminated at the donor and acceptor excitation wavelengths. Algorithms are described that pseudocolor the image to display pixels exhibiting radiometrically-corrected fluorescence emission from the donor (blue), the acceptor (green) and FRET (red). The method is demonstrated on samples exhibiting FRET between genetically engineered derivatives of the Green Fluorescent Protein (GFP) bound to the surface of Ni chelating beads by histidine-tags.

  1. Upconversion luminescence resonance energy transfer-based aptasensor for the sensitive detection of oxytetracycline.

    PubMed

    Zhang, Hui; Fang, Congcong; Wu, Shijia; Duan, Nuo; Wang, Zhouping

    2015-11-15

    In this work, a biosensor based on luminescence resonance energy transfer (LRET) from NaYF4:Yb,Tm upconversion nanoparticles (UCNPs) to SYBR Green I has been developed. The aptamers are covalently linked to UCNPs and hybridized with their complementary strands. The subsequent addition of SYBR Green allows SYBR Green I to insert into the formed double-stranded DNA (dsDNA) duplex and brings the energy donor and acceptor into close proximity, leading to the fluorescence of UCNPs transferred to SYBR Green I. When excited at 980 nm, the UCNPs emit luminescence at 477 nm, and this energy is transferred to SYBR Green I, which emits luminescence at 530 nm. In the presence of oxytetracycline (OTC), the aptamers prefer to bind to its corresponding analyte and dehybridize with the complementary DNA. This dehybridization leads to the liberation of SYBR Green I, which distances SYBR Green I from the UCNPs and recovers the UCNPs' luminescence. Under optimal conditions, a linear calibration is obtained between the ratio of I530 to I477 nm (I530/I477) and the OTC concentration, which ranges from 0.1 to 10 ng/ml with a limit of detection (LOD) of 0.054 ng/ml. PMID:26302361

  2. Energy transfer and light tolerance studies in a fluorescent tandem phycobiliprotein conjugate.

    PubMed

    Tian, Yu; Pappas, Dimitri

    2011-09-01

    Light harvesting and energy transfer between allophycocyanin (APC) and a tandem conjugate dye was investigated using single-molecule recrossings in the probe volume. By comparing saturation irradiance and recrossing events of APC and the tandem conjugate Streptavidin Allophycocyanin-AlexaFluor-680 (APC-680), it was demonstrated that the light tolerance and photostability of APC-680 were improved over APC. This improvement was due to conjugating a tandem dye to APC, which provided an alternative pathway for energy transfer. This additional pathway decreases photobleaching and triplet-state conversion. In this study, the average fluorescence intensity at different laser powers was calculated from extracted signal peaks. Saturation irradiance was determined by interpolating the average intensity as a function of excitation power. By comparing the saturation irradiance of APC and APC-680, it was demonstrated that light tolerance was not significantly increased by having a small fluorophore covalently linked to the protein. The molecular recrossing method was used to determine triplet-state conversion and photobleaching effects. The number of molecules that were detected within 2 ms of each other was defined as the number of recrossing events (N(r)). The total number of molecules detected was defined as N(t). The normalized number of recrossings events (N(r)/N(t)) showed that energy transfer between APC and AlexaFluor-680 could reduce triplet-state formation of phycobiliproteins. In this case, the saturation irradiance was not improved, but the resistance to photobleaching and triplet-state conversion was improved. PMID:21929852

  3. Fluorescence energy transfer efficiency in labeled yeast cytochrome c: a rapid screen for ion biocompatibility in aqueous ionic liquids

    SciTech Connect

    Baker, Sheila N; Zhao, Hua; Pandey, Siddharth; Heller, William T; Bright, Frank; Baker, Gary A

    2011-01-01

    A fluorescence energy transfer de-quenching assay was implemented to follow the equilibrium unfolding behaviour of site-specific tetramethylrhodamine-labelled yeast cytochrome c in aqueous ionic liquid solutions; additionally, this approach offers the prospect of naked eye screening for biocompatible ion combinations in hydrated ionic liquids.

  4. Ion transfer battery: storing energy by transferring ions across liquid-liquid interfaces.

    PubMed

    Peljo, Pekka; Bichon, Marie; Girault, Hubert H

    2016-07-28

    A battery utilizing the Galvani potential difference between aqueous and organic phases is demonstrated. The battery consists of two organic redox electrolytes separated by an immiscible aqueous phase. The charge is stored by transferring a salt from the aqueous phase into organic phases in ion transfer coupled electron transfer reactions. PMID:27327108

  5. Adiabatic principles in atom-diatom collisional energy transfer

    SciTech Connect

    Hovingh, W.J.

    1993-01-01

    This work describes the application of numerical methods to the solution of the time dependent Schroedinger equation for non-reactive atom-diatom collisions in which only one of the degrees of freedom has been removed. The basic method involves expanding the wave function in a basis set in two of the diatomic coordinates in a body-fixed frame (with respect to the triatomic complex) and defining the coefficients in that expansion as functions on a grid in the collision coordinate. The wave function is then propagated in time using a split operator method. The bulk of this work is devoted to the application of this formalism to the study of internal rotational predissociation in NeHF, in which quasibound states of the triatom predissociate through the transfer of energy from rotation of the diatom into translational energy in the atom-diatom separation coordinate. The author analyzes the computed time dependent wave functions to calculate the lifetimes for several quasibound states; these are in agreement with time independent quantum calculations using the same potential. Moreover, the time dependent behavior of the wave functions themselves sheds light on the dynamics of the predissociation processes. Finally, the partial cross sections of the products in those processes is determined with multiple exit channels. These show strong selectivity in the orbital angular momentum of the outgoing fragments, which the author explains with an adiabatic channel interpretation of the wave function's dynamics. The author also suggests that the same formalism might profitably be used to investigate the quantum dynamics of [open quotes]quasiresonant vibration-rotation transfer[close quotes], in which remarkably strong propensity rules in certain inelastic atom-diatom collision arise from classical adiabatic invariance theory.

  6. Fluorescence resonance energy transfer-based stoichiometry in living cells.

    PubMed Central

    Hoppe, Adam; Christensen, Kenneth; Swanson, Joel A

    2002-01-01

    Imaging of fluorescence resonance energy transfer (FRET) between fluorescently labeled molecules can measure the timing and location of intermolecular interactions inside living cells. Present microscopic methods measure FRET in arbitrary units, and cannot discriminate FRET efficiency and the fractions of donor and acceptor in complex. Here we describe a stoichiometric method that uses three microscopic fluorescence images to measure FRET efficiency, the relative concentrations of donor and acceptor, and the fractions of donor and acceptor in complex in living cells. FRET stoichiometry derives from the concept that specific donor-acceptor complexes will give rise to a characteristic FRET efficiency, which, if measured, can allow stoichiometric discrimination of interacting components. A first equation determines FRET efficiency and the fraction of acceptor molecules in complex with donor. A second equation determines the fraction of donor molecules in complex by estimating the donor fluorescence lost due to energy transfer. This eliminates the need for acceptor photobleaching to determine total donor concentrations and allows for repeated measurements from the same cell. A third equation obtains the ratio of total acceptor to total donor molecules. The theory and method were confirmed by microscopic measurements of fluorescence from cyan fluorescent protein (CFP), citrine, and linked CFP-Citrine fusion protein, in solutions and inside cells. Together, the methods derived from these equations allow sensitive, rapid, and repeatable detection of donor-, acceptor-, and donor-acceptor complex stoichiometry at each pixel in an image. By accurately imaging molecular interactions, FRET stoichiometry opens new areas for quantitative study of intracellular molecular networks. PMID:12496132

  7. Energy Transfer Based Nanocomposite Scintillator for Radiation Detection

    NASA Astrophysics Data System (ADS)

    Aslam, Soha; Sahi, Sunil; Chen, Wei; Ma, Lun; Kenarangui, Rasool

    2014-09-01

    Scintillators are the materials that emit light upon irradiation with high energy radiation like X-ray or gamma-ray. Inorganic single crystal and organic (plastic and liquid) are the two most used scintillator types. Both of these scintillator kinds have advantages and disadvantages. Inorganic single crystals are expensive and difficult to grow in desire shape and size. Also, single crystal scintillator such as NaI and CsI are very hygroscopic. On the other hand, organic scintillators have low density which limits their applications in gamma spectroscopy. Due to high quantum yield and size dependent emission, nanoparticles have attracted interested in various field of research. Here, we have studies the nanoparticles for radiation detection. We have synthesized nanoparticles of Cerium fluoride (CeF3), Zinc Oxide (ZnO), Cadmium Telluride (CdTe), Copper complex and Zinc sulfide (ZnS). We have used Fluorescence Resonance Energy Transfer (FRET) principle to enhance the luminescence properties of nanocomposite scintillator. Nanocomposites scintillators are structurally characterized with X-ray diffraction (XRD) and Transmission Electron Microscopy (TEM). Optical properties are studied using Photoluminescence, UV-Visible and X-ray. Enhancements in the luminescence are observed under UV and X-ray excitation. Preliminary studies shows nanocomposite scintillators are promising for radiation detection. Scintillators are the materials that emit light upon irradiation with high energy radiation like X-ray or gamma-ray. Inorganic single crystal and organic (plastic and liquid) are the two most used scintillator types. Both of these scintillator kinds have advantages and disadvantages. Inorganic single crystals are expensive and difficult to grow in desire shape and size. Also, single crystal scintillator such as NaI and CsI are very hygroscopic. On the other hand, organic scintillators have low density which limits their applications in gamma spectroscopy. Due to high quantum

  8. In situ energy transfer quenching of quantum dot electrochemiluminescence for sensitive detection of cancer biomarkers.

    PubMed

    Yang, Mengli; Chen, Ying; Xiang, Yun; Yuan, Ruo; Chai, Yaqin

    2013-12-15

    In this work, we develop a sensitive and selective method for the detection of a cancer biomarker (carcinoembryonic antigen, CEA) based on a new electrochemiluminescence (ECL) energy transfer mechanism, in which the energy transfer occurs from the excited quantum dots (QDs) to the in situ electro-generated quenchers. A CdTe QD-containing composite film is first deposited on the electrode followed by the conjugation of the primary antibody (Ab1) on the film. Subsequent incubation of the modified sensing electrode with CEA and the secondary antibody-alkaline phosphatase-gold nanoparticle labels (Ab2-ALP-AuNP) leads to the formation of the Ab1/CEA/Ab2-ALP-AuNPs immunocomplexes on the electrode surface. The captured ALP catalyzes the p-nitrophenyl phosphate disodium salt (p-NPP) substrate in the ECL detection buffer to p-nitrophenol (p-NP). The potential sweep on the electrode results in the oxidation of p-NP to p-benzoquinone (p-BQ) and the generation of excited QDs. The ECL emission of the excited QDs is therefore quenched through direct energy transfer from the excited QDs to p-BQ. This ECL quenching effect is significantly amplified because of the numerous ALP enzymes involved in each antibody-antigen recognition event. This proposed method of amplified quenching of QD ECL emission offers a low detection limit of 1.67 pg mL(-1) for CEA. In addition, this method exhibits high reproducibility and selectivity and can also be applied to serum samples. Given these advantages, this new ECL energy transfer approach holds great promise for the detection of other biological targets and has potential applications in clinical diagnoses. PMID:23891869

  9. On the use of Lineal Energy Measurements to Estimate Linear Energy Transfer Spectra

    NASA Technical Reports Server (NTRS)

    Adams, David A.; Howell, Leonard W., Jr.; Adam, James H., Jr.

    2007-01-01

    This paper examines the error resulting from using a lineal energy spectrum to represent a linear energy transfer spectrum for applications in the space radiation environment. Lineal energy and linear energy transfer spectra are compared in three diverse but typical space radiation environments. Different detector geometries are also studied to determine how they affect the error. LET spectra are typically used to compute dose equivalent for radiation hazard estimation and single event effect rates to estimate radiation effects on electronics. The errors in the estimations of dose equivalent and single event rates that result from substituting lineal energy spectra for linear energy spectra are examined. It is found that this substitution has little effect on dose equivalent estimates in interplanetary quiet-time environment regardless of detector shape. The substitution has more of an effect when the environment is dominated by solar energetic particles or trapped radiation, but even then the errors are minor especially if a spherical detector is used. For single event estimation, the effect of the substitution can be large if the threshold for the single event effect is near where the linear energy spectrum drops suddenly. It is judged that single event rate estimates made from lineal energy spectra are unreliable and the use of lineal energy spectra for single event rate estimation should be avoided.

  10. Simultaneous backward data transmission and power harvesting in an ultrasonic transcutaneous energy transfer link employing acoustically dependent electric impedance modulation.

    PubMed

    Ozeri, Shaul; Shmilovitz, Doron

    2014-09-01

    The advancement and miniaturization of body implanted medical devices pose several challenges to Ultrasonic Transcutaneous Energy Transfer (UTET), such as the need to reduce the size of the piezoelectric resonator, and the need to maximize the UTET link power-transfer efficiency. Accordingly, the same piezoelectric resonator that is used for energy harvesting at the body implant, may also be used for ultrasonic backward data transfer, for instance, through impedance modulation. This paper presents physical considerations and design guidelines of the body implanted transducer of a UTET link with impedance modulation for a backward data transfer. The acoustic matching design procedure was based on the 2×2 transfer matrix chain analysis, in addition to the Krimholtz Leedom and Matthaei KLM transmission line model. The UTET power transfer was carried out at a frequency of 765 kHz, continuous wave (CW) mode. The backward data transfer was attained by inserting a 9% load resistance variation around its matched value (550 Ohm), resulting in a 12% increase in the acoustic reflection coefficient. A backward data transmission rate of 1200 bits/s was experimentally demonstrated using amplitude shift keying, simultaneously with an acoustic power transfer of 20 mW to the implant. PMID:24861424

  11. Inter-and intraspecific variation in excited-state triplet energy transfer rates in reaction centers of photosynthetic bacteria.

    SciTech Connect

    Laible, P. D.; Morris, Z. S.; Thurnauer, M. C.; Schiffer, M.; Hanson, D. K.

    2003-08-01

    In protein-cofactor reaction center (RC) complexes of purple photosynthetic bacteria, the major role of the bound carotenoid (C) is to quench the triplet state formed on the primary electron donor (P) before its sensitization of the excited singlet state of molecular oxygen from its ground triplet state. This triplet energy is transferred from P to C via the bacteriochlorophyll monomer B{sub B}. Using time-resolved electron paramagnetic resonance (TREPR), we have examined the temperature dependence of the rates of this triplet energy transfer reaction in the RC of three wild-type species of purple nonsulfur bacteria. Species-specific differences in the rate of transfer were observed. Wild-type Rhodobacter capsulatus RCs were less efficient at the triplet transfer reaction than Rhodobacter sphaeroides RCs, but were more efficient than Rhodospirillum rubrum RCs. In addition, RCs from three mutant strains of R. capsulatus carrying substitutions of amino acids near P and B{sub B} were examined. Two of the mutant RCs showed decreased triplet transfer rates compared with wild-type RCs, whereas one of the mutant RCs demonstrated a slight increase in triplet transfer rate at low temperatures. The results show that site-specific changes within the RC of R. capsulatus can mimic interspecies differences in the rates of triplet energy transfer. This application of TREPR was instrumental in defining critical energetic and coupling factors that dictate the efficiency of this photoprotective process.

  12. Novel Dental Restorative Materials having Low Polymerization Shrinkage Stress via Stress Relaxation by Addition-Fragmentation Chain Transfer

    PubMed Central

    Park, Hee Young; Kloxin, Christopher J.; Abuelyaman, Ahmed S.; Oxman, Joe D.; Bowman, Christopher N.

    2012-01-01

    Objectives To produce a reduced stress dental restorative material while simultaneously maintaining excellent mechanical properties, we have incorporated an allyl sulfide functional group into norbornene-methacrylate comonomer resins. We hypothesize that the addition-fragmentation chain transfer (AFCT) enabled by the presence of the allyl sulfide relieves stress in these methacrylate-based systems while retaining excellent mechanical properties owing to the high glass transition temperature of norbornene-containing resins. Methods An allyl sulfide-containing dinorbornene was stoichiometrically formulated with a ring-containing allyl sulfide-possessing methacrylate. To evaluate the stress relaxation effect as a function of the allyl sulfide concentration, a propyl sulfide-based dinorbornene, not capable of addition-fragmentation, was also formulated with the methacrylate monomer. Shrinkage stress, the glass transition temperature and the elastic modulus were all measured. The composite flexural strength and modulus were also measured. ANOVA (CI 95%) was conducted to determine differences between the means. Results Increasing the allyl sulfide content in the resin dramatically reduces the final stress in the norbornene-methacrylate systems. Both norbornene-methacrylate resins demonstrated almost zero stress (more than 96% stress reduction) compared with the conventional BisGMA/TEGDMA 70/30 wt% control. Mechanical properties of the allyl sulfide-based dental composites were improved to the point of being statistically indistinguishable from the control BisGMA-TEGDMA by changing the molar ratio between the methacrylate and norbornene functionalities. Significance The allyl sulfide-containing norbornene-methacrylate networks possessed super-ambient Tg, and demonstrated significantly lower shrinkage stress when compared with the control (BisGMA/TEGDMA 70 to 30 wt%). Although additional development remains, these low stress materials exhibit excellent mechanical

  13. Harvesting singlet fission for solar energy conversion via triplet energy transfer

    NASA Astrophysics Data System (ADS)

    Tritsch, John R.; Chan, Wai-Lun; Wu, Xiaoxi; Monahan, Nicholas R.; Zhu, X.-Y.

    2013-10-01

    The efficiency of a conventional solar cell may be enhanced if one incorporates a molecular material capable of singlet fission, that is, the production of two triplet excitons from the absorption of a single photon. To implement this, we need to successfully harvest the two triplets from the singlet fission material. Here we show in the tetracene (Tc)/copper phthalocyanine (CuPc) model system that triplets produced from singlet fission in the former can transfer to the later on the timescale of 45±5 ps. However, the efficiency of triplet energy transfer is limited by a loss channel due to faster formation (400±100 fs) and recombination (2.6±0.5 ps) of charge transfer excitons at the interface. These findings suggest a design principle for efficient energy harvesting from singlet fission: one must reduce interfacial area between the two organic chromophores to minimize charge transfer/recombination while optimizing light absorption, singlet fission and triplet rather than singlet transfer.

  14. Investigation of spectroscopy and the dual energy transfer mechanisms of Sm3+-doped telluroborate glasses

    NASA Astrophysics Data System (ADS)

    Van Do, Phan; Tuyen, Vu Phi; Quang, Vu Xuan; Hung, Le Xuan; Thanh, Luong Duy; Ngoc, Tran; Van Tam, Ngo; Huy, Bui The

    2016-05-01

    The absorption, luminescence, Raman spectra and lifetimes of Sm-doped alkali telluroborate glasses (TB glasses) TB:Sm3+ have been investigated. The dual energy transfers including energy transfer between Sm3+ - Sm3+ pairs and Sm3+ - non-bridging oxygen (NBO) intrinsic defects were investigated. The concentration quenching of luminescence intensity was explained by the non-radiative energy transfer between the Sm3+ ions through the cross-relaxation mechanism. The decay curves are single exponentials with low concentrations (lower 0.10 mol%) and become non-exponentials at higher concentrations. The non-exponential decay curves are fitted to the Inokuti and Hirayama model to give the energy transfer parameters between Sm3+ ions. The dominant interaction mechanism for energy transfer process is dipole-dipole interaction. The energy transfer induced Sm3+ photoluminescence enhancement in tellurite glass was experimentally studied and confirmed.

  15. Methods and kits for nucleic acid analysis using fluorescence resonance energy transfer

    DOEpatents

    Kwok, Pui-Yan; Chen, Xiangning

    1999-01-01

    A method for detecting the presence of a target nucleotide or sequence of nucleotides in a nucleic acid is disclosed. The method is comprised of forming an oligonucleotide labeled with two fluorophores on the nucleic acid target site. The doubly labeled oligonucleotide is formed by addition of a singly labeled dideoxynucleoside triphosphate to a singly labeled polynucleotide or by ligation of two singly labeled polynucleotides. Detection of fluorescence resonance energy transfer upon denaturation indicates the presence of the target. Kits are also provided. The method is particularly applicable to genotyping.

  16. Immobilization of antimony in waste-to-energy bottom ash by addition of calcium and iron containing additives.

    PubMed

    Van Caneghem, Jo; Verbinnen, Bram; Cornelis, Geert; de Wijs, Joost; Mulder, Rob; Billen, Pieter; Vandecasteele, Carlo

    2016-08-01

    The leaching of Sb from waste-to-energy (WtE) bottom ash (BA) often exceeds the Dutch limit value of 0.32mgkg(-1) for recycling of BA in open construction applications. From the immobilization mechanisms described in the literature, it could be concluded that both Ca and Fe play an important role in the immobilization of Sb in WtE BA. Therefore, Ca and Fe containing compounds were added to the samples of the sand fraction of WtE BA, which in contrast to the granulate fraction is not recyclable to date, and the effect on the Sb leaching was studied by means of batch leaching tests. Results showed that addition of 0.5 and 2.5% CaO, 5% CaCl2, 2.5% Fe2(SO4)3 and 1% FeCl3 decreased the Sb leaching from 0.62±0.02mgkgDM(-1) to 0.20±0.02, 0.083±0.044, 0.25±0.01, 0.27±0.002 and 0.29±0.02mgkgDM(-1), respectively. Due to the increase in pH from 11.41 to 12.53 when 2.5% CaO was added, Pb and Zn leaching increased and exceeded the respective leaching limits. Addition of 5% CaCO3 had almost no effect on the Sb leaching, as evidenced by the resulting 0.53mgkgDM(-1) leaching concentration. This paper shows a complementary enhancement of the effect of Ca and Fe, by comparing the aforementioned Sb leaching results with those of WtE BA with combined addition of 2.5% CaO or 5% CaCl2 with 2.5% Fe2(SO4)3 or 1% FeCl3. These lab scale results suggest that formation of romeites with a high Ca content and formation of iron antimonate (tripuhyite) with a very low solubility are the main immobilization mechanisms of Sb in WtE BA. Besides the pure compounds and their mixtures, also addition of 10% of two Ca and Fe containing residues of the steel industry, hereafter referred to as R1 and R2, was effective in decreasing the Sb leaching from WtE BA below the Dutch limit value for reuse in open construction applications. To evaluate the long term effect of the additives, pilot plots of WtE BA with 10% of R1 and 5% and 10% of R2 were built and samples were submitted to leaching tests at

  17. Study of Coherent Raman Energy Transfer in Molecular Liquids with Strong Field Laser Excitation

    NASA Astrophysics Data System (ADS)

    Pearson, B. J.; Morris, D. S.; Bucksbaum, P. H.; Weinacht, T. C.

