Science.gov

Sample records for energy transfer spfret

  1. Miniature fiber optic spectrometer-based quantitative fluorescence resonance energy transfer measurement in single living cells

    NASA Astrophysics Data System (ADS)

    Chai, Liuying; Zhang, Jianwei; Zhang, Lili; Chen, Tongsheng

    2015-03-01

    Spectral measurement of fluorescence resonance energy transfer (FRET), spFRET, is a widely used FRET quantification method in living cells today. We set up a spectrometer-microscope platform that consists of a miniature fiber optic spectrometer and a widefield fluorescence microscope for the spectral measurement of absolute FRET efficiency (E) and acceptor-to-donor concentration ratio (RC) in single living cells. The microscope was used for guiding cells and the spectra were simultaneously detected by the miniature fiber optic spectrometer. Moreover, our platform has independent excitation and emission controllers, so different excitations can share the same emission channel. In addition, we developed a modified spectral FRET quantification method (mlux-FRET) for the multiple donors and multiple acceptors FRET construct (mD˜nA) sample, and we also developed a spectra-based 2-channel acceptor-sensitized FRET quantification method (spE-FRET). We implemented these modified FRET quantification methods on our platform to measure the absolute E and RC values of tandem constructs with different acceptor/donor stoichiometries in single living Huh-7 cells.

  2. 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…

  3. 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

  4. 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)

  5. 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

  6. Observation of an angular change in the structure of an RNA complex using Fluorescence Resonance Energy Transfer

    NASA Astrophysics Data System (ADS)

    Rahmanseresht, Sheema; Milas, Peker; Parrot, Louis; Goldner, Lori S.

    Single-molecular-pair FRET is often used to study distance fluctuations of single molecules. It is harder to capture angular changes using FRET, because rotational motion of the dyes tends to wash out the angular sensitivity. Using a dye labeling scheme that minimizes the rotational motion of the dyes with respect to the RNA, we use spFRET to measure an angular change in structure of an RNA kissing complex upon protein binding. The model system studied here, R1inv-R2inv, is derived from the RNAI-RNAII complex in E.coli. RNA II is a primer for replication of the ColE1 plasmid; its function is modulated by interaction with RNA I, Rop protein is known to stabilize the bent R1inv-R2inv kissing complex against dissociation. The effect, if any, of Rop protein on the conformation of the kissing complex is not known. The eight minimized-energy NMR structures reported for R1inv-R2inv show a small difference in end-to-end distances and much larger differences in twist and bend angles. We compare a first-principles model with spFRET data to determine if the observed change in FRET is consistent with an angular change in structure, as suggested by the model. Grant Number: NSF DBI-1152386.

  7. 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.

  8. 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.

  9. 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.

  10. 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.

  11. 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

  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. 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.

  14. 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

  15. 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.

  16. 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.

  17. 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.

  18. 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

  19. 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)

  20. Single-pair fluorescence resonance energy transfer analysis of mRNA transcripts for highly sensitive gene expression profiling in near real time.

    PubMed

    Peng, Zhiyong; Young, Brandon; Baird, Alison E; Soper, Steven A

    2013-08-20

    Expression analysis of mRNAs transcribed from certain genes can be used as important sources of biomarkers for in vitro diagnostics. While the use of reverse transcription quantitative PCR (RT-qPCR) can provide excellent analytical sensitivity for monitoring transcript numbers, more sensitive approaches for expression analysis that can report results in near real-time are needed for many critical applications. We report a novel assay that can provide exquisite limits-of-quantitation and consists of reverse transcription (RT) followed by a ligase detection reaction (LDR) with single-pair fluorescence resonance energy transfer (spFRET) to provide digital readout through molecular counting. For this assay, no PCR was employed, which enabled short assay turnaround times. To facilitate implementation of the assay, a cyclic olefin copolymer (COC) microchip, which was fabricated using hot embossing, was employed to carry out the LDR in a continuous flow format with online single-molecule detection following the LDR. As demonstrators of the assay's utility, MMP-7 mRNA was expression profiled from several colorectal cancer cell lines. It was found that the RT-LDR/spFRET assay produced highly linear calibration plots even in the low copy number regime. Comparison to RT-qPCR indicated a better linearity over the low copy number range investigated (10-10,000 copies) with an R(2) = 0.9995 for RT-LDR/spFRET and R(2) = 0.98 for RT-qPCR. In addition, differentiating between copy numbers of 10 and 50 could be performed with higher confidence using RT-LDR/spFRET. To demonstrate the short assay turnaround times obtainable using the RT-LDR/spFRET assay, a two thermal cycle LDR was carried out on amphiphysin gene transcripts that can serve as important diagnostic markers for ischemic stroke. The ability to supply diagnostic information on possible stroke events in short turnaround times using RT-LDR/spFRET will enable clinicians to treat patients effectively with appropriate time

  1. 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.

  2. 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

  3. 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.

  4. 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.

  5. 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.

  6. 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.

  7. 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%.

  8. 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.

  9. 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

  10. 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.

  11. 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.

  12. 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.

  13. 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.

  14. 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.

  15. 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.

  16. 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.

  17. 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.

  18. 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

  19. 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

  20. 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.

  1. 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.

  2. 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

  3. 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

  4. 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.

  5. 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}.

  6. 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

  7. 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.

  8. 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.

  9. 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.

  10. 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

  11. 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.

  12. 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.

  13. 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

  14. 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.

  15. 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.

  16. 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.

  17. 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.

  18. 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.

  19. 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

  20. 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.

  1. 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.

  2. 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.

  3. 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.

  4. 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

  5. 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.

  6. 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

  7. 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.

  8. 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.

  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. 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.

  11. 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

  12. 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.

  13. 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.

  14. 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.

  15. 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

  16. 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.

  17. 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.

  18. 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.

  19. 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…

  20. 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.

  1. 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.

  2. 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

  3. 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.

  4. 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.

  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. 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

  7. 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.

  8. 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

  9. 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

  10. 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

  11. 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.

  12. 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.

  13. 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%.

  14. 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

  15. 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

  16. 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

  17. 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.

  18. 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.

  19. 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

  20. 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.

  1. 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.

  2. 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.

  3. 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.

  4. 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.

  5. 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.

  6. 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

  7. 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.

  8. 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.

  9. 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.

  10. 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

  11. 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

  12. 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.

  13. 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.

  14. 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.

  15. 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

  16. 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.

  17. 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

  18. 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.

  19. 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.

  20. 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.

  1. 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.

  2. 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.

  3. 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.

  4. 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

  5. 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

  6. 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.

  7. 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

  8. 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

  9. 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

  10. 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

  11. 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

  12. 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

  13. 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.

  14. 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

  15. 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

  16. 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.

  17. 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.

  18. 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?

  19. 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.

  20. 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

  1. 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.

  2. 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.

  3. 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.

  4. 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.

  5. 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

  6. 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.

  7. 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.

  8. 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.

  9. 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.

  10. 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.

  11. 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.

  12. 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.

  13. 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.

  14. 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

  15. 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.

  16. 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.

  17. 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.

  18. 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.

  19. 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.

  20. 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.

  1. 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

  2. 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.

  3. 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.

  4. 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)

  5. 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.

  6. 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

  7. 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.

  8. 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

  9. 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.

  10. 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.

  11. 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

  12. 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

  13. 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.

  14. 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.

  15. 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.

  16. 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.

  17. 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

  18. 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.

  19. 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.

  20. 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

  1. 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.

  2. 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.

  3. 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.

  4. 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

  5. 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.

  6. 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

  7. 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

  8. 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

  9. 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

  10. 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.

  11. 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.

  12. 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.

  13. 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.

  14. 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

  15. 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.

  16. 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.

  17. 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

  18. 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.

  19. 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.

  20. 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

  1. 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.

  2. 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.

  3. 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.

  4. 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.

  5. 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.

  6. 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.

  7. 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

  8. 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

  9. 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

  10. 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.

  11. 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

  12. 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.

  13. 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

  14. 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.

  15. 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.

  16. 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).

  17. 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.

  18. 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.

  19. 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

  20. 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

  1. 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.

  2. 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.

  3. 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

  4. 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.

  5. 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.

  6. 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).

  7. 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.

  8. 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.

  9. 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.

  10. 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...

  11. 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

  12. 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

  13. 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

  14. 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

  15. 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

  16. 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

  17. 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.

  18. 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.

  19. 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.

  20. 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.

  1. 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.

  2. 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

  3. 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

  4. 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.

  5. 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.

  6. 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

  7. 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.

  8. 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

  9. 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

  10. 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.

  11. 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.

  12. 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.

  13. 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.

  14. 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.

  15. 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

  16. 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.

  17. 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''.

  18. 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

  19. 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

  20. 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

  1. 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

  2. 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.

  3. 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.

  4. 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...

  5. 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.

  6. 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 .

  7. 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.

  8. 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

  9. 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

  10. 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.

  11. 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.

  12. 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.

  13. 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.

  14. 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

  15. 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.

  16. 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

  17. 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.

  18. 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

  19. 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

  20. 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.

  1. 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

  2. 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.

  3. 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

  4. 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.

  5. 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.

  6. 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

  7. 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

  8. 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.

  9. 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.

  10. 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.

  11. 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.

  12. 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.

  13. 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

  14. 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

  15. 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.

  16. 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

  17. 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

  18. 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.

  19. 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.

  20. 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.

  1. 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.

  2. 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.

  3. 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.

  4. 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

  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. 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.

  7. 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

  8. 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

  9. 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

  10. 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

  11. 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.

  12. 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.

  13. 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.

  14. 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.

  15. 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.

  16. 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.

  17. 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

  18. 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.

  19. 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.

  20. 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.

  1. 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

  2. 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

  3. 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.

  4. 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

  5. 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...

  6. 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

  7. 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

  8. 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,...

  9. 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.

  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. 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

  16. 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.

  17. 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.

  18. 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.

  19. 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.

  20. 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.

  1. 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

  2. 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.%.

  3. 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

  4. 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

  5. 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

  6. 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

  7. 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.

  8. 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.

  9. 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.

  10. 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

  11. 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.

  12. 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.

  13. 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.

  14. Energy transfer between a nanosystem and its host fluid: A multiscale factorization approach

    SciTech Connect

    Sereda, Yuriy V.; Espinosa-Duran, John M.; Ortoleva, Peter J.

    2014-02-21

    Energy transfer between a macromolecule or supramolecular assembly and a host medium is considered from the perspective of Newton's equations and Lie-Trotter factorization. The development starts by demonstrating that the energy of the molecule evolves slowly relative to the time scale of atomic collisions-vibrations. The energy is envisioned to be a coarse-grained variable that coevolves with the rapidly fluctuating atomistic degrees of freedom. Lie-Trotter factorization is shown to be a natural framework for expressing this coevolution. A mathematical formalism and workflow for efficient multiscale simulation of energy transfer is presented. Lactoferrin and human papilloma virus capsid-like structure are used for validation.

  15. Combining semiconductor quantum dots and bioscaffolds into nanoscale energy transfer devices.

    PubMed

    Spillmann, Christopher M; Stewart, Michael H; Susumu, Kimihiro; Medintz, Igor L

    2015-11-01

    Significant advances have been made in the development of nanoscale devices capable of exciton transport via Förster resonance energy transfer. Several requirements must be met for effective operation, including a reliable energy-harvesting source along with highly organized, precisely placed energy relay elements. For the latter, biological scaffolds such as DNA provide a customizable, symmetric, and stable structure that can be site-specifically modified with organic fluorophores. Here, advancements in nanoscale energy transfer devices incorporating semiconductor nanocrystals and bioscaffolds are reviewed with discussion of biofunctionalization, linker chemistries, design considerations, and concluding with applications in light harvesting, multiplexed biosensing, and optical logic. PMID:26560627

  16. Energy transfer between a nanosystem and its host fluid: A multiscale factorization approach

    NASA Astrophysics Data System (ADS)

    Sereda, Yuriy V.; Espinosa-Duran, John M.; Ortoleva, Peter J.

    2014-02-01

    Energy transfer between a macromolecule or supramolecular assembly and a host medium is considered from the perspective of Newton's equations and Lie-Trotter factorization. The development starts by demonstrating that the energy of the molecule evolves slowly relative to the time scale of atomic collisions-vibrations. The energy is envisioned to be a coarse-grained variable that coevolves with the rapidly fluctuating atomistic degrees of freedom. Lie-Trotter factorization is shown to be a natural framework for expressing this coevolution. A mathematical formalism and workflow for efficient multiscale simulation of energy transfer is presented. Lactoferrin and human papilloma virus capsid-like structure are used for validation.

  17. Quantum coherent energy transfer over varying pathways in single light-harvesting complexes.

    PubMed

    Hildner, Richard; Brinks, Daan; Nieder, Jana B; Cogdell, Richard J; van Hulst, Niek F

    2013-06-21

    The initial steps of photosynthesis comprise the absorption of sunlight by pigment-protein antenna complexes followed by rapid and highly efficient funneling of excitation energy to a reaction center. In these transport processes, signatures of unexpectedly long-lived coherences have emerged in two-dimensional ensemble spectra of various light-harvesting complexes. Here, we demonstrate ultrafast quantum coherent energy transfer within individual antenna complexes of a purple bacterium under physiological conditions. We find that quantum coherences between electronically coupled energy eigenstates persist at least 400 femtoseconds and that distinct energy-transfer pathways that change with time can be identified in each complex. Our data suggest that long-lived quantum coherence renders energy transfer in photosynthetic systems robust in the presence of disorder, which is a prerequisite for efficient light harvesting. PMID:23788794

  18. Chemical process yielding stimulating emission of visible radiation via fast near resonant energy transfer

    SciTech Connect

    Gole, J.L.; Woodward, J.R.; Cobb, S.H.

    1991-05-28

    This patent describes a chemical process yielding stimulated emission of visible radiation via fast rear resonant intermolecular energy transfer. It comprises: providing a first source of vapor selected from the group consisting of metal or semimetal vapor; providing a second source of atomic vapor selected from the group consisting of metal or semimetal vapor to serve as receptor atoms to receive the energy; providing a source of reactant to react with the first source of vapor in a highly exothermic reaction which liberates energy exceeding 2.5 eV; chemically reacting the reactant and the first source of vapor to form metastable states of a final reaction product; transferring energy stored in the metastable states of the the reaction product to the second source of atomic vapor serving as receptor atoms by means of near resonant energy transfer; and providing a mirror configuration having first and second mirrors and windows associated with the mirrors.

  19. Modeling of energy transfer between two crossing smoothed laser beams in a plasma with flow profile

    NASA Astrophysics Data System (ADS)

    Colaitis, A.; Hüller, S.; Tikhonchuk, V. T.; Pesme, D.; Duchateau, G.; Porzio, A.

    2016-05-01

    We study the crossed beam energy transfer (CBET) between laser fields generated by optical smoothing methods. The energy transfer, as well as the angular distribution of the outgoing light fields are investigated for two incident smoothed laser beams in a plasma with a flow gradient, allowing for resonant transfer close to the sonic point. Simulations with the code HARMONY based on time-dependent paraxial light propagation are compared to simulations using a new approach based on paraxial complex geometrical optics (PCGO). Both approaches show good agreement for the average energy transfer past a short transient period, which is a promising result for the use of the PCGO method as a module within a hydrodynamics code to efficiently compute CBET in mm-scale plasma configurations. Statistical aspects related to role of laser speckles in CBET are considered via an ensemble of different phase plate realizations.

  20. Local intermodal energy transfer of the secondary instability in a plane channel

    NASA Technical Reports Server (NTRS)

    Singer, Bart A.; Ferziger, Joel H.; Spalart, Philippe R.; Reed, Helen L.

    1987-01-01

    A mathematical technique for analyzing local energy-transfer rates among wave-vector triads is developed and applied to the data generated by direct numerical simulations of waves with various types of initial conditions. Starting the simulation with a primary two-dimensional wave and random noise produced structures very similar to those which evolved from three-dimensional center modes. The local transfer rates determined in this case help to explain the eventual deformation of the primary two-dimensional wave which was observed in wind-tunnel experiments. Including weak streamwise vortices in the initial flow field results in large amounts of energy being transferred to the K-type modes early in the simulation. The later development of the waves (and hence the energy-transfer rates) is similar to the previous case.

  1. Mid-range adiabatic wireless energy transfer via a mediator coil

    SciTech Connect

    Rangelov, A.A. Vitanov, N.V.

    2012-09-15

    A technique for efficient mid-range wireless energy transfer between two coils via a mediator coil is proposed. By varying the coil frequencies, three resonances are created: emitter-mediator (EM), mediator-receiver (MR) and emitter-receiver (ER). If the frequency sweeps are adiabatic and such that the EM resonance precedes the MR resonance, the energy flows sequentially along the chain emitter-mediator-receiver. If the MR resonance precedes the EM resonance, then the energy flows directly from the emitter to the receiver via the ER resonance; then the losses from the mediator are suppressed. This technique is robust against noise, resonant constraints and external interferences. - Highlights: Black-Right-Pointing-Pointer Efficient and robust mid-range wireless energy transfer via a mediator coil. Black-Right-Pointing-Pointer The adiabatic energy transfer is analogous to adiabatic passage in quantum optics. Black-Right-Pointing-Pointer Wireless energy transfer is insensitive to any resonant constraints. Black-Right-Pointing-Pointer Wireless energy transfer is insensitive to noise in the neighborhood of the coils.