    2001-05-01

    We investigate coherent population transfer among vibrational states in molecular liquids via stimulated Raman scattering. A learning algorithm and ultrafast optical pulse shaper are able to selectively excite or suppress excitation in adjacent vibrational modes. In particular, results with deuterated methanol (CD3OD) are compared to previous results in methanol (CH3OH) in order to test possible control mechanisms for the observed energy transfer. Analysis includes examination of both the optimal pulse shapes as well as the spectrum of the pulse intensity envelope. Although the interaction is non-impulsive, control is still achieved. Further investigations with other molecular liquids including ethanol should provide additional information. This work is supported by the National Science Foundation, grant 9987916.

  18. Monthly Variations of Low-Energy Ballistic Transfers to Lunar Halo Orbits

    NASA Technical Reports Server (NTRS)

    Parker, Jeffrey S.

    2010-01-01

    The characteristics of low-energy transfers between the Earth and Moon vary from one month to the next largely due to the Earth's and Moon's non-circular, non-coplanar orbits in the solar system. This paper characterizes those monthly variations as it explores the trade space of low-energy lunar transfers across many months. Mission designers may use knowledge of these variations to swiftly design desirable low-energy lunar transfers in any given month.

  19. Proton Linear Energy Transfer measurement using Emulsion Cloud Chamber

    NASA Astrophysics Data System (ADS)

    Shin, Jae-ik; Park, Seyjoon; Kim, Haksoo; Kim, Meyoung; Jeong, Chiyoung; Cho, Sungkoo; Lim, Young Kyung; Shin, Dongho; Lee, Se Byeong; Morishima, Kunihiro; Naganawa, Naotaka; Sato, Osamu; Kwak, Jungwon; Kim, Sung Hyun; Cho, Jung Sook; Ahn, Jung Keun; Kim, Ji Hyun; Yoon, Chun Sil; Incerti, Sebastien

    2015-04-01

    This study proposes to determine the correlation between the Volume Pulse Height (VPH) measured by nuclear emulsion and Linear Energy Transfer (LET) calculated by Monte Carlo simulation based on Geant4. The nuclear emulsion was irradiated at the National Cancer Center (NCC) with a therapeutic proton beam and was installed at 5.2 m distance from the beam nozzle structure with various thicknesses of water-equivalent material (PMMA) blocks to position with specific positions along the Bragg curve. After the beam exposure and development of the emulsion films, the films were scanned by S-UTS developed in Nagoya University. The proton tracks in the scanned films were reconstructed using the 'NETSCAN' method. Through this procedure, the VPH can be derived from each reconstructed proton track at each position along the Bragg curve. The VPH value indicates the magnitude of energy loss in proton track. By comparison with the simulation results obtained using Geant4, we found the correlation between the LET calculated by Monte Carlo simulation and the VPH measured by the nuclear emulsion.

  20. Exciton-plasmon interactions and energy transfer in nanoparticles

    NASA Astrophysics Data System (ADS)

    Govorov, Alexander

    2009-03-01

    Energy transfer between optically-excited nanocrystals coupled by the Coulomb interaction can be very efficient. The interaction of excitons and plasmons in nanocrystals leads to several effects: energy transfer between nanoparticles (NPs), electromagnetic enhancement, reduced exciton diffusion in nanowires (NWs), exciton energy shifts, and interference and non-linear phenomena [1-3]. Using kinetic equations for excitons, we model exciton transport in a NW and explain the origin of the blue shift of exciton emission observed in the recent experiments on hybrid NW-NP assemblies [2]. We also model artificial light-harvesting complexes composed of chlorophylls, bacterial reaction centers, and NPs [3]. Using superior optical properties of metal and semiconductor NPs, one can strongly enhance the efficiency of light harvesting [3]. An interaction between a discrete state of exciton and a continuum of plasmonic states can give rise to interference effects (Fano-like asymmetric resonances). These interference effects greatly enhance visibility of relatively weak exciton signals and can be used for spectroscopy of single nanoparticle and molecules. In the nonlinear regime, the Fano effect becomes strongly amplified [4]. In conclusion, our theory explains present experimental results and also provides motivation for future experiments and applications. Potential applications of dynamical exciton-plasmon systems include sensors and light-harvesting. The above theoretical studies were performed in collaboration with several groups [1-4]. [4pt] [1] A. O. Govorov, G. W. Bryant, W. Zhang, T. Skeini, J. Lee, N. A. Kotov, J. M. Slocik, and R. R. Naik, Nano Letters 6, 984 (2006).[0pt] [2] J. Lee, P. Hernandez, J. Lee, A. Govorov, and N. Kotov, Nature Materials 6, 291 (2007).[0pt] [3] A. O. Govorov and I. Carmeli, Nano Lett. 7, 620 (2007); S. Mackowski, S. W"ormke, A.J. Maier, T.H.P. Brotosudarmo, H. Harutyunyan, A. Hartschuh, A.O. Govorov, H. Scheer, C. Br"auchle, Nano Lett. 8, 558

  1. Relaxation dynamics and exciton energy transfer in the low-temperature phase of MEH-PPV

    SciTech Connect

    Consani, Cristina; Koch, Federico; Panzer, Fabian; Unger, Thomas; Köhler, Anna; Brixner, Tobias

    2015-06-07

    Understanding the effects of aggregation on exciton relaxation and energy transfer is relevant to control photoinduced function in organic electronics and photovoltaics. Here, we explore the photoinduced dynamics in the low-temperature aggregated phase of a conjugated polymer by transient absorption and coherent electronic two-dimensional (2D) spectroscopy. Coherent 2D spectroscopy allows observing couplings among photoexcited states and discriminating band shifts from homogeneous broadening, additionally accessing the ultrafast dynamics at various excitation energies simultaneously with high spectral resolution. By combining the results of the two techniques, we differentiate between an initial exciton relaxation, which is not characterized by significant exciton mobility, and energy transport between different chromophores in the aggregate.

  2. Role of Tensorial Electronic Friction in Energy Transfer at Metal Surfaces.

    PubMed

    Askerka, Mikhail; Maurer, Reinhard J; Batista, Victor S; Tully, John C

    2016-05-27

    An accurate description of nonadiabatic energy relaxation is crucial for modeling atomistic dynamics at metal surfaces. Interfacial energy transfer due to electron-hole pair excitations coupled to motion of molecular adsorbates is often simulated by Langevin molecular dynamics with electronic friction. Here, we present calculations of the full electronic friction tensor by using first order time-dependent perturbation theory at the density functional theory level. We show that the friction tensor is generally anisotropic and nondiagonal, as found for hydrogen atom on Pd(100) and CO on Cu(100) surfaces. This implies that electron-hole pair induced nonadiabatic coupling at metal surfaces leads to friction-induced mode coupling, therefore, opening an additional channel for energy redistribution. We demonstrate the robustness and accuracy of our results by direct comparison to established methods and experimental data. PMID:27284673

  3. Role of Tensorial Electronic Friction in Energy Transfer at Metal Surfaces

    NASA Astrophysics Data System (ADS)

    Askerka, Mikhail; Maurer, Reinhard J.; Batista, Victor S.; Tully, John C.

    2016-05-01

    An accurate description of nonadiabatic energy relaxation is crucial for modeling atomistic dynamics at metal surfaces. Interfacial energy transfer due to electron-hole pair excitations coupled to motion of molecular adsorbates is often simulated by Langevin molecular dynamics with electronic friction. Here, we present calculations of the full electronic friction tensor by using first order time-dependent perturbation theory at the density functional theory level. We show that the friction tensor is generally anisotropic and nondiagonal, as found for hydrogen atom on Pd(100) and CO on Cu(100) surfaces. This implies that electron-hole pair induced nonadiabatic coupling at metal surfaces leads to friction-induced mode coupling, therefore, opening an additional channel for energy redistribution. We demonstrate the robustness and accuracy of our results by direct comparison to established methods and experimental data.

  4. Electronic energy transfer in model photosynthetic systems: Markovian vs. non-Markovian dynamics.

    PubMed

    Singh, Navinder; Brumer, Paul

    2011-01-01

    A simple numerical algorithm for solving the non-Markovian master equation in the second Born approximation is developed and used to propagate the traditional dimer system that models electronic energy transfer in photosynthetic systems. Specifically, the coupled integro-differential equations for the reduced density matrix are solved by an efficient auxiliary function method in both the energy and site representations. In addition to giving exact results to this order, the approach allows us to access the range of the reorganization energy and decay rates of the phonon auto-correlation function for which the Markovian Redfield theory and the second-order approximation is useful. For example, the use of Redfield theory for lambda > 10 cm(-1) in Fenna-Mathews-Olson (FMO) type systems is shown to be fundamentally inaccurate. PMID:22452072

  5. Pressure drop and heat transfer in turbulent non-Newtonian pipe flow of advanced energy transmission fluids

    NASA Astrophysics Data System (ADS)

    Choi, U. S.; Liu, K. V.; Kasza, K. E.

    1988-03-01

    Argonne National Laboratory (ANL), under sponsorship of the U.S. Department of Energy, is making significant progress on the development of advanced energy transmission fluids for thermal systems, in particular district heating and cooling systems. ANL has identified two concepts for developing advanced energy transmission fluids. Tests have been conducted at ANL to prove these concepts. This paper presents experimental results and discusses the degradation behavior of linear polymer additives and the flow and heat transfer characteristics of non-melting slurry flows. The experimental data obtained in this study provide support for the use of friction reducing additives and slurries in thermal system applications.

  6. Local Measurement of Fuel Energy Deposition and Heat Transfer Environment During Fuel Lifetime Using Controlled Calorimetry

    SciTech Connect

    Don W. Miller; Andrew Kauffmann; Eric Kreidler; Dongxu Li; Hanying Liu; Daniel Mills; Thomas D. Radcliff; Joseph Talnagi

    2001-12-31

    A comprehensive description of the accomplishments of the DOE grant titled, ''Local Measurement of Fuel Energy Deposition and Heat Transfer Environment During Fuel Lifetime using Controlled Calorimetry''.

  7. Organic Solar Cells: Understanding the Role of Förster Resonance Energy Transfer

    PubMed Central

    Feron, Krishna; Belcher, Warwick J.; Fell, Christopher J.; Dastoor, Paul C.

    2012-01-01

    Organic solar cells have the potential to become a low-cost sustainable energy source. Understanding the photoconversion mechanism is key to the design of efficient organic solar cells. In this review, we discuss the processes involved in the photo-electron conversion mechanism, which may be subdivided into exciton harvesting, exciton transport, exciton dissociation, charge transport and extraction stages. In particular, we focus on the role of energy transfer as described by Förster resonance energy transfer (FRET) theory in the photoconversion mechanism. FRET plays a major role in exciton transport, harvesting and dissociation. The spectral absorption range of organic solar cells may be extended using sensitizers that efficiently transfer absorbed energy to the photoactive materials. The limitations of Förster theory to accurately calculate energy transfer rates are discussed. Energy transfer is the first step of an efficient two-step exciton dissociation process and may also be used to preferentially transport excitons to the heterointerface, where efficient exciton dissociation may occur. However, FRET also competes with charge transfer at the heterointerface turning it in a potential loss mechanism. An energy cascade comprising both energy transfer and charge transfer may aid in separating charges and is briefly discussed. Considering the extent to which the photo-electron conversion efficiency is governed by energy transfer, optimisation of this process offers the prospect of improved organic photovoltaic performance and thus aids in realising the potential of organic solar cells. PMID:23235328

  8. Heat Transfer Analysis of Encapsulated Phase Change Materials for Thermal Energy Storage

    NASA Astrophysics Data System (ADS)

    Elmozughi, Ali F.

    process are investigated. The charging and discharging into and from the capsule wall is simulated for different boundary conditions and is applied with both laminar and turbulent flow conditions. Computational models are conducted by applying an enthalpy -- porosity method and volume of fluid method (VOF) to calculate the transport phenomena within the PCM capsule, including an internal air void. Energy storage and retrieval in different sized capsules is simulated. A cylindrical shaped EPCM capsule or tube is considered in simulations using both gas (air) and liquid (Therminol/VP-1) as the heat transfer fluid in a cross flow arrangement. The presence of the void has profound effects on the thermal response of the EPCM during both energy storage and retrieval process. Melting and solidification per unit mass of the PCM takes longer when the void is present. Additionally, due to material properties and the lack of convective effects, the solidification process is much slower than the melting process. One of the most significant outcomes of the present work is that the thermal energy module in the power generation systems has to be designed properly by careful consideration of the heat transfer from HTF to the EPCM as well as the heat transport inside the EPCM.

  9. Shell-to-shell energy transfer in magnetohydrodynamics. I. Steady state turbulence.

    PubMed

    Alexakis, Alexandros; Mininni, Pablo D; Pouquet, Annick

    2005-10-01

    We investigate the transfer of energy from large scales to small scales in fully developed forced three-dimensional magnetohydrodynamics (MHD) turbulence by analyzing the results of direct numerical simulations in the absence of an externally imposed uniform magnetic field. Our results show that the transfer of kinetic energy from large scales to kinetic energy at smaller scales and the transfer of magnetic energy from large scales to magnetic energy at smaller scales are local, as is also found in the case of neutral fluids and in a way that is compatible with the Kolmogorov theory of turbulence. However, the transfer of energy from the velocity field to the magnetic field is a highly nonlocal process in Fourier space. Energy from the velocity field at large scales can be transferred directly into small-scale magnetic fields without the participation of intermediate scales. Some implications of our results to MHD turbulence modeling are also discussed. PMID:16383527

  10. Non-Radiative Energy Transfer Mediated by Hybrid Light-Matter States.

    PubMed

    Zhong, Xiaolan; Chervy, Thibault; Wang, Shaojun; George, Jino; Thomas, Anoop; Hutchison, James A; Devaux, Eloise; Genet, Cyriaque; Ebbesen, Thomas W

    2016-05-17

    We present direct evidence of enhanced non-radiative energy transfer between two J-aggregated cyanine dyes strongly coupled to the vacuum field of a cavity. Excitation spectroscopy and femtosecond pump-probe measurements show that the energy transfer is highly efficient when both the donor and acceptor form light-matter hybrid states with the vacuum field. The rate of energy transfer is increased by a factor of seven under those conditions as compared to the normal situation outside the cavity, with a corresponding effect on the energy transfer efficiency. The delocalized hybrid states connect the donor and acceptor molecules and clearly play the role of a bridge to enhance the rate of energy transfer. This finding has fundamental implications for coherent energy transport and light-energy harvesting. PMID:27072296

  11. The role of charge-transfer states in energy transfer and dissipation within natural and artificial bacteriochlorophyll-proteins

    PubMed Central

    Wahadoszamen, Md.; Margalit, Iris; Ara, Anjue Mane; van Grondelle, Rienk; Noy, Dror

    2014-01-01

    Understanding how specific protein environments affect the mechanisms of non-radiative energy dissipation within densely assembled chlorophylls in photosynthetic protein complexes is of great interest to the construction of bioinspired solar energy conversion devices. Mixing of charge-transfer and excitonic states in excitonically interacting chlorophylls was implicated in shortening excited states lifetimes but its relevance to active control of energy dissipation in natural systems is under considerable debate. Here we show that the degree of fluorescence quenching in two similar pairs of excitonically interacting bacteriochlorophyll derivatives is directly associated with increasing charge transfer character in the excited state, and that the protein environment may control non-radiative dissipation by affecting the mixing of charge transfer and excitonic states. The capability of local protein environments to determine the fate of excited states, and thereby to confer different functionalities to excitonically coupled dimers substantiates the dimer as the basic functional element of photosynthetic enzymes. PMID:25342121

  12. Interaction mechanism for energy transfer from Ce to Tb ions in silica

    NASA Astrophysics Data System (ADS)

    Seed Ahmed, H. A. A.; Chae, W. S.; Ntwaeaborwa, O. M.; Kroon, R. E.

    2016-01-01

    Energy transfer phenomena can play an important role in the development of luminescent materials. In this study, numerical simulations based on theoretical models of non-radiative energy transfer are compared to experimental results for Ce, Tb co-doped silica. Energy transfer from the donor (Ce) to the acceptor (Tb) resulted in a decrease in the Ce luminescence intensity and lifetime. The decrease in intensity corresponded best with the energy transfer models based on the exchange interaction and the dipole-dipole interaction. The critical transfer distance obtained from the fitting using both these models is around 2 nm. Since the exchange interaction requires a distance shorter than 1 nm to occur, the mechanism most likely to account for the energy transfer is concluded to be the dipole-dipole interaction. This is supported by an analysis of the lifetime data.

  13. Gamma radiation induced synthesis of poly(N-isopropylacrylamide) mediated by Reversible Addition-Fragmentation Chain Transfer (RAFT) process

    NASA Astrophysics Data System (ADS)

    Kiraç, Feyza; Güven, Olgun

    2015-07-01

    Poly(N-isopropylacrylamide) (PNiPAAm) is synthesized by gamma radiation induced Reversible Addition-Fragmentation Chain Transfer (RAFT) polymerization. The monomer is polymerized in the presence of two different trithiocarbonate-based RAFT agents i.e., Cyanomethyldodecyltrithiocarbonate (CDTC) and 2-(Dodecylthiocarbonothioylthio)-2-methylpropionic acid (DMPA) in dimethylformamide (DMF) at room temperature under nitrogen atmosphere. Number-average molecular weights (Mn) and dispersities of the polymers were determined by Size Exclusion Chromatography (SEC). Dispersities (Ɖ) of the resulting polymers are narrow, i.e., Ɖ≤1.18, indicating the occurrence of well-controlled polymerization via radiation induced RAFT process. %Conversion is determined by gravimetric method and also confirmed by Proton Nuclear Magnetic Resonance (1H-NMR) Spectroscopy. By selecting proper [Monomer]/[RAFT] ratio and controlling conversion it is possible to synthesize PNiPAAm in the molecular weight range of 2400-72400 with extremely low molecular weight distributions with the anticipation of preparing corresponding size-controlled nanogels. The phase transition of PNiPAAm with low dispersity synthesized by RAFT is sharper than PNiPAAm synthesized by free radical polymerization.

  14. The transfer between electron bulk kinetic energy and thermal energy in collisionless magnetic reconnection

    SciTech Connect

    Lu, San; Lu, Quanming; Huang, Can; Wang, Shui

    2013-06-15

    By performing two-dimensional particle-in-cell simulations, we investigate the transfer between electron bulk kinetic and electron thermal energy in collisionless magnetic reconnection. In the vicinity of the X line, the electron bulk kinetic energy density is much larger than the electron thermal energy density. The evolution of the electron bulk kinetic energy is mainly determined by the work done by the electric field force and electron pressure gradient force. The work done by the electron gradient pressure force in the vicinity of the X line is changed to the electron enthalpy flux. In the magnetic island, the electron enthalpy flux is transferred to the electron thermal energy due to the compressibility of the plasma in the magnetic island. The compression of the plasma in the magnetic island is the consequence of the electromagnetic force acting on the plasma as the magnetic field lines release their tension after being reconnected. Therefore, we can observe that in the magnetic island the electron thermal energy density is much larger than the electron bulk kinetic energy density.

  15. Luminescence and energy transfer from açai oil in polystyrene matrix

    NASA Astrophysics Data System (ADS)

    Pereira, N. S.; Monte, A. F. G.; Reis, A.; Morais, P. C.; Sales, M. J. A.

    2010-07-01

    This work aims to examine the optical properties of the açai oil embedded in polystyrene (PS) matrix. By doing this, we expect to introduce new properties in the polymeric matrix and check their availability for the construction of light-emitting devices. Energy transfer experiments were conducted using a confocal microscope adapted for scanning the luminescence on the sample surface with micrometer spatial resolution. The luminescence from the sample was provided by the large amount of chlorophyll molecules found in the açai oil. Two main emission peaks were observed, one peaked at 621 nm and the other at 654 nm. The photon migration length increases by increasing the oil concentration. The migration length is larger at 654 nm compared to that at 621 nm wavelength, showing the energy transfer from higher energy states to lower energy states. Indeed, addition of açai oil changed the optical properties of the PS template, thus making this material a promising candidate for optical applications.

  16. 77 FR 2293 - AmeriGas Propane, L.P., AmeriGas Propane, Inc., Energy Transfer Partners, L.P., and Energy...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-01-17

    ... AmeriGas Propane, L.P., AmeriGas Propane, Inc., Energy Transfer Partners, L.P., and Energy Transfer...'') with AmeriGas Propane, L.P. (``AmeriGas''), AmeriGas Propane, Inc., Energy Transfer Partners, L.P. (``ETP''), and Energy Transfer Partners GP, L.P. (``ETP GP''), which is designed to guard...

  17. Peculiarities of collisional excitation transfer with excited screened energy levels of atoms

    SciTech Connect

    Gerasimov, V. A.; Gerasimov, V. V.; Pavlinskiy, A. V.

    2007-09-15

    We report an experimental discovery of deviations from the known regularities in collisional excitation transfer processes for metal atoms. The collisional excitation transfer with excited screened energy levels of thulium and dysprosium atoms is studied. The selecting role of the screening 6s shell in collisional excitation transfer is shown.

  18. Rapid and facile ratiometric detection of an anthrax biomarker by regulating energy transfer process in bio-metal-organic framework.

    PubMed

    Zhang, Yihe; Li, Bin; Ma, Heping; Zhang, Liming; Zheng, Youxuan

    2016-11-15

    A ratiometric fluorescent sensor based on luminescent bio-metal-organic framework was prepared by exchanging both Tb(3+) and Eu(3+) cations into anionic bio-MOF-1. Due to a highly efficient energy transfer from Tb(3+) to Eu(3+) (>89%), emission color of Tb/Eu@bio-MOF-1 was orange-red even though Tb(3+) was the dominant content in this Tb/Eu co-doping material. More interestingly, this energy transfer process could be modulated by dipicolinic acid (DPA), an unique biomarker for bacillus spores. With DPA addition, corresponding DPA-to-Tb(3+) energy transfer was gradually enhanced while the energy transfer from Tb(3+) to Eu(3+) was significantly weakened. By regulating the energy transfer process in Tb/Eu@bio-MOF-1, visual colorimetric sensing of DPA in porous MOF was realized for the first time. Detection limit of Tb/Eu@bio-MOF-1 for DPA was 34nM, which was much lower than an infectious dosage of Bacillus anthracis spores (60μM) for human being. Besides, Tb/Eu@bio-MOF-1 showed a remarkable selectivity over other aromatic ligands and amino acids. More importantly, this porous ratiometric sensor worked equally well in human serum. These particularly attractive features of Tb/Eu@bio-MOF-1 made the direct, rapid and naked-eye detection of DPA for practical application possible. PMID:27183278

  19. Complete and Partial Transfer of Energy in Bremsstrahlung Should Include Rotational and Vibrational Kinetic Energies

    NASA Astrophysics Data System (ADS)

    Brekke, Stewart

    2015-03-01

    In complete braking achievement the rotational and vibrational as well as the linear kinetic energies of the charged particle results in a photon: hν = 1 / 2 mv2 + 1 / 2 Iω2 + 1 / 2 kx2 . In partial transfer of kinetic energies of the deccelerating particle the resulting photon is hν = [(1 / 2 mv2) 1 +(1 / 2 Iω2) 1 +(1 / 2 kx2) 1 ] - [(1 / 2 mv2) 2 +(1 / 2 Iω2) 2 +(1 / 2 kx2) 2 ] . The linear kinetic energy of the charged particle is 1 / 2 mv2 , the rotational kinetic energy is 1 / 2 Iω2 and the vibrational kinetic energy is given by 1 / 2 kx2 .

  20. Low-energy plasma immersion ion implantation to induce DNA transfer into bacterial E. coli

    NASA Astrophysics Data System (ADS)

    Sangwijit, K.; Yu, L. D.; Sarapirom, S.; Pitakrattananukool, S.; Anuntalabhochai, S.

    2015-12-01

    Plasma immersion ion implantation (PIII) at low energy was for the first time applied as a novel biotechnology to induce DNA transfer into bacterial cells. Argon or nitrogen PIII at low bias voltages of 2.5, 5 and 10 kV and fluences ranging from 1 × 1012 to 1 × 1017 ions/cm2 treated cells of Escherichia coli (E. coli). Subsequently, DNA transfer was operated by mixing the PIII-treated cells with DNA. Successes in PIII-induced DNA transfer were demonstrated by marker gene expressions. The induction of DNA transfer was ion-energy, fluence and DNA-size dependent. The DNA transferred in the cells was confirmed functioning. Mechanisms of the PIII-induced DNA transfer were investigated and discussed in terms of the E. coli cell envelope anatomy. Compared with conventional ion-beam-induced DNA transfer, PIII-induced DNA transfer was simpler with lower cost but higher efficiency.

  1. Nonresonant energy transfers independent on the phonon densities in polyatomic liquids.

    PubMed

    Chen, Hailong; Zhang, Qiang; Guo, Xunmin; Wen, Xiewen; Li, Jiebo; Zhuang, Wei; Zheng, Junrong

    2015-01-29

    Energy-gap-dependent vibrational-energy transfers among the nitrile stretches of KSCN/KS(13)CN/KS(13)C(15)N in D2O, DMF, and formamide liquid solutions at room temperature were measured by the vibrational-energy-exchange method. The energy transfers are slower with a larger energy donor/acceptor gap, independent of the calculated instantaneous normal mode ("phonons" in liquids) densities or the terahertz absorption spectra. The energy-gap dependences of the nonresonant energy transfers cannot be described by phonon compensation mechanisms with the assumption that phonons are the instantaneous normal modes of the liquids. Instead, the experimental energy-gap dependences can be quantitatively reproduced by the dephasing mechanism. A simple theoretical derivation shows that the fast molecular motions in liquids randomize the modulations on the energy donor and acceptor by phonons and diminish the phonon compensation efficiency on energy transfer. Estimations based on the theoretical derivations suggest that, for most nonresonant intermolecular vibrational-energy transfers in liquids with energy gaps smaller than the thermal energy, the dephasing mechanism dominates the energy-transfer process. PMID:25549247

  2. Nonresonant and resonant mode-specific intermolecular vibrational energy transfers in electrolyte aqueous solutions.

    PubMed

    Bian, Hongtao; Chen, Hailong; Li, Jiebo; Wen, Xiewen; Zheng, Junrong

    2011-10-27

    The donor/acceptor energy mismatch and vibrational coupling strength dependences of interionic vibrational energy transfer kinetics in electrolyte aqueous solutions were investigated with ultrafast multiple-dimensional vibrational spectroscopy. An analytical equation derived from the Fermi's Golden rule that correlates molecular structural parameters and vibrational energy transfer kinetics was found to be able to describe the intermolecular mode specific vibrational energy transfer. Under the assumption of the dipole-dipole approximation, the distance between anions in the aqueous solutions was obtained from the vibrational energy transfer measurements, confirmed with measurements on the corresponding crystalline samples. The result demonstrates that the mode-specific vibrational energy transfer method holds promise as an angstrom molecular ruler. PMID:21916443

  3. Generalized Förster-Dexter theory of photoinduced intramolecular energy transfer

    NASA Astrophysics Data System (ADS)

    Lin, S. H.; Xiao, W. Z.; Dietz, W.

    1993-05-01

    In this paper, we generalize the Förster-Dexter theory to treat photoinduced electronic energy transfer for a system in dense media and for an isolated system (i.e., a system in the collision-free condition). Instead of expressing the rate of energy transfer in terms of spectral overlap, we obtain the expression of the energy-transfer rate constant by evaluating a Fourier integral using the saddle-point method. In this way, the energy-gap dependence and the effect of temperature and the isotope effect on the energy transfer can be easily studied. The effect of bridge groups connecting between donor and acceptor on the energy transfer is also studied.

  4. Efficient near-field wireless energy transfer using adiabatic system variations

    DOEpatents

    Hamam, Rafif E.; Karalis, Aristeidis; Joannopoulos, John D.; Soljacic, Marin

    2013-01-29

    Disclosed is a method for transferring energy wirelessly including transferring energy wirelessly from a first resonator structure to an intermediate resonator structure, wherein the coupling rate between the first resonator structure and the intermediate resonator structure is .kappa..sub.1B, transferring energy wirelessly from the intermediate resonator structure to a second resonator structure, wherein the coupling rate between the intermediate resonator structure and the second resonator structure is .kappa..sub.B2, and during the wireless energy transfers, adjusting at least one of the coupling rates .kappa..sub.1B and .kappa..sub.B2 to reduce energy accumulation in the intermediate resonator structure and improve wireless energy transfer from the first resonator structure to the second resonator structure through the intermediate resonator structure.

  5. Efficient near-field wireless energy transfer using adiabatic system variations

    DOEpatents

    Hamam, Rafif E; Karalis, Aristeidis; Joannopoulos, John D; Soljacic, Marin

    2014-09-16

    Disclosed is a method for transferring energy wirelessly including transferring energy wirelessly from a first resonator structure to an intermediate resonator structure, wherein the coupling rate between the first resonator structure and the intermediate resonator structure is .kappa..sub.1B, transferring energy wirelessly from the intermediate resonator structure to a second resonator structure, wherein the coupling rate between the intermediate resonator structure and the second resonator structure is .kappa..sub.B2, and during the wireless energy transfers, adjusting at least one of the coupling rates .kappa..sub.1B and .kappa..sub.B2 to reduce energy accumulation in the intermediate resonator structure and improve wireless energy transfer from the first resonator structure to the second resonator structure through the intermediate resonator structure.

  6. Single-collision studies of energy transfer and chemical reaction

    SciTech Connect

    Valentini, J.J.

    1993-12-01

    The research focus in this group is state-to-state dynamics of reaction and energy transfer in collisions of free radicals such as H, OH, and CH{sub 3} with H{sub 2}, alkanes, alcohols and other hydrogen-containing molecules. The motivation for the work is the desire to provide a detailed understanding of the chemical dynamics of prototype reactions that are important in the production and utilization of energy sources, most importantly in combustion. The work is primarily experimental, but with an important and growing theoretical/computational component. The focus of this research program is now on reactions in which at least one of the reactants and one of the products is polyatomic. The objective is to determine how the high dimensionality of the reactants and products differentiates such reactions from atom + diatom reactions of the same kinematics and energetics. The experiments use highly time-resolved laser spectroscopic methods to prepare reactant states and analyze the states of the products on a single-collision time scale. The primary spectroscopic tool for product state analysis is coherent anti-Stokes Raman scattering (CARS) spectroscopy. CARS is used because of its generality and because the extraction of quantum state populations from CARS spectra is straightforward. The combination of the generality and easy analysis of CARS makes possible absolute cross section measurements (both state-to-state and total), a particularly valuable capability for characterizing reactive and inelastic collisions. Reactant free radicals are produced by laser photolysis of appropriate precursors. For reactant vibrational excitation stimulated Raman techniques are being developed and implemented.

  7. Modeling the Transfer Function for the Dark Energy Survey

    DOE PAGESBeta

    Chang, C.

    2015-03-04

    We present a forward-modeling simulation framework designed to model the data products from the Dark Energy Survey (DES). This forward-model process can be thought of as a transfer function—a mapping from cosmological/astronomical signals to the final data products used by the scientists. Using output from the cosmological simulations (the Blind Cosmology Challenge), we generate simulated images (the Ultra Fast Image Simulator) and catalogs representative of the DES data. In this work we demonstrate the framework by simulating the 244 deg2 coadd images and catalogs in five bands for the DES Science Verification data. The simulation output is compared with themore » corresponding data to show that major characteristics of the images and catalogs can be captured. We also point out several directions of future improvements. Two practical examples—star-galaxy classification and proximity effects on object detection—are then used to illustrate how one can use the simulations to address systematics issues in data analysis. With clear understanding of the simplifications in our model, we show that one can use the simulations side-by-side with data products to interpret the measurements. This forward modeling approach is generally applicable for other upcoming and future surveys. It provides a powerful tool for systematics studies that is sufficiently realistic and highly controllable.« less

  8. Modeling the Transfer Function for the Dark Energy Survey

    NASA Astrophysics Data System (ADS)

    Chang, C.; Busha, M. T.; Wechsler, R. H.; Refregier, A.; Amara, A.; Rykoff, E.; Becker, M. R.; Bruderer, C.; Gamper, L.; Leistedt, B.; Peiris, H.; Abbott, T.; Abdalla, F. B.; Balbinot, E.; Banerji, M.; Bernstein, R. A.; Bertin, E.; Brooks, D.; Carnero, A.; Desai, S.; da Costa, L. N.; Cunha, C. E.; Eifler, T.; Evrard, A. E.; Fausti Neto, A.; Gerdes, D.; Gruen, D.; James, D.; Kuehn, K.; Maia, M. A. G.; Makler, M.; Ogando, R.; Plazas, A.; Sanchez, E.; Santiago, B.; Schubnell, M.; Sevilla-Noarbe, I.; Smith, C.; Soares-Santos, M.; Suchyta, E.; Swanson, M. E. C.; Tarle, G.; Zuntz, J.

    2015-03-01

    We present a forward-modeling simulation framework designed to model the data products from the Dark Energy Survey (DES). This forward-model process can be thought of as a transfer function—a mapping from cosmological/astronomical signals to the final data products used by the scientists. Using output from the cosmological simulations (the Blind Cosmology Challenge), we generate simulated images (the Ultra Fast Image Simulator) and catalogs representative of the DES data. In this work we demonstrate the framework by simulating the 244 deg2 coadd images and catalogs in five bands for the DES Science Verification data. The simulation output is compared with the corresponding data to show that major characteristics of the images and catalogs can be captured. We also point out several directions of future improvements. Two practical examples—star-galaxy classification and proximity effects on object detection—are then used to illustrate how one can use the simulations to address systematics issues in data analysis. With clear understanding of the simplifications in our model, we show that one can use the simulations side-by-side with data products to interpret the measurements. This forward modeling approach is generally applicable for other upcoming and future surveys. It provides a powerful tool for systematics studies that is sufficiently realistic and highly controllable.

  9. Mutation induction by charged particles of defined linear energy transfer.

    PubMed

    Hei, T K; Chen, D J; Brenner, D J; Hall, E J

    1988-07-01

    The mutagenic potential of charged particles of defined linear energy transfer (LET) was assessed using the hypoxanthine-guanine phosphoribosyl transferase locus (HGPRT) in primary human fibroblasts. Exponentially growing cultures of early passaged fibroblasts were grown as monolayers on thin mylar sheets and were irradiated with accelerated protons, deuterons or helium-3 ions. The mutation rates were compared with those generated by 137Cs gamma-rays. LET values for charged particles accelerated at the Radiological Research Accelerator Facility, using the track segment mode, ranged from 10 to 150 keV/micron. After irradiation, cells were trypsinized, subcultured and assayed for both cytotoxicity and 6-thioguanine resistance. For gamma-rays, and for the charged particles of lower LET, the dose-response curves for cell survival were characterized by a marked initial shoulder, but approximated to an exponential function of dose for higher LETs. Mutation frequencies, likewise, showed a direct correlation to LET over the dose range examined. Relative biological effectiveness (RBE) for mutagenesis, based on the initial slopes of the dose-response curves, ranged from 1.30 for 10 keV/micron protons to 9.40 for 150 keV/micron helium-3 ions. Results of the present studies indicate that high-LET radiations, apart from being efficient inducers of cell lethality, are even more efficient in mutation induction as compared to low-LET ionizing radiation. These data are consistent with results previously obtained with both rodent and human fibroblast cell lines. PMID:3383341

  10. Fluorescence resonance energy transfer in the studies of guanine quadruplexes.

    PubMed

    Juskowiak, Bernard; Takenaka, Shigeori

    2006-01-01

    A guanine (G)-quadruplex DNA motif has recently emerged as a biologically important structure that is believed to interfere with telomere maintenance by telomerase. G-quadruplexes exhibit four-stranded structures containing one or more nucleic acid strands with central channel able to accommodate metal cations. Coordination of certain metal cations stabilizes G-quadruplex as with some promising small organic molecules that promote the formation and/or stabilization of G-quadruplex. Among many techniques employed to explore properties of G-quadruplexes, the fluorescence resonance energy transfer (FRET) technique has been recognized as a powerful tool to study G-quadruplex formation. This review summarizes the current developments in the uses of FRET technique for the fundamental structural investigations and its practical applications. Applications include FRET-based selection of efficient quadruplex-binding ligands, design of a nanomolecular machine, and a molecular aptamer beacon for protein recognition. We also describe a technique for detection of potassium ions in aqueous solution with the use of quadruplex-based sensor (potassium-sensing oligonucleotide). PMID:16785636

  11. Ultrafast energy transfer in water-AOT reverse micelles.

    PubMed

    Cringus, Dan; Bakulin, Artem; Lindner, Jörg; Vöhringer, Peter; Pshenichnikov, Maxim S; Wiersma, Douwe A

    2007-12-27

    A spectroscopic investigation of the vibrational dynamics of water in a geometrically confined environment is presented. Reverse micelles of the ternary microemulsion H2O/AOT/n-octane (AOT = bis-2-ethylhexyl sulfosuccinate or aerosol-OT) with diameters ranging from 1 to 10 nm are used as a model system for nanoscopic water droplets surrounded by a soft-matter boundary. Femtosecond nonlinear infrared spectroscopy in the OH-stretching region of H2O fully confirms the core/shell model, in which the entrapped water molecules partition onto two molecular subensembles: a bulk-like water core and a hydration layer near the ionic surfactant headgroups. These two distinct water species display different relaxation kinetics, as they do not exchange vibrational energy. The observed spectrotemporal ultrafast response exhibits a local character, indicating that the spatial confinement influences approximately one molecular layer located near the water-amphiphile boundary. The core of the encapsulated water droplet is similar in its spectroscopic properties to the bulk phase of liquid water, i.e., it does not display any true confinement effects such as droplet-size-dependent vibrational lifetimes or rotational correlation times. Unlike in bulk water, no intermolecular transfer of OH-stretching quanta occurs among the interfacial water molecules or from the hydration shell to the bulk-like core, indicating that the hydrogen bond network near the H2O/AOT interface is strongly disrupted. PMID:18047308

  12. Modeling the Transfer Function for the Dark Energy Survey

    SciTech Connect

    Chang, C.

    2015-03-04

    We present a forward-modeling simulation framework designed to model the data products from the Dark Energy Survey (DES). This forward-model process can be thought of as a transfer function—a mapping from cosmological/astronomical signals to the final data products used by the scientists. Using output from the cosmological simulations (the Blind Cosmology Challenge), we generate simulated images (the Ultra Fast Image Simulator) and catalogs representative of the DES data. In this work we demonstrate the framework by simulating the 244 deg2 coadd images and catalogs in five bands for the DES Science Verification data. The simulation output is compared with the corresponding data to show that major characteristics of the images and catalogs can be captured. We also point out several directions of future improvements. Two practical examples—star-galaxy classification and proximity effects on object detection—are then used to illustrate how one can use the simulations to address systematics issues in data analysis. With clear understanding of the simplifications in our model, we show that one can use the simulations side-by-side with data products to interpret the measurements. This forward modeling approach is generally applicable for other upcoming and future surveys. It provides a powerful tool for systematics studies that is sufficiently realistic and highly controllable.

  13. Concentric Förster resonance energy transfer imaging.

    PubMed

    Wu, Miao; Algar, W Russ

    2015-08-18

    Concentric Förster resonance energy transfer (cFRET) configurations based on semiconductor quantum dots (QDs) are promising probes for biological sensing because they offer multiplexing capability in a single vector with robust ratiometric detection by exploiting a network of FRET pathways. To expand the scope and utility of cFRET probes, it is necessary to develop and validate cFRET imaging methodology. In this technical note, we present such a methodology using a protease-sensitive cFRET configuration that comprises a green-emitting QD, Alexa Fluor 555 (A555), and Alexa Fluor 647 (A647). Photoluminescence (PL) images were acquired with three filter-based emission channels to permit measurement of A555/QD and A647/QD PL ratios. With reference to calibration samples, these PL ratios were used to calculate quantitative progress curves for proteolytic activity in regions of interest in the acquired images. Importantly, the imaging methodology reproduces quantitative results obtained with a monochromator-based fluorescence plate reader. Spatiotemporal resolution is demonstrated by tracking the activity of two prototypical proteases, trypsin and chymotrypsin, as they diffuse down the length of a capillary. This methodology is expected to enable the future use of cFRET probes for cellular sensing and other imaging assays. PMID:26214686

  14. Resonant energy transfer of triplet excitons from pentacene to PbSe nanocrystals

    NASA Astrophysics Data System (ADS)

    Tabachnyk, Maxim; Ehrler, Bruno; Gélinas, Simon; Böhm, Marcus L.; Walker, Brian J.; Musselman, Kevin P.; Greenham, Neil C.; Friend, Richard H.; Rao, Akshay

    2014-11-01

    The efficient transfer of energy between organic and inorganic semiconductors is a widely sought after property, but has so far been limited to the transfer of spin-singlet excitons. Here we report efficient resonant-energy transfer of molecular spin-triplet excitons from organic semiconductors to inorganic semiconductors. We use ultrafast optical absorption spectroscopy to track the dynamics of triplets, generated in pentacene through singlet exciton fission, at the interface with lead selenide (PbSe) nanocrystals. We show that triplets transfer to PbSe rapidly (<1 ps) and efficiently, with 1.9 triplets transferred for every photon absorbed in pentacene, but only when the bandgap of the nanocrystals is close to resonance (±0.2 eV) with the triplet energy. Following triplet transfer, the excitation can undergo either charge separation, allowing photovoltaic operation, or radiative recombination in the nanocrystal, enabling luminescent harvesting of triplet exciton energy in light-emitting structures.

  15. Resonant energy transfer of triplet excitons from pentacene to PbSe nanocrystals.

    PubMed

    Tabachnyk, Maxim; Ehrler, Bruno; Gélinas, Simon; Böhm, Marcus L; Walker, Brian J; Musselman, Kevin P; Greenham, Neil C; Friend, Richard H; Rao, Akshay

    2014-11-01

    The efficient transfer of energy between organic and inorganic semiconductors is a widely sought after property, but has so far been limited to the transfer of spin-singlet excitons. Here we report efficient resonant-energy transfer of molecular spin-triplet excitons from organic semiconductors to inorganic semiconductors. We use ultrafast optical absorption spectroscopy to track the dynamics of triplets, generated in pentacene through singlet exciton fission, at the interface with lead selenide (PbSe) nanocrystals. We show that triplets transfer to PbSe rapidly (<1 ps) and efficiently, with 1.9 triplets transferred for every photon absorbed in pentacene, but only when the bandgap of the nanocrystals is close to resonance (±0.2 eV) with the triplet energy. Following triplet transfer, the excitation can undergo either charge separation, allowing photovoltaic operation, or radiative recombination in the nanocrystal, enabling luminescent harvesting of triplet exciton energy in light-emitting structures. PMID:25282509

  16. Electronic resonance with anticorrelated pigment vibrations drives photosynthetic energy transfer outside the adiabatic framework

    PubMed Central

    Tiwari, Vivek; Peters, William K.; Jonas, David M.

    2013-01-01

    The delocalized, anticorrelated component of pigment vibrations can drive nonadiabatic electronic energy transfer in photosynthetic light-harvesting antennas. In femtosecond experiments, this energy transfer mechanism leads to excitation of delocalized, anticorrelated vibrational wavepackets on the ground electronic state that exhibit not only 2D spectroscopic signatures attributed to electronic coherence and oscillatory quantum energy transport but also a cross-peak asymmetry not previously explained by theory. A number of antennas have electronic energy gaps matching a pigment vibrational frequency with a small vibrational coordinate change on electronic excitation. Such photosynthetic energy transfer steps resemble molecular internal conversion through a nested intermolecular funnel. PMID:23267114

  17. Reorganization energy of electron transfer processes in ionic fluids: A molecular Debye-Hueckel approach

    SciTech Connect

    Xiao Tiejun; Song Xueyu

    2013-03-21

    The reorganization energy of electron transfer processes in ionic fluids is studied under the linear response approximation using a molecule Debye-Hueckel theory. Reorganization energies of some model reactants of electron transfer reactions in molten salts are obtained from molecular simulations and a molecule Debye-Hueckel approach. Good agreements between simulation results and the results from our theoretical calculations using the same model Hamiltonian are found. Applications of our theory to electron transfer reactions in room temperature ionic liquids further demonstrate that our theoretical approach presents a reliable and accurate methodology for the estimation of reorganization energies of electron transfer reactions in ionic fluids.

  18. Cyanine dyes with high-absorbance cross section as donor chromophores in energy transfer labels

    DOEpatents

    Glazer, Alexander N.; Mathies, Richard A.; Hung, Su-Chun; Ju, Jingyue

    1998-01-01

    Cyanine dyes are used as the donor fluorophore in energy transfer labels in which light energy is absorbed by a donor fluorophore and transferred to an acceptor fluorophore which responds to the transfer by emitting fluorescent light for detection. The cyanine dyes impart an unusually high sensitivity to the labels thereby improving their usefulness in a wide variety of biochemical procedures, particularly nucleic acid sequencing, nucleic acid fragment sizing, and related procedures.