  2. New model of calculating the energy transfer efficiency for the spherical theta-pinch device

    SciTech Connect

    Xu, G.; Hock, C.; Loisch, G.; Jacoby, J.; Xiao, G.; Zhao, Y.; Weyrich, K.; Li, Y.

    2015-05-15

    Ion-beam-plasma-interaction plays an important role in the field of warm dense matter and inertial confinement fusion. A spherical theta pinch is proposed to act as a plasma target in various applications including a plasma stripper cell. One key parameter for such applications is the free electron density. A linear dependency of this density to the amount of energy transferred into the plasma from an energy storage was found by Teske. Since the amount of stored energy is known, the energy transfer efficiency is a reliable parameter for the design of a spherical theta pinch device. As the main assumption of a constant reflected plasma resistance is contradictory by the measured data, the traditional two models of energy transfer efficiency will lead to wrong results. From measurements, the parasitic resistance is derived as constant. Based on this key parameter, a new model is proposed. Due to no assumption, the new model is considered as exact. Further, a comparison of these three different models is given at a fixed operation voltage for the full range of working gas pressures. Due to the inappropriate assumptions included in the traditional models, one owns a tendency to overestimate the energy transfer efficiency whereas the other leads to an underestimation. Applying our new model to a wide spread set of operation voltages and gas pressures, an overall picture of the energy transfer efficiency results.

  3. Introducing novel amorphous carbon nanoparticles as energy acceptors into a chemiluminescence resonance energy transfer immunoassay system.

    PubMed

    Wang, Zhenxing; Gao, Hongfei; Fu, Zhifeng

    2013-11-21

    A novel chemiluminescence resonance energy transfer (CRET) system for competitive immunoassay of biomolecules was developed by using novel amorphous carbon nanoparticles (CNPs) prepared from candle soot as energy acceptors. The CNPs were firstly prepared to bind with the antigen (Ag) for obtaining the nanocomposite CNP-Ag, and this obtained CNP-Ag was then reacted with the horseradish peroxidase-labeled antibody (HRP-Ab) to assemble the CRET system. The luminol catalyzed by HRP serving as the energy donor for CNPs triggered the CRET phenomenon between luminol and CNPs, which led to the chemiluminescence signal decrease. Due to the competitive immunoreaction of the target antigen and the CNP-Ag, a part of the CNP-Ag was replaced from the HRP-Ab, and then resulted in a weaker interaction between luminol and CNPs. Thus the competitive immunoreaction led to a higher chemiluminescence emission. This CNP-based CRET system was successfully applied to detect the human IgG as a model analyte, and a linear range of 10-200 ng mL(-1) and a detection limit of 1.9 ng mL(-1) (S/N = 3) were obtained. The results for real sample analysis demonstrated its application potential in some important areas such as clinical diagnosis. PMID:23979821

  4. Morphology-dependent energy transfer within polyfluorene thin films

    NASA Astrophysics Data System (ADS)

    Khan, Amena L.; Sreearunothai, Paiboon; Herz, Laura M.; Banach, Michael J.; Köhler, Anna

    2004-02-01

    We have performed a detailed study of the photoluminescence from thin films of blue-light-emitting poly(9,9-dioctylfluorene) containing different fractions of planarized (β-phase) chains within the glassy polymer film. By choosing solvents with a range of polarities and boiling points we were able to cast films with reliable control of the relative amounts of β-phase chains present. We analyzed the emission spectra in terms of Franck-Condon progressions and found that, at low temperatures (8 K), the luminescence can be modeled accurately by considering two distinct contributions from the two phases present in the film. The Huang-Rhys parameter for the β phase is shown to be approximately half the value obtained for the glassy phase, in agreement with a more delocalized exciton in the β phase. Time-resolved photoluminescence measurements on a film containing roughly 25% of β phase reveal a fast transfer of excitations from the glassy to the β phase, indicating that the two phases are well intermixed. Assuming the transfer dynamics to be governed by dipole-dipole coupling, we obtain a Förster radius of 8.2±0.6 nm, significantly larger than the radius typically found for excitation transfer within the glassy phase. These results are consistent with the large spectral overlap between the emission of the glassy phase and the absorption of the β phase and explain why the latter dominates the emission even from films containing only a small fraction of β-phase chains.

  5. Non-contact pumping of light emitters via non-radiative energy transfer

    DOEpatents

    Klimov, Victor I.; Achermann, Marc

    2010-01-05

    A light emitting device is disclosed including a primary light source having a defined emission photon energy output, and, a light emitting material situated near to said primary light source, said light emitting material having an absorption onset equal to or less in photon energy than the emission photon energy output of the primary light source whereby non-radiative energy transfer from said primary light source to said light emitting material can occur yielding light emission from said light emitting material.

  6. Large cross section for super energy transfer from hyperthermal atoms to ambient molecules

    NASA Astrophysics Data System (ADS)

    Ma, Jianqiang; Wilhelm, Michael J.; Smith, Jonathan M.; Dai, Hai-Lung

    2016-04-01

    The experimentally measured cross section for super energy transfer collisions between a hyperthermal H atom and an ambient molecule is presented here. This measurement substantiates an emerging energy transfer mechanism with significant cross section, whereby a major fraction of atomic translational energy is converted into molecular vibrational energy through a transient collision-induced reactive complex. Specifically, using nanosecond time-resolved infrared emission spectroscopy, it is revealed that collisions between hyperthermal hydrogen atoms (with 59 kcal/mol of kinetic energy) and ambient SO2 result in the production of vibrationally highly excited SO2 with >14 000 cm-1 of internal energy. The lower limit of the cross section for this super energy transfer process is determined to be 0.53 ±0.05 Å2, i.e., 2% of all hard-sphere collisions. This cross section is orders of magnitude greater than that predicted by the exponential energy gap law, which is commonly used for describing collisional energy transfer through repulsive interactions.

  7. 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

  8. 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.

  9. Radiative and nonradiative exciton energy transfer in monolayers of two-dimensional group-VI transition metal dichalcogenides

    NASA Astrophysics Data System (ADS)

    Manolatou, Christina; Wang, Haining; Chan, Weimin; Tiwari, Sandip; Rana, Farhan

    2016-04-01

    We present results on the rates of interlayer energy transfer between excitons in monolayers of two-dimensional group-VI transition metal dichalcogenides (TMDs). We consider both radiative (mediated by real photons) and nonradiative (mediated by virtual photons) mechanisms of energy transfer using a unified Green's function approach that takes into account modification of the exciton energy dispersions as a result of interactions. The large optical oscillator strengths associated with excitons in TMDs result in very fast energy transfer rates. The energy transfer times depend on the exciton momentum, exciton linewidth, and the interlayer separation and can range from values less than 100 femtoseconds to more than tens of picoseconds. Whereas inside the light cone the energy transfer rates of longitudinal and transverse excitons are comparable, outside the light cone the energy transfer rates of longitudinal excitons far exceed those of transverse excitons. Average energy transfer times for a thermal ensemble of longitudinal and transverse excitons is temperature dependent and can be smaller than a picosecond at room temperature for interlayer separations smaller than 10 nm. Energy transfer times of localized excitons range from values less than a picosecond to several tens of picoseconds. When the exciton scattering and dephasing rates are small, energy transfer dynamics exhibit coherent oscillations. Our results show that electromagnetic interlayer energy transfer can be an efficient mechanism for energy exchange between TMD monolayers.

  10. Simulations of fluorescence quenching using theoretical models of energy and electron transfer in random arrays

    NASA Astrophysics Data System (ADS)

    Boulu, Laurent G.; Kozak, John J.

    A master equation is solved numerically for investigating energy transfer and trapping in two-dimensional disordered systems of chlorophylls and quinones. Quenching of the excitation occurs both by electron transfer from a chlorophyll to a neighbouring quinone and by energy transfer to self-quenching traps consisting of statistical pairs of chlorophyll molecules closer than a critical distance. The quinone concentration dependence of the average lifetime of the calculated fluorescence decay is determined for different values of the Förster transfer radius 0 and A, the microscopic electron transfer rate at 'zero distance'. Quasi-Stern-Volmer behaviour is obtained. The half-quenching concentration and the quenching rate kQ depend strongly on A; they increase little with faster energy transfer because of competing self-quenching and slow electron transfer. Our results are compared to recent fluorescence quenching data that Chauvet and Patterson obtained from real-time measurements in monolayers of chlorophyll a and vitamin K1 diluted in dioleylphosphatidylcholine (DOL). Our convoluted decays fit the experimental data if A = 50-100 ns-1 and tMPH0193_images = 60-70 Å. Accordingly, kQ = 3-5 × 10-5 cm2/molecules·s. These values are in close agreement with those reported in the literature.

  11. Energy-Efficient Information Transfer by Visual Pathway Synapses

    PubMed Central

    Harris, Julia J.; Jolivet, Renaud; Engl, Elisabeth; Attwell, David

    2015-01-01

    Summary The architecture of computational devices is shaped by their energy consumption. Energetic constraints are used to design silicon-based computers but are poorly understood for neural computation. In the brain, most energy is used to reverse ion influxes generating excitatory postsynaptic currents (EPSCs) and action potentials. Thus, EPSCs should be small to minimize energy use, but not so small as to impair information transmission. We quantified information flow through the retinothalamic synapse in the visual pathway in brain slices, with cortical and inhibitory input to the postsynaptic cell blocked. Altering EPSC size with dynamic clamp, we found that a larger-than-normal EPSC increased information flow through the synapse. Thus, the evolutionarily selected EPSC size does not maximize retinal information flow to the cortex. By assessing the energy used on postsynaptic ion pumping and action potentials, we show that, instead, the EPSC size optimizes the ratio of retinal information transmitted to energy consumed. These data suggest maximization of information transmission per energy used as a synaptic design principle. PMID:26671670

  12. 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

  13. Role of an elliptical structure in photosynthetic energy transfer: Collaboration between quantum entanglement and thermal fluctuation

    PubMed Central

    Oka, Hisaki

    2016-01-01

    Recent experiments have revealed that the light-harvesting complex 1 (LH1) in purple photosynthetic bacteria has an elliptical structure. Generally, symmetry lowering in a structure leads to a decrease in quantum effects (quantum coherence and entanglement), which have recently been considered to play a role in photosynthetic energy transfer, and hence, elliptical structure seems to work against efficient photosynthetic energy transfer. Here we analyse the effect of an elliptical structure on energy transfer in a purple photosynthetic bacterium and reveal that the elliptical distortion rather enhances energy transfer from peripheral LH2 to LH1 at room temperature. Numerical results show that quantum entanglement between LH1 and LH2 is formed over a wider range of high energy levels than would have been the case with circular LH1. Light energy absorbed by LH2 is thermally pumped via thermal fluctuation and is effectively transferred to LH1 through the entangled states at room temperature rather than at low temperature. This result indicates the possibility that photosynthetic systems adopt an elliptical structure to effectively utilise both quantum entanglement and thermal fluctuation at physiological temperature. PMID:27173144

  14. Role of an elliptical structure in photosynthetic energy transfer: Collaboration between quantum entanglement and thermal fluctuation.

    PubMed

    Oka, Hisaki

    2016-01-01

    Recent experiments have revealed that the light-harvesting complex 1 (LH1) in purple photosynthetic bacteria has an elliptical structure. Generally, symmetry lowering in a structure leads to a decrease in quantum effects (quantum coherence and entanglement), which have recently been considered to play a role in photosynthetic energy transfer, and hence, elliptical structure seems to work against efficient photosynthetic energy transfer. Here we analyse the effect of an elliptical structure on energy transfer in a purple photosynthetic bacterium and reveal that the elliptical distortion rather enhances energy transfer from peripheral LH2 to LH1 at room temperature. Numerical results show that quantum entanglement between LH1 and LH2 is formed over a wider range of high energy levels than would have been the case with circular LH1. Light energy absorbed by LH2 is thermally pumped via thermal fluctuation and is effectively transferred to LH1 through the entangled states at room temperature rather than at low temperature. This result indicates the possibility that photosynthetic systems adopt an elliptical structure to effectively utilise both quantum entanglement and thermal fluctuation at physiological temperature. PMID:27173144

  15. Role of an elliptical structure in photosynthetic energy transfer: Collaboration between quantum entanglement and thermal fluctuation

    NASA Astrophysics Data System (ADS)

    Oka, Hisaki

    2016-05-01

    Recent experiments have revealed that the light-harvesting complex 1 (LH1) in purple photosynthetic bacteria has an elliptical structure. Generally, symmetry lowering in a structure leads to a decrease in quantum effects (quantum coherence and entanglement), which have recently been considered to play a role in photosynthetic energy transfer, and hence, elliptical structure seems to work against efficient photosynthetic energy transfer. Here we analyse the effect of an elliptical structure on energy transfer in a purple photosynthetic bacterium and reveal that the elliptical distortion rather enhances energy transfer from peripheral LH2 to LH1 at room temperature. Numerical results show that quantum entanglement between LH1 and LH2 is formed over a wider range of high energy levels than would have been the case with circular LH1. Light energy absorbed by LH2 is thermally pumped via thermal fluctuation and is effectively transferred to LH1 through the entangled states at room temperature rather than at low temperature. This result indicates the possibility that photosynthetic systems adopt an elliptical structure to effectively utilise both quantum entanglement and thermal fluctuation at physiological temperature.

  16. Solar wind energy transfer through the magnetopause of an open magnetosphere

    NASA Technical Reports Server (NTRS)

    Lee, L. C.; Roederer, J. G.

    1982-01-01

    An expression is derived for the total power, transferred from the solar wind to an open magnetosphere, which consists of the electromagnetic energy rate and the particle kinetic energy rate. The total rate of energy transferred from the solar wind to an open magnetosphere mainly consists of kinetic energy, and the kinetic energy flux is carried by particles, penetrating from the solar wind into the magnetosphere, which may contribute to the observed flow in the plasma mantle and which will eventually be convected slowly toward the plasma sheet by the electric field as they flow down the tail. While the electromagnetic energy rate controls the near-earth magnetospheric activity, the kinetic energy rate should dominate the dynamics of the distant magnetotail.

  17. 77 FR 73654 - Eau Galle Renewable Energy Company, Eau Galle Hydro, LLC; Notice of Transfer of Exemption

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-12-11

    ... Energy Regulatory Commission Eau Galle Renewable Energy Company, Eau Galle Hydro, LLC; Notice of Transfer of Exemption 1. By letter filed October 12, 2012, Eau Galle Renewable Energy Company informed the..., originally issued March 10, 1987,\\1\\ and transferred to Eau Galle Renewable Energy Company by letter.\\2\\...

  18. Energy transfer during freeze-drying in dual-chamber cartridges.

    PubMed

    Korpus, Christoph; Haase, Thomas; Sönnichsen, Caren; Friess, Wolfgang

    2015-05-01

    Freeze-drying essentially requires knowledge about the heat and mass transfer characteristics to assure product quality. Whereas this understanding has been created for freeze-drying in vials, only limited information is available for state-of-the-art multiple compartment container systems such as dual-chamber cartridges (DCCs). Therefore, the aim of this study was to investigate the heat transfer characteristics of this novel container format. Sublimation tests were carried out using pure water at 60, 100, 150, and 200 mTorr chamber pressure at a shelf temperature of 0°C. Custom-made aluminum blocks were used as holder systems. Two heat transfer coefficients could be identified: the coefficient characterizing heat transfer between shelf and block, KAl , and between block and cartridge, KDCC . KAl was dependent on all three modes of heat transfer: contact conduction, gas conduction, and radiation. For KDCC , contact conduction was negligible. Radiation strongly influenced the overall energy transfer as it is the major mode of heat transfer for KDCC and contributes up to 44% to KAl . A third coefficient, Ktot , was defined as an overall heat transfer coefficient. This knowledge about heat transfer enables a purposeful development and control of optimized lyophilization processes for this novel container system. PMID:25712903

  19. A simple model for exploring the role of quantum coherence and the environment in excitonic energy transfer.

    PubMed

    Manikandan, Sreenath K; Shaji, Anil

    2015-07-28

    We investigate the role of quantum coherence in modulating the energy transfer rate between two independent energy donors and a single acceptor participating in an excitonic energy transfer process. The energy transfer rate depends explicitly on the nature of the initial coherent superposition state of the two donors and we connect it to the observed absorption profile of the acceptor and the stimulated emission profile of the energy donors. We consider simple models with mesoscopic environments interacting with the donors and the acceptor and compare the expression we obtained for the energy transfer rate with the results of numerical integration. PMID:26123739

  20. Why are the Interaction Energies of Charge-Transfer Complexes Challenging for DFT?

    PubMed

    Steinmann, Stephan N; Piemontesi, Cyril; Delachat, Aurore; Corminboeuf, Clemence

    2012-05-01

    The description of ground state charge-transfer complexes is highly challenging. Illustrative examples include large overestimations of charge-transfer by local and semilocal density functional approximations as well as inaccurate binding energies. It is demonstrated here that standard density functionals fail to accurately describe interaction energies of charge-transfer complexes not only because of the missing long-range exchange as generally assumed but also as a result of the neglect of weak interactions. Thus, accounting for the missing van der Waals interactions is of key importance. These assertions, based on the evaluation of the extent of stabilization due to dispersion using both DFT coupled with our recent density-dependent dispersion correction (dDsC) and high-level ab initio computations, reflect the imperfect error-cancellation between the overestimation of charge-transfer and the missing long-range interactions. An in-depth energy decomposition analysis of an illustrative series of four small ambidentate molecules (HCN, HNC, HF, and ClF) bound together with NF3 provides the main conclusions, which are validated on a prototypical organic charge-transfer complex (i.e., tetrathiafulvalene-tetracyanoquinodimethane, TTF-TCNQ). We establish that the interaction energies for charge-transfer complexes can only be properly described when using well-balanced functionals such as PBE0-dDsC, M06-2X, and LC-BOP-LRD. PMID:26593656

  1. Charge transfer and association of protons colliding with potassium from very low to intermediate energies

    SciTech Connect

    Liu, C. H.; Qu, Y. Z.; Wang, J. G.; Li, Y.; Buenker, R. J.

    2010-01-15

    The nonradiative charge-transfer process for H{sup +}+K(4s) collision is investigated using the quantum-mechanical molecular-orbital close-coupling method for collision energies from 1 eV to 10 keV. The radiative-decay and radiative charge transfer cross sections are calculated using the optical potential approach and the fully quantal method, respectively, for the energy range of 10{sup -5}-10 eV. The radiative-association cross sections are obtained by subtracting the radiative charge-transfer part from total radiative-decay cross sections. The relevant molecular data are calculated from the multireference single- and double-excitation configuration interaction approach. The nonradiative charge transfer is the dominant mechanism at energies above 2 eV, whereas the radiative charge transfer becomes primary in the low-energy region of E<1.5 eV. The present radiative-decay cross sections disagree with the calculations of Watanabe et al. [Phys. Rev. A 66, 044701 (2002)]. The total charge-transfer rate coefficient is obtained in the temperature range of 1-20000 K.

  2. The local field dependent effect of the critical distance of energy transfer between nanoparticles

    NASA Astrophysics Data System (ADS)

    Viet Ha, Chu; Thi Nga, Do; Ai Viet, Nguyen; Hong Nhung, Tran

    2015-10-01

    The fluorescence resonance energy transfer between various types of fluorophore pairs was investigated. Dye molecules, quantum dots, fluorescent nanoparticles (dye molecules encapsulated in polymer matrices) were used as donor D. Dye molecules and gold nanoparticles were used as acceptor A. We found that the experimental Förster critical transfer distance R0 is 1-10 nm when both D and A are dye molecules, and becomes larger than 10 nm when the donor is fluorescent nanoparticles. When the acceptors A are gold nanoparticles, the case is considered as localized plasmon coupled nanosurface energy transfer (NSET), the experimental critical distance d0 increases up to few ten nanometers when D are dye molecules or quantum dots. For the first time, un-expected giant resonance energy transfer (G-RET) phenomenon is observed in our experiments with very large critical transfer distance d0, which increases from few ten nanometers to micrometers when the donors are fluorescent and the acceptors are gold nanoparticles. A model "nanowave emitter station and antenna" is given to explain the local field dependence of the critical distance of energy transfer between those nanoparticles. Moreover, a simple theoretical model with size-number contribution (for fluorescent nanoparticles) and surface plasmon coupled enhancement effect (for gold nanoparticles) is proposed to explain these obtained experimental results.

  3. PRELIMINARY ASSESSMENT OF THE USE OF HEAT TRANSFER FLUIDS FOR SOLAR THERMAL ENERGY SYSTEMS

    EPA Science Inventory

    The report contains a preliminary assessment, based on available data, of the extent to which various materials will be used as heat transfer media in solar energy systems and of mechanisms for their release to the environment. The emphasis is on solar thermal energy systems for ...

  4. Experimental studies and computer simulation of the control of energy transfer using inductor-converter bridges

    SciTech Connect

    Hirano, M.; Kustom, R.L.

    1984-03-01

    An inductor-converter bridge (ICB) is a solid state DC-AC-DC power converter system for bidirectional, controllable, energy transfer between two coils. The ICB is suitable for supplying large pulsed power to such magnets as the superconducting equilibrium field coil of the proposed tokamak power reactors from another superconducting energy storage coil.

  5. Network-based representation of energy transfer in unsteady separated flow

    NASA Astrophysics Data System (ADS)

    Nair, Aditya; Taira, Kunihiko

    2015-11-01

    We construct a network-based representation of energy pathways in unsteady separated flows using a POD-Galerkin projection model. In this formulation, we regard the POD modes as the network nodes and the energy transfer between the modes as the network edges. Based on the energy transfer analysis performed by Noack et al. (2008), edge weights are characterized on the interaction graph. As an example, we examine the energy transfer within the two-dimensional incompressible flow over a circular cylinder. In particular, we analyze the energy pathways involved in flow transition from the unstable symmetric steady state to periodic shedding cycle. The growth of perturbation energy over the network is examined to highlight key features of flow physics and to determine how the energy transfer can be influenced. Furthermore, we implement closed-loop flow control on the POD-Galerkin model to alter the energy interaction path and modify the global behavior of the wake dynamics. The insights gained will be used to perform further network analysis on fluid flows with added complexity. Work supported by US Army Research Office (W911NF-14-1-0386) and US Air Force Office of Scientific Research (YIP: FA9550-13-1-0183).

  6. Measurements of pressure drop, heat transfer coefficient and critical energy of a bundle conductor

    SciTech Connect

    Junghans, D.

    1981-09-01

    Friction factor, saturation temperature, heat transfer coefficient and critical energy of an eight strand bundle conductor were measured in the test facility SULTAN at SIN in Switzerland. The measured values of the critical energy are in good agreement with those calculated by the computer code LONSA. 10 refs.

  7. 76 FR 49764 - Steve Mason Enterprises, Inc., Green Energy Trans, LLC; Notice of Transfer of Exemption

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-11

    ... Energy Regulatory Commission Steve Mason Enterprises, Inc., Green Energy Trans, LLC; Notice of Transfer... Enterprises, Inc., exemptee for the Long Shoals Project No. 7742,\\2\\ informed the Commission that it... Hydro, Inc., 28 FERC ] 62,067 (1984). \\3\\ See filing of May 26, 2011 from Steve Mason Enterprises,...

  8. A Conceptual Change Model for Teaching Heat Energy, Heat Transfer and Insulation

    ERIC Educational Resources Information Center

    Lee, C. K.

    2014-01-01

    This study examines the existing knowledge that pre-service elementary teachers (PSETs) have regarding heat energy, heat transfer and insulation. The PSETs' knowledge of heat energy was initially assessed by using an activity: determining which container would be best to keep hot water warm for the longest period of time. Results showed that…

  9. Generating Excitement: Build Your Own Generator to Study the Transfer of Energy

    ERIC Educational Resources Information Center

    Fletcher, Kurt; Rommel-Esham, Katie; Farthing, Dori; Sheldon, Amy

    2011-01-01

    The transfer of energy from one form to another can be difficult to understand. The electrical energy that turns on a lamp may come from the burning of coal, water falling at a hydroelectric plant, nuclear reactions, or gusts of wind caused by the uneven heating of the Earth. The authors have developed and tested an exciting hands-on activity to…

  10. Energy transfer in volume-reflecting heat shields

    NASA Technical Reports Server (NTRS)

    Weston, K. C.

    1974-01-01

    An approximate analysis of radiative transfer in highly scattering materials was developed based on the Kubelka-Munk differential equations--a set of two differential equations representing the spatial rate of change of radiative half-fluxes within the scattering media. These approximate solutions of the Kubelka-Munk equations together with analytic solutions for the steady state temperature distribution for two types of boundary conditions are given. These solutions show the influence of back surface reflectance, scattering power, incident radiative flux parameter and boundary conductive flux parameter on overall reflectance and temperature distributions. This radiation field analysis, adapted to spherical geometry, was applied to the evaluation of the thermal performance of teflon and fritted quartz as heat protection materials for entry into the atmosphere of Jupiter.

  11. Dynamics of ultrafast photoinduced heterogeneous electron transfer, implications for recent solar energy conversion scenarios

    NASA Astrophysics Data System (ADS)

    Gundlach, Lars; Burfeindt, Bernd; Mahrt, Jürgen; Willig, Frank

    2012-08-01

    The general case of a heterogeneous electron transfer reaction is realized by ultrafast electron transfer from a photo-excited molecule to a wide continuum of electronic acceptor states. Two different theoretical model calculations addressing the injection dynamics have recently been presented. The first scenario predicts a wide energy distribution for the injected electron via excitations of high-energy vibrational modes in the ionized molecule, whereas the second scenario ascribes the width to thermal fluctuations. We present experimental data at different temperatures and identify the valid injection scenario for perylene/TiO2 systems. The results are discussed in view of recent solar energy conversion scenarios.

  12. Observation of anisotropic energy transfer in magnetically coupled magnetic vortex pair

    NASA Astrophysics Data System (ADS)

    Hasegawa, N.; Sugimoto, S.; Kumar, D.; Barman, S.; Barman, A.; Kondou, K.; Otani, Y.

    2016-06-01

    We have experimentally investigated the energy transfer and storage in the magnetostatically coupled vortices in a pair of disks. By measuring the frequency dependence of the rectified dc voltage, we observed a specific gyrating motion due to anomalous energy storage at the off-resonant frequency for anti-parallel polarities. Micromagnetic simulations based on the Landau-Lifshitz-Gilbert equation qualitatively reproduce the experimental results and reveal that the behavior arises from the anisotropic energy transfer, i.e., the modulation of effective damping constant of the pair disks, originating from the phase difference between coupled vortex cores. These findings can be of use in magnetic vortex based logic operations.

  13. Nonequilibrium Energy Transfer at Nanoscale: A Unified Theory from Weak to Strong Coupling

    PubMed Central

    Wang, Chen; Ren, Jie; Cao, Jianshu

    2015-01-01

    Unraveling the microscopic mechanism of quantum energy transfer across two-level systems provides crucial insights to the optimal design and potential applications of low-dimensional nanodevices. Here, we study the non-equilibrium spin-boson model as a minimal prototype and develop a fluctuation-decoupled quantum master equation approach that is valid ranging from the weak to the strong system-bath coupling regime. The exact expression of energy flux is analytically established, which dissects the energy transfer as multiple boson processes with even and odd parity. Our analysis provides a unified interpretation of several observations, including coherence-enhanced heat flux and negative differential thermal conductance. The results will have broad implications for the fine control of energy transfer in nano-structural devices. PMID:26152705

  14. Energy and Electron Transfer Dynamics within a Series of Perylene Diimide/Cyclophane Systems.

    PubMed

    Ryan, Seán T J; Young, Ryan M; Henkelis, James J; Hafezi, Nema; Vermeulen, Nicolaas A; Hennig, Andreas; Dale, Edward J; Wu, Yilei; Krzyaniak, Matthew D; Fox, Athan; Nau, Werner M; Wasielewski, Michael R; Stoddart, J Fraser; Scherman, Oren A

    2015-12-01

    Artificial photosynthetic systems for solar energy conversion exploit both covalent and supramolecular chemistry to produce favorable arrangements of light-harvesting and redox-active chromophores in space. An understanding of the interplay between key processes for photosynthesis, namely light-harvesting, energy transfer, and photoinduced charge separation and the design of novel, self-assembling components capable of these processes are imperative for the realization of multifunctional integrated systems. We report our investigations on the potential of extended tetracationic cyclophane/perylene diimide systems as components for artificial photosynthetic applications. We show how the selection of appropriate heterocycles, as extending units, allows for tuning of the electron accumulation and photophysical properties of the extended tetracationic cyclophanes. Spectroscopic techniques confirm energy transfer between the extended tetracationic cyclophanes and perylene diimide is ultrafast and quantitative, while the heterocycle specifically influences the energy transfer related parameters and the acceptor excited state. PMID:26551041

  15. Analysis of optical near-field energy transfer by stochastic model unifying architectural dependencies

    SciTech Connect

    Naruse, Makoto; Akahane, Kouichi; Yamamoto, Naokatsu; Holmström, Petter; Thylén, Lars; Huant, Serge; Ohtsu, Motoichi

    2014-04-21

    We theoretically and experimentally demonstrate energy transfer mediated by optical near-field interactions in a multi-layer InAs quantum dot (QD) structure composed of a single layer of larger dots and N layers of smaller ones. We construct a stochastic model in which optical near-field interactions that follow a Yukawa potential, QD size fluctuations, and temperature-dependent energy level broadening are unified, enabling us to examine device-architecture-dependent energy transfer efficiencies. The model results are consistent with the experiments. This study provides an insight into optical energy transfer involving inherent disorders in materials and paves the way to systematic design principles of nanophotonic devices that will allow optimized performance and the realization of designated functions.

  16. Theoretical study of vibrational energy transfer of free OH groups at the water-air interface

    NASA Astrophysics Data System (ADS)

    Zheng, Renhui; Wei, Wenmei; Sun, Yuanyuan; Song, Kai; Shi, Qiang

    2016-04-01

    Recent experimental studies have shown that the vibrational dynamics of free OH groups at the water-air interface is significantly different from that in bulk water. In this work, by performing molecular dynamics simulations and mixed quantum/classical calculations, we investigate different vibrational energy transfer pathways of free OH groups at the water-air interface. The calculated intramolecular vibrational energy transfer rate constant and the free OH bond reorientation time scale agree well with the experiment. It is also found that, due to the small intermolecular vibrational couplings, the intermolecular vibrational energy transfer pathway that is very important in bulk water plays a much less significant role in the vibrational energy relaxation of the free OH groups at the water-air interface.

  17. Theoretical study of vibrational energy transfer of free OH groups at the water-air interface.

    PubMed

    Zheng, Renhui; Wei, Wenmei; Sun, Yuanyuan; Song, Kai; Shi, Qiang

    2016-04-14

    Recent experimental studies have shown that the vibrational dynamics of free OH groups at the water-air interface is significantly different from that in bulk water. In this work, by performing molecular dynamics simulations and mixed quantum/classical calculations, we investigate different vibrational energy transfer pathways of free OH groups at the water-air interface. The calculated intramolecular vibrational energy transfer rate constant and the free OH bond reorientation time scale agree well with the experiment. It is also found that, due to the small intermolecular vibrational couplings, the intermolecular vibrational energy transfer pathway that is very important in bulk water plays a much less significant role in the vibrational energy relaxation of the free OH groups at the water-air interface. PMID:27083739

  18. Nonequilibrium Energy Transfer at Nanoscale: A Unified Theory from Weak to Strong Coupling.

    PubMed

    Wang, Chen; Ren, Jie; Cao, Jianshu

    2015-01-01

    Unraveling the microscopic mechanism of quantum energy transfer across two-level systems provides crucial insights to the optimal design and potential applications of low-dimensional nanodevices. Here, we study the non-equilibrium spin-boson model as a minimal prototype and develop a fluctuation-decoupled quantum master equation approach that is valid ranging from the weak to the strong system-bath coupling regime. The exact expression of energy flux is analytically established, which dissects the energy transfer as multiple boson processes with even and odd parity. Our analysis provides a unified interpretation of several observations, including coherence-enhanced heat flux and negative differential thermal conductance. The results will have broad implications for the fine control of energy transfer in nano-structural devices. PMID:26152705

  19. Rovibrational energy transfer and dissociation in O2-O collisions

    NASA Astrophysics Data System (ADS)

    Andrienko, Daniil A.; Boyd, Iain D.

    2016-03-01

    A set of state-specific transition rates for each rovibrational level is generated for the O 2 ( X 3 Σg - ) - O (" separators=" 3 P ) system using the quasi-classical trajectory method at temperatures observed in hypersonic flows. A system of master equations describes the relaxation of the rovibrational ensemble to thermal equilibrium under ideal heat bath conditions at a constant translational temperature. Vibrational and rotational relaxation times, obtained from the average internal energies, exhibit a pattern inherent in a chemically reactive collisional pair. An intrinsic feature of the O3 molecular system with a large attractive potential is a weak temperature dependence of the rovibrational transition rates. For this reason, the quasi-steady vibrational and rotational temperatures experience a maximum at increasing translational temperature. The energy rate coefficients, that characterize the average loss of internal energy due to dissociation, quickly diminish at high temperatures, compared to other molecular systems.

  20. Rovibrational energy transfer and dissociation in O2-O collisions.

    PubMed

    Andrienko, Daniil A; Boyd, Iain D

    2016-03-14

    A set of state-specific transition rates for each rovibrational level is generated for the O2(X(3)Σ(g)(-))-O(3)P system using the quasi-classical trajectory method at temperatures observed in hypersonic flows. A system of master equations describes the relaxation of the rovibrational ensemble to thermal equilibrium under ideal heat bath conditions at a constant translational temperature. Vibrational and rotational relaxation times, obtained from the average internal energies, exhibit a pattern inherent in a chemically reactive collisional pair. An intrinsic feature of the O3 molecular system with a large attractive potential is a weak temperature dependence of the rovibrational transition rates. For this reason, the quasi-steady vibrational and rotational temperatures experience a maximum at increasing translational temperature. The energy rate coefficients, that characterize the average loss of internal energy due to dissociation, quickly diminish at high temperatures, compared to other molecular systems. PMID:26979687

  1. Electronic Energy Transfer on CaO Surfaces

    SciTech Connect

    Joly, Alan G.; Beck, Kenneth M.; Hess, Wayne P.