  19. Methods of sequencing and detection using energy transfer labels with cyanine dyes as donor chromophores

    DOEpatents

    Glazer, Alexander N.; Mathies, Richard A.; Hung, Su-Chun; Ju, Jingyue

    2000-01-01

    Cyanine dyes are used as the donor fluorophore in energy transfer labels in which light energy is absorbed by a donor fluorophore and transferred to an acceptor fluorophore which responds to the transfer by emitting fluorescent light for detection. The cyanine dyes impart an unusually high sensitivity to the labels thereby improving their usefulness in a wide variety of biochemical procedures, particularly nucleic acid sequencing, nucleic acid fragment sizing, and related procedures.

  20. Cyanine dyes with high-absorbance cross section as donor chromophores in energy transfer labels

    DOEpatents

    Glazer, A.N.; Mathies, R.A.; Hung, S.C.; Ju, J.

    1998-12-29

    Cyanine dyes are used as the donor fluorophore in energy transfer labels in which light energy is absorbed by a donor fluorophore and transferred to an acceptor fluorophore which responds to the transfer by emitting fluorescent light for detection. The cyanine dyes impart an unusually high sensitivity to the labels thereby improving their usefulness in a wide variety of biochemical procedures, particularly nucleic acid sequencing, nucleic acid fragment sizing, and related procedures. 22 figs.

  1. Forster resonance energy transfer in the system of human serum albumin-xanthene dyes

    NASA Astrophysics Data System (ADS)

    Kochubey, V. I.; Pravdin, A. B.; Melnikov, A. G.; Konstantinova, I.; Alonova, I. V.

    2016-04-01

    The processes of interaction of fluorescent probes: eosin and erythrosine with human serum albumin (HSA) were studied by the methods of absorption and fluorescence spectroscopy. Extinction coefficients of probes were determined. Critical transfer radius and the energy transfer efficiency were defined by fluorescence quenching of HSA. Analysis of the excitation spectra of HSA revealed that the energy transfer process is carried out mainly between tryptophanyl and probes.

  2. Spiranic BODIPYs: a ground-breaking design to improve the energy transfer in molecular cassettes.

    PubMed

    Sánchez-Carnerero, Esther M; Gartzia-Rivero, Leire; Moreno, Florencio; Maroto, Beatriz L; Agarrabeitia, Antonia R; Ortiz, María J; Bañuelos, Jorge; López-Arbeloa, Íñigo; de la Moya, Santiago

    2014-10-28

    Boosted excitation energy transfer in spiranic O-BODIPY/polyarene cassettes, when compared with the parent non-spiranic (flexible) system, is highlighted as a proof for the ability of a new structural design to improve the energy transfer in molecular cassettes. PMID:25207836

  3. Ratio-metric sensor to detect riboflavin via fluorescence resonance energy transfer with ultrahigh sensitivity

    NASA Astrophysics Data System (ADS)

    Wang, Jilong; Su, Siheng; Wei, Junhua; Bahgi, Roya; Hope-Weeks, Louisa; Qiu, Jingjing; Wang, Shiren

    2015-08-01

    In this paper, a novel fluorescence resonance energy transfer (FRET) ration-metric fluorescent probe based on heteroatom N, S doped carbon dots (N, S-CDs) was developed to determine riboflavin in aqueous solutions. The ratio of two emission intensities at different wavelengths is applied to determine the concentration of riboflavin (RF). This method is more effective in reducing the background interference and fluctuation of diverse conditions. Therefore, this probe obtains high sensitivity with a low limit of detection (LOD) of 1.9 nM (0.7 ng/ml) which is in the highest level of all riboflavin detection approaches and higher than single wavelength intensity detection (1.9 μM). In addition, this sensor has a high selectivity of detecting riboflavin in deionized water (pH=7) with other biochemical like amino acids. Moreover, riboflavin in aqueous solution is very sensitive to sunlight and can be degraded to lumiflavin, which is toxic. Because the N, S doped carbon dots cannot serve as an energy donor for N, S doped carbon dots and lumiflavin system, this system makes it easy to determine whether the riboflavin is degraded or not, which is first to be reported. This platform may provide possibilities to build a new and facile fluorescence resonance energy transfer based sensor to detect analytes and metamorphous analytes in aqueous solution.

  4. Equilibrium structure of solar magnetic flux tubes: Energy transport with multistream radiative transfer

    NASA Technical Reports Server (NTRS)

    Hasan, S. S.; Kalkofen, W.

    1994-01-01

    We examine the equilibrium structure of vertical intense magnetic flux tubes on the Sun. Assuming cylindrical geometry, we solve the magnetohydrostatic equations in the thin flux-tube approximation, allowing for energy transport by radiation and convection. The radiative transfer equation is solved in the six-stream approximation, assuming gray opacity and local thermodynamic equilibrium. This constitutes a significant improvement over a previous study, in which the transfer was solved using the multidimensional generalization of the Eddington approximation. Convection in the flux tube is treated using mixing-length theory, with an additional parameter alpha, characterizing the suppression of convective energy transport in the tube by the strong magnetic field. The equations are solved using the method of partial linearization. We present results for tubes with different values of the magnetic field strength and radius at a fixed depth in the atmosphere. In general, we find that, at equal geometric heights, the temperature on the tube axis, compared to the ambient medium, is higher in the photosphere and lower in the convection zone, with the difference becoming larger for thicker tubes. At equal optical depths the tubes are generally hotter than their surroundings. The results are comparatively insensitive to alpha but depend upon whether radiative and convective energy transport operate simultaneously or in separate layers. A comparison of our results with semiempirical models shows that the temperature and intensity contrast are in broad agreement. However, the field strengths of the flux-tube models are somewhat lower than the values inferred from observations.

  5. Rapid Energy Transfer Enabling Control of Emission Polarization in Perylene Bisimide Donor-Acceptor Triads.

    PubMed

    Menelaou, Christopher; ter Schiphorst, Jeroen; Kendhale, Amol M; Parkinson, Patrick; Debije, Michael G; Schenning, Albertus P H J; Herz, Laura M

    2015-04-01

    Materials showing rapid intramolecular energy transfer and polarization switching are of interest for both their fundamental photophysics and potential for use in real-world applications. Here, we report two donor-acceptor-donor triad dyes based on perylene-bisimide subunits, with the long axis of the donors arranged either parallel or perpendicular to that of the central acceptor. We observe rapid energy transfer (<2 ps) and effective polarization control in both dye molecules in solution. A distributed-dipole Förster model predicts the excitation energy transfer rate for the linearly arranged triad but severely underestimates it for the orthogonal case. We show that the rapid energy transfer arises from a combination of through-bond coupling and through-space transfer between donor and acceptor units. As they allow energy cascading to an excited state with controllable polarization, these triad dyes show high potential for use in luminescent solar concentrator devices. PMID:26262968

  6. Energy transfer and energy level decay processes in Tm{sup 3+}-doped tellurite glass

    SciTech Connect

    Gomes, Laercio; Lousteau, Joris; Milanese, Daniel; Scarpignato, Gerardo C.; Jackson, Stuart D.

    2012-03-15

    The primary excited state decay and energy transfer processes in singly Tm{sup 3+}-doped TeO{sub 2}:ZnO:Bi{sub 2}O{sub 3}:GeO{sub 2} (TZBG) glass relating to the {sup 3}F{sub 4}{yields}{sup 3}H{sub 6}{approx}1.85 {mu}m laser transition have been investigated in detail using time-resolved fluorescence spectroscopy. Selective laser excitation of the {sup 3}H{sub 4} manifold at 794 nm, the {sup 3}H{sub 5} manifold at 1220 nm, and {sup 3}F{sub 4} manifold at 1760 nm has established that the {sup 3}H{sub 5} manifold is entirely quenched by multiphonon relaxation in tellurite glass. The luminescence from the {sup 3}H{sub 4} manifold with an emission peak at 1465 nm suffers strong suppression due to cross relaxation that populates the {sup 3}F{sub 4} level with a near quadratic dependence on the Tm{sup 3+} concentration. The {sup 3}F{sub 4} lifetime becomes longer as the Tm{sup 3+} concentration increases due to energy migration and decreases to 2.92 ms when [Tm{sup 3+}] = 4 mol. % as a result of quasi-resonant energy transfer to free OH{sup -} radicals present in the glass at concentrations between 1 x 10{sup 18} cm{sup -3} and 2 x 10{sup 18} cm{sup -3}. Judd-Ofelt theory in conjunction with absorption measurements were used to obtain the radiative lifetimes and branching ratios of the energy levels located below 25 000 cm{sup -1}. The spectroscopic parameters, the cross relaxation and Tm{sup 3+}({sup 3}F{sub 4}) {yields} OH{sup -} energy transfer rates were used in a numerical model for laser transitions emitting at 2335 nm and 1865 nm.

  7. Chemiluminescence resonance energy transfer-based detection for microchip electrophoresis.

    PubMed

    Zhao, Shulin; Huang, Yong; Shi, Ming; Liu, Rongjun; Liu, Yi-Ming

    2010-03-01

    Since the channels in micro- and nanofluidic devices are extremely small, a sensitive detection is required following microchip electrophoresis (MCE). This work describes a highly sensitive and yet universal detection scheme based on chemiluminescence resonance energy transfer (CRET) for MCE. It was found that an efficient CRET occurred between a luminol donor and a CdTe quantum dot (QD) acceptor in the luminol-NaBrO-QD system and that it was sensitively suppressed by the presence of certain organic compounds of biological interest including biogenic amines and thiols, amino acids, organic acids, and steroids. These findings allowed developing sensitive MCE-CL assays for the tested compounds. The proposed MCE-CL methods showed desired analytical figures of merit such as a wide concentration range of linear response. Detection limits obtained were approximately 10(-9) M for biogenic amines including dopamine and epinephrine and approximately 10(-8) M for biogenic thiols (e.g., glutathione and acetylcysteine), organic acids (i.e., ascorbic acid and uric acid), estrogens, and native amino acids. These were 10-1000 times more sensitive than those of previously reported MCE-based methods with chemiluminescence, electrochemical, or laser-induced fluorescence detection for quantifying corresponding compounds. To evaluate the applicability of the present MCE-CL method for analyzing real biological samples, it was used to determine amino acids in individual human red blood cells. Nine amino acids, including Lys, Ser, Ala, Glu, Trp, etc., were detected. The contents ranged from 3 to 31 amol/cell. The assay proved to be simple, quick, reproducible, and very sensitive. PMID:20121202

  8. Förster Resonance Energy Transfer between Core/Shell Quantum Dots and Bacteriorhodopsin

    PubMed Central

    Griep, Mark H.; Winder, Eric M.; Lueking, Donald R.; Garrett, Gregory A.; Karna, Shashi P.; Friedrich, Craig R.

    2012-01-01

    An energy transfer relationship between core-shell CdSe/ZnS quantum dots (QDs) and the optical protein bacteriorhodopsin (bR) is shown, demonstrating a distance-dependent energy transfer with 88.2% and 51.1% of the QD energy being transferred to the bR monomer at separation distances of 3.5 nm and 8.5 nm, respectively. Fluorescence lifetime measurements isolate nonradiative energy transfer, other than optical absorptive mechanisms, with the effective QD excited state lifetime reducing from 18.0 ns to 13.3 ns with bR integration, demonstrating the Förster resonance energy transfer contributes to 26.1% of the transferred QD energy at the 3.5 nm separation distance. The established direct energy transfer mechanism holds the potential to enhance the bR spectral range and sensitivity of energies that the protein can utilize, increasing its subsequent photocurrent generation, a significant potential expansion of the applicability of bR in solar cell, biosensing, biocomputing, optoelectronic, and imaging technologies. PMID:22737583

  9. Energy transfers in large-scale and small-scale dynamos

    NASA Astrophysics Data System (ADS)

    Samtaney, Ravi; Kumar, Rohit; Verma, Mahendra

    2015-11-01

    We present the energy transfers, mainly energy fluxes and shell-to-shell energy transfers in small-scale dynamo (SSD) and large-scale dynamo (LSD) using numerical simulations of MHD turbulence for Pm = 20 (SSD) and for Pm = 0.2 on 10243 grid. For SSD, we demonstrate that the magnetic energy growth is caused by nonlocal energy transfers from the large-scale or forcing-scale velocity field to small-scale magnetic field. The peak of these energy transfers move towards lower wavenumbers as dynamo evolves, which is the reason for the growth of the magnetic fields at the large scales. The energy transfers U2U (velocity to velocity) and B2B (magnetic to magnetic) are forward and local. For LSD, we show that the magnetic energy growth takes place via energy transfers from large-scale velocity field to large-scale magnetic field. We observe forward U2U and B2B energy flux, similar to SSD.

  10. Yield Improvement and Energy Savings Uing Phosphonates as Additives in Kraft pulping

    SciTech Connect

    Ulrike W. Tschirner; Timothy Smith

    2007-03-31

    Project Objective: Develop a commercially viable modification to the Kraft process resulting in energy savings, increased yield and improved bleachability. Evaluate the feasibility of this technology across a spectrum of wood species used in North America. Develop detailed fundamental understanding of the mechanism by which phosphonates improve KAPPA number and yield. Evaluate the North American market potential for the use of phosphonates in the Kraft pulping process. Examine determinants of customer perceived value and explore organizational and operational factors influencing attitudes and behaviors. Provide an economic feasibility assessment for the supply chain, both suppliers (chemical supply companies) and buyers (Kraft mills). Provide background to most effectively transfer this new technology to commercial mills.

  11. The determination of energy transfer rates in the Ho:Tm:Cr:YAG laser material

    NASA Technical Reports Server (NTRS)

    Koker, Edmond B.

    1988-01-01

    Energy transfer processes occurring between atomic, ionic, or molecular systems are very widespread in nature. The applications of such processes range form radiation physics and chemistry to biology. In the field of laser physics, energy transfer processes have been used to extend the lasing range, increase the output efficiency, and influence the spectral and temporal characteristics of the output pulses of energy transfer dye lasers or solid-state laser materials. Thus in the development of solid state lasers, it is important to investigate the basic energy transfer (ET) mechanisms and processes in order to gain detailed knowledge so that successful technical utilization can be achieved. The aim of the present research is to measure the ET rate from a given manifold associated with the chromium sensitizer atom to a given manifold in the holmium activator atom via the thulium transfer atom, in the Ho:Cr:YAG laser material.

  12. Local structure of intercomponent energy transfer in homogeneous turbulent shear flow

    NASA Technical Reports Server (NTRS)

    Brasseur, James G.; Lee, Moon J.

    1987-01-01

    Intercomponent energy transfer by pressure-strain-rate was investigated for homogeneous turbulent shear flow. The rapid and slow parts of turbulent pressure (decomposed according to the influence of the mean deformation rate) are found to be uncorrelated; this finding provides strong justification for current modeling procedure in which the pressure-strain-rate term is split into the corresponding parts. Issues pertinent to scales involved in the intercomponent energy transfer are addressed in comparison with those for the Reynolds-stress and vorticity fields. A physical picture of the energy transfer process is described from a detailed study of instantaneous events of high transfer regions. It was found that the most significant intercomponent energy transfer events are highly localized in space and are imbedded within a region of concentrated vorticity.

  13. Plasmon Enhancement of Electronic Energy Transfer Between Quantum Dots on the Surface of Nanoporous Silica

    NASA Astrophysics Data System (ADS)

    Tikhomirova, N. S.; Myslitskaya, N. A.; Samusev, I. G.; Bryukhanov, V. V.

    2016-01-01

    We use spectral kinetic methods to study electronic energy transfer processes between semiconductor quantum dots on the surface of wide-pore silica in the absence of and in the presence of silver nanoparticles, obtained by laser ablation methods. We have determined the efficiencies of dipole-dipole energy transfer between two-shell (CdSe/CdS/ZnS) and one-shell (CdSe/ZnS) quantum dots on the surface, the luminescence lifetimes and quantum yields, transfer distances and transfer rate constants. We have studied enhancement of photoprocesses in individual quantum dots and in a pair under the influence of resonant localized plasmons of ablative silver nanoparticles.

  14. Analytic Methods for Predicting Significant Multi-Quanta Effects in Collisional Molecular Energy Transfer

    NASA Technical Reports Server (NTRS)

    Bieniek, Ronald J.

    1996-01-01

    Collision-induced transitions can significantly affect molecular vibrational-rotational populations and energy transfer in atmospheres and gaseous systems. This, in turn. can strongly influence convective heat transfer through dissociation and recombination of diatomics. and radiative heat transfer due to strong vibrational coupling. It is necessary to know state-to-state rates to predict engine performance and aerothermodynamic behavior of hypersonic flows, to analyze diagnostic radiative data obtained from experimental test facilities, and to design heat shields and other thermal protective systems. Furthermore, transfer rates between vibrational and translational modes can strongly influence energy flow in various 'disturbed' environments, particularly where the vibrational and translational temperatures are not equilibrated.

  15. An enzymatically-sensitized sequential and concentric energy transfer relay self-assembled around semiconductor quantum dots

    NASA Astrophysics Data System (ADS)

    Samanta, Anirban; Walper, Scott A.; Susumu, Kimihiro; Dwyer, Chris L.; Medintz, Igor L.

    2015-04-01

    The ability to control light energy within de novo nanoscale structures and devices will greatly benefit their continuing development and ultimate application. Ideally, this control should extend from generating the light itself to its spatial propagation within the device along with providing defined emission wavelength(s), all in a stand-alone modality. Here we design and characterize macromolecular nanoassemblies consisting of semiconductor quantum dots (QDs), several differentially dye-labeled peptides and the enzyme luciferase which cumulatively demonstrate many of these capabilities by engaging in multiple-sequential energy transfer steps. To create these structures, recombinantly-expressed luciferase and the dye-labeled peptides were appended with a terminal polyhistidine sequence allowing for controlled ratiometric self-assembly around the QDs via metal-affinity coordination. The QDs serve to provide multiple roles in these structures including as central assembly platforms or nanoscaffolds along with acting as a potent energy harvesting and transfer relay. The devices are activated by addition of coelenterazine H substrate which is oxidized by luciferase producing light energy which sensitizes the central 625 nm emitting QD acceptor by bioluminescence resonance energy transfer (BRET). The sensitized QD, in turn, acts as a relay and transfers the energy to a first peptide-labeled Alexa Fluor 647 acceptor dye displayed on its surface. This dye then transfers energy to a second red-shifted peptide-labeled dye acceptor on the QD surface through a second concentric Förster resonance energy transfer (FRET) process. Alexa Fluor 700 and Cy5.5 are both tested in the role of this terminal FRET acceptor. Photophysical analysis of spectral profiles from the resulting sequential BRET-FRET-FRET processes allow us to estimate the efficiency of each of the transfer steps. Importantly, the efficiency of each step within this energy transfer cascade can be controlled to

  16. Time-dependent energy transfer rates in a conjugated polymer guest-host system

    NASA Astrophysics Data System (ADS)

    Herz, L. M.; Silva, C.; Grimsdale, A. C.; Müllen, K.; Phillips, R. T.

    2004-10-01

    We have investigated the energy transfer dynamics in films of a conjugated polyindenofluorene host doped with covalently attached perylene guests. By performing time-resolved measurements of the host luminescence decay under site-selective excitation conditions, we have examined the influence of exciton migration within the host on the temporal evolution of the host-guest energy transfer. We find that highly mobile excitons created at the peak of the host’s inhomogeneous density of states transfer to guests considerably faster than more localized excitons created in the low-energy tail, indicating a strong contribution of exciton migration to the overall energy transfer. These effects are significantly more pronounced at low temperature (7K) than at ambient temperature, suggesting that for the latter, up-hill migration of excitons in the host and a broadening of their homogeneous linewidth may prevent truly site-selective excitation of localized excitons. In the asymptotic long-time limit, the observed dynamics are compatible with long-range single-step Förster energy transfer. However, at early times (≲10ps) after excitation, the behavior notably deviates from this description, suggesting that diffusion-assisted energy transfer is more important in this regime. The measured changes in excitation transfer rates with temperature and excitation energy correlate well with those observed for the dynamic energy shifts of the vibronic emission peaks from the undoped polymer. Our results therefore indicate that energy-transfer rates in polymeric guest-host systems are strongly time-dependent, owing to a contribution both from exciton relaxation through incoherent hopping within the host’s density of states and direct Förster energy transfer.

  17. Development of flexible, free-standing, thin films for additive manufacturing and localized energy generation

    SciTech Connect

    Clark, Billy; McCollum, Jena; Pantoya, Michelle L.; Heaps, Ronald J.; Daniels, Michael A.

    2015-08-01

    Film energetics are becoming increasingly popular because a variety of technologies are driving a need for localized energy generation in a stable, safe and flexible form. Aluminum (Al) and molybdenum trioxide (MoO₃) composites were mixed into a silicon binder and extruded using a blade casting technique to form flexible free-standing films ideal for localized energy generation. Since this material can be extruded onto a surface it is well suited to additive manufacturing applications. This study examines the influence of 0-35% by mass potassium perchlorate (KClO₄) additive on the combustion behavior of these energetic films. Without KClO₄ the film exhibits thermal instabilities that produce unsteady energy propagation upon reaction. All films were cast at a thickness of 1 mm with constant volume percent solids to ensure consistent rheological properties. The films were ignited and flame propagation was measured. The results show that as the mass percent KClO₄ increased, the flame speed increased and peaked at 0.43 cm/s and 30 wt% KClO₄. Thermochemical equilibrium simulations show that the heat of combustion increases with increasing KClO₄ concentration up to a maximum at 20 wt% when the heat of combustion plateaus, indicating that the increased chemical energy liberated by the additional KClO₄ promotes stable energy propagation. Differential scanning calorimeter and thermogravimetric analysis show that the silicone binder participates as a fuel and reacts with KClO₄ adding energy to the reaction and promoting propagation.

  18. Energy transfer properties of Rhodobacter sphaeroides chromatophores during adaptation to low light intensity.

    PubMed

    Driscoll, B; Lunceford, C; Lin, S; Woronowicz, K; Niederman, R A; Woodbury, N W

    2014-08-28

    Time-resolved fluorescence spectroscopy was used to explore the pathway and kinetics of energy transfer in photosynthetic membrane vesicles (chromatophores) isolated from Rhodobacter (Rba.) sphaeroides cells harvested 2, 4, 6 or 24 hours after a transition from growth in high to low level illumination. As previously observed, this light intensity transition initiates the remodeling of the photosynthetic apparatus and an increase in the number of light harvesting 2 (LH2) complexes relative to light harvesting 1 (LH1) and reaction center (RC) complexes. It has generally been thought that the increase in LH2 complexes served the purpose of increasing the overall energy transmission to the RC. However, fluorescence lifetime measurements and analysis in terms of energy transfer within LH2 and between LH2 and LH1 indicate that, during the remodeling time period measured, only a portion of the additional LH2 generated are well connected to LH1 and the reaction center. The majority of the additional LH2 fluorescence decays with a lifetime comparable to that of free, unconnected LH2 complexes. The presence of large LH2-only domains has been observed by atomic force microscopy in Rba. sphaeroides chromatophores (Bahatyrova et al., Nature, 2004, 430, 1058), providing structural support for the existence of pools of partially connected LH2 complexes. These LH2-only domains represent the light-responsive antenna complement formed after a switch in growth conditions from high to low illumination, while the remaining LH2 complexes occupy membrane regions containing mixtures of LH2 and LH1-RC core complexes. The current study utilized a multi-parameter approach to explore the fluorescence spectroscopic properties related to the remodeling process, shedding light on the structure-function relationship of the photosynthetic assembles. Possible reasons for the accumulation of these largely disconnected LH2-only pools are discussed. PMID:25008288

  19. Quantum dots arrangement and energy transfer control via charge-transfer complex achieved on poly(phenylene ethynylene)/schizophyllan nanowires.