    2008-09-28

    We excite low-coordinated surface sites of nanostructured CaO samples using tunable UV laser pulses and observe hyperthermal O-atom emission indicative of an electronic excited-state desorption mechanism. The O-atom yield increases dramatically with photon energy, between 3.75 and 5.4 eV, below the bulk absorption threshold. The peak of the kinetic energy distribution does not increase with photon energy in the range 3.9 to 5.15 eV. These results are analyzed in the context of a laser desorption model developed previously for nanostructured MgO samples. The data are consistent with desorption induced by exciton localization at corner-hole trapped surface sites following either direct corner excitation or diffusion and localization of excitons from higher coordinated surface sites.

  2. Remote Electric Power Transfer Between Spacecrafts by Infrared Beamed Energy

    NASA Astrophysics Data System (ADS)

    Chertok, Boris E.; Evdokimov, Roman A.; Legostaev, Victor P.; Lopota, Vitaliy A.; Sokolov, Boris A.; Tugaenko, Vjacheslav Yu.

    2011-11-01

    High efficient wireless electric energy transmission (WET) technology between spacecrafts by laser channel is proposed. WET systems could be used for remote power supplying of different consumers in space. First of all, there are autonomous technology modules for microgravity experiments, micro and nano satellites, different equipment for explorations of planetary surfaces, space transport vehicles with electric rocket propulsion systems. The main components of the WET technology consist of radiation sources on the base of semiconductor IR laser diodes; systems for narrow laser beam creation; special photovoltaic receivers for conversion of monochromatic IR radiation with high energy density to electric power. The multistage space experiment for WET technology testing is described. During this experiment energy will be transmitted from International Space Station to another spacecrafts like cargo transport vehicles (Progress or/and ATV) and micro satellites.

  3. Assessing Locations of Energy Transfer/Deposit in the Ionosphere-Thermosphere System

    NASA Astrophysics Data System (ADS)

    Tu, J.; Song, P.

    2014-12-01

    It has long been believed that most of energy transferred from the magnetosphere and deposited in the ionosphere-thermosphere system occurs in the auroral zone, the region of strong field-aligned current density. Recent observations of the Poynting flux to the ionosphere and theoretical investigations of the magnetosphere-ionosphere coupling show that the strongest energy transfer may be in the polar cap proper where the plasma flow speed is high and not where the flow reverses. This implies that the field-aligned current is not the primary agent of the energy transfer into the ionosphere-thermosphere system and that other physical progresses are at play. Recent simulation studies using an inductive-dynamic approach (including self-consistent solutions of Faraday's law and retaining inertia terms in the ion momentum equations) on the magnetosphere-ionosphere-thermosphere coupling indicate that the energy transfer is through Alfven waves propagating to the ionosphere/thermosphere and the energy deposition is via the frictional heating caused by relative motion between ions and neutrals. In this study we assess the locations of the energy transfer and deposition by employing a self-consistent inductive-dynamic ionosphere-thermosphere model. In a 2-D numerical simulation (dawn-dusk meridian plane), we solve the continuity, momentum, and energy equations for multiple species of ions and neutrals including photochemistry and Maxwell's equations. By simulating responses of the ionosphere-thermosphere system to enhanced magnetosphere convection, we show that the strongest energy transfer occurs in the polar cap proper instead of the auroral zone.

  4. Triplet energy transfer in conjugated polymers. I. Experimental investigation of a weakly disordered compound

    NASA Astrophysics Data System (ADS)

    Sudha Devi, Lekshmi; Al-Suti, Mohammad K.; Dosche, Carsten; Khan, Muhammad S.; Friend, Richard H.; Köhler, Anna

    2008-07-01

    Efficient triplet exciton emission has allowed improved operation of organic light-emitting diodes (LEDs). To enhance the device performance, it is necessary to understand what governs the motion of triplet excitons through the organic semiconductor. Here, we have investigated triplet diffusion using a model compound that has weak energetic disorder. The Dexter-type triplet energy transfer is found to be thermally activated down to a transition temperature TT , below which the transfer rate is only weakly temperature dependent. We show that above the transition temperature, Dexter energy transfer can be described within the framework of Marcus theory. We suggest that below TT , the nature of the transfer changes from phonon-assisted hopping to quantum-mechanical tunneling. The lower electron-phonon coupling and higher electronic coupling in the polymer compared to the monomer results in an enhanced triplet diffusion rate.

  5. Designing matrix models for fluorescence energy transfer between moving donors and acceptors.

    PubMed Central

    van der Meer, B W; Raymer, M A; Wagoner, S L; Hackney, R L; Beechem, J M; Gratton, E

    1993-01-01

    A recipe is given for designing theoretical models for donor-acceptor systems in which fluorescence energy transfer and motion takes place simultaneously. This recipe is based on the idea that a system exhibiting both motion and fluorescence energy transfer can be modeled by specifying a number of "states" and the rates of transitions between them. A state in this context is a set of specific coordinates and conditions that describe the system at a certain moment in time. As time goes on, the coordinates and conditions for the system change, and this evolution can be described as a series of transitions from one state to the next. The recipe is applied to a number of example systems in which the donors and/or acceptors undergo either rotational or translational motion. In each example, fluorescence intensities and anisotropies for the donor and acceptor are calculated from solutions of eigensystems. The proposed method allows for analyzing time-resolved fluorescence energy transfer data without restrictive assumptions for motional averaging regimes and the orientation factor. It is shown that the fluorescence quantities depend on the size of the motional step (i.e., on the number of states), only if fluorescence energy transfer occurs. This finding indicates that fluorescence energy transfer studies may reveal whether the dynamics of a system (e.g., a protein) is better described in terms of transitions between a relatively small number of discrete states (jumping) or a large number of dense states (diffusion). PMID:8494980

  6. Direct effects of ionizing radiation on integral membrane proteins. Noncovalent energy transfer requires specific interpeptide interactions

    SciTech Connect

    Jhun, E.; Jhun, B.H.; Jones, L.R.; Jung, C.Y. )

    1991-05-25

    The 12 transmembrane alpha helices (TMHs) of human erythrocyte glucose transporter were individually cut by pepsin digestion as membrane-bound 2.5-3.5-kDa peptide fragments. Radiation-induced chemical degradation of these fragments showed an average target size of 34 kDa. This is 10-12 x larger than the average size of an individual TMH, demonstrating that a significant energy transfer occurs among these TMHs in the absence of covalent linkage. Heating this TMH preparation at 100{degree}C for 15 min reduced the target size to 5 kDa or less, suggesting that the noncovalent energy transfer requires specific helix-helix interactions. Purified phospholamban, a small (6-kDa) integral membrane protein containing a single TMH, formed a pentameric assembly in sodium dodecyl sulfate. The chemical degradation target size of this phospholamban pentamer was 5-6 kDa, illustrating that not all integral membrane protein assemblies permit intersubunit energy transfer. These findings together with other published observations suggest strongly that significant noncovalent energy transfer can occur within the tertiary and quaternary structure of membrane proteins and that as yet undefined proper molecular interactions are required for such covalent energy transfer. Our results with pepsin-digested glucose transporter also illustrate the importance of the interhelical interaction as a predominating force in maintaining the tertiary structure of a transmembrane protein.

  7. Energy transfer between quantum dots and 2D materials: graphene versus MoS2

    NASA Astrophysics Data System (ADS)

    Raja, Archana; Zultak, Johanna; Zhang, Xiaoxiao; Montoya-Castillo, Andres; Ye, Ziliang; Roquelet, Cyrielle; van der Zande, Arend; Chenet, Daniel; Brus, Louis; Heinz, Tony

    2015-03-01

    Understanding charge and energy transfer processes at the interface of nanostructures is an important area of research, both from the fundamental and application points of view. Interactions between 0D semiconductor quantum dots and 2D van der Waals materials have been a subject of recent investigations. Here, we report highly efficient near-field energy transfer from core-shell quantum dots to monolayer and few layer graphene, a semi-metal and MoS2, a semiconductor. We observe both quenching of single quantum dot photoluminescence (PL) and decreasing lifetime in time resolved PL. Our measurements show that increasing the number of layers in the acceptor van der Waals material results in contrasting trends in the rate of non-radiative energy transfer. The energy-transfer rate increases significantly with increasing layer thickness for graphene, but decreases with increasing thickness for MoS2 layers. Energy transfer rates on the order of 1-10ns-1 are determined. We interpret the results in terms of differences in the interplay between dielectric loss and screening.

  8. Study of energy transfer mechanism from ZnO nanocrystals to Eu3+ ions

    NASA Astrophysics Data System (ADS)

    Mangalam, Vivek; Pita, Kantisara; Couteau, Christophe

    2016-02-01

    In this work, we investigate the efficient energy transfer occurring between ZnO nanocrystals (ZnO-nc) and europium (Eu3+) ions embedded in a SiO2 matrix prepared using the sol-gel technique. We show that a strong red emission was observed at 614 nm when the ZnO-nc were excited using a continuous optical excitation at 325 nm. This emission is due to the radiative 5D0 → 7F2 de-excitation of the Eu3+ ions and has been conclusively shown to be due to the energy transfer from the excited ZnO-nc to the Eu3+ ions. The photoluminescence excitation spectra are also examined in this work to confirm the energy transfer from ZnO-nc to the Eu3+ ions. Furthermore, we study various de-excitation processes from the excited ZnO-nc and their contribution to the energy transfer to Eu3+ ions. We also report the optimum fabrication process for maximum red emission at 614 nm from the samples where we show a strong dependence on the annealing temperature and the Eu3+ concentration in the sample. The maximum red emission is observed with 12 mol% Eu3+ annealed at 450 °C. This work provides a better understanding of the energy transfer mechanism from ZnO-nc to Eu3+ ions and is important for applications in photonics, especially for light emitting devices.

  9. Tunable negligible-loss energy transfer between dipolar-coupled magnetic disks by stimulated vortex gyration

    PubMed Central

    Jung, Hyunsung; Lee, Ki-Suk; Jeong, Dae-Eun; Choi, Youn-Seok; Yu, Young-Sang; Han, Dong-Soo; Vogel, Andreas; Bocklage, Lars; Meier, Guido; Im, Mi-Young; Fischer, Peter; Kim, Sang-Koog

    2011-01-01

    A wide variety of coupled harmonic oscillators exist in nature. Coupling between different oscillators allows for the possibility of mutual energy transfer between them and the information-signal propagation. Low-energy input signals and their transport with negligible energy loss are the key technological factors in the design of information-signal processing devices. Here, utilizing the concept of coupled oscillators, we experimentally demonstrated a robust new mechanism for energy transfer between spatially separated dipolar-coupled magnetic disks - stimulated vortex gyration. Direct experimental evidence was obtained by a state-of-the-art experimental time-resolved soft X-ray microscopy probe. The rate of energy transfer from one disk to the other was deduced from the two normal modes' frequency splitting caused by dipolar interaction. This mechanism provides the advantages of tunable energy transfer rates, low-power input signals and negligible energy loss in the case of negligible intrinsic damping. Coupled vortex-state disks might be implemented in applications for information-signal processing. PMID:22355578

  10. 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

  11. 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.

  12. Excitonic energy transfer in light-harvesting complexes in purple bacteria

    NASA Astrophysics Data System (ADS)

    Ye, Jun; Sun, Kewei; Zhao, Yang; Yu, Yunjin; Kong Lee, Chee; Cao, Jianshu

    2012-06-01

    Two distinct approaches, the Frenkel-Dirac time-dependent variation and the Haken-Strobl model, are adopted to study energy transfer dynamics in single-ring and double-ring light-harvesting (LH) systems in purple bacteria. It is found that the inclusion of long-range dipolar interactions in the two methods results in significant increase in intra- or inter-ring exciton transfer efficiency. The dependence of exciton transfer efficiency on trapping positions on single rings of LH2 (B850) and LH1 is similar to that in toy models with nearest-neighbor coupling only. However, owing to the symmetry breaking caused by the dimerization of BChls and dipolar couplings, such dependence has been largely suppressed. In the studies of coupled-ring systems, both methods reveal an interesting role of dipolar interactions in increasing energy transfer efficiency by introducing multiple intra/inter-ring transfer paths. Importantly, the time scale (4 ps) of inter-ring exciton transfer obtained from polaron dynamics is in good agreement with previous studies. In a double-ring LH2 system, non-nearest neighbor interactions can induce symmetry breaking, which leads to global and local minima of the average trapping time in the presence of a non-zero dephasing rate, suggesting that environment dephasing helps preserve quantum coherent energy transfer when the perfect circular symmetry in the hypothetic system is broken. This study reveals that dipolar coupling between chromophores may play an important role in the high energy transfer efficiency in the LH systems of purple bacteria and many other natural photosynthetic systems.

  13. Intramolecular energy transfer reactions in polymetallic complexes.. Progress report, 1991--1992

    SciTech Connect

    Petersen, J.

    1992-12-01

    (1) Excited-state energy transfer: The major effort was an attempt to sensitize the photoelimination of H{sub 2} from a bimetallic, metal-dihydride complex. These complexes have involved Fe, Ru, and Co complexes. (2) Excited-state electron transfer (charge separation): A series of diad and triad complexes were prepared in order to sustain charge separation in an artificial photosynthetic system.

  14. The flash photodissociation of nitrosyl chloride: Vibrational energy-transfer processes

    NASA Astrophysics Data System (ADS)

    Bechara, J.; Morrow, T.; McGrath, W. D.

    1985-12-01

    Vibrationally excited NOCl (NOCl *) has been observed, via its strong continuous absorption in the 230-280 nm region, following partial flash photodissociation of gaseous nitrosyl chloride mixtures. The formation of NOCl * is attributed to a vibrational energy transfer from Cl 2*, formed in the reaction of Cl with NOCl. The possibility of vibrational transfer from NO * to NOCl is also discussed. Rate constants for quenching of NOCl * and its precursor (Cl 2*) by NOCl, CO 2 and Ar are reported.

  15. Computing intramolecular charge and energy transfer rates using optimal modes

    SciTech Connect

    Yang, Xunmo; Bittner, Eric R.

    2015-06-28

    In our recent work [X. Yang and E. R. Bittner, J. Phys. Chem. A 118, 5196 (2014)], we showed how to construct a reduced set of nuclear motions that capture the coupling between electronic and nuclear degrees of freedom over the course of an electronic transition. We construct these modes, referred to as “Lanczos modes,” by applying a search algorithm to find linear combinations of vibrational normal modes that optimize the electronic/nuclear coupling operator. Here, we analyze the irreducible representations of the dominant contributions of these modes and find that for the cases considered here, these belong to totally symmetric irreducible representations of the donor and acceptor moieties. Upon investigating the molecular geometry changes following the transition, we propose that the electronic transition process can be broken into two steps, in the agreement of Born-Oppenheimer approximation: a fast excitation transfer occurs, facilitated by the “primary Lanczos mode,” followed by slow nuclear relaxation on the final electronic diabatic surface.

  16. Charge transfer activation energy for alkali atoms on Re and Ta

    NASA Astrophysics Data System (ADS)

    Gładyszewski, Longin

    1993-09-01

    Ion and atom desorption energies for five alkali metals on Re and Ta were determined using the ion thermal emission noise method. The activation energies for the charge transfer process in the adsorbed state were calculated using a special energetic balance equation, which describes the surface ionization and thermal desorption effect. Energies for desorption of Li, Na, K, Rb and Cs from Re and Ta surfaces were determined by measuring the time autocorrelation function of the ion thermoemission current fluctuations.

  17. A study of the generation of linear energy transfer spectra for space radiations

    NASA Technical Reports Server (NTRS)

    Wilson, John W.; Badavi, Francis F.

    1992-01-01

    The conversion of particle-energy spectra into a linear energy transfer (LET) distribution is a guide in assessing biologically significant components. The mapping of LET to energy is triple valued and can be defined only on open subintervals. A well-defined numerical procedure is found to allow generation of LET spectra on the open subintervals that are integrable in spite of their singular nature.

  18. A simple parameterization for quality factor as a function of linear energy transfer

    NASA Technical Reports Server (NTRS)

    Townsend, Lawrence W.; Wilson, John; Cucinotta, Francis A.

    1987-01-01

    The paper presents a simple analytic approximation of the radiation quality factor (Q) as a function of linear energy transfer for use in radiation protection calculations. The paper also presents estimated quality factors in water for protons over a broad range of incident energies. It is shown that the quality factors are less than unity for all proton energies greater than 13 MeV.