    PubMed

    Shiraki, Tomohiro; Haraguchi, Shuichi; Tsuchiya, Youichi; Shinkai, Seiji

    2009-09-01

    Assemblies of organic and inorganic compounds in the nanoscale region have contributed to the development of novel functional materials toward future applications, including sensors and opto-electronics. We succeed in fabricating hybrid nanowires composed of a conjugated polymer and semiconductor quantum dots (QDs) by a supramolecular assembly technique. The 1-D fashion of the nanowire structure is obtained by the polymer wrapping of cationic poly(phenylene ethynylene) (PPE) with helix-forming polysaccharide schizophyllan (SPG). The electrostatic interaction between cationic PPE and anionic QDs affords the nanowires decorated with QDs. Upon addition of an acceptor molecule, tetranitrofluorenone (TNF), the charge-transfer (CT) complex between PPE and TNF is formed, resulting in energy transfer from the QDs to PPE arising from the induced spectral overlap. Furthermore, the employment of the conjugated polymer allows highly sensitive quenching of the QD's emission by raising the transmission efficiency to the CT complexed electron deficient sites along the polymer backbone. PMID:19629958

  20. Sequential energy and electron transfer in a three-component system aligned on a clay nanosheet.

    PubMed

    Fujimura, Takuya; Ramasamy, Elamparuthi; Ishida, Yohei; Shimada, Tetsuya; Takagi, Shinsuke; Ramamurthy, Vaidhyanathan

    2016-02-21

    To achieve the goal of energy transfer and subsequent electron transfer across three molecules, a phenomenon often utilized in artificial light harvesting systems, we have assembled a light absorber (that also serves as an energy donor), an energy acceptor (that also serves as an electron donor) and an electron acceptor on the surface of an anionic clay nanosheet. Since neutral organic molecules have no tendency to adsorb onto the anionic surface of clay, a positively charged water-soluble organic capsule was used to hold neutral light absorbers on the above surface. A three-component assembly was prepared by the co-adsorption of a cationic bipyridinium derivative, cationic zinc porphyrin and cationic octaamine encapsulated 2-acetylanthracene on an exfoliated anionic clay surface in water. Energy and electron transfer phenomena were monitored by steady state fluorescence and picosecond time resolved fluorescence decay. The excitation of 2-acetylanthracene in the three-component system resulted in energy transfer from 2-acetylanthracene to zinc porphyrin with 71% efficiency. Very little loss due to electron transfer from 2-acetylanthracene in the cavitand to the bipyridinium derivative was noticed. Energy transfer was followed by electron transfer from the zinc porphyrin to the cationic bipyridinium derivative with 81% efficiency. Analyses of fluorescence decay profiles confirmed the occurrence of energy transfer and subsequent electron transfer. Merging the concepts of supramolecular chemistry and surface chemistry we realized sequential energy and electron transfer between three hydrophobic molecules in water. Exfoliated transparent saponite clay served as a matrix to align the three photoactive molecules at a close distance in aqueous solutions. PMID:26820105

  1. Zonal-flow-driven nonlinear energy transfer in experiment and simulation

    SciTech Connect

    Holland, C.; Tynan, G. R.; Fonck, R. J.; McKee, G. R.; Candy, J.; Waltz, R. E.

    2007-05-15

    Using a newly developed algorithm, the nonlinear transfer of internal fluctuation energy vertical bar n-tilde vertical bar{sup 2} due to convection of drift-wave turbulence by a geodesic acoustic mode (GAM, a finite-frequency zonal flow) has now been measured directly in a high-temperature plasma. By combining spatially resolved density fluctuation measurements obtained via an upgraded beam emission spectroscopy system in the edge region of the DIII-D tokamak [J. L. Luxon, Nucl. Fusion 42, 614 (2002)] with a velocity inference algorithm, the convection of turbulent fluctuations by the GAM has been measured. Taken together, the results strongly suggest that GAM convection of turbulence leads to a transfer of internal fluctuation energy from low to high frequencies, in agreement with expectations from theory and simulation. In addition, the GAM is found to modulate the intensity of the density fluctuations. Calculations of the measured nonlinear interactions in the gyrokinetic code GYRO are found to be in good qualitative agreement with the experimental observations.

  2. Intra-molecular Triplet Energy Transfer is a General Approach to Improve Organic Fluorophore Photostability

    PubMed Central

    Zheng, Qinsi; Jockusch, Steffen; Rodríguez-Calero, Gabriel G.; Zhou, Zhou; Zhao, Hong; Altman, Roger B.; Abruña, Héctor D.; Blanchard, Scott C.

    2015-01-01

    Bright, long-lasting and non-phototoxic organic fluorophores are essential to the continued advancement of biological imaging. Traditional approaches towards achieving photostability, such as the removal of molecular oxygen and the use of small-molecule additives in solution, suffer from potentially toxic side effects, particularly in the context of living cells. The direct conjugation of small-molecule triplet state quenchers, such as cyclooctatetraene (COT), to organic fluorophores has the potential to bypass these issues by restoring reactive fluorophore triplet states to the ground state through intra-molecular triplet energy transfer. Such methods have enabled marked improvement in cyanine fluorophore photostability spanning the visible spectrum. However, the generality of this strategy to chemically and structurally diverse fluorophore species has yet to be examined. Here, we show that the proximal linkage of COT increases the photon yield of a diverse range of organic fluorophores widely used in biological imaging applications, demonstrating that the intra-molecular triplet energy transfer mechanism is a potentially general approach for improving organic fluorophore performance and photostability. PMID:26700693

  3. Intramolecular fluorescence resonance energy transfer and living cell imaging of novel pyridyltriphenylamine dye

    NASA Astrophysics Data System (ADS)

    Cao, Duojun; Qian, Ying

    2016-07-01

    A novel pyridyltriphenylamine-rhodamine dye PTRh and a pyridyltriphenylamine derivative PTO were synthesized and characterized by 1H NMR and HRMS-MALDI-TOF. PTRh performed typical fluorescence resonance energy transfer (FRET) signal from pyridyltriphenylamine to rhodamine along with notable color change from green to rose when interacting with Hg2+ in EtOH/H2O. And PTRh as a ratiometric probe for Hg2+ based on FRET could achieve a very low detection limit of 32 nM and energy transfer efficiency of 83.7% in aqueous organic system. On the other hand, spectra properties of PTO in its aggregates, THF/H2O mixed solution and silica nanoparticles (Si-NPs) dispersed in water were investigated. And the results indicated PTO exhibited bright green fluorescence in solid state, and PTO was successfully encapsulated in silica matrix (30-40 nm), emitting bright blue fluorescence with 11.7% quantum yield. Additionally, living cell imaging experiments demonstrated that PTRh could effectively response to intracellular Hg2+ and PTO-doped Si-NPs were well uptaken by MCF-7 breast cancer cells. It could be concluded that the chromophores are promising materials used as biosensors.

  4. Free energy calculation of water addition coupled to reduction of aqueous RuO4-

    NASA Astrophysics Data System (ADS)

    Tateyama, Yoshitaka; Blumberger, Jochen; Ohno, Takahisa; Sprik, Michiel

    2007-05-01

    Free energy calculations were carried out for water addition coupled reduction of aqueous ruthenate, RuO4-+H2O +e-→[RuO3(OH)2]2-, using Car-Parrinello molecular dynamics simulations. The full reaction is divided into the reduction of the tetrahedral monoanion, RuO4-+e-→RuO42-, followed by water addition, RuO42-+H2O →[RuO3(OH)2]2-. The free energy of reduction is computed from the fluctuations of the vertical energy gap using the MnO4-+e -→MnO42- reaction as reference. The free energy for water addition is estimated using constrained molecular dynamics methods. While the description of this complex reaction, in principle, involves multiple reaction coordinates, we found that reversible transformation of the reactant into the product can be achieved by control of a single reaction coordinate consisting of a suitable linear combination of atomic distances. The free energy difference of the full reaction is computed to be -0.62eV relative to the normal hydrogen electrode. This is in good agreement with the experimental value of -0.59eV, lending further support to the hypothesis that, contrary to the ruthenate monoanion, the dianion is not tetrahedral but forms a trigonal-bipyramidal dihydroxo complex in aqueous solution. We construct an approximate two-dimensional free energy surface using the coupling parameter for reduction and the mechanical constraint for water addition as variables. Analyzing this surface we find that in the most favorable reaction pathway the reduction reaction precedes water addition. The latter takes place via the protonated complex [RuO3(OH)]- and subsequent transport of the created hydroxide ion to the fifth coordination site of Ru.

  5. Inter- and intra-molecular energy transfers of encapsulate dyes in dendrimers

    NASA Astrophysics Data System (ADS)

    Otomo, Akira; Zhou, Minniu; Furumi, Seiichi; Yokoyama, Shiyoshi; Mashiko, Shinro

    2002-12-01

    Dendrimers are capable to encapsulate small molecules inside them. Because three-dimensional structures of dendrimers are highly controllable, energy transfers among dye molecules encapsulated inside them can be controlled precisely. Electronic energy transfers from optical excited molecules are categorized into two classes, Forster and Dexter types. Inter-molecular interactions between encapsulated dyes can be expressed as the Forster (singlet-singlet) energy transfer, because the size of dendrimers extends to a few nanometers. We have evaluated time resolved optical responses in rhodamine-cored dendrimer films. Fast decay in fluorescent lifetime is observed and it depends on the dendrimer size. A low generation dendrimer shows lifetime as short as 10 psec without severe quenching of fluorescence. A quadratic dependence of the emission intensity on density of molecules indicates that the origin of the short lifetime is not only energy transfer, but also super-radiance. Since the Dexter (triplet-triplet) energy transfer occurs in short range of 1.0 nm, we attached both donor and acceptor molecules to a dendrimer for investigation. We demonstrated photocrosslinking via triplet-triplet energy transfer from donor molecules encapsulated to acceptors attached at the surface. This procedure of triplet-triplet energy transfer in dendritic molecules opens up way to design novel optical and electrical molecular devices.

  6. An energy transfer method for 4D Monte Carlo dose calculation

    PubMed Central

    Siebers, Jeffrey V.; Zhong, Hualiang

    2008-01-01

    This article presents a new method for four-dimensional Monte Carlo dose calculations which properly addresses dose mapping for deforming anatomy. The method, called the energy transfer method (ETM), separates the particle transport and particle scoring geometries: Particle transport takes place in the typical rectilinear coordinate system of the source image, while energy deposition scoring takes place in a desired reference image via use of deformable image registration. Dose is the energy deposited per unit mass in the reference image. ETM has been implemented into DOSXYZnrc and compared with a conventional dose interpolation method (DIM) on deformable phantoms. For voxels whose contents merge in the deforming phantom, the doses calculated by ETM are exactly the same as an analytical solution, contrasting to the DIM which has an average 1.1% dose discrepancy in the beam direction with a maximum error of 24.9% found in the penumbra of a 6 MV beam. The DIM error observed persists even if voxel subdivision is used. The ETM is computationally efficient and will be useful for 4D dose addition and benchmarking alternative 4D dose addition algorithms. PMID:18841862

  7. An energy transfer method for 4D Monte Carlo dose calculation.

    PubMed

    Siebers, Jeffrey V; Zhong, Hualiang

    2008-09-01

    This article presents a new method for four-dimensional Monte Carlo dose calculations which properly addresses dose mapping for deforming anatomy. The method, called the energy transfer method (ETM), separates the particle transport and particle scoring geometries: Particle transport takes place in the typical rectilinear coordinate system of the source image, while energy deposition scoring takes place in a desired reference image via use of deformable image registration. Dose is the energy deposited per unit mass in the reference image. ETM has been implemented into DOSXYZnrc and compared with a conventional dose interpolation method (DIM) on deformable phantoms. For voxels whose contents merge in the deforming phantom, the doses calculated by ETM are exactly the same as an analytical solution, contrasting to the DIM which has an average 1.1% dose discrepancy in the beam direction with a maximum error of 24.9% found in the penumbra of a 6 MV beam. The DIM error observed persists even if voxel subdivision is used. The ETM is computationally efficient and will be useful for 4D dose addition and benchmarking alternative 4D dose addition algorithms. PMID:18841862

  8. Mutations to R. sphaeroides Reaction Center Perturb Energy Levels and Vibronic Coupling but Not Observed Energy Transfer Rates.

    PubMed

    Flanagan, Moira L; Long, Phillip D; Dahlberg, Peter D; Rolczynski, Brian S; Massey, Sara C; Engel, Gregory S

    2016-03-10

    The bacterial reaction center is capable of both efficiently collecting and quickly transferring energy within the complex; therefore, the reaction center serves as a convenient model for both energy transfer and charge separation. To spectroscopically probe the interactions between the electronic excited states on the chromophores and their intricate relationship with vibrational motions in their environment, we examine coherences between the excited states. Here, we investigate this question by introducing a series of point mutations within 12 Å of the special pair of bacteriochlorophylls in the Rhodobacter sphaeroides reaction center. Using two-dimensional spectroscopy, we find that the time scales of energy transfer dynamics remain unperturbed by these mutations. However, within these spectra, we detect changes in the mixed vibrational-electronic coherences in these reaction centers. Our results indicate that resonance between bacteriochlorophyll vibrational modes and excitonic energy gaps promote electronic coherences and support current vibronic models of photosynthetic energy transfer. PMID:26630123

  9. Biomolecular interactions probed by fluorescence resonance energy transfer

    NASA Astrophysics Data System (ADS)

    Lange, Daniela Charlotte

    2000-09-01

    This thesis describes how a physical phenomenon, Fluorescence Resonance Energy Transfer (FRET), can be exploited for the study of interactions between biomolecules. The physical basis of this phenomenon is discussed and it is described how some of its characteristics can be exploited in measurement. A recently introduced method, photobleaching FRET microscopy, was implemented and its image analysis refined to suit our biological context. Further, a new technique is proposed, which combines FRET with confocal laser scanning microscopy to optimize resolution and to allow for 3D-studies in living cells. The first part of this thesis presents the application of FRET to the study of oligomerization of G-protein coupled receptors (GPCRs), which was performed at the Fraser Laboratories at McGill University in Montreal. It is demonstrated how FRET microscopy allowed us to circumvent problems of traditional biochemical approaches and provided the first direct evidence for GPCR oligomerization in intact cells. We found that somatostatin receptors (SSTRs) functionally interact by forming oligomers with their own kind, with different SSTR isoforms, and even with distantly related GPCRs, such as dopamine receptors, the latter of which is breaking with the dogma that GPCRs would only pair up with their own kind. The high sensitivity of the FRET technique allowed us to characterize these interactions under more physiological conditions, which lead to the observation that oligomerization is induced by receptor agonist. We further studied the differential effects of agonists and antagonists on receptor oligomerization, leading to a model for the molecular mechanism underlying agonist/antagonist function and receptor activation. The second part was carried out at the Neurobiology Laboratory of the VA Medical Center in Newington, CT. The objective was to further our understanding of Niemann- Pick type C disease, which is characterized by a defect in intracellular cholesterol

  10. Nanoscale heat transfer and thermoelectrics for alternative energy

    NASA Astrophysics Data System (ADS)

    Robinson, Richard

    2011-03-01

    In the area of alternative energy, thermoelectrics have experienced an unprecedented growth in popularity because of their ability to convert waste heat into electricity. Wired in reverse, thermoelectrics can act as refrigeration devices, where they are promising because they are small in size and lightweight, have no moving parts, and have rapid on/off cycles. However, due to their low efficiencies bulk thermoelectrics have historically been a niche market. Only in the last decade has thermoelectric efficiency exceeded ~ 20 % due to fabrication of nanostructured materials. Nanoscale materials have this advantage because electronic and acoustic confinement effects can greatly increase thermoelectric efficiency beyond bulk values. In this talk, I will introduce our work in the area of nanoscale heat transfer with the goal of more efficient thermoelectrics. I will discuss our experiments and methods to study acoustic confinement in nanostructures and present some of our new nanostructured thermoelectric materials. To study acoustic confinement we are building a nanoscale phonon spectrometer. The instrument can excite phonon modes in nanostructures in the ~ 100 s of GHz. Ballistic phonons from the generator are used to probe acoustic confinement and surface scattering effects. Transmission studies using this device will help optimize materials and morphologies for more efficient nanomaterial-based thermoelectrics. For materials, our group has synthesized nano-layer superlattices of Na x Co O2 . Sodium cobaltate was recently discovered to have a high Seebeck coeficent and is being studied as an oxide thermoelectric material. The thickness of our nano-layers ranges from 5 nm to 300 nm while the lengths can be varied between 10 μ m and 4 mm. Typical aspect ratios are 40 nm: 4 mm, or 1:100,000. Thermoelectric characterization of samples with tilted multiple-grains along the measurement axis indicate a thermoelectric efficiency on par with current polycrystalline samples

  11. Design, Development and Testing of an Energy-Environment Information Transfer System: Final Report August 16, 1977 through October 15, 1978. Volume I.

    ERIC Educational Resources Information Center

    Cornog, Martha; And Others

    Documented in this project report are efforts to create and evaluate an Energy-Environment Information Transfer System (EEITS) for Region VIII of the Environmental Protection Agency (EPA). This system is designed to support government policy-making and implementation decisions regarding energy and the environment. In addition to assisting federal,…

  12. Chemo- and Enantioselective Addition and β-Hydrogen Transfer Reduction of Carbonyl Compounds with Diethylzinc Reagent in One Pot Catalyzed by a Single Chiral Organometallic Catalyst.

    PubMed

    Huang, Huayin; Zong, Hua; Bian, Guangling; Song, Ling

    2015-12-18

    Using a single chiral phosphoramide-Zn(II) complex as the catalyst, the asymmetric β-H transfer reduction of aromatic α-trifluoromethyl ketones and enantioselective addition of aromatic aldehydes with Et2Zn in one pot were successfully realized, affording the corresponding additive products of secondary alcohols in high yields (up to 99%) with excellent enantioselectivities (up to 98% ee) and the reduction products of α-trifluoromethyl alcohols in good to excellent yields with up to 77% ee. PMID:26579727

  13. Radiation and collisional energy transfer among the A 2Pi(i) and X 2Sigma(+) states of CN

    NASA Technical Reports Server (NTRS)

    Huang, Yuhui; Lu, Richang; Halpern, Joshua B.

    1993-01-01

    Laser-photolysis-laser-induced-fluorescence methods are used to characterize the collisional energy transfer between CN (A 2Pi(i) and (X 2Sigma(+)) states and to measure radiative lifetimes of the (A 2Pi(i)) v-prime = 2-7 vibrational levels. In addition, use of the A 2Pi(i) - X 2Sigma(+) system for the laser-induced-fluorescence determination of (X 2Sig(+)) populations is demonstrated and discussed.

  14. Modulation of energy transfer pathways between mitochondria and myofibrils by changes in performance of perfused heart.

    PubMed

    Vendelin, Marko; Hoerter, Jacqueline A; Mateo, Philippe; Soboll, Sibylle; Gillet, Brigitte; Mazet, Jean-Luc

    2010-11-26

    In the heart, the energy supplied by mitochondria to myofibrils is continuously and finely tuned to the contraction requirement over a wide range of cardiac loads. This process is mediated both by the creatine kinase (CK) shuttle and by direct ATP transfer. The aim of this study was to identify the contribution of energy transfer pathways at different cardiac performance levels. For this, five protocols of (31)P NMR inversion and saturation transfer experiments were performed at different performance levels on Langendorff perfused rat hearts. The cardiac performance was changed either through variation of external calcium in the presence or absence of isoprenaline or through variation of LV balloon inflation. The recordings were analyzed by mathematical models composed on the basis of different energy transfer pathway configurations. According to our results, the total CK unidirectional flux was relatively stable when the cardiac performance was changed by increasing the calcium concentration or variation of LV balloon volume. The stability of total CK unidirectional flux is lost at extreme energy demand levels leading to a rise in inorganic phosphate, a drop of ATP and phosphocreatine, a drop of total CK unidirectional flux, and to a bypass of CK shuttle by direct ATP transfer. Our results provide experimental evidence for the existence of two pathways of energy transfer, direct ATP transfer, and PCr transfer through the CK shuttle, whose contribution may vary depending on the metabolic status of the heart. PMID:20847056

  15. Energy transfer and photochemistry in biomimetic solar conversion

    NASA Astrophysics Data System (ADS)

    Boxer, S. G.

    1987-09-01

    Electron transfer is being studied in several well-defined molecular systems, and techniques for studying electron transfer are being developed. Photo-induced electron transfer lies at the heart of photosynthesis and forms the basis for the approach to biomimetic solar conversion. Electron donors and acceptors are covalently connected to molecular frameworks which permit variation of the distance between sites and the nature of the intervening medium. Myoglobin produced by recombinant DNA methods was modified to place a free sulfhydryl group at various positions on the surface for attachment of electron acceptors. Surface histidine residues are modified with Ru-reagents. Electron donors and acceptors were also attached to double-helical DNA as a first approach to polymer-based donor/acceptor systems. The effects of applied electric fields on the absorption and emission spectra of compounds undergoing electron transfer were studied. The Stark effect spectra of several Ru-complexes were obtained, from which quantitative information on changes in the permanent dipole moment between the ground and the excited state was extracted. It was also shown that, under certain conditions, the electric field can change the rate of electron transfer reactions, and that the effect is easily detected in the electric-field-modulated fluorescence spectrum. These effects were demonstrated for bacterial reaction centers and certain Ru-complexes.

  16. Spectroscopic investigation on the energy transfer process in photosynthetic apparatus of cyanobacteria

    NASA Astrophysics Data System (ADS)

    Li, Ye; Wang, Bei; Ai, Xi-Cheng; Zhang, Xing-Kang; Zhao, Jing-Quan; Jiang, Li-Jin

    2004-06-01

    In this work, we employ cyanobacteria, Spirulina platensis, and separate their photosynthetic apparatus, phycobilisome (PBS), thylakoid membrane and phycobilisome-thylakoid membrane complex. The steady state absorption spectra, fluorescence spectra and corresponding deconvoluted spectra and picosecond time-resolved spectra are used to investigate the energy transfer process in phycobilisome-thylakoid membrane complex. The results on steady state spectra show chlorophylls of the photosystem II are able to transfer excitation energy to phycobilisome with Chl a molecules selectively excited. The decomposition of the steady state spectra further suggest the uphill energy transfer originate from chlorophylls of photosystem II to cores of phycobilisome, while rods and cores of phycobilisome cannot receive energy from the chlorophylls of photosystem I. The time constant for the back energy transfer process is 18 ps.

  17. The geometry effect on energy transfer rate in a coupled-quantum-wires structure

    NASA Astrophysics Data System (ADS)

    Rafee, Vahdat

    2016-03-01

    The geometry effect on energy transfer rate in a coupled cylindrical quantum wires system is investigated. The corrected random phase approximation by the zero-temperature static Hubbard correction is employed to calculate dielectric function of the system. The geometry effect on energy transfer rate is studied for statically and dynamically screened electron-electron interaction. Both the linear and nonlinear regimes correspond respectively to weak and strong external field are considered. The calculations show that increasing wire radius increases energy transfer rate in both the static and dynamic screening approximations for electron-electron interactions. Moreover, the same trend is predicted by the calculations for both the linear and nonlinear regimes.

  18. Energy Transfer Process of Eu3+ Ions Doped in Tellurite Glass

    NASA Astrophysics Data System (ADS)

    Hong, Tran Thi; Dung, Phan Tien; Quang, Vu Xuan

    2016-05-01

    Tellurite glass doped with different concentrations of Eu3+ ions has been prepared by the conventional melting process. Photoluminescence, Raman spectra, phonon side-band spectra, and Judd-Ofelt analysis were carried out. Some spectroscopic parameters were estimated to predict the luminescence efficiency of the materials. The energy transfer between the rare-earth ions was observed, and a model for its cross-relaxation was proposed and quantitatively estimated. The charged intrinsic defects in the form of nonbridging oxygen (NBO) were determined, and the energy transfer between NBO and rare-earth ions observed. The energy-transfer-induced Eu3+ photoluminescence enhancement in tellurite glass is studied.

  19. Energy Transfer of Excitons Between Quantum Wells Separated by a Wide Barrier

    SciTech Connect

    LYO,SUNGKWUN K.

    1999-12-06

    We present a microscopic theory of the excitonic Stokes and anti-Stokes energy transfer mechanisms between two widely separated unequal quantum wells with a large energy mismatch ({Delta}) at low temperatures (T). Exciton transfer through dipolar coupling, photon-exchange coupling and over-barrier ionization of the excitons through exciton-exciton Auger processes are examined. The energy transfer rate is calculated as a function of T and the center-to-center distance d between the two wells. The rates depend sensitively on T for plane-wave excitons. For located excitons, the rates depend on T only through the T-dependence of the localization radius.

  20. Excitation energy transfer from long-persistent phosphors for enhancing power conversion of dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Puntambekar, Ajinkya; Chakrapani, Vidhya

    2016-06-01

    Incorporation of inorganic phosphors to improve the spectral absorption range of a dye-sensitized solar cell (DSSC) is a promising strategy to enhance efficiency beyond 15%. However, only marginal improvements have been achieved so far, which is mainly due to the use of nonoptimized device architecture and the lack of understanding of the energy transfer mechanism. Here we report results of DSSCs employing long-persistence phosphor coupled to the sensitizing dye. Detailed time-resolved photoluminescence measurements suggest that excitation energy is transferred radiatively as opposed to Förster resonance energy transfer. As a result of efficient energy transfer, large-area solar cells show a 63% increase in the photocurrent density along with a 54% increase in power conversion efficiency. In addition, the device works as a "nighttime solar cell" with generation of 52 μ W c m-2 power density in the dark. Under short-circuit conditions, the device can output 300 mV for 30 h in the dark.

  1. CRISPR-Cas and Restriction-Modification Act Additively against Conjugative Antibiotic Resistance Plasmid Transfer in Enterococcus faecalis

    PubMed Central

    Price, Valerie J.; Huo, Wenwen; Sharifi, Ardalan

    2016-01-01

    ABSTRACT Enterococcus faecalis is an opportunistic pathogen and a leading cause of nosocomial infections. Conjugative pheromone-responsive plasmids are narrow-host-range mobile genetic elements (MGEs) that are rapid disseminators of antibiotic resistance in the faecalis species. Clustered regularly interspaced short palindromic repeat (CRISPR)-Cas and restriction-modification confer acquired and innate immunity, respectively, against MGE acquisition in bacteria. Most multidrug-resistant E. faecalis isolates lack CRISPR-Cas and possess an orphan locus lacking cas genes, CRISPR2, that is of unknown function. Little is known about restriction-modification defense in E. faecalis. Here, we explore the hypothesis that multidrug-resistant E. faecalis strains are immunocompromised. We assessed MGE acquisition by E. faecalis T11, a strain closely related to the multidrug-resistant hospital isolate V583 but which lacks the ~620 kb of horizontally acquired genome content that characterizes V583. T11 possesses the E. faecalis CRISPR3-cas locus and a predicted restriction-modification system, neither of which occurs in V583. We demonstrate that CRISPR-Cas and restriction-modification together confer a 4-log reduction in acquisition of the pheromone-responsive plasmid pAM714 in biofilm matings. Additionally, we show that the orphan CRISPR2 locus is functional for genome defense against another pheromone-responsive plasmid, pCF10, only in the presence of cas9 derived from the E. faecalis CRISPR1-cas locus, which most multidrug-resistant E. faecalis isolates lack. Overall, our work demonstrated that the loss of only two loci led to a dramatic reduction in genome defense against a clinically relevant MGE, highlighting the critical importance of the E. faecalis accessory genome in modulating horizontal gene transfer. Our results rationalize the development of antimicrobial strategies that capitalize upon the immunocompromised status of multidrug-resistant E

  2. CRISPR-Cas and Restriction-Modification Act Additively against Conjugative Antibiotic Resistance Plasmid Transfer in Enterococcus faecalis.

    PubMed

    Price, Valerie J; Huo, Wenwen; Sharifi, Ardalan; Palmer, Kelli L

    2016-01-01

    Enterococcus faecalis is an opportunistic pathogen and a leading cause of nosocomial infections. Conjugative pheromone-responsive plasmids are narrow-host-range mobile genetic elements (MGEs) that are rapid disseminators of antibiotic resistance in the faecalis species. Clustered regularly interspaced short palindromic repeat (CRISPR)-Cas and restriction-modification confer acquired and innate immunity, respectively, against MGE acquisition in bacteria. Most multidrug-resistant E. faecalis isolates lack CRISPR-Cas and possess an orphan locus lacking cas genes, CRISPR2, that is of unknown function. Little is known about restriction-modification defense in E. faecalis. Here, we explore the hypothesis that multidrug-resistant E. faecalis strains are immunocompromised. We assessed MGE acquisition by E. faecalis T11, a strain closely related to the multidrug-resistant hospital isolate V583 but which lacks the ~620 kb of horizontally acquired genome content that characterizes V583. T11 possesses the E. faecalis CRISPR3-cas locus and a predicted restriction-modification system, neither of which occurs in V583. We demonstrate that CRISPR-Cas and restriction-modification together confer a 4-log reduction in acquisition of the pheromone-responsive plasmid pAM714 in biofilm matings. Additionally, we show that the orphan CRISPR2 locus is functional for genome defense against another pheromone-responsive plasmid, pCF10, only in the presence of cas9 derived from the E. faecalis CRISPR1-cas locus, which most multidrug-resistant E. faecalis isolates lack. Overall, our work demonstrated that the loss of only two loci led to a dramatic reduction in genome defense against a clinically relevant MGE, highlighting the critical importance of the E. faecalis accessory genome in modulating horizontal gene transfer. Our results rationalize the development of antimicrobial strategies that capitalize upon the immunocompromised status of multidrug-resistant E. faecalis. IMPORTANCE

  3. Activation energies for addition of O/3P/ to simple olefins.

    NASA Technical Reports Server (NTRS)

    Demore, W. B.

    1972-01-01

    Description of relative rate measurements for the addition of O(3P) to C2H4, C2F4, C3H6, and C4H8-1 in liquid argon at 87.5 K. The data strongly indicate that the activation energies for the addition of O(3P) to the double bonds of propylene and butene-1 are identical, probably to within 0.1 kcal/mole. It is very doubtful that differences in pre-exponential factors or other factors such as solvent effects, could invalidate this conclusion. A similar argument holds for the C2H4 and C2F4 reactions. Furthermore, the experiments suggest that the activation energy for addition of O(3P) to the double bond of butene-1 is about 0.1 kcal/mole.

  4. Electrochemical Electron Transfer and Proton-Coupled Electron Transfer: Effects of Double Layer and Ionic Environment on Solvent Reorganization Energies.

    PubMed

    Ghosh, Soumya; Soudackov, Alexander V; Hammes-Schiffer, Sharon

    2016-06-14

    Electron transfer and proton coupled electron transfer (PCET) reactions at electrochemical interfaces play an essential role in a broad range of energy conversion processes. The reorganization energy, which is a measure of the free-energy change associated with solute and solvent rearrangements, is a key quantity for calculating rate constants for these reactions. We present a computational method for including the effects of the double layer and ionic environment of the diffuse layer in calculations of electrochemical solvent reorganization energies. This approach incorporates an accurate electronic charge distribution of the solute within a molecular-shaped cavity in conjunction with a dielectric continuum treatment of the solvent, ions, and electrode using the integral equations formalism polarizable continuum model. The molecule-solvent boundary is treated explicitly, but the effects of the electrode-double layer and double layer-diffuse layer boundaries, as well as the effects of the ionic strength of the solvent, are included through an external Green's function. The calculated total reorganization energies agree well with experimentally measured values for a series of electrochemical systems, and the effects of including both the double layer and ionic environment are found to be very small. This general approach was also extended to electrochemical PCET and produced total reorganization energies in close agreement with experimental values for two experimentally studied PCET systems. PMID:27111050

  5. Drag Reduction by Laser-Plasma Energy Addition in Hypersonic Flow

    SciTech Connect

    Oliveira, A. C.; Minucci, M. A. S.; Toro, P. G. P.; Chanes, J. B. Jr; Myrabo, L. N.

    2008-04-28

    An experimental study was conducted to investigate the drag reduction by laser-plasma energy addition in a low density Mach 7 hypersonic flow. The experiments were conducted in a shock tunnel and the optical beam of a high power pulsed CO{sub 2} TEA laser operating with 7 J of energy and 30 MW peak power was focused to generate the plasma upstream of a hemispherical model installed in the tunnel test section. The non-intrusive schlieren optical technique was used to visualize the effects of the energy addition to hypersonic flow, from the plasma generation until the mitigation of the shock wave profile over the model surface. Aside the optical technique, a piezoelectric pressure transducer was used to measure the impact pressure at stagnation point of the hemispherical model and the pressure reduction could be observed.

  6. 40 CFR 80.591 - What are the product transfer document requirements for additives to be used in diesel fuel?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... requirements for additives to be used in diesel fuel? 80.591 Section 80.591 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) REGULATION OF FUELS AND FUEL ADDITIVES... additives to be used in diesel fuel? (a) Except as provided in paragraphs (b) and (d) of this section,...

  7. 40 CFR 80.591 - What are the product transfer document requirements for additives to be used in diesel fuel?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... requirements for additives to be used in diesel fuel? 80.591 Section 80.591 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) REGULATION OF FUELS AND FUEL ADDITIVES... additives to be used in diesel fuel? (a) Except as provided in paragraphs (b) and (d) of this section,...

  8. Efficient photoinduced orthogonal energy and electron transfer reactions via phospholipid membrane-bound donors and acceptors

    SciTech Connect

    Clapp, P.J.; Armitage, B.; Roosa, P.; O'Brien, D.F. )

    1994-10-05

    A three component, liposome-bound photochemical molecular device (PMD) consisting of energy and electron transfer reactions is described. Bilayer membrane surface-associated dyes, 5,10,15,20-tetrakis[4-(trimethylammonio)-phenyl]-21H,2 3H-porphine tetra-p-tosylate salt and N,N[prime]-bis[(3-trimethylammonio)propyl]thiadicarbocya nine tribromide, are the energy donor and acceptor, respectively, in a blue light stimulated energy transfer reaction along the vesicle surface. The electronically excited cyanine is quenched by electron transfer from the phospholipid membrane bound triphenylbenzyl borate anion, which is located in the lipid bilayer interior. The PMD exhibits sequential reactions following electronic excitation with the novel feature that the steps proceed with orthogonal orientation: energy transfer occurs parallel to the membrane surface, and electron transfer occurs perpendicular to the surface. Photobleaching and fluorescence quenching experiments verify the transfer reactions, and Stern-Volmer analysis was used to estimate the reaction rate constants. At the highest concentrations examined of energy and electron acceptor ca. 60% of the photoexcited porphyrins were quenched by energy transfer to the cyanine. 56 refs., 6 figs., 3 tabs.

  9. Surfactant-enhanced singlet energy transfer from the charge-transfer excited state of tris(2,2-bipyridine) ruthenium(II)

    NASA Astrophysics Data System (ADS)

    Mandal, Krishnagopal; Demas, J. N.

    1981-12-01

    Very efficient (45-75%) sodium lauryl sulfate (NaLS) enhanced singlet enengy transfer has been demonstrated from the spin-orbit charge-transfer excited state of [Ru(bpy) 3] 2+ (bpy = 2,2'-bipyridine) to the xxx violet, oxazine 1, and rhodamine 101 at concentrations of 10 -5 M, Energy transfer occurs in xxx.

  10. Rotational Energy Transfer of N2 Determined Using a New Ab Initio Potential Energy Surface

    NASA Technical Reports Server (NTRS)

    Huo, Winifred M.; Stallcop, James R.; Partridge, Harry; Langhoff, Stephen R. (Technical Monitor)

    1997-01-01

    A new N2-N2 rigid-rotor surface has been determined using extensive Ab Initio quantum chemistry calculations together with recent experimental data for the second virial coefficient. Rotational energy transfer is studied using the new potential energy surface (PES) employing the close coupling method below 200 cm(exp -1) and coupled state approximation above that. Comparing with a previous calculation based on the PES of van der Avoird et al.,3 it is found that the new PES generally gives larger cross sections for large (delta)J transitions, but for small (delta)J transitions the cross sections are either comparable or smaller. Correlation between the differences in the cross sections and the two PES will be attempted. The computed cross sections will also be compared with available experimental data.

  11. Time-resolved Förster-resonance-energy-transfer DNA assay on an active CMOS microarray

    PubMed Central

    Schwartz, David Eric; Gong, Ping; Shepard, Kenneth L.

    2008-01-01

    We present an active oligonucleotide microarray platform for time-resolved Förster resonance energy transfer (TR-FRET) assays. In these assays, immobilized probe is labeled with a donor fluorophore and analyte target is labeled with a fluorescence quencher. Changes in the fluorescence decay lifetime of the donor are measured to determine the extent of hybridization. In this work, we demonstrate that TR-FRET assays have reduced sensitivity to variances in probe surface density compared with standard fluorescence-based microarray assays. Use of an active array substrate, fabricated in a standard complementary metal-oxide-semiconductor (CMOS) process, provides the additional benefits of reduced system complexity and cost. The array consists of 4096 independent single-photon avalanche diode (SPAD) pixel sites and features on-chip time-to-digital conversion. We demonstrate the functionality of our system by measuring a DNA target concentration series using TR-FRET with semiconductor quantum dot donors. PMID:18515059

  12. Communication: Exciton-phonon information flow in the energy transfer process of photosynthetic complexes

    SciTech Connect

    Rebentrost, P.; Aspuru-Guzik, Alan

    2011-03-14

    Non-Markovian and nonequilibrium phonon effects are believed to be key ingredients in the energy transfer in photosynthetic complexes, especially in complexes which exhibit a regime of intermediate exciton–phonon coupling. In this work, we utilize a recently developed measure for non-Markovianity to elucidate the exciton–phonon dynamics in terms of the information flow between electronic and vibrational degrees of freedom. We study the measure in the hierarchical equation of motion approach which captures strong coupling effects and nonequilibrium molecular reorganization. We propose an additional trace distance measure for the information flow that could be extended to other master equations. We find that for a model dimer system and for the Fenna–Matthews–Olson complex the non-Markovianity is significant under physiological conditions.

  13. Proposal for probing energy transfer pathway by single-molecule pump-dump experiment

    PubMed Central

    Tao, Ming-Jie; Ai, Qing; Deng, Fu-Guo; Cheng, Yuan-Chung

    2016-01-01

    The structure of Fenna-Matthews-Olson (FMO) light-harvesting complex had long been recognized as containing seven bacteriochlorophyll (BChl) molecules. Recently, an additional BChl molecule was discovered in the crystal structure of the FMO complex, which may serve as a link between baseplate and the remaining seven molecules. Here, we investigate excitation energy transfer (EET) process by simulating single-molecule pump-dump experiment in the eight-molecules complex. We adopt the coherent modified Redfield theory and non-Markovian quantum jump method to simulate EET dynamics. This scheme provides a practical approach of detecting the realistic EET pathway in BChl complexes with currently available experimental technology. And it may assist optimizing design of artificial light-harvesting devices. PMID:27277702

  14. Proposal for probing energy transfer pathway by single-molecule pump-dump experiment

    NASA Astrophysics Data System (ADS)

    Tao, Ming-Jie; Ai, Qing; Deng, Fu-Guo; Cheng, Yuan-Chung

    2016-06-01

    The structure of Fenna-Matthews-Olson (FMO) light-harvesting complex had long been recognized as containing seven bacteriochlorophyll (BChl) molecules. Recently, an additional BChl molecule was discovered in the crystal structure of the FMO complex, which may serve as a link between baseplate and the remaining seven molecules. Here, we investigate excitation energy transfer (EET) process by simulating single-molecule pump-dump experiment in the eight-molecules complex. We adopt the coherent modified Redfield theory and non-Markovian quantum jump method to simulate EET dynamics. This scheme provides a practical approach of detecting the realistic EET pathway in BChl complexes with currently available experimental technology. And it may assist optimizing design of artificial light-harvesting devices.

  15. Prolonged irradiation of enhanced cyan fluorescent protein or Cerulean can invalidate Forster resonance energy transfer measurements.

    PubMed

    Hoffmann, Birgit; Zimmer, Thomas; Klöcker, Nikolaj; Kelbauskas, Laimonas; König, Karsten; Benndorf, Klaus; Biskup, Christoph

    2008-01-01

    Since its discovery, green fluorescent protein (GFP) and its variants have proven to be a good and convenient fluorescent label for proteins: GFP and other visible fluorescent proteins (VFPs) can be fused selectively to the protein of interest by simple cloning techniques and develop fluorescence without additional cofactors. Among the steadily growing collection of VFPs, several pairs can be chosen that can serve as donor and acceptor fluorophores in Forster resonance energy transfer (FRET) experiments. Among them, the cyan fluorescent proteins (ECFP/Cerulean) and the enhanced yellow fluorescent protein (EYFP) are most commonly used. We show that ECFP and Cerulean have some disadvantages despite their common use: Upon irradiation with light intensities that are commonly used for intensity- and lifetime-based FRET measurements, both the fluorescence intensity and the fluorescence lifetime of ECFP and Cerulean decrease. This can hamper both intensity- and lifetime-based FRET measurements and emphasizes the need for control measurements to exclude these artifacts. PMID:18601529

  16. Highly efficient energy transfer from quantum dot to allophycocyanin in hybrid structures.

    PubMed

    Karpulevich, A A; Maksimov, E G; Sluchanko, N N; Vasiliev, A N; Paschenko, V Z

    2016-07-01

    Excitation energy transfer (EET) is observed in hybrid structures that composed of allophycocyanin and CdSe/ZnS core-shell quantum dot (QD). We demonstrate that the EET efficiency in such systems could be significantly increased under conditions inducing monomerization of allophycocyanin trimers. For these purposes, the EET efficiency was estimated under different experimental conditions (pH, high temperature or the presence of NaSCN) for self-assembled hybrid structures. Additionally, the hybrid structures were stabilized by covalent coupling which resulted in approximately 20-fold enhancement of allophycocyanin fluorescence upon excitation of QDs. The observed effect provides new opportunities for the practical implementation of hybrid systems as fluorescent markers. PMID:27101277

  17. Proposal for probing energy transfer pathway by single-molecule pump-dump experiment.

    PubMed

    Tao, Ming-Jie; Ai, Qing; Deng, Fu-Guo; Cheng, Yuan-Chung

    2016-01-01

    The structure of Fenna-Matthews-Olson (FMO) light-harvesting complex had long been recognized as containing seven bacteriochlorophyll (BChl) molecules. Recently, an additional BChl molecule was discovered in the crystal structure of the FMO complex, which may serve as a link between baseplate and the remaining seven molecules. Here, we investigate excitation energy transfer (EET) process by simulating single-molecule pump-dump experiment in the eight-molecules complex. We adopt the coherent modified Redfield theory and non-Markovian quantum jump method to simulate EET dynamics. This scheme provides a practical approach of detecting the realistic EET pathway in BChl complexes with currently available experimental technology. And it may assist optimizing design of artificial light-harvesting devices. PMID:27277702

  18. A spectroscopist's view of energy states, energy transfers, and chemical reactions.

    PubMed

    Moore, C Bradley

    2007-01-01

    This chapter describes a research career beginning at Berkeley in 1960, shortly after Sputnik and the invention of the laser. Following thesis work on vibrational spectroscopy and the chemical reactivity of small molecules, we studied vibrational energy transfers in my own lab. Collision-induced transfers among vibrations of a single molecule, from one molecule to another, and from vibration to rotation and translation were elucidated. My research group also studied the competition between vibrational relaxation and chemical reaction for potentially reactive collisions with one molecule vibrationally excited. Lasers were used to enrich isotopes by the excitation of a predissociative transition of a selected isotopomer. We also tested the hypotheses of transition-state theory for unimolecular reactions of ketene, formaldehyde, and formyl fluoride by (a) resolving individual molecular eigenstates above a dissociation threshold, (b) locating vibrational levels at the transition state, (c) observing quantum resonances in the barrier region for motion along a reaction coordinate, and (d) studying energy release to fragments. PMID:17034339

  19. Energy spectrum transfer equations of solar wind turbulence

    NASA Technical Reports Server (NTRS)

    Tu, C.-Y.