  19. Protein modifications affecting triplet energy transfer in bacterial photosynthetic reaction centers.

    SciTech Connect

    Laible, P. D.; Chynwat, V.; Thurnauer, M. C.; Schiffer, M.; Hanson, D. K.; Frank, H. A.; Univ.of Connecticut; Univ. of Connecticut

    1998-05-01

    The efficiency of triplet energy transfer from the special pair (P) to the carotenoid (C) in photosynthetic reaction centers (RCs) from a large family of mutant strains has been investigated. The mutants carry substitutions at positions L181 and/or M208 near chlorophyll-based cofactors on the inactive and active sides of the complex, respectively. Light-modulated electron paramagnetic resonance at 10 K, where triplet energy transfer is thermally prohibited, reveals that the mutations do not perturb the electronic distribution of P. At temperatures > or = 70 K, we observe reduced signals from the carotenoid in most of the RCs with L181 substitutions. In particular, triplet transfer efficiency is reduced in all RCs in which a lysine at L181 donates a sixth ligand to the monomeric bacteriochlorophyll B(B). Replacement of the native Tyr at M208 on the active side of the complex with several polar residues increased transfer efficiency. The difference in the efficiencies of transfer in the RCs demonstrates the ability of the protein environment to influence the electronic overlap of the chromophores and thus the thermal barrier for triplet energy transfer.

  20. Energy and angular momentum transfer in binary galaxies

    NASA Technical Reports Server (NTRS)

    Namboodiri, P. M. S.; Kochhar, R. K.

    1990-01-01

    The authors numerically studied tidal effects of a massive perturber on a satellite galaxy. The model consists of a spherical satellite galaxy and a point mass perturber and the encounter is non-penetrating. A wide range of density ratios and eccentricities of the relative orbits have been considered. The disruption of the satellite galaxy has been observed when the numerical value of the fractional change in the energy is greater than two. The changes in the energy and angular momentum show smooth variation in the case of unbound orbits and irregular variation in the bound orbit cases. It is shown that for a constant pericentral distance, increasing the density ratio decreases the tidal effects; and for a given density ratio an increase in the eccentricity decreases the tidal effects.

  1. Photoexcited energy transfer in a weakly coupled dimer

    NASA Astrophysics Data System (ADS)

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

    2015-03-01

    Cycloalkanes are important components in conventional fuels and oil shale derived fuels and the combustion of cyclohexane fuels leads to the production of benzene, a pollutant precursor. One of the pathways from cyclohexane to benzene is through sequential hydrogen loss, including the cyclohexyl radical as an intermediate. The ultraviolet (UV) photodissociation dynamics of the cyclohexyl (c-C6H11) radical was studied for the first time using the high- n Rydberg atom time-of-flight (HRTOF) technique in the range of 232-262 nm. The translational energy distributions of the H-atom loss product channel, P (ET) 's, show a large translational energy release and a large fraction of average translational energy in the total excess energy, , from 232-262 nm. The H-atom product angular distribution is anisotropic with a positive β parameter. The most likely H-atom loss pathway is an axial H ejection from the β-carbon in cyclohexyl to form cyclohexene + H, which along with the positive β parameter, indicates that the transition dipole moment, μ, is perpendicular to the ring. The P (ET) and anisotropy of the H-atom loss product channel are significantly larger than those expected for a statistical unimolecular dissociation of a hot radical, indicating a non-statistical dissociation mechanism. The dissociation mechanism is consistent with direct dissociation on a repulsive excited state surface or on the repulsive part of the ground state surface to produce cyclohexene + H, possibly mediated by a conical intersection. Cyclohexyl is the largest radical so far showing a direct dissociation mechanism.

  2. Energy Transfer in a Fast-Slow Hamiltonian System

    NASA Astrophysics Data System (ADS)

    Dolgopyat, Dmitry; Liverani, Carlangelo

    2011-11-01

    We consider a finite region of a lattice of weakly interacting geodesic flows on manifolds of negative curvature and we show that, when rescaling the interactions and the time appropriately, the energies of the flows evolve according to a nonlinear diffusion equation. This is a first step toward the derivation of macroscopic equations from a Hamiltonian microscopic dynamics in the case of weakly coupled systems.

  3. A state-space analysis of mechanical energy generation, absorption, and transfer during pedaling.

    PubMed

    Fregly, B J; Zajac, F E

    1996-01-01

    Seated ergometer pedaling is a motor task ideal for studying basic mechanisms of human bipedal coordination because, in contrast to standing and walking, fewer degrees of freedom are being controlled and upright balance is not a factor. As a step toward understanding how individual muscles coordinate pedaling, we investigated how individual net muscle joint torques and non-muscular (e.g. centripetal, coriolis, and gravity) forces of the lower limbs generate, absorb, and transfer mechanical energy in order to propel the crank and recover the limb. This was accomplished using a mechanical power analysis derived entirely from the closed-form state-space dynamical equations of a two-legged pedaling model that accounted for both the limb segmental and crank load dynamics. Based on a pedaling simulation that reproduced experimental kinematic and kinetic trajectories, we found that the net ankle and hip extensor joint torques function 'synergistically' to deliver energy to the crank during the downstroke. The net hip extensor joint torque generates energy to the limb, while the net ankle extensor joint torque transfers this energy from the limb to the crank. In contrast, net knee extensor and flexor joint torques function 'independently' by generating energy to the crank through the top and bottom of the stroke, respectively. The net ankle joint torque transfers and the net knee joint torque generates energy to the crank by contributing to the driving component of the pedal reaction force. During the upstroke, net ankle extensor joint torque transfers energy from the crank to the limb to restore the potential energy of the limb. In both halves of the crank cycle, gravity forces augment the crank-limb energy transfer performed by the net ankle extensor joint torque. PMID:8839020

  4. ISTP Global Geospace Science. Energy transfer in geospace

    NASA Technical Reports Server (NTRS)

    1990-01-01

    Solar-terrestrial physics concerns the study of the generation, flow, and dissipation of mass, momentum, and energy between the Sun and the Earth. Mass, momentum, and energy are carried by charged particles that compose the solar wind. When the solar wind reaches the Earth, some solar-wind particles enter the magnetosphere; this coupling between the solar wind and the Earth means that the solar wind can influence the Earth's upper atmosphere. As the first step in addressing the behavior of this solar-terrestrial system, the Global Geospace Science (GGS) Initiative will use the Wind and Polar satellites, provided by NASA, and the Geotail satellite provided by the Japanese Institute of Space and Astronautical Science (ISAS), to perform simultaneous and closely coordinated measurements of the key geospace regions and will add data from equatorial missions. Magnetic field and particle changes that occur when particles are energized during auroral events will be monitored. The intention behind the GGS Initiative is to understand the physical mechanisms and various regions controlling the transport of mass, momentum, and energy in geospace. A summary of the GGS Initiative is presented.

  5. Energy transfer to low energy chlorophyll species prior to trapping by P700 and subsequent electron transfer.

    PubMed

    Klug, D R; Giorgi, L B; Crystall, B; Barber, J; Porter, G

    1989-12-01

    It is found that the two singlet state lifetimes observed in medium sized isolated Photosystem One reaction centres belong to two distinct sets of particles. The nanosecond lifetime is due to PS1 particles in which P700 does not trap excitation energy, and the excitation energy is homogeneously distributed within the antennae of these particles. The spectral features of the picosecond component show that excitation energy in the antenna has become largely concentrated in one or more low energy (red) chlorophyll species within 3.5 ps. Antennae which have become decoupled from P700 also appear to be decoupled from these red "ancillary" chlorophylls, and this suggests that some substructure or level of organisation links them to P700.The rate of quenching of antenna singlet states appears to be independent of the redox state of P700 under the conditions used here, and oxidising P700 does not prevent excitation energy from reaching the red chlorophyll species in the antenna.We find no evidence in the data presented here of a chlorophyll molecule acting as a "metastable" primary acceptor (A0). The lower limit for the detection of such a species in these data is 20% of the optical density of the transient P700 bleach. PMID:24424816

  6. Ultrafast Studies of Resonance Energy Transfer in Myoglobin: A-Helix and Local Conformational Fluctuations

    NASA Astrophysics Data System (ADS)

    Stevens, Jeffrey A.; Link, Justin J.; Kao, Ya-Ting; Zang, Chen; Guo, Lijun; Zhong, Dongping

    2009-06-01

    Myoglobin (Mb), a heme containing protein, is involved in the storage and release of ligands. We report here our studies of resonance energy transfer in Mb using an intrinsic tryptophan (Trp) and the prosthetic heme as an energy transfer pair. With site-directed mutagenesis, we placed one-at-a-time a single Trp donor into four locations on the A-helix. Utilizing the femtosecond up-conversion method, we examined a series of energy transfer dynamics in Mb. A molecular dynamics (MD) simulation was also used to infer structure and dipole orientation fluctuations for specific Trp. Both methodologies were used to characterize the local dynamic nature of Mb in solution compared to the static crystal structure.

  7. Theory of energy transfer interactions near sphere and nanoshell based plasmonic nanostructures

    NASA Astrophysics Data System (ADS)

    Shishodia, Manmohan S.; Fainberg, Boris D.; Nitzan, Abraham

    2011-10-01

    Theory of energy transfer interactions between a pair of two level molecules in the molecular nanojunction including surface plasmon (SP) dressed interaction of plasmonic nanostructure, replicating metallic leads is presented. Results on the modification of bare dipolar interaction, known to be responsible for molecular energy transfer processes, in the proximity of metallic nanosystem are presented. Specifically, the manuscript includes theoretical investigation of nanosphere (NSP) monomer, nanoshell (NSH) monomer, and coupled nanosphere pair (dimer) based nanosystems. Closed form analytical expressions for NSP and NSH structures tailored for molecular nanojunction geometry are derived in the theoretical framework of multipole spectral expansion (MSE) method, which is straightforwardly extendible to dimers and multimers. The role of size and dielectric environment on energy transfer is investigated and interpreted. Theory predicts that the monomer and dimer both enhance the dipolar interaction, yet, dimer geometry is favorable due to its spectral tuning potential originated from plasmon hybridization and true resemblance with typical molecular nanojunctions.

  8. Resonant energy transfer between Eu luminescent sites and their local geometry in GaN

    SciTech Connect

    Timmerman, Dolf; Wakamatsu, Ryuta; Tanaka, Kazuteru; Lee, Dong-gun; Koizumi, Atsushi; Fujiwara, Yasufumi

    2015-10-12

    Eu-doped GaN is a solid state material with promising features for quantum manipulation. In this study, we investigate the population dynamics of Eu in ions in this system by resonant excitation. From differences in the emission related to transitions between the {sup 5}D{sub 0} and {sup 7}F{sub 2} manifold in the Eu ions, we can distinguish different luminescence sites and observe that a resonant energy transfer takes place between two of these sites which are in proximity of each other. The time constants related to this energy transfer are on the order of 100 μs. By using different substrates, the energy transfer efficiency could be strongly altered, and it is demonstrated that the coupling between ions has an out-of-plane character. Based on these results, a microscopic model of this combined center is presented.

  9. Upconversion energy transfer in Yb3+/Tm3+ doped tellurite glass

    NASA Astrophysics Data System (ADS)

    Żmojda, J.; Dorosz, D.; Kochanowicz, M.; Dorosz, J.

    2011-06-01

    The paper presents energy transfer in tellurite glass from the system TeO2 - GeO2 - PbO - PbF2- BaO - Nb2O5 - LaF3 doped with Yb3+/Tm3+ ions. Under the excitation of 976 nm laser a strong blue emission (477 nm) corresponding to the transition 1G4 --> 3H6 in thulium ions was observed. Analysing the influence of the content of Tm3+ ions on the level of luminescence obtained by the mechanism of upconversion it was established that the most effective energy transfer between Yb 3+--> Tm3+ ions took place in the matrix doped in the following proportion: 1 Yb3+:0.1 Tm3+ (%mol). Based on the non-resonant process of energy transfer between Yb3+ and Tm3+ ions the mechanism of upconversion was discussed.

  10. Energy transfer from Rhodamine-B to Oxazine-170 in the presence of photonic stop band

    NASA Astrophysics Data System (ADS)

    Kedia, Sunita; Sinha, Sucharita

    2015-03-01

    Photonic crystals can effectively suppress spontaneous emission of embedded emitter in the direction were photonic stop band overlaps emission band of emitter. This property of PhC has been successfully exploited to enhance energy transfer from a donor Rhodamine-B dye to an acceptor Oxazine-170 dye by inhibiting the fluorescence emission of donor in a controlled manner. Self-assembled PhC were synthesized using RhB dye doped polystyrene microspheres subsequently infiltrated with O-170 dye molecules dissolved in ethanol. An angle dependent enhancement of emission intensity of acceptor via energy transfer in photonic crystal environment was observed. These results were compared with observations made on a dye mixture solution of the same two dyes. Restricted number of available modes in photonic crystal inhibited de-excitation of donor thereby enabling efficient transfer of energy from excited donor to acceptor dye molecules.

  11. Nanophotonic Control of the Förster Resonance Energy Transfer Efficiency

    NASA Astrophysics Data System (ADS)

    Blum, Christian; Zijlstra, Niels; Lagendijk, Ad; Wubs, Martijn; Mosk, Allard P.; Subramaniam, Vinod; Vos, Willem L.

    2012-11-01

    We have studied the influence of the local density of optical states (LDOS) on the rate and efficiency of Förster resonance energy transfer (FRET) from a donor to an acceptor. The donors and acceptors are dye molecules that are separated by a short strand of double-stranded DNA. The LDOS is controlled by carefully positioning the FRET pairs near a mirror. We find that the energy transfer efficiency changes with LDOS, and that, in agreement with theory, the energy transfer rate is independent of the LDOS, which allows one to quantitatively control FRET systems in a new way. Our results imply a change in the characteristic Förster distance, in contrast to common lore that this distance is fixed for a given FRET pair.

  12. Energy (mass) transfer processes in low-temperature plasma as applied to forming ordered structures

    NASA Astrophysics Data System (ADS)

    Abramenko, T. N.; Laktyushina, T. V.; Laktyushin, A. N.

    2000-03-01

    The methods of irreversible thermodynamics are adopted to analyze the energy (mass) transfer in gases (their mixtures) over a wide temperature range up to 20000 K. An energy transfer process is considered as a path in the state space, and a concept of non-Euclidean state space is postulated. Experimental data on the gas thermal conductivity over a wide temperature range is generalized by the methods of thermodynamic similarity theory. Thermal conductivities of CH4-O2 and CH4-H2O mixtures are calculated for technological applications. The process of forming a space-time structure is analyzed by using the experimental data on the gas thermal conductivity over a wide temperature range. An attempt is made to interpret the mechanism of the thermal diffusion in gases due to the forming of ordered structures. A contribution of the diffusional thermoeffect to the energy transfer processes in a three-component nitrogen plasma is calculated.

  13. Geometrical effects in the energy transfer mechanism for silicon nanocrystals and Er3+

    NASA Astrophysics Data System (ADS)

    Choy, K.; Lenz, F.; Liang, X. X.; Marsiglio, F.; Meldrum, A.

    2008-12-01

    Silicon nanoclusters (NCs) strongly sensitize the luminescence of Er3+ ions. Attempts to calculate the interaction distance have assumed that the Förster [Ann. Phys. 437, 55 (1948)] and Dexter [J. Chem. Phys. 21, 836 (1953)] relationships for point-to-point energy transfer can be applied to experiments based on multilayered thin-film specimens. Here, the effective finite plane-to-plane relationships are derived for both interaction mechanisms. These relationships show that energy transfer can result from the Förster interaction despite the fact that the measured luminescence intensity varies much more weakly with NC-Er3+ separation than predicted by theory for point dipoles. An effective energy transfer distance is found for the NC-Er3+ system.

  14. Studies of Photosynthetic Energy and Charge Transfer by Two-dimensional Fourier transform electronic spectroscopy

    NASA Astrophysics Data System (ADS)

    Ogilvie, Jennifer

    2010-03-01

    Two-dimensional (2D) Fourier transform electronic spectroscopy has recently emerged as a powerful tool for the study of energy transfer in complex condensed-phase systems. Its experimental implementation is challenging but can be greatly simplified by implementing a pump-probe geometry, where the two phase-stable collinear pump pulses are created with an acousto-optic pulse-shaper. This approach also allows the use of a continuum probe pulse, expanding the available frequency range of the detection axis and allowing studies of energy transfer and electronic coupling over a broad range of frequencies. We discuss several benefits of 2D electronic spectroscopy and present 2D data on the D1-D2 reaction center complex of Photosystem II from spinach. We discuss the ability of 2D spectroscopy to distinguish between current models of energy and charge transfer in this system.

  15. [Improvement of anti-stokes energy transfer between rare earth ions--2. Numerical calculation and analysis].

    PubMed

    Chen, Xiao-bo; Wang, Ce; Kang, Dong-guo; Sawanobori, Naruhito; Wang, Shui-feng; Li, Yong-liang; Wang, Ping

    2010-08-01

    The dynamics of all levels were calculated numerically in the present article for Er(0.5)Yb(3):FOV oxyfluoride nanophase vitroceramics. The population dynamical processes were analyzed carefully. It was found for the first time that traditional phonon-assisted energy transfer theory of rare earth ion energy transfer can not well explain the observed experimental calibrated results, as it does not take into account the difference between Stokes and anti-Stokes process. A coefficient, the improved factor of the intensity ratio of Stokes to anti-Stokes process in quantum Raman theory compared to classical Raman theory, was introduced for the first time to successfully describe the anti-Stokes energy transfer. The theoretical improvement results are coincident with experiments very well. This improvement is very significant and indispensable when the photonics of nanomaterials is probed. PMID:20939297

  16. 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.

  17. Energy Transfer with Hydrogen and Superconductivity - The Review of the First Experimental Results

    NASA Astrophysics Data System (ADS)

    Vysotsky, V. S.; Antyukhov, I. V.; Firsov, V. P.; Blagov, E. V.; Kostyuk, V. V.; Nosov, A. A.; Fetisov, S. S.; Zanegin, S. Yu.; Rachuk, V. S.; Katorgin, B. I.

    The transfer of massive amounts of both electrical and chemical power over long distances will present a major challenge for the global energy enterprise in future. Attraction of hydrogen is apparent as a chemical energy agent, possessing among the highest energy density content of various common fuels, whose combustive "waste" is simply water. The usage of "gratis" cold to cool a superconducting cable made of proper superconductor permits to deliver extra electrical power with the same line. This, rather old theoretical idea recently found its experimental realization. The team of Russian institutes and organizations with using Italian-produced MgB2 wire has made and successfully tested two hybrid energy transfer lines with liquid hydrogen as a chemical source of power and superconducting cable as a source of electricity. The first line has been tested in 2011. It has length ∼10 m, maximum liquid hydrogen flow ∼250 g/s and maximum current of MgB2 superconducting cable 2600 A @ 20K. This test was the first experimental proof of conception of the hybrid energy transfer line. The second line has been tested in October 2013. It has length ∼30 m. The new MgB2 cable has critical current at 21 K ∼3500 A and successfully passed high voltage DC test of 50 kV. New hydrogen cryostat has three sections with different types of thermal insulation in each section. The idea of hybrid energy transfer is formulated and details of first experiments are reviewed.

  18. Long-range plasmon-assisted energy transfer over doped graphene

    NASA Astrophysics Data System (ADS)

    Velizhanin, Kirill; Shahbazyan, Tigran

    2013-03-01

    Förster resonance energy transfer (FRET) between spatially separated donor and acceptor fluorophores, such as dye molecules or semiconductors quantum dots, underpins diverse phenomena in physics, chemistry and biology. However, the range of present and potential applications of FRET is limited by its intrinsically short-range nature (~ 1 /R6). We demonstrate that longitudinal plasmons in doped monolayer graphene can mediate highly efficient long-range (~ 1 / R) energy transfer between nearby fluorophores, e.g., semiconductor quantum dots. We derive a simple analytical expression for the energy transfer efficiency that incorporates all the essential processes involved. We perform numerical calculations of the transfer efficiency for a pair of PbSe quantum dots near graphene for inter-fluorophore distances of up to 1 μm and find that the plasmon-assisted long-range energy transfer can be enhanced by up to a factor of ~104 relative to FRET in vacuum. Work at LANL was performed under the NNSA of the U.S. DOE at LANL under Contract No. DE-AC52- 06NA25396. Work at JSU was supported by the NSF under Grants No. DMR-1206975 and No. HRD-0833178 and under EPSCOR program.

  19. Tunable and long-range energy transfer efficiency through a graphene nanodisk

    NASA Astrophysics Data System (ADS)

    Karanikolas, Vasilios D.; Marocico, Cristian A.; Bradley, A. Louise

    2016-01-01

    In this paper, we present a theoretical investigation of the energy transfer efficiency between a pair of quantum emitters placed in proximity to a conducting graphene nanodisk. The energy transfer efficiency quantifies the contribution of the energy transfer process to the relaxation of the donor quantum system, as compared to the spontaneous emission rate of the donor in the absence of the acceptor. We use in our calculations the Green's tensor formalism in the electrostatic limit. This approximation works very well for the nanodisks considered here, for which the radius is much smaller than the emission wavelength of the donor. The approximate analytical solutions obtained are used to investigate the decay rate of a single quantum emitter and the energy transfer rate between quantum emitters in the vicinity of the graphene nanodisk. We find that these rates are enhanced several orders of magnitude compared with their free-space values. We determine the resonance frequencies of the spontaneous emission rate of a single quantum emitter to a graphene nanodisk, and the energy transfer rate between a pair of quantum emitters in proximity to a graphene nanodisk. We identify the surface modes which give the largest contributions to the energy transfer function. We connect the resonance frequency values and their surface plasmon wave numbers, which depend on the radius of the graphene nanodisk, with the dispersion relation of an infinite graphene monolayer at the same chemical potential. Analyzing the distance dependence of these rates, we are able to fit the full numerical results with a simple analytical expression which depends only on the geometrical characteristics of the graphene nanodisk, i.e., its radius. We show that the interaction distance depends on the transition dipole moment orientation and the different order resonance frequencies. The interaction distance between a pair of quantum emitters increases from a free-space value of 20 nm to reach values of

  20. Supramolecular Surface Photochemistry: Cascade Energy Transfer between Encapsulated Dyes Aligned on a Clay Nanosheet Surface.

    PubMed

    Tsukamoto, Takamasa; Ramasamy, Elamparuthi; Shimada, Tetsuya; Takagi, Shinsuke; Ramamurthy, V

    2016-03-29

    Three coumarin derivatives (7-propoxy coumarin, coumarin-480, and coumarin-540a, 2, 3, and 4, respectively) having different absorption and emission spectra were encapsulated within a water-soluble organic capsule formed by the two positively charged ammonium-functionalized cavitand octaamine (OAm, 1). Guests 2, 3, and 4 absorb in ultraviolet, violet, and blue regions and emit in violet, blue, and green regions, respectively. Energy transfer between the above three coumarin@(OAm)2 complexes assembled on the surface of a saponite clay nanosheet was investigated by steady-state and time-resolved emission techniques. Judging from their emission and excitation spectra, we concluded that the singlet-singlet energy transfer proceeded from 2 to 3, from 2 to 4, and from 3 to 4 when OAm-encapsulated 2, 3, and 4 were aligned on a clay surface as two-component systems. Under such conditions, the energy transfer efficiencies for the paths 2* to 3, 2* to 4, and 3* to 4 were calculated to be 33, 36, and 50% in two-component systems. When all three coumarins were assembled on the surface and 2 was excited, the energy transfer efficiencies for the paths 2* to 3, 2* to 4, and 3* to 4 were estimated to be 32, 34, and 33%. A comparison of energy transfer efficiencies of the two-component and three-component systems revealed that excitation of 2 leads to emission from 4. Successful merging of supramolecular chemistry and surface chemistry by demonstrating novel multi-step energy transfer in a three-component dye encapsulated system on a clay surface opens up newer opportunities for exploring such systems in an artificial light-harvesting phenomenon. PMID:26963843

  1. Energy transfer from a pulsed thermal source to He II below 0.3 K.

    NASA Technical Reports Server (NTRS)

    Pfeifer, C. D.; Luszczynski, K.

    1973-01-01

    Results of measurements of the angular distribution of the energy flux radiated from a pulsed heater immersed in He II at low temperatures (around 230 mK). It is shown that the energy transfer from a pulsed carbon heater at a relatively high temperature to ambient liquid helium maintained at low temperature cannot be adequately described by the phonon-coupling models. The experimental data on the velocity and angular distribution of the energy flux radiated from the plane of the heater indicate that the energy from the heater is transferred to a layer of hot helium adjacent to the surface of the heater and that this layer acts as the effective source of excitations radiated into the ambient liquid helium. The extent and shape of this source depend on the total energy flux produced by the heater.

  2. Systematic gas gain measurements and Penning energy transfer rates in Ne - CO2 mixtures

    NASA Astrophysics Data System (ADS)

    Şahin, Ö.; Kowalski, T. Z.; Veenhof, R.

    2016-01-01

    In Ne - CO2 mixtures, excitation energy of Ne atom can be used to ionize CO2 molecule by the mechanisms called Penning transfers. In the present work, we have measured the gas gain systematically in various Ne - CO2 mixtures (Ne + 0.6 - 60% CO2) at 0.4, 0.8, 1.2, 1.8 atm. The experimental data have been fitted to investigate the Penning energy transfer rates and the secondary processes playing a role in avalanche formations.

  3. Brightening Gold Nanoparticles: New Sensing Approach Based on Plasmon Resonance Energy Transfer

    PubMed Central

    Shi, Lei; Jing, Chao; Gu, Zhen; Long, Yi-Tao

    2015-01-01

    Scattering recovered plasmonic resonance energy transfer (SR-PRET) was reported by blocking the plasmon resonance energy transfer (PRET) from gold nanoparticle (GNP) to the adsorbed molecules (RdBS). Due to the selective cleavage of the Si-O bond by F− ions, the quenching is switched off causing an increase in the brightness of the GNPs,detected using dark-field microscopy (DFM) were brightened. This method was successfully applied to the determination of fluoride ions in water. The SR-PRET provides a potential approach for a vitro/vivo sensing with high sensitivity and selectivity. PMID:25959016

  4. 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

  5. Amino-functionalized green fluorescent carbon dots as surface energy transfer biosensors for hyaluronidase.

    PubMed

    Liu, Siyu; Zhao, Ning; Cheng, Zhen; Liu, Hongguang

    2015-04-21

    Amino-functionalized fluorescent carbon dots have been prepared by hydrothermal treatment of glucosamine with excess pyrophosphate. The produced carbon dots showed stabilized green emission fluorescence at various excitation wavelengths and pH environments. Herein, we demonstrate the surface energy transfer between the amino-functionalized carbon dots and negatively charged hyaluronate stabilized gold nanoparticles. Hyaluronidase can degrade hyaluronate and break down the hyaluronate stabilized gold nanoparticles to inhibit the surface energy transfer. The developed fluorescent carbon dot/gold nanoparticle system can be utilized as a biosensor for sensitive and selective detection of hyaluronidase by two modes which include fluorescence measurements and colorimetric analysis. PMID:25807038

  6. Light yield and energy transfer in a new Gd-loaded liquid scintillator

    NASA Astrophysics Data System (ADS)

    Aberle, C.; Buck, C.; Hartmann, F. X.; Schönert, S.

    2011-11-01

    We investigate a new gadolinium-loaded organic liquid scintillator which is designed to detect electron antineutrinos. A model has been developed to account for the various energy transfer paths possible in a liquid scintillator with multiple solvents, one fluor and a quenching component. Experimental light yield measurements were carried out to determine the relative rates for the energy transfers included in the model. Model predictions were used to tune the luminescent properties of the Gd-loaded target scintillator and the unloaded Gamma Catcher scintillator for the reactor neutrino experiment Double Chooz.

  7. Mechanism for the thermal dependence of the Cr to Nd energy transfer in garnets

    NASA Technical Reports Server (NTRS)

    Armagan, Guzin; Di Bartolo, Baldassare

    1988-01-01

    The temperature dependence of the Cr-Nd energy transfer is found to be due to the thermal variation of the radiative decay probability of Cr. The validity of this conjecture is checked in the Gd3Sc2Ga3O12 and CaMg2Y2Ge3O12 crystals. It is also found that above 200 K, the nonradiative energy transfer rate from Cr to Nd is greater in Gd3Sc2Ga3O12 than in CaMg2Y2Ge3O12.

  8. Computation studies into architecture and energy transfer properties of photosynthetic units from filamentous anoxygenic phototrophs

    SciTech Connect

    Linnanto, Juha Matti; Freiberg, Arvi

    2014-10-06

    We have used different computational methods to study structural architecture, and light-harvesting and energy transfer properties of the photosynthetic unit of filamentous anoxygenic phototrophs. Due to the huge number of atoms in the photosynthetic unit, a combination of atomistic and coarse methods was used for electronic structure calculations. The calculations reveal that the light energy absorbed by the peripheral chlorosome antenna complex transfers efficiently via the baseplate and the core B808–866 antenna complexes to the reaction center complex, in general agreement with the present understanding of this complex system.

  9. Mesoscopic order and the dimensionality of long-range resonance energy transfer in supramolecular semiconductors

    NASA Astrophysics Data System (ADS)

    Daniel, Clément; Makereel, François; Herz, Laura M.; Hoeben, Freek J. M.; Jonkheijm, Pascal; Schenning, Albertus P. H. J.; Meijer, E. W.; Silva, Carlos

    2008-09-01

    We present time-resolved photoluminescence measurements on two series of oligo-p-phenylenevinylene materials that self-assemble into supramolecular nanostructures with thermotropic reversibility in dodecane. One set of derivatives form chiral helical stacks, while the second set form less organized "frustrated" stacks. Here we study the effects of supramolecular organization on the resonance energy transfer rates. We measure these rates in nanoassemblies formed with mixed blends of oligomers and compare them with the rates predicted by Förster theory. Our results and analysis show that control of supramolecular order in the nanometer length scale has a dominant effect on the efficiency and dimensionality of resonance energy transfer.

  10. On Energy-Momentum Transfer of Quantum Fields

    NASA Astrophysics Data System (ADS)

    Herdegen, Andrzej

    2014-10-01

    We prove the following theorem on bounded operators in quantum field theory: if , then , where D( x) is a function weakly decaying in spacelike directions, are creation/annihilation parts of an appropriate time derivative of B, G is any positive, bounded, non-increasing function in , and is any finite complex Borel measure; creation/annihilation operators may be also replaced by with . We also use the notion of energy-momentum scaling degree of B with respect to a submanifold (Steinmann-type, but in momentum space, and applied to the norm of an operator). These two tools are applied to the analysis of singularities of . We prove, among others, the following statement (modulo some more specific assumptions): outside p = 0 the only allowed contributions to this functional which are concentrated on a submanifold (including the trivial one—a single point) are Dirac measures on hypersurfaces (if the decay of D is not to slow).

  11. Energy Transfers in Coupled Ordered Granular Chains with No Precompression

    NASA Astrophysics Data System (ADS)

    Vakakis, Alexander; Hasan, Arif M.; Starosvetsky, Yuli; Manevitch, Leonid I.

    2013-03-01

    We study the dynamics of coupled one-dimensional granular chains mounted on elastic foundations. No dissipative effects, such as plasticity or dry friction effects are taken into account in our analysis. Assuming no pre-compression between beads, the dynamics of the system under consideration is strongly nonlinear and, in an acoustic analogy they can be viewed as `sonic vacua'. Sources of strong nonlinearity in these systems are nonlinearizable Hertzian interactions between adjacent beads in compression, and also possible separations between beads in the absence of compressive forces leading to bead collisions. We find that demonstrate that in weakly coupled granular chains there can occur strong energy exchanges in the form of nonlinear beat phenomena of spatially periodic traveling waves, stationary breathers or propagating breathers. We employ analytical techniques to study these dynamical phenomena. This work was supported by MURI grant US ARO W911NF-09-1-0436. Dr. David Stepp is the grant monitor.

  12. Tracing of backward energy transfer from LH1 to LH2 in photosynthetic membranes grown under high and low irradiation.

    NASA Astrophysics Data System (ADS)

    Lüer, L.; Moulisová, V.; Henry, S.; Polli, D.; Brotosudarmo, T. H. P.; Hoseinkhani, S.; Brida, D.; Lanzani, G.; Cerullo, G.; Cogdell, R. J.

    2013-03-01

    By introducing derivative transient absorption spectroscopy, we obtain rate constants for backward and forward energy transfer between LH1 and LH2 complexes in purple bacterial membranes. We find that backward energy transfer is strongly reduced in membranes grown under low irradiation conditions, compared to high light grown ones. We conclude that backward energy transfer is managed actively by the bacteria to avoid LH1 exciton deactivation under high irradiation conditions. The analytical method is generally applicable to excitonically coupled systems.

  13. Energy transfer mechanism and Auger effect in Er{sup 3+} coupled silicon nanoparticle samples

    SciTech Connect

    Pitanti, A.; Navarro-Urrios, D.; Garrido, B.; Prtljaga, N.; Daldosso, N.; Pavesi, L.; Gourbilleau, F.; Rizk, R.

    2010-09-15

    We report a spectroscopic study about the energy transfer mechanism among silicon nanoparticles (Si-np), both amorphous and crystalline, and Er ions in a silicon dioxide matrix. From infrared spectroscopic analysis, we have determined that the physics of the transfer mechanism does not depend on the Si-np nature, finding a fast (<200 ns) energy transfer in both cases, while the amorphous nanoclusters reveal a larger transfer efficiency than the nanocrystals. Moreover, the detailed spectroscopic results in the visible range here reported are essential to understand the physics behind the sensitization effect, whose knowledge assumes a crucial role to enhance the transfer rate and possibly employing the material in optical amplifier devices. Joining the experimental data, performed with pulsed and continuous-wave excitation, we develop a model in which the internal intraband recombination within Si-np is competitive with the transfer process via an Auger electron-''recycling'' effect. Posing a different light on some detrimental mechanism such as Auger processes, our findings clearly recast the role of Si-np in the sensitization scheme, where they are able to excite very efficiently ions in close proximity to their surface.

  14. Energy transfer and clustering of photosynthetic light-harvesting complexes in reconstituted lipid membranes

    NASA Astrophysics Data System (ADS)

    Dewa, Takehisa; Sumino, Ayumi; Watanabe, Natsuko; Noji, Tomoyasu; Nango, Mamoru

    2013-06-01

    In purple photosynthetic bacteria, light-harvesting complex 2 (LH2) and light harvesting/reaction centre core complex (LH1-RC) play the key roles of capturing and transferring light energy and subsequent charge separation. These photosynthetic apparatuses form a supramolecular assembly; however, how the assembly influences the efficiency of energy conversion is not yet clear. We addressed this issue by evaluating the energy transfer in reconstituted photosynthetic protein complexes LH2 and LH1-RC and studying the structures and the membrane environment of the LH2/LH1-RC assemblies, which had been embedded into various lipid bilayers. Thus, LH2 and LH1-RC from Rhodopseudomonas palustris 2.1.6 were reconstituted in phosphatidylglycerol (PG), phosphatidylcholine (PC), and phosphatidylethanolamine (PE)/PG/cardiolipin (CL). Efficient energy transfer from LH2 to LH1-RC was observed in the PC and PE/PG/CL membranes. Atomic force microscopy revealed that LH2 and LH1-RC were heterogeneously distributed to form clusters in the PC and PE/PG/CL membranes. The results indicated that the phospholipid species influenced the cluster formation of LH2 and LH1-RC as well as the energy transfer efficiency.

  15. Photophysics, Dynamics, and Energy Transfer in Rigid Mimics of GFP-based Systems.

    PubMed

    Dolgopolova, Ekaterina A; Rice, Allison M; Smith, Mark D; Shustova, Natalia B

    2016-08-01

    Engineering of novel systems capable of efficient energy capture and transfer in a predesigned pathway could potentially boost applications varying from organic photovoltaics to catalytic platforms and have implications for energy sustainability and green chemistry. While light-harvesting properties of different materials have been studied for decades, recently, there has been great progress in the understanding and modeling of short- and long-range energy transfer processes through utilization of metal-organic frameworks (MOFs). In this Forum Article, the recent advances in efficient multiple-chromophore coupling in well-defined metal-organic materials through mimicking a protein system possessing near 100% energy transfer are discussed. Utilization of a MOF as an efficient replica of a protein β-barrel to maintain chromophore emission was also demonstrated. Furthermore, we established a novel dependence of a photophysical response on an electronic configuration for chromophores with the benzylidene imidazolinone core. For that, we prepared 16 chromophores, in which the benzylidene imidazolinone core was modified with electron-donating and electron-withdrawing substituents. To establish the structure-dependent photophysical properties of the prepared chromophores, 11 novel molecular structures were determined by single-crystal X-ray diffraction. These findings allow one to predict the chromophore emission profile inside a rigid framework as a function of the substituent, a key parameter for achieving the spectral overlap necessary to study and increase resonance energy transfer efficiency in MOF-based materials. PMID:27304253

  16. Mode-specific intermolecular vibrational energy transfer. I. Phenyl selenocyanate and deuterated chloroform mixture

    NASA Astrophysics Data System (ADS)

    Bian, Hongtao; Li, Jiebo; Wen, Xiewen; Zheng, Junrong

    2010-05-01

    Vibrational energy transfer from the first excited state (2252 cm-1) of the C-D stretch of deuterated chloroform (DCCl3) to the 0-1 transition (2155 cm-1) of the CN stretch of phenyl selenocyanate (C6H5SeCN) in their 1:1 liquid mixture was observed with a pump/probe two-color two dimensional infrared spectroscopic technique. The mode-specific energy transfer can occur mainly because of the long vibrational lifetime of the CN stretch first excited state (˜300 ps) and the relatively strong hydrogen-bond between the C-D and CN (calculated H-bond formation energy in gas phase ˜-5.4 kcal/mol). The mode-specific energy transfer is relatively low efficient (only ˜2%), which is mainly because of the relatively short vibrational lifetime (˜9 ps) of the C-D stretch first excited state and the big donor/acceptor energy mismatch (97 cm-1) and the slow transfer kinetics (1/kCD→CN=330 ps).

  17. Applications of free-electron lasers to measurements of energy transfer in biopolymers and materials

    NASA Astrophysics Data System (ADS)

    Edwards, Glenn S.; Johnson, J. B.; Kozub, John A.; Tribble, Jerri A.; Wagner, Katrina

    1992-08-01

    Free-electron lasers (FELs) provide tunable, pulsed radiation in the infrared. Using the FEL as a pump beam, we are investigating the mechanisms for energy transfer between localized vibrational modes and between vibrational modes and lattice or phonon modes. Either a laser-Raman system or a Fourier transform infrared (FTIR) spectrometer will serve as the probe beam, with the attribute of placing the burden of detection on two conventional spectroscopic techniques that circumvent the limited response of infrared detectors. More specifically, the Raman effect inelastically shifts an exciting laser line, typically a visible frequency, by the energy of the vibrational mode; however, the shifted Raman lines also lie in the visible, allowing for detection with highly efficient visible detectors. With regards to FTIR spectroscopy, the multiplex advantage yields a distinct benefit for infrared detector response. Our group is investigating intramolecular and intermolecular energy transfer processes in both biopolymers and more traditional materials. For example, alkali halides contain a number of defect types that effectively transfer energy in an intermolecular process. Similarly, the functioning of biopolymers depends on efficient intramolecular energy transfer. Understanding these mechanisms will enhance our ability to modify biopolymers and materials with applications to biology, medecine, and materials science.

  18. Upconversion-induced delayed fluorescence in multicomponent organic systems: Role of Dexter energy transfer

    NASA Astrophysics Data System (ADS)

    Monguzzi, A.; Tubino, R.; Meinardi, F.

    2008-04-01

    The efficiency of the upconversion-induced delayed fluorescence in a solution of multicomponent organic systems is limited by two steps of the overall process: (i) a triplet-triplet energy transfer between a phosphorescent donor and an emitting acceptor, and (ii) a bimolecular acceptor triplet-triplet annihilation generating acceptor singlet excited states from which the high-energy emission takes place. In this work, the energy transfer process has been investigated in a model system constituted by solutions of Pt(II)octaethylporphyrin, which acts as a donor, and 9,10 diphenylanthracene, which acts as an acceptor. At low temperature, the experimental data have been interpreted in the frame of a pure Dexter energy transfer by using the Perrin approximation. A Dexter radius as large as 26.5 Å has been found. At room temperature, the fast diffusion of the molecules in the solution is no longer negligible, which gives rise to a strong increase in the energy transfer rates.

  19. Inhibition of plasmonically enhanced interdot energy transfer in quantum dot solids via photo-oxidation

    SciTech Connect

    Sadeghi, S. M.; Nejat, A.; West, R. G.

    2012-11-15

    We studied the impact of photophysical and photochemical processes on the interdot Forster energy transfer in monodisperse CdSe/ZnS quantum dot solids. For this, we investigated emission spectra of CdSe/ZnS quantum dot solids in the vicinity of gold metallic nanoparticles coated with chromium oxide. The metallic nanoparticles were used to enhance the rate of the energy transfer between the quantum dots, while the chromium oxide coating led to significant increase of their photo-oxidation rates. Our results showed that irradiation of such solids with a laser beam can lead to unique spectral changes, including narrowing and blue shift. We investigate these effects in terms of inhibition of the plasmonically enhanced interdot energy transfer between quantum dots via the chromium-oxide accelerated photo-oxidation process. We demonstrate this considering energy-dependent rate of the interdot energy transfer process, plasmonic effects, and the way photo-oxidation enhances non-radiative decay rates of quantum dots with different sizes.

  20. Forster Energy Transfer Theory as Reflected in the Structures of Photosynthetic Light-Harvesting Systems

    SciTech Connect

    Sener, Melih; Strumpfer, Johan; Hsin, Jen; Chandler, Danielle; Scheuring, Simon; Hunter, C. Neil; Schulten, Klaus

    2011-02-22

    Förster's theory of resonant energy transfer underlies a fundamental process in nature, namely the harvesting of sunlight by photosynthetic life forms. The theoretical framework developed by Förster and others describes how electronic excitation migrates in the photosynthetic apparatus of plants, algae, and bacteria from light absorbing pigments to reaction centers where light energy is utilized for the eventual conversion into chemical energy. The demand for highest possible efficiency of light harvesting appears to have shaped the evolution of photosynthetic species from bacteria to plants which, despite a great variation in architecture, display common structural themes founded on the quantum physics of energy transfer as described first by Förster. Herein, Förster’s theory of excitation transfer is summarized, including recent extensions, and the relevance of the theory to photosynthetic systems as evolved in purple bacteria, cyanobacteria, and plants is demonstrated. Förster's energy transfer formula, as used widely today in many fields of science, is also derived.

  1. Photoinduced proton transfer coupled with energy transfer: Mechanism of sensitized luminescence of terbium ion by salicylic acid doped in polymer.

    PubMed

    Misra, Vinita; Mishra, Hirdyesh

    2008-06-28

    In the present work, excited state intramolecular proton transfer (ESIPT) in salicylic acid (SA) monoanion and subsequent sensitization of Tb(3+) ion in polyvinyl alcohol (PVA) have been studied. The study has been carried out both by steady state and time domain fluorescence measurement techniques at room temperature. It is found that the SA completely ionizes and exists as monoanion in PVA. It exhibits a large Stokes shifted blue emission (10 000 cm(-1)) due to ESIPT and shows a decay time of 6.85 ns. On the other hand, Tb(3+) ion shows a very weak green emission and a decay time of approximately 641 mus in PVA film. Upon incorporating Tb(3+) ion in SA doped PVA film, both intensity and decay time of SA decrease and sensitized emission from Tb(+3) ion along with 3.8 mus rise time is observed. Energy transfer is found to take place both from excited singlet as well as triplet states. A brief description of the properties of the present system from the viewpoint of luminescent solar collector material is addressed. PMID:18601359

  2. Imaging charge and energy transfer in molecules using free-electron lasers

    NASA Astrophysics Data System (ADS)

    Rudenko, Artem

    2014-05-01

    Charge and energy transfer reactions drive numerous important processes in physics, chemistry and biology, with applications ranging from X-ray astrophysics to artificial photosynthesis and molecular electronics. Experimentally, the central goal in studies of transfer phenomena is to trace the spatial localization of charge at a given time. Because of their element and site sensitivity, ultrafast X-rays provide a promising tool to address this goal. In this talk I will discuss several experiments where free-electron lasers were employed to study charge and energy transfer dynamics in fragmenting molecules. In a first example, we used intense, 70 femtosecond 1.5 keV pulses from the Linac Coherent Light Source (LCLS) to study distance dependence of electron transfer in laser-dissociated methyl iodide molecules. Inducing well-localized positive charge on the heavy iodine atom, we observe signature of electron transition from the separated methyl group up to the distances of 35 atomic units. In a complementary experiment, we studied charge exchange between two partners in a dissociating molecular iodine employing a pump-probe arrangement with two identical 90 eV pulses from the Free-Electron LASer in Hamburg (FLASH). In both cases, the effective spatial range of the electron transfer can be reasonably described by a classical over-the-barrier model developed for ion-atom collisions. Finally, I will discuss a time-resolved measurement on non-local relaxation mechanism based on a long-range energy transfer, the so-called interatomic Coulombic decay. This work was supported by Chemical Sciences, Geosciences, and Biosciences Division, Office of Basic Energy Sciences, Office of Science, US Department of Energy and by the Kansas NSF ``First Award'' program.

  3. Transferring building energy technologies by linking government and private-sector programs

    SciTech Connect

    Farhar, B.C.

    1990-07-01

    The US Department of Energy's Office of Building Technologies (OBT) may wish to use existing networks and infrastructures wherever possible to transfer energy-efficiency technologies for buildings. The advantages of relying on already existing networks are numerous. These networks have in place mechanisms for reaching audiences interested in energy-efficiency technologies in buildings. Because staffs in trade and professional organizations and in state and local programs have responsibilities for brokering information for their members or client organizations, they are open to opportunities to improve their performance in information transfer. OBT, as an entity with primarily R D functions, is, by cooperating with other programs, spared the necessity of developing an extensive technology transfer program of its own, thus reinventing the wheel.'' Instead, OBT can minimize its investment in technology transfer by relying extensively on programs and networks already in place. OBT can work carefully with staff in other organizations to support and facilitate their efforts at information transfer and getting energy-efficiency tools and technologies into actual use. Consequently, representatives of some 22 programs and organizations were contacted, and face-to-face conversations held, to explore what the potential might be for transferring technology by linking with OBT. The briefs included in this document were derived from the discussions, the newly published Directory of Energy Efficiency Information Services for the Residential and Commercial Sectors, and other sources provided by respondents. Each brief has been sent to persons contacted for their review and comment one or more times, and each has been revised to reflect the review comments.

  4. Vibrational spectroscopy and intramolecular energy transfer in isocyanic acid (HNCO)

    SciTech Connect

    Coffey, M.J.; Berghout, H.L.; Woods, E. III; Crim, F.F.

    1999-06-01

    Room temperature photoacoustic spectra in the region of the first through the fourth overtones (2{nu}{sub 1} to 5{nu}{sub 1}) and free-jet action spectra of the second through the fourth overtones (3{nu}{sub 1} to 5{nu}{sub 1}) of the N{endash}H stretching vibration permit analysis of the vibrational and rotational structure of HNCO. The analysis identifies the strong intramolecular couplings that control the early stages of intramolecular vibrational energy redistribution (IVR) and gives the interaction matrix elements between the zero-order N{endash}H stretching states and the other zero-order states with which they interact. The experimentally determined couplings and zero-order state separations are consistent with {ital ab initio} calculations of East, Johnson, and Allen [J. Chem. Phys. {bold 98}, 1299 (1993)], and comparison with the calculation identifies the coupled states and likely interactions. The states most strongly coupled to the pure N{endash}H stretching zero-order states are ones with a quantum of N{endash}H stretching excitation ({nu}{sub 1}) replaced by different combinations of N{endash}C{endash}O asymmetric or symmetric stretching excitation ({nu}{sub 2} or {nu}{sub 3}) and {ital trans}-bending excitation ({nu}{sub 4}). The two strongest couplings of the n{nu}{sub 1} state are to the states (n{minus}1){nu}{sub 1}+{nu}{sub 2}+{nu}{sub 4} and (n{minus}1){nu}{sub 1}+{nu}{sub 3}+2{nu}{sub 4}, and sequential couplings through a series of low order resonances potentially play a role. The analysis shows that if the pure N{endash}H stretch zero-order state were excited, energy would initially flow out of that mode into the strongly coupled mode in 100 fs to 700 fs, depending on the level of initial excitation. {copyright} {ital 1999 American Institute of Physics.}

  5. Targeted energy transfer between a system with a set of Saint-Venant elements and a nonlinear energy sink

    NASA Astrophysics Data System (ADS)

    Lamarque, C.-H.; Ture Savadkoohi, A.

    2015-09-01

    Targeted energy transfer between a main oscillator with a set of parallel Saint-Venant elements and a nonlinear energy sink with a general nonlinear and odd potential function around 1:1 resonance is studied. The complexified system has been investigated at fast and slow time scales by detecting its invariant manifold, equilibrium and singular points, which can explain bifurcation(s) and different regimes of the system. Then, we introduce an example which treats vibratory energy exchanges between a main oscillator with two parallel Saint-Venant elements and a coupled cubic nonlinear energy sink. Finally, analytical predictions are compared with results obtained by numerical integrations of system equations.

  6. The influence of triplet energy levels of bridging ligands on energy transfer processes in Ir(III)/Eu(III) dyads.

    PubMed

    Jiang, Weili; Lou, Bin; Wang, Jianqiang; Lv, Hongbin; Bian, Zuqiang; Huang, Chunhui

    2011-11-21

    A series of N^N,O^O-bridging ligands based on substituted 1-(pyridin-2-yl)-3-methyl-5-pyrazolone and their corresponding heteroleptic iridium(III) complexes as well as Ir-Eu bimetallic complexes were synthesized and fully characterized. The influence of the triplet energy levels of the bridging ligands on the energy transfer (ET) process from the Ir(III) complexes to Eu(III) ions in solution was investigated at 77 K in Ir(III)/Eu(III) dyads. Photophysical experiment results show the bridging ligands play an important role in the ET process. Only when the triplet energy level of the bridging ligand was lower than the triplet metal-to-ligand charge transfer ((3)MLCT) energy level of the Ir moiety, was pure emission from the Eu(III) ion observed, implying complete ET took place from the Ir moiety to the Eu(III) ion. PMID:21931913

  7. The free-energy barrier to hydride transfer across a dipalladium complex.

    PubMed

    Vanston, C R; Kearley, G J; Edwards, A J; Darwish, T A; de Souza, N R; Ramirez-Cuesta, A J; Gardiner, M G

    2015-01-01

    We use density-functional theory molecular dynamics (DFT-MD) simulations to determine the hydride transfer coordinate between palladium centres of the crystallographically observed terminal hydride locations, Pd-Pd-H, originally postulated for the solution dynamics of the complex bis-NHC dipalladium hydride [{(MesIm)2CH2}2Pd2H][PF6], and then calculate the free-energy along this coordinate. We estimate the transfer barrier-height to be about 20 kcal mol(-1) with a hydride transfer rate in the order of seconds at room temperature. We validate our DFT-MD modelling using inelastic neutron scattering which reveals anharmonicity of the hydride environment that is so pronounced that there is complete failure of the harmonic model for the hydride ligand. The simulations are extended to high temperature to bring the H-transfer to a rate that is accessible to the simulation technique. PMID:25652724

  8. Energy transfer efficiency in the chromophore network strongly coupled to a vibrational mode

    NASA Astrophysics Data System (ADS)

    Mourokh, Lev G.; Nori, Franco

    2015-11-01

    Using methods from condensed matter and statistical physics, we examine the transport of excitons through the photosynthetic complex from a receiving antenna to a reaction center. Writing the equations of motion for the exciton creation-annihilation operators, we are able to describe the exciton dynamics, even in the regime when the reorganization energy is of the order of the intrasystem couplings. We determine the exciton transfer efficiency in the presence of a quenching field and protein environment. While the majority of the protein vibrational modes are treated as a heat bath, we address the situation when specific modes are strongly coupled to excitons and examine the effects of these modes on the energy transfer efficiency in the steady-state regime. Using the structural parameters of the Fenna-Matthews-Olson complex, we find that, for vibrational frequencies below 16 meV, the exciton transfer is drastically suppressed. We attribute this effect to the formation of a "mixed exciton-vibrational mode" where the exciton is transferred back and forth between the two pigments with the absorption or emission of vibrational quanta, instead of proceeding to the reaction center. The same effect suppresses the quantum beating at the vibrational frequency of 25 meV. We also show that the efficiency of the energy transfer can be enhanced when the vibrational mode strongly couples to the third pigment only, instead of coupling to the entire system.

  9. 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.

  10. Energy transfer in spectrally inhomogeneous light-harvesting pigment-protein complexes of purple bacteria.

    PubMed Central

    Hess, S; Akesson, E; Cogdell, R J; Pullerits, T; Sundström, V

    1995-01-01

    Energy transfer within the peripheral light-harvesting antenna of the purple bacteria Rhodobacter sphaeroides and Rhodopseudomonas palustris was studied by one- and two-color pump-probe absorption spectroscopy with approximately 100-fs tunable pulses at room temperature and at 77 K. The energy transfer from B800 to B850 occurs with a time constant of 0.7 +/- 0.05 ps at room temperature and 1.8 +/- 0.2 ps at 77 K and is similar in both species. Anisotropy measurements suggest a limited but fast B800 <--> B800 transfer time (tau approximately 0.3 ps). This is analyzed as incoherent hopping of the excitation in a system of spectrally inhomogeneous antenna pigment-protein complexes, by a master equation approach. The simulations show that the measured B800 dynamics is well described as energy transfer with a characteristic average nearest-neighbor pairwise transfer time of 0.35 ps among approximately 10 Bchl molecules in a circular arrangement, in good agreement with the recent high-resolution structure of LH2. The possible presence of fast intramolecular relaxation processes within the Bchl a molecule was investigated by measurement of time-resolved difference absorption spectra and kinetics of Bchl a in solution and in low-temperature glasses. From these measurements it is concluded that fast transients observed at room temperature are due mainly to solvation processes, whereas at 77 K predominantly slower (> 10-ps) relaxation occurs. Images FIGURE 11 PMID:8599629

  11. Site-sensitive energy transfer modes in Ca3Al2O6: Ce(3+)/Tb(3+)/Mn(2+) phosphors.

    PubMed

    Zhang, Jilin; He, Yani; Qiu, Zhongxian; Zhang, Weilu; Zhou, Wenli; Yu, Liping; Lian, Shixun

    2014-12-28

    Ce(3+)/Eu(2+), Tb(3+) and Mn(2+) co-doping in single-phase hosts is a common strategy to achieve white-light phosphors via energy transfer, which provides a high color rendering index (CRI) value and good color stability. However, not all hosts are suitable for white-light phosphors due to inefficient energy transfer. In this study, the site-sensitive energy transfer from different crystallographic sites of Ce(3+) to Tb(3+)/Mn(2+) in Ca3Al2O6 has been investigated in detail. The energy transfer from purplish-blue Ce(3+) to Tb(3+) is an electric dipole-dipole mode, and the calculated critical distance (Rc) suggests the existence of purplish-blue Ce(3+)-Tb(3+) clusters. No energy transfer is observed from purplish-blue Ce(3+) to Mn(2+). In co-doped phosphors based on greenish-blue Ce(3+), however, the radiative mode dominates the energy transfer from Ce(3+) to Tb(3+), and an electric dipole-quadrupole interaction is responsible for the energy transfer from Ce(3+) to Mn(2+). A detailed discussion on the site-sensitive energy transfer modes might provide a new aspect to discuss and understand the possibilities and mechanisms of energy transfer, according to certain crystallographic sites in a complex host with different cation sites, as well as provide a possible approach in searching for single-phase white-light-emitting phosphors. PMID:25354712

  12. Scale-to-scale energy transfer in mixing flow induced by the Richtmyer-Meshkov instability

    NASA Astrophysics Data System (ADS)

    Liu, Han; Xiao, Zuoli

    2016-05-01

    The Richtmyer-Meshkov instability (RMI) mixing flow induced by a planar shock wave of Mach 1.6 is investigated using direct numerical simulation method. Interfacial perturbations of different scales between air and sulfur hexafluoride are introduced to study the effect of the initial conditions. Focus is placed on the analysis of the scale-to-scale transfer of kinetic energy in both Fourier and physical spaces. The kinetic energy injected from the perturbation scales is transferred to both larger and smaller scales in an average sense within the inner mixing zone (IMZ) at early times and is mainly passed down into smaller scales at the late stage. The physical-space energy flux due to the subgrid-scale (SGS) stress is studied using a filtering approach in order to shed light on the physical origin of the scale-to-scale kinetic energy transfer. It is found that the pointwise SGS energy flux is highly correlated with the local spike and bubble structures in the IMZ. Moreover, it turns out that the mean SGS energy flux is mainly ascribed to the component in the direction of shock wave propagation. An analysis using the method of conditional averaging manifests that the generation of local SGS energy flux is associated with the property of the surrounding flow induced by quadrupolar or dipolar vortex structures.

  13. Higher-order processes of excitation energy transfer in supramolecular complexes: Liouville space analysis of bridge molecule mediated transfer and direct photon exchange.

    PubMed

    May, Volkhard

    2008-09-21

    Long-range electronic excitation energy transfer is studied in the framework of a generalized master equation approach, which offers a systematic account for higher-order processes. Bridge molecule mediated transfer is confronted with the direct excitation energy exchange via photon emission and absorption. It is the central aim of this paper to present a systematic study of fourth-order rates, which describe both types of transfer processes characterized by the presence of intermediate states. While such a Liouville space formulation of rates is known from bridge mediated transfer, it is new for the case of photon mediated processes. In the former case, however, a novel approach to account for intermediate state relaxation is introduced. Finally and for illustration, some estimates are offered for the length dependence of the various discussed transfer rates. PMID:19044952

  14. Dynamics of Energy Transfer in a Conjugated Dendrimer Driven by Ultrafast Localization of Excitations.

    PubMed

    Galindo, Johan F; Atas, Evrim; Altan, Aysun; Kuroda, Daniel G; Fernandez-Alberti, Sebastian; Tretiak, Sergei; Roitberg, Adrian E; Kleiman, Valeria D

    2015-09-16

    Solar energy conversion starts with the harvest of light, and its efficacy depends on the spatial transfer of the light energy to where it can be transduced into other forms of energy. Harnessing solar power as a clean energy source requires the continuous development of new synthetic materials that can harvest photon energy and transport it without significant losses. With chemically-controlled branched architectures, dendrimers are ideally suited for these initial steps, since they consist of arrays of chromophores with relative positioning and orientations to create energy gradients and to spatially focus excitation energies. The spatial localization of the energy delimits its efficacy and has been a point of intense research for synthetic light harvesters. We present the results of a combined theoretical experimental study elucidating ultrafast, unidirectional, electronic energy transfer on a complex molecule designed to spatially focus the initial excitation onto an energy sink. The study explores the complex interplay between atomic motions, excited-state populations, and localization/delocalization of excitations. Our findings show that the electronic energy-transfer mechanism involves the ultrafast collapse of the photoexcited wave function due to nonadiabatic electronic transitions. The localization of the wave function is driven by the efficient coupling to high-frequency vibrational modes leading to ultrafast excited-state dynamics and unidirectional efficient energy funneling. This work provides a long-awaited consistent experiment-theoretical description of excited-state dynamics in organic conjugated dendrimers with atomistic resolution, a phenomenon expected to universally appear in a variety of synthetic conjugated materials. PMID:26122872

  15. 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.

  16. Energy transfer processes in solar energy conversion. Progress report, March 1, 1991--February 29, 1992

    SciTech Connect

    Fayer, M.D.

    1992-07-01

    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.

  17. Collective Förster energy transfer modified by planar plasmonic mirror (Presentation Recording)

    NASA Astrophysics Data System (ADS)

    Poddubny, Alexander N.

    2015-09-01

    This is an invited presentation devoted to the Förster energy transfer in plasmonic systems. Förster energy transfer processes are now actively studied in various fields that bridge physics, biology and medicine. One can try to control the efficiency of the transfer by embedding the donors and acceptors into the structured electromagnetic environment. Available experimental studies yields contradictory reports on suppressed [1], enhanced [2] or unaffected [3] transfer. We present a rigorous Green function theory of the collective Förster energy transfer between the arrays of donor and acceptor molecules lying on the planar metallic mirror that has been previously available only for spherical nanoparticles [4]. We reveal strong modification of the effective transfer rate by the mirror. The rate can be either suppressed or enhanced depending on the relative positions between acceptor and donor arrays. This is a collective effect, completely absent for a single donor-acceptor pair put above the mirror. Our results may explain the slowdown of the transfer rate recently observed in experiment for dye molecules put on top of plasmonic mirrors and layered hyperbolic metamaterials [1]. [1] T. Tumkur, J. Kitur, C. Bonner, A. Poddubny, E. Narimanov and M. Noginov , Faraday Discuss., 2014 , DOI: 10.1039/C4FD00184B [2] C. Blum, N. Zijlstra, A. Lagendijk, M. Wubs, A. P. Mosk, V. Subramaniam, and W. L. Vos, Phys. Rev. Lett. 109, 203601 (2012). [3] P. Andrew and W. L. Barnes, Science 290, 785 (2000). [4] V.N. Pustovit, A.M. Urbas, and T.V. Shahbazyan, Phys. Rev. B 88, 245427(2013)

  18. Energy transfer by inertial waves during the buildup of turbulence in a rotating system.

    PubMed

    Kolvin, Itamar; Cohen, Kobi; Vardi, Yuval; Sharon, Eran

    2009-01-01

    We study the transition from fluid at rest to turbulence in a rotating tank. The energy is transported by inertial wave packets through the fluid volume. These high amplitude waves propagate at velocities consistent with those calculated from linearized theory [H. P. Greenspan, (Cambridge University Press, Cambridge, England, 1968)]. A "front" in the temporal evolution of the energy power spectrum indicates a time scale for energy transport at the linear wave speed. Nonlinear energy transfer between modes is governed by a different, longer, time scale. The observed mechanisms can lead to significant differences between rotating and two-dimensional turbulent flows. PMID:19257200

  19. Light Harvesting in Microscale Metal-Organic Frameworks by Energy Migration and Interfacial Electron Transfer Quenching

    SciTech Connect

    Kent, Caleb A.; Liu, Demin; Ma, Liqing; Papanikolas, John M.; Meyer, Thomas J.; Lin, Wenbin

    2011-08-24

    Microscale metal–organic frameworks (MOFs) were synthesized from photoactive Ru(II)-bpy building blocks with strong visible light absorption and long-lived triplet metal-to-ligand charge transfer (³MLCT) excited states. These MOFs underwent efficient luminescence quenching in the presence of either oxidative or reductive quenchers. Up to 98% emission quenching was achieved with either an oxidative quencher (1,4-benzoquinone) or a reductive quencher (N,N,N',N'-tetramethylbenzidine), as a result of rapid energy migration over several hundred nanometers followed by efficient electron transfer quenching at the MOF/solution interface. The photoactive MOFs act as an excellent light-harvesting system by combining intraframework energy migration and interfacial electron transfer quenching.

  20. Effective bridge spectral density for long-range biological energy and charge transfer

    NASA Astrophysics Data System (ADS)

    Kühn, Oliver; Rupasov, Valery; Mukamel, Shaul

    1996-04-01

    The role of medium-induced relaxation of intermediate (bridge) sites in energy and charge transfer processes in molecular aggregates of arbitrary size and geometry is explored by means of Green's function techniques. The coupling of electronic and (solvent and intramolecular) nuclear degrees of freedom is incorporated using the Brownian oscillator model, which allows an exact calculation of the necessary two-point and four-point correlation functions of exciton operators. The signatures of energy transfer and spectral diffusion in time- and frequency-resolved fluorescence spectroscopy are studied. A unified expression for the frequency-dependent transfer rate is derived, which interpolates between the sequential and superexchange limits. Numerical results and a Liouville space pathway analysis for a donor-acceptor system coupled through a single bridge molecule are presented.

  1. Horizontal versus vertical charge and energy transfer in hybrid assemblies of semiconductor nanoparticles

    PubMed Central

    Gotesman, Gilad; Guliamov, Rahamim

    2012-01-01

    Summary We studied the photoluminescence and time-resolved photoluminescence from self-assembled bilayers of donor and acceptor nanoparticles (NPs) adsorbed on a quartz substrate through organic linkers. Charge and energy transfer processes within the assemblies were investigated as a function of the length of the dithiolated linker (DT) between the donors and acceptors. We found an unusual linker-length-dependency in the emission of the donors. This dependency may be explained by charge and energy transfer processes in the vertical direction (from the donors to the acceptors) that depend strongly on charge transfer processes occurring in the horizontal plane (within the monolayer of the acceptor), namely, parallel to the substrate. PMID:23019559

  2. Study of energy transfer between molecules placed in the vicinity of a bimetal composite nanoparticle

    SciTech Connect

    Daneshfar, Nader E-mail: ndaneshfar@razi.ac.ir

    2015-10-15

    In this study, the problem of energy transfer between two molecules near a bimetallic composite nanoparticle is investigated. The influence of the interaction between metal particles on the intermolecular energy is studied, because when two metal nanoparticles are placed close to each other, their plasmons coupling giving rise to new features. On the other hand, we discuss the transfer of resonance energy between donor and acceptor molecules (a single donor and a single acceptor) in the presence of a nanocomposite containing gold and silver nanoparticles based on the Maxwell-Garnett effective medium theory and within the quasistatic limit. We show that the interaction energy strongly depends on the particle size, the filling factor of metal particles, the intermolecular distance (the distance between the donor and acceptor molecules), and the dielectric constant of host matrix.

  3. Collisional vibrational energy transfer of OH (A 2Sigma + , v'=1)

    NASA Astrophysics Data System (ADS)

    Williams, Leah R.; Crosley, David R.

    1996-05-01

    Vibrational energy transfer (VET) and quenching of the v'=1 level of A 2Σ+ OH have been studied using laser-induced fluorescence in a discharge flow cell at room temperature. VET cross sections (Å2) are N2, 30.1±2.8; O2, 2.8±0.3; Ar, 0.56±0.05; H2O, 8.6±0.6. The rotational energy distribution in v'=0 following the VET event was determined for nine colliders. It is nonthermal, generally populating high rotational levels. There are three broad categories of colliders that cause varying degrees of vibrational to rotational energy transfer; H2, D2, and CH4 show the least; N2, CO2, CF4, and N2O more; and O2 and Ar the most, with about one-third of the vibrational energy appearing as OH rotation.

  4. DEPENDENCE OF THE SNS TRANSFER LINES AND ACCUMULATOR RING ON LINAC ENERGY.

    SciTech Connect

    RAPARIA,D.; LEE,Y.Y.; WEI,J.; WENG,W.T.

    2001-06-18

    One of the options considered for the SNS linac, to reduce the cost, was to lower the energy to 840 MeV and leave space in the tunnel for a future upgrade to 1.3 GeV either by adding cryo-modules or increasing the gradient in the SC linac. A linac energy other than 1.0 GeV will have an impact on the transfer line and accumulator ring. The energy impacts the location of the corrector cavity in the HEBT, the injection magnet, beam power, dE/dx, multiple scattering and H stripping, neutron production at the target etc. These issues will be discussed, and changes required in the transfer lines and accumulator ring to accommodate lower energy beam are presented.

  5. Rotational energy transfer in HF(v = 2): Double resonance measurements and fitting law analysis

    SciTech Connect

    Copeland, R.A.; Crim, F.F.

    1983-05-01

    Data from overtone vibration-laser double resonance experiments show extremely rapid rotational relaxation in HF (v = 2) for rotational states up to J = 6 and serve to test energy based fitting laws for rotational energy transfer rate constants. The observed rotational states equilibrate in less than a gas kinetic collision with some individual rates being more than twice the hard sphere collision rate. Energy based fitting laws reproduce the observed evolution of the state populations to within 30% but fail systematically for higher (J = 5 and 6) rotational levels. Fitting laws formulated for collisions between an atom and a molecule are virtually as successful as those for collisions between two molecules. The extracted rate constants show that multiple rotational quantum energy transfer is an important aspect of relaxation dynamics.

  6. Toward understanding as photosynthetic biosignatures: light harvesting and energy transfer calculation

    NASA Astrophysics Data System (ADS)

    Komatsu, Y.; Umemura, M.; Shoji, M.; Shiraishi, K.; Kayanuma, M.; Yabana, K.

    2014-03-01

    Among several proposed biosignatures, red edge