    1995-01-01

    The recent studies of transfer equations for solar wind magnetohydrodynamic (MHD) turbulence are reviewed with emphasis on the comparison with the statistical observational results. Helios and Voyager missions provide an opportunity to study the the radial evolution of the power spectrum. the cross-helicity the Alfven ratio and the minimum variance direction. Spectrum transfer equations are considered as a tool to explore the nature of this radial evolution of the fluctuations. The transfer equations are derived from incompressible MHD equations. Generally one needs to make assumptions about the nature of the fluctuations and the nature of the turbulent non-linear interactions to obtain numerical results which can be compared with the observations. Some special model results for several simple cases SUCH as for structures or strong mixing. for Alfven waves with weak turbulent interactions. and for a superposition of structures and Alfven waves. are discussed. The difference between the various approaches to derive and handle the transfer equations are also addressed. Finally some theoretical description of the compressible fluctuations are also briefly reviewed.

  20. Inter-phase heat transfer and energy coupling in turbulent dispersed multiphase flows

    NASA Astrophysics Data System (ADS)

    Ling, Y.; Balachandar, S.; Parmar, M.

    2016-03-01

    The present paper addresses important fundamental issues of inter-phase heat transfer and energy coupling in turbulent dispersed multiphase flows through scaling analysis. In typical point-particle or two-fluid approaches, the fluid motion and convective heat transfer at the particle scale are not resolved and the momentum and energy coupling between fluid and particles are provided by proper closure models. By examining the kinetic energy transfer due to the coupling forces from the macroscale to microscale fluid motion, closure models are obtained for the contributions of the coupling forces to the energy coupling. Due to the inviscid origin of the added-mass force, its contribution to the microscale kinetic energy does not contribute to dissipative transfer to fluid internal energy as was done by the quasi-steady force. Time scale analysis shows that when the particle is larger than a critical diameter, the diffusive-unsteady kernel decays at a time scale that is smaller than the Kolmogorov time scale. As a result, the computationally costly Basset-like integral form of diffusive-unsteady heat transfer can be simplified to a non-integral form. Conventionally, the fluid-to-particle volumetric heat capacity ratio is used to evaluate the relative importance of the unsteady heat transfer to the energy balance of the particles. Therefore, for gas-particle flows, where the fluid-to-particle volumetric heat capacity ratio is small, unsteady heat transfer is usually ignored. However, the present scaling analysis shows that for small fluid-to-particle volumetric heat capacity ratio, the importance of the unsteady heat transfer actually depends on the ratio between the particle size and the Kolmogorov scale. Furthermore, the particle mass loading multiplied by the heat capacity ratio is usually used to estimate the importance of the thermal two-way coupling effect. Through scaling argument, improved estimates are established for the energy coupling parameters of each

  1. High Energy Density Additives for Hybrid Fuel Rockets to Improve Performance and Enhance Safety

    NASA Technical Reports Server (NTRS)

    Jaffe, Richard L.

    2014-01-01

    We propose a conceptual study of prototype strained hydrocarbon molecules as high energy density additives for hybrid rocket fuels to boost the performance of these rockets without compromising safety and reliability. Use of these additives could extend the range of applications for which hybrid rockets become an attractive alternative to conventional solid or liquid fuel rockets. The objectives of the study were to confirm and quantify the high enthalpy of these strained molecules and to assess improvement in rocket performance that would be expected if these additives were blended with conventional fuels. We confirmed the chemical properties (including enthalpy) of these additives. However, the predicted improvement in rocket performance was too small to make this a useful strategy for boosting hybrid rocket performance.

  2. 40 CFR 74.47 - Transfer of allowances from the replacement of thermal energy-combustion sources.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... and End of Year Compliance § 74.47 Transfer of allowances from the replacement of thermal energy... seeking to transfer allowances based on the replacement of thermal energy. (3) Contents. Each thermal... energy plan, the Administrator will annually transfer allowances to the compliance account of each...

  3. A model for energy transfer in collisions of atoms with highly excited molecules.

    PubMed

    Houston, Paul L; Conte, Riccardo; Bowman, Joel M

    2015-05-21

    A model for energy transfer in the collision between an atom and a highly excited target molecule has been developed on the basis of classical mechanics and turning point analysis. The predictions of the model have been tested against the results of trajectory calculations for collisions of five different target molecules with argon or helium under a variety of temperatures, collision energies, and initial rotational levels. The model predicts selected moments of the joint probability distribution, P(Jf,ΔE) with an R(2) ≈ 0.90. The calculation is efficient, in most cases taking less than one CPU-hour. The model provides several insights into the energy transfer process. The joint probability distribution is strongly dependent on rotational energy transfer and conservation laws and less dependent on vibrational energy transfer. There are two mechanisms for rotational excitation, one due to motion normal to the intermolecular potential and one due to motion tangential to it and perpendicular to the line of centers. Energy transfer is found to depend strongly on the intermolecular potential and only weakly on the intramolecular potential. Highly efficient collisions are a natural consequence of the energy transfer and arise due to collisions at "sweet spots" in the space of impact parameter and molecular orientation. PMID:25907301

  4. Energy transfer between rhodamine 3B and oxazine 4 in synthetic-saponite dispersions and films.

    PubMed

    Czímerová, A; Iyi, N; Bujdák, J

    2007-02-15

    The objective of this study was the investigation of energy transfer between the laser dyes rhodamine 3B (R3B) and oxazine 4 (Ox4) adsorbed on the surface of synthetic Sumecton saponite (Sum). The process of energy transfer was studied for both saponite dispersions and oriented solid films. The electronic properties, luminescence, and the energy transfer process were described by UV-vis absorption and fluorescence spectroscopy. For the efficiency of the energy transfer process, the concentrations of energy donor and acceptor components on a clay mineral surface were found to be essential. A side reaction of the molecular assembly formation reduced both the luminescence and energy-transfer yields, mainly due to fluorescence quenching. The quenching was more problematic for the solid film specimens, where an appropriate modification of the inorganic host with hydrophobic alkylammonium cations was used to achieve a higher luminescence. Due to the higher tendency of Ox4 to form nonluminescent aggregates at higher concentrations, the lowering of the Ox4 concentration further improved the luminescent properties of the films. In this case, the energy transfer occurring in the solid film from R3B to Ox4 was clearly proven. PMID:17118384

  5. Restricted access chiral stationary phase synthesized via reversible addition-fragmentation chain-transfer polymerization for direct analysis of biological samples by high performance liquid chromatography.

    PubMed

    Song, Wen-Jun; Wei, Ji-Ping; Wang, Su-Ying; Wang, Huai-Song

    2014-06-17

    Novel hydrophilic microparticles containing β-cyclodextrin (β-CD) were prepared via one-pot synthesis using reversible addition-fragmentation chain-transfer (RAFT) precipitation polymerization, a "controlled/living" radical polymerization technique. The polymerization was initiated by hydrophilic macromolecular chain-transfer agent [poly(2-hydroxyethyl methacrylate), PHEMA]. The hydrophilic PHEMA on the surface of microparticles can well improve their surface hydrophilicity and lead to their biological compatibility. As chiral restricted access material (RAM), the hydrophilic microparticles can be used for determination of enantiomers in biological samples with direct injection via HPLC analysis. PMID:24890695

  6. Reduction of ammonia emission by shallow slurry injection: injection efficiency and additional energy demand.

    PubMed

    Hansen, Martin N; Sommer, Sven G; Madsen, Niels P

    2003-01-01

    Ammonia (NH3) emission from livestock production causes undesirable environmental effects and a loss of plant-available nitrogen. Much atmospheric NH3 is lost from livestock manure applied in the field. The NH3 emission may be reduced by slurry injection, but slurry injection in general, and especially on grassland, increases the energy demand and places heavy demands on the slurry injection techniques used. The reduction in NH3 emission, injection efficiency, and energy demand of six different shallow slurry-injection techniques was examined. The NH3 emission from cattle slurry applied to grassland was reduced by all the injectors tested in the study, but there were major differences in the NH3 reduction potential of the different types of injectors. Compared with the trailing hose spreading technique, the NH3 loss was reduced by 75% when cattle slurry was injected using the most efficient slurry injection technique, and by 20% when incorporated by the least efficient injection technique. The reduction in NH3 emission was correlated with injection depth and the volume of the slot created. The additional energy demand for reducing ammonia emissions by slurry injection was approximately 13 000 kJ ha(-1) for a 20% reduction and 34 000 kJ ha(-1) for a 75% reduction. The additional energy demand corresponds to additional emissions of, respectively, 5.6 and 14.5 kg CO2 per ha injected. PMID:12809311

  7. 78 FR 2985 - Moretown Hydro Energy Company; Ampersand Moretown Hydro, LLC; Notice of Application for Transfer...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-01-15

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF ENERGY Federal Energy Regulatory Commission Moretown Hydro Energy Company; Ampersand Moretown Hydro, LLC; Notice of Application for Transfer of License, and Soliciting Comments and Motions To Intervene On September 25,...

  8. Non-pairwise additivity of the leading-order dispersion energy

    SciTech Connect

    Hollett, Joshua W.

    2015-02-28

    The leading-order (i.e., dipole-dipole) dispersion energy is calculated for one-dimensional (1D) and two-dimensional (2D) infinite lattices, and an infinite 1D array of infinitely long lines, of doubly occupied locally harmonic wells. The dispersion energy is decomposed into pairwise and non-pairwise additive components. By varying the force constant and separation of the wells, the non-pairwise additive contribution to the dispersion energy is shown to depend on the overlap of density between neighboring wells. As well separation is increased, the non-pairwise additivity of the dispersion energy decays. The different rates of decay for 1D and 2D lattices of wells is explained in terms of a Jacobian effect that influences the number of nearest neighbors. For an array of infinitely long lines of wells spaced 5 bohrs apart, and an inter-well spacing of 3 bohrs within a line, the non-pairwise additive component of the leading-order dispersion energy is −0.11 kJ mol{sup −1} well{sup −1}, which is 7% of the total. The polarizability of the wells and the density overlap between them are small in comparison to that of the atomic densities that arise from the molecular density partitioning used in post-density-functional theory (DFT) damped dispersion corrections, or DFT-D methods. Therefore, the nonadditivity of the leading-order dispersion observed here is a conservative estimate of that in molecular clusters.

  9. Excitation energy transfer in photosynthetic protein-pigment complexes

    NASA Astrophysics Data System (ADS)

    Yeh, Shu-Hao

    Quantum biology is a relatively new research area which investigates the rules that quantum mechanics plays in biology. One of the most intriguing systems in this field is the coherent excitation energy transport (EET) in photosynthesis. In this document I will discuss the theories that are suitable for describing the photosynthetic EET process and the corresponding numerical results on several photosynthetic protein-pigment complexes (PPCs). In some photosynthetic EET processes, because of the electronic coupling between the chromophores within the system is about the same order of magnitude as system-bath coupling (electron-phonon coupling), a non-perturbative method called hierarchy equation of motion (HEOM) is applied to study the EET dynamics. The first part of this thesis includes brief introduction and derivation to the HEOM approach. The second part of this thesis the HEOM method will be applied to investigate the EET process within the B850 ring of the light harvesting complex 2 (LH2) from purple bacteria, Rhodopseudomonas acidophila. The dynamics of the exciton population and coherence will be analyzed under different initial excitation configurations and temperatures. Finally, how HEOM can be implemented to simulate the two-dimensional electronic spectra of photosynthetic PPCs will be discussed. Two-dimensional electronic spectroscopy is a crucial experimental technique to probe EET dynamics in multi-chromophoric systems. The system we are interested in is the 7-chromophore Fenna-Matthews-Olson (FMO) complex from green sulfur bacteria, Prosthecochloris aestuarii. Recent crystallographic studies report the existence of an additional (eighth) chromophore in some of the FMO monomers. By applying HEOM we are able to calculate the two-dimensional electronic spectra of the 7-site and 8-site FMO complexes and investigate the functionality of the eighth chromophore.

  10. Temperature dependence of vibrational energy transfer between vibrationally excited polyatomic molecules and bath gases

    NASA Astrophysics Data System (ADS)

    Zalesskaya, G. A.; Yakovlev, D. L.; Sambor, E. G.

    2000-08-01

    Efficiency of vibrational energy transfer (VET) in vibrational quasicontinuum of triplet states was estimated from the dependence of time-resolved delayed fluorescence of benzophenone and anthraquinone on bath gas pressure. The negative temperature dependence for vibration-vibration (V-V) and positive for vibration-translation (V-T) energy transfers from benzophenone and anthraquinone to bath gases (C 2H 4, SF 6, CCl 4, C 5H 12) were obtained between 373 and 553 K. Polarizability and dipole moment of colliding molecules seem to affect the efficiency of V-V relaxation. These data reflect the dominance of long-range attractive interactions in V-V energy transfer and short-range repulsive interactions in V-T energy transfer.

  11. Investigation of Fluorescence Resonance Energy Transfer between Fluorescein and Rhodamine 6G

    NASA Astrophysics Data System (ADS)

    Saha, Jaba; Datta Roy, Arpan; Dey, Dibyendu; Chakraborty, Santanu; Bhattacharjee, D.; Paul, P. K.; Hussain, Syed Arshad

    2015-10-01

    Fluorescence Resonance Energy Transfer between two organic dyes Fluorescein and Rhodamine 6G was investigated in aqueous solution in presence and absence of synthetic clay laponite. Spectroscopic studies suggest that both the dyes were present mainly as monomer in solution. Fluorescence Resonance Energy Transfer occurred from Fluorescein to Rhodamine 6G in solutions. Energy transfer efficiency increases in presence of laponite and the maximum efficiency was 72.00% in aqueous laponite dispersion. Energy transfer efficiency was found to be pH sensitive. It has been demonstrated that with proper calibration it is possible to use the present system under investigation to sense pH over a wide range from 1.5 to 8.0.

  12. Color-Tunable Resonant Photoluminescence and Cavity-Mediated Multistep Energy Transfer Cascade.

    PubMed

    Okada, Daichi; Nakamura, Takashi; Braam, Daniel; Dao, Thang Duy; Ishii, Satoshi; Nagao, Tadaaki; Lorke, Axel; Nabeshima, Tatsuya; Yamamoto, Yohei

    2016-07-26

    Color-tunable resonant photoluminescence (PL) was attained from polystyrene microspheres doped with a single polymorphic fluorescent dye, boron-dipyrrin (BODIPY) 1. The color of the resonant PL depends on the assembling morphology of 1 in the microspheres, which can be selectively controlled from green to red by the initial concentration of 1 in the preparation process of the microspheres. Studies on intersphere PL propagation with multicoupled microspheres, prepared by micromanipulation technique, revealed that multistep photon transfer takes place through the microspheres, accompanying energy transfer cascade with stepwise PL color change. The intersphere energy transfer cascade is direction selective, where energy donor-to-acceptor down conversion direction is only allowed. Such cavity-mediated long-distance and multistep energy transfer will be advantageous for polymer photonics device application. PMID:27348045

  13. Electronic coherence and the kinetics of energy transfer in light-harvesting systems

    NASA Astrophysics Data System (ADS)

    Huo, Pengfei; Coker, David; Miller, Thomas

    Recent 2D-spectroscopy experiments have observed transient electronic coherence in natural and artificial light harvesting systems, which raises questions about the role of electronic coherence in facilitating excitation energy transfer (EET) processes. In this talk, we introduce the recently developed partial linearized path-integral (PLPI) method, which can accurately simulate exciton transfer dynamics across multiple reaction regimes, as well as reliably describe the electronic coherence among excitonic states. Further, we develop a strategy that enables the analysis of the relative impact of static and dynamic electronic coherence. With PLPI simulations, we find that energy transfer dynamics are almost entirely dominated by static coherence effects; dynamic coherence is found to cause only minor effects. These conclusions are consistent with the historical view that emphasizes the importance of energy-level alignment for efficient incoherent energy transfer,while suggesting a less important role for more exotic electronic coherence effects that have been recently emphasized.

  14. Simple Model for Gold Nano Particles Concentration Dependence of Resonance Energy Transfer Intensity

    NASA Astrophysics Data System (ADS)

    Hoa, N. M.; Ha, C. V.; Nga, D. T.; Lan, N. T.; Nhung, T. H.; Viet, N. A.

    2016-06-01

    Gold nano particles (GNPs) concentration dependence of the energy transfer occurs between the fluorophores and GNPs is investigated. In the case of theses pairs, GNPs can enhance or quench the fluorescence of fluorophores depending upon the relative magnitudes of two energy transfer mechanisms: i) the plasmonic field enhancement at the fluorophores emission frequencies (plasmon coupled fluorescence enhancement) and ii) the localized plasmon coupled Forster energy transfer from fluorescent particles to gold particles, which quenches the fluorescence. The competition of these mechanisms is depending on the spectral overlap of fluorophores and GNPs, their relative concentration, excitation wavelength. Simple two branches surface plasmon polariton model for GNPs concentration dependence of the energy transfer is proposed. The experimental data and theoretical results confirm our findings.

  15. Development of flexible, free-standing, thin films for additive manufacturing and localized energy generation

    SciTech Connect

    Clark, Billy; McCollum, Jena; Pantoya, Michelle L.; Heaps, Ronald J.; Daniels, Michael A.

    2015-08-15

    Film energetics are becoming increasingly popular because a variety of technologies are driving a need for localized energy generation in a stable, safe and flexible form. Aluminum (Al) and molybdenum trioxide (MoO{sub 3}) composites were mixed into a silicon binder and extruded using a blade casting technique to form flexible free-standing films ideal for localized energy generation. Since this material can be extruded onto a surface it is well suited to additive manufacturing applications. This study examines the influence of 0-35% by mass potassium perchlorate (KClO{sub 4}) additive on the combustion behavior of these energetic films. Without KClO{sub 4} the film exhibits thermal instabilities that produce unsteady energy propagation upon reaction. All films were cast at a thickness of 1 mm with constant volume percent solids to ensure consistent rheological properties. The films were ignited and flame propagation was measured. The results show that as the mass percent KClO{sub 4} increased, the flame speed increased and peaked at 0.43 cm/s and 30 wt% KClO{sub 4}. Thermochemical equilibrium simulations show that the heat of combustion increases with increasing KClO{sub 4} concentration up to a maximum at 20 wt% when the heat of combustion plateaus, indicating that the increased chemical energy liberated by the additional KClO{sub 4} promotes stable energy propagation. Differential scanning calorimeter and thermogravimetric analysis show that the silicone binder participates as a fuel and reacts with KClO{sub 4} adding energy to the reaction and promoting propagation.

  16. Development of flexible, free-standing, thin films for additive manufacturing and localized energy generation

    DOE PAGESBeta

    Clark, Billy; McCollum, Jena; Pantoya, Michelle L.; Heaps, Ronald J.; Daniels, Michael A.

    2015-08-01

    Film energetics are becoming increasingly popular because a variety of technologies are driving a need for localized energy generation in a stable, safe and flexible form. Aluminum (Al) and molybdenum trioxide (MoO₃) composites were mixed into a silicon binder and extruded using a blade casting technique to form flexible free-standing films ideal for localized energy generation. Since this material can be extruded onto a surface it is well suited to additive manufacturing applications. This study examines the influence of 0-35% by mass potassium perchlorate (KClO₄) additive on the combustion behavior of these energetic films. Without KClO₄ the film exhibits thermalmore » instabilities that produce unsteady energy propagation upon reaction. All films were cast at a thickness of 1 mm with constant volume percent solids to ensure consistent rheological properties. The films were ignited and flame propagation was measured. The results show that as the mass percent KClO₄ increased, the flame speed increased and peaked at 0.43 cm/s and 30 wt% KClO₄. Thermochemical equilibrium simulations show that the heat of combustion increases with increasing KClO₄ concentration up to a maximum at 20 wt% when the heat of combustion plateaus, indicating that the increased chemical energy liberated by the additional KClO₄ promotes stable energy propagation. Differential scanning calorimeter and thermogravimetric analysis show that the silicone binder participates as a fuel and reacts with KClO₄ adding energy to the reaction and promoting propagation.« less

  17. Molecular level energy and electron transfer processes at nanocrystalline titanium dioxide interfaces

    NASA Astrophysics Data System (ADS)

    Farzad, Fereshteh

    This thesis describes photo-induced molecular electron and energy transfer processes occurring at nanocrystalline semiconductor interfaces. The Introductory Chapter provides background and describes how these materials may be useful for solar energy conversion. In Chapter 2, results describing excitation of Ru(deeb)(bpy)2 2+, bis(2,2'-bipyridine)(2,2'-bipyridine-4,4 '-diethylester)ruthenium(II) hexafluorophosphate, bound to nanocrystalline TiO2 thin films, immersed in an acetonitrile bath are presented. The data indicates that light excitation forms predominately long-lived metal-to-ligand charge-transfer, MLCT, excited states under these conditions. Modeling of the data as a function of irradiance has been accomplished assuming parallel unimolecular and bimolecular excited state deactivation processes. The quantum yield for excited state formation depends on the excitation irradiance, consistent with triplet-triplet annihilation processes that occur with k > 1 x 108 s-1. Chapter 3 extends the work described in Chapter 2 to LiClO4 acetonitrile solutions. Li+ addition results in a red shift in the MLCT absorption and photoluminescence, PL, and a concentration dependent quenching of the PL intensity on TiO2. The Li+ induced spectroscopic changes were found to be reversible by varying the electrolyte composition. A second-order kinetic model quantified charge recombination transients. A model is proposed wherein Li+ ion adsorption stabilizes TiO2 acceptor states resulting in energetically more favorable interfacial electron transfer. The photophysical and photoelectrochemical properties of porous nanocrystalline anatase TiO2 electrodes modified with Ru(deeb)(bpy)2 2+, Os(deeb)(bpy)22+, and mixtures of both are described in Chapters 4 and 5. In regenerative solar cells with 0.5 M LiI/0.05 M I2 acetonitrile electrolyte, both compounds efficiently inject electrons into TiO2 producing monochromatic incident photon-to-current efficiencies (IPCE), IPCE (460 nm) = 0.70 + 0

  18. Spectral Properties and Energy Transfer between Ce(3+) and Yb(3+) in the Ca3Sc2Si3O12 Host: Is It an Electron Transfer Mechanism?

    PubMed

    Zhou, Lei; Tanner, Peter A; Ning, Lixin; Zhou, Weijie; Liang, Hongbin; Zheng, Lirong

    2016-07-21

    The downshifting from Ce(3+) blue emission to Yb(3+) near-infrared emission has been studied in the garnet host Ca2.8-2xCe0.1YbxNa0.1+xSc2Si3O12 (x = 0-0.36). The downshifting does not involve quantum cutting, but one incident blue photon is transferred from Ce(3+) to Yb(3+) with an energy transfer efficiency up to 90% when x = 0.36 for the Yb(3+) dopant ion. For x ≤ 0.15, a multiphonon-assisted electric dipole-electric quadrupole mechanism of energy transfer dominates, while for the highest concentration of Yb(3+) employed, the electron transfer mechanism is confirmed. A temperature-dependent increase of the Ce(3+) → Yb(3+) energy transfer rate does not exclusively indicate the electron transfer mechanism. The application of the material to solar energy conversion is indicated. PMID:27331405

  19. The energy transfer in the TEMP-4M pulsed ion beam accelerator

    SciTech Connect

    Isakova, Y. I.; Pushkarev, A. I.; Khaylov, I. P.

    2013-07-15

    The results of a study of the energy transfer in the TEMP-4M pulsed ion beam accelerator are presented. The energy transfer efficiency in the Blumlein and a self-magnetically insulated ion diode was analyzed. Optimization of the design of the accelerator allows for 85% of energy transferred from Blumlein to the diode (including after-pulses), which indicates that the energy loss in Blumlein and spark gaps is insignificant and not exceeds 10%–12%. Most losses occur in the diode. The efficiency of energy supplied to the diode to the energy of accelerated ions is 8%–9% for a planar strip self-magnetic MID, 12%–15% for focusing diode and 20% for a spiral self-magnetic MID.

  20. Methods and energy storage devices utilizing electrolytes having surface-smoothing additives

    SciTech Connect

    Xu, Wu; Zhang, Jiguang; Graff, Gordon L; Chen, Xilin; Ding, Fei

    2015-11-12

    Electrodeposition and energy storage devices utilizing an electrolyte having a surface-smoothing additive can result in self-healing, instead of self-amplification, of initial protuberant tips that give rise to roughness and/or dendrite formation on the substrate and anode surface. For electrodeposition of a first metal (M1) on a substrate or anode from one or more cations of M1 in an electrolyte solution, the electrolyte solution is characterized by a surface-smoothing additive containing cations of a second metal (M2), wherein cations of M2 have an effective electrochemical reduction potential in the solution lower than that of the cations of M1.

  1. Evidence of energy transfer in nanoparticle-porphyrins conjugates for radiation therapy enhancement

    NASA Astrophysics Data System (ADS)

    Kudinov, Konstantin; Cooper, Daniel; Tyagi, Pooja; Bekah, Devesh; Bhattacharyya, Dhrittiman; Hill, Colin; Ha, Jonathan Kin; Nadeau, Jay; Bradforth, Stephen

    2015-03-01

    We report progress towards combining radiation therapy (RT) and photodynamic therapy (PDT) using scintillating nanoparticle (NP)-photosensitizer conjugates. In this approach, scintillating NPs are excited by clinically relevant ionizing radiation sources and subsequently transfer energy to conjugated photosensitizers via FRET, acting as an energy mediator between ionizing radiation and photosensitizer molecules. The excited photosensitizers generate reactive oxygen species that can induce local damage and immune response. Advantages of the scheme include: 1) Compared with traditional radiation therapy, a possible decrease of the total radiation dose needed to eliminate the lesion; 2) Compared with traditional PDT, the ability to target deeper and more highly pigmented lesions; 3) The possibility of additional photosensitizing effects due to the scintillation of the nanoparticles. In this work, the photosensitizer molecule chlorin e6 was covalently bound to the surface of LaF3:Ce NPs. After conjugation, the photoluminescence intensity of NPs decreased, and fluorescence lifetime of conjugated chlorin e6 became sensitive to excitation wavelength, suggesting rapid FRET. In addition, scintillation spectra of nanoparticles were measured. Preliminary calculations suggest that the observed scintillation efficiencies are sufficient to enhance RT. In vitro cancer cell studies suggest conjugates are taken up by cells. Survival curves with radiation exposure suggest that the particles alone cause radiosensitization comparable to that seen with gold nanoparticles.

  2. Efficient evaluation of collisional energy transfer terms for plasma particle simulations

    NASA Astrophysics Data System (ADS)

    Turrell, A. E.; Sherlock, M.; Rose, S. J.

    2016-01-01

    Particle-based simulations, such as in particle-in-cell (PIC) codes, are widely used in plasma physics research. The analysis of particle energy transfers, as described by the second moment of the Boltzmann equation, is often necessary within these simulations. We present computationally efficient, analytically derived equations for evaluating collisional energy transfer terms from simulations using discrete particles. The equations are expressed as a sum over the properties of the discrete particles.

  3. Tuning the implosion symmetry of ICF targets via controlled crossed-beam energy transfer

    SciTech Connect

    Michel, P; Divol, L; Williams, E; Weber, S; Thomas, C A; Callahan, D A; Haan, S W; Salmonson, J D; Dixit, S; Hinkel, D E; Edwards, M J; MacGowan, B J; Lindl, J D; Glenzer, S H; Suter, L

    2008-07-29

    Radiative hydrodynamics simulations of ignition experiments show that energy transfer between crossing laser beams allows tuning of the implosion symmetry. A new full-scale, three dimensional quantitative model has been developed for crossed-beam energy transfer, allowing calculations of the propagation and coupling of multiple laser beams and their associated plasma waves in ignition hohlraums. This model has been implemented in a radiative-hydrodynamics code, demonstrating control of the implosion symmetry by a wavelength separation between cones of laser beams.

  4. Energy transfer enhancement by oxygen perturbation of spin-forbidden electronic transitions in aromatic systems

    NASA Astrophysics Data System (ADS)

    Monguzzi, A.; Tubino, R.; Salamone, M. M.; Meinardi, F.

    2010-09-01

    Triplet-triplet energy transfer in multicomponent organic systems is usually entirely ascribed to a Dexter-type mechanism involving only short-range donor/acceptor interactions. We demonstrate that the presence of molecular oxygen introduces a perturbation to the electronic structure of one of the involved moieties which can induce a large increase in the spin-forbidden transition oscillator strength so that the otherwise negligible Förster contribution dominates the overall energy transfer rate.

  5. Fluorescence energy transfer in quantum dot/azo dye complexes in polymer track membranes

    NASA Astrophysics Data System (ADS)

    Gromova, Yulia A.; Orlova, Anna O.; Maslov, Vladimir G.; Fedorov, Anatoly V.; Baranov, Alexander V.

    2013-10-01

    Fluorescence resonance energy transfer in complexes of semiconductor CdSe/ZnS quantum dots with molecules of heterocyclic azo dyes, 1-(2-pyridylazo)-2-naphthol and 4-(2-pyridylazo) resorcinol, formed at high quantum dot concentration in the polymer pore track membranes were studied by steady-state and transient PL spectroscopy. The effect of interaction between the complexes and free quantum dots on the efficiency of the fluorescence energy transfer and quantum dot luminescence quenching was found and discussed.

  6. Energy transfers in shell models for magnetohydrodynamics turbulence.

    PubMed

    Lessinnes, Thomas; Carati, Daniele; Verma, Mahendra K

    2009-06-01

    A systematic procedure to derive shell models for magnetohydrodynamic turbulence is proposed. It takes into account the conservation of ideal quadratic invariants such as the total energy, the cross helicity, and the magnetic helicity, as well as the conservation of the magnetic energy by the advection term in the induction equation. This approach also leads to simple expressions for the energy exchanges as well as to unambiguous definitions for the energy fluxes. When applied to the existing shell models with nonlinear interactions limited to the nearest-neighbor shells, this procedure reproduces well-known models but suggests a reinterpretation of the energy fluxes. PMID:19658594

  7. Energy transfer and energy level decay processes of Er3+ in water-free tellurite glass

    NASA Astrophysics Data System (ADS)

    Gomes, Laercio; Rhonehouse, Daniel; Nguyen, Dan T.; Zong, Jie; Chavez-Pirson, Arturo; Jackson, Stuart D.

    2015-12-01

    This report details the fundamental spectroscopic properties of a new class of water-free tellurite glasses studied for future applications in mid-infrared light generation. The fundamental excited state decay processes relating to the 4I11/2 → 4I13/2 transition in singly Er3+-doped Tellurium Zinc Lanthanum glass have been investigated using time-resolved fluorescence spectroscopy. The excited state dynamics was analyzed for Er2O3 concentrations between 0.5 mol% and 4 mol%. Selective laser excitation of the 4I11/2 energy level at 972 nm and selective laser excitation of the 4I13/2 energy level at 1485 nm has established that in a similar way to other Er3+-doped glasses, a strong energy-transfer upconversion by way of a dipole-dipole interaction between two excited erbium ions in the 4I13/2 level populates the 4I11/2 upper laser level of the 3 μm transition. The 4I13/2 and 4I11/2 energy levels emitted luminescence with peaks located at 1532 nm and 2734 nm respectively with luminescence efficiencies of 100% and 8% for the higher (4 mol.%) concentration sample. Results from numerical simulations showed that a population inversion is reached at a threshold pumping intensity of ∼57 kW cm-2 for a CW laser pump at 976 nm for [Er2O3] = 2 mol.%.

  8. Methanol Oxidative Dehydrogenation on Oxide Catalysts: Molecular and Dissociative Routes and Hydrogen Addition Energies as Descriptors of Reactivity

    SciTech Connect

    Deshlahra, Prashant; Iglesia, Enrique

    2014-11-13

    The oxidative dehydrogenation (ODH) of alkanols on oxide catalysts is generally described as involving H-abstraction from alkoxy species formed via O–H dissociation. Kinetic and isotopic data cannot discern between such routes and those involving kinetically-relevant H-abstraction from undissociated alkanols. Here, we combine such experiments with theoretical estimates of activation energies and entropies to show that the latter molecular routes prevail over dissociative routes for methanol reactions on polyoxometalate (POM) clusters at all practical reaction temperatures. The stability of the late transition states that mediate H-abstraction depend predominantly on the stability of the O–H bond formed, making H-addition energies (HAE) accurate and single-valued descriptors of reactivity. Density functional theory-derived activation energies depend linearly on HAE values at each O-atom location on clusters with a range of composition (H3PMo12, H4SiMo12, H3PW12, H4PV1Mo11, and H4PV1W11); both barriers and HAE values reflect the lowest unoccupied molecular orbital energy of metal centers that accept the electron and the protonation energy of O-atoms that accept the proton involved in the H-atom transfer. Bridging O-atoms form O–H bonds that are stronger than those of terminal atoms and therefore exhibit more negative HAE values and higher ODH reactivity on all POM clusters. For each cluster composition, ODH turnover rates reflect the reactivity-averaged HAE of all accessible O-atoms, which can be evaluated for each cluster composition to provide a rigorous and accurate predictor of ODH reactivity for catalysts with known structure. These relations together with oxidation reactivity measurements can then be used to estimate HAE values and to infer plausible structures for catalysts with uncertain active site structures.

  9. Sequential Energy and Electron Transfer in Polynuclear Complex Sensitized TiO2 Nanoparticles.

    PubMed

    Verma, Sandeep; Kar, Prasenjit; Banerjee, Tanmay; Das, Amitava; Ghosh, Hirendra N

    2012-06-01

    Polynuclear-polypyridyl complexes exhibit a directional energy-transfer property that can improve their photosensitization activity. In the present work, the energy-transfer process is explored in a trinuclear Ru2(∧)Os1 complex using transient absorption spectroscopy. This study reveals an efficient excitation energy transfer from the terminal (Ru(II) complex) to the core (Os(II) complex) region in the ultrafast time domain (400 fs-40 ps). The excitation energy funnel is useful in improving the functionalized core activity. This is evidenced in an interfacial electron-transfer study of Ru2(∧)Os1, Ru2(∧)Ru1, and Os1 complex sensitized TiO2 nanoparticle (TiO2 NP) systems. The intramolecular energy transfer causes sequential excitation of the core part of the Ru2(∧)Os1 complex, which leads to multiexponential electron injection into TiO2 NP. Besides this, the electronic coupling between the metal ion centers stabilizes the positive charge within the trinuclear complex, which results in a slow charge recombination reaction. This study shows that polynuclear complexes can be very useful for their panchromatic effects, unidirectional energy- and electron-transfer properties. PMID:26285635

  10. Linker proteins enable ultrafast excitation energy transfer in the phycobilisome antenna system of Thermosynechococcus vulcanus.

    PubMed

    Nganou, C; David, L; Adir, N; Mkandawire, M

    2016-01-01

    We applied a femtosecond flash method, using induced transient absorption changes, to obtain a time-resolved view of excitation energy transfer in intact phycobilisomes of Thermosynechococcus vulcanus at room temperature. Our measurement of an excitation energy transfer rate of 888 fs in phycobilisomes shows the existence of ultrafast kinetics along the phycocyanin rod subcomplex to the allophycocyanin core that is faster than expected for previous excitation energy transfer based on Förster theory in phycobilisomes. Allophycocyanin in the core further transfers energy to the terminal emitter(s) in 17 ps. In the phycobilisome, rod doublets composed of hexameric phycocyanin discs and internal linker proteins are arranged in a parallel fashion, facilitating direct rod-rod interactions. Excitonic splitting likely drives rod absorption at 635 nm as a result of strong coupling between β84 chromophores (20 ± 1 Å) in adjacent hexamers. In comparison to the absorbance of the phycobilisome antenna system of the cyanobacterium Acaryochloris marina, which possesses a single rod structure, the linkers in T. vulcanus rods induce a 17 nm red shift in the absorbance spectrum. Furthermore, the kinetics of 888 fs indicates that the presence of the linker protein induces ultrafast excitation energy transfer between phycocyanin and allophycocyanin inside the phycobilisome, which is faster than all previous excitation energy transfer in phycobilisome subunits or sub-complexes reported to date. PMID:26537632

  11. Ultrafast Charge- and Energy-Transfer Dynamics in Conjugated Polymer: Cadmium Selenide Nanocrystal Blends

    PubMed Central

    2014-01-01

    Hybrid nanocrystal–polymer systems are promising candidates for photovoltaic applications, but the processes controlling charge generation are poorly understood. Here, we disentangle the energy- and charge-transfer processes occurring in a model system based on blends of cadmium selenide nanocrystals (CdSe-NC) with poly[2-methoxy-5-(3′,7′-dimethyloctyloxy)-1,4-phenylene vinylene] (MDMO-PPV) using a combination of time-resolved absorption and luminescence measurements. The use of different capping ligands (n-butylamine, oleic acid) as well as thermal annealing allows tuning of the polymer–nanocrystal interaction. We demonstrate that energy transfer from MDMO-PPV to CdSe-NCs is the dominant exciton quenching mechanism in nonannealed blends and occurs on ultrafast time scales (<1 ps). Upon thermal annealing electron transfer becomes competitive with energy transfer, with a transfer rate of 800 fs independent of the choice of the ligand. Interestingly, we find hole transfer to be much less efficient than electron transfer and to extend over several nanoseconds. Our results emphasize the importance of tuning the organic–nanocrystal interaction to achieve efficient charge separation and highlight the unfavorable hole-transfer dynamics in these blends. PMID:24490650

  12. Bond-Specific Dissociation Following Excitation Energy Transfer for Distance Constraint Determination in the Gas Phase

    PubMed Central

    2015-01-01

    Herein, we report chemistry that enables excitation energy transfer (EET) to be accurately measured via action spectroscopy on gaseous ions in an ion trap. It is demonstrated that EET between tryptophan or tyrosine and a disulfide bond leads to excited state, homolytic fragmentation of the disulfide bond. This phenomenon exhibits a tight distance dependence, which is consistent with Dexter exchange transfer. The extent of fragmentation of the disulfide bond can be used to determine the distance between the chromophore and disulfide bond. The chemistry is well suited for the examination of protein structure in the gas phase because native amino acids can serve as the donor/acceptor moieties. Furthermore, both tyrosine and tryptophan exhibit unique action spectra, meaning that the identity of the donating chromophore can be easily determined in addition to the distance between donor/acceptor. Application of the method to the Trpcage miniprotein reveals distance constraints that are consistent with a native-like fold for the +2 charge state in the gas phase. This structure is stabilized by several salt bridges, which have also been observed to be important previously in proteins that retain native-like structures in the gas phase. The ability of this method to measure specific distance constraints, potentially at numerous positions if combined with site-directed mutagenesis, significantly enhances our ability to examine protein structure in the gas phase. PMID:25174489

  13. Bond-specific dissociation following excitation energy transfer for distance constraint determination in the gas phase.

    PubMed

    Hendricks, Nathan G; Lareau, Nichole M; Stow, Sarah M; McLean, John A; Julian, Ryan R

    2014-09-24

    Herein, we report chemistry that enables excitation energy transfer (EET) to be accurately measured via action spectroscopy on gaseous ions in an ion trap. It is demonstrated that EET between tryptophan or tyrosine and a disulfide bond leads to excited state, homolytic fragmentation of the disulfide bond. This phenomenon exhibits a tight distance dependence, which is consistent with Dexter exchange transfer. The extent of fragmentation of the disulfide bond can be used to determine the distance between the chromophore and disulfide bond. The chemistry is well suited for the examination of protein structure in the gas phase because native amino acids can serve as the donor/acceptor moieties. Furthermore, both tyrosine and tryptophan exhibit unique action spectra, meaning that the identity of the donating chromophore can be easily determined in addition to the distance between donor/acceptor. Application of the method to the Trpcage miniprotein reveals distance constraints that are consistent with a native-like fold for the +2 charge state in the gas phase. This structure is stabilized by several salt bridges, which have also been observed to be important previously in proteins that retain native-like structures in the gas phase. The ability of this method to measure specific distance constraints, potentially at numerous positions if combined with site-directed mutagenesis, significantly enhances our ability to examine protein structure in the gas phase. PMID:25174489

  14. Laboratory Studies of Thermal Energy Charge Transfer of Silicon and Iron Ions in Astrophysical Plasmas

    NASA Technical Reports Server (NTRS)

    Kwong, Victor H. S.

    1996-01-01

    Charge transfer at electron-volt energies between multiply charged atomic ions and neutral atoms and molecules is of considerable importance in astrophysics, plasma physics, and in particular, fusion plasmas. In the year covered by this report, several major tasks were completed. These include: (1) the re-calibration of the ion gauge to measure the absolute particle densities of H2, He, N2, and CO for our current measurements; (2) the analysis of data for charge transfer reactions of N(exp 2 plus) ion and He, H2, N2, and CO; (3) measurement and data analysis of the charge transfer reaction of (Fe(exp 2 plus) ion and H2; (4) charge transfer measurement of Fe(exp 2 plus) ion and H2; and (5) redesign and modification of the ion detection and data acquisition system for the low energy beam facility (reflection time of flight mass spectrometer) dedicated to the study of state select charge transfer.

  15. Observation of the one- to six-neutron transfer reactions at sub-barrier energies

    SciTech Connect

    Jiang, C.L.; Rehm, K.E.; Gehring, J.

    1995-08-01

    It was suggested many years ago that when two heavy nuclei are in contact during a grazing collision, the transfer of several correlated neutron-pairs could occur. Despite considerable experimental effort, however, so far only cross sections for up to four-neutron transfers have been uniquely identified. The main difficulties in the study of multi-neutron transfer reactions are the small cross sections encountered at incident energies close to the barrier, and various experimental uncertainties which can complicate the analysis of these reactions. We have for the first time found evidence for multi-neutron transfer reactions covering the full sequence from one- to six-neutron transfer reactions at sub-barrier energies in the system {sup 58}Ni + {sup 100}Mo.

  16. Path induced coherent energy transfer in light-harvesting complexes in purple bacteria

    NASA Astrophysics Data System (ADS)

    Sun, Kewei; Ye, Jun; Zhao, Yang

    2014-09-01

    Features of path dependent energy transfer in a dual-ring light-harvesting (LH2) complexes (B850) system have been examined in detail systematically. The Frenkel-Dirac time dependent variational method with the Davydov D1 Ansatz is employed with detailed evolution of polaron dynamics in real space readily obtained. It is found that the phase of the transmission amplitude through the LH2 complexes plays an important role in constructing the coherent excitonic energy transfer. It is also found that the symmetry breaking caused by the dimerization of bacteriochlorophylls and coherence or correlation between two rings will be conducive in enhancing the exciton transfer efficiency.

  17. Path induced coherent energy transfer in light-harvesting complexes in purple bacteria.

    PubMed

    Sun, Kewei; Ye, Jun; Zhao, Yang

    2014-09-28

    Features of path dependent energy transfer in a dual-ring light-harvesting (LH2) complexes (B850) system have been examined in detail systematically. The Frenkel-Dirac time dependent variational method with the Davydov D1 Ansatz is employed with detailed evolution of polaron dynamics in real space readily obtained. It is found that the phase of the transmission amplitude through the LH2 complexes plays an important role in constructing the coherent excitonic energy transfer. It is also found that the symmetry breaking caused by the dimerization of bacteriochlorophylls and coherence or correlation between two rings will be conducive in enhancing the exciton transfer efficiency. PMID:25273408

  18. An electron energy-loss study of picene and chrysene based charge transfer salts

    SciTech Connect

    Müller, Eric; Mahns, Benjamin; Büchner, Bernd; Knupfer, Martin

    2015-05-14

    The electronic excitation spectra of charge transfer compounds built from the hydrocarbons picene and chrysene, and the strong electron acceptors F{sub 4}TCNQ (2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane) and TCNQ (7,7,8,8-tetracyanoquinodimethan) have been investigated using electron energy-loss spectroscopy. The corresponding charge transfer compounds have been prepared by co-evaporation of the pristine constituents. We demonstrate that all investigated combinations support charge transfer, which results in new electronic excitation features at low energy. This might represent a way to synthesize low band gap organic semiconductors.

  19. Spectroscopic properties, energy transfer dynamics, and laser performance of thulium-holmium doped laser systems

    SciTech Connect

    Kalisky, Y.; Rotman, S.R.; Boulon, G.; Pedrini, C.; Brenier, A.

    1994-12-31

    Spectroscopic studies using laser induced fluorescence and numerical modeling of energy transfer and back transfer mechanism are reported in Er:Tm:Ho:YLF, Cr:Tm:Ho:YAG and Cr:Tm:YAG laser crystals at various temperatures (10 K-300 K). Direct energy transfer from Tm{sup 3+} excited states to Ho{sup 3+} {sup 5}I{sub 7} emitting level was observed and analyzed both in YAG and YLF. Further analysis of Cr{sup 3+} and Tm{sup 3+} time-dependent emission curves indicate a strong correlation of chromium-thulium pairs. Pulsed operation of holmium laser at high temperature will be presented.

  20. Degrees of locality of energy transfer in the inertial range. [Kolmogoroff notion in turbulence theory

    NASA Technical Reports Server (NTRS)

    Zhou, YE

    1993-01-01

    Measured raw transfer interactions from which local energy transfer is argued to result are summed in a way that directly indicates the scale disparity (s) of contributions to the net energy flux across the spectrum. It is found that the dependence upon s closely follows the s exp -4/3 form predicted by classical arguments. As a result, it is concluded that direct numerical simulation measurements lend support to the classical Kolmogorov phenomenology of local interactions and local transfer in an inertial range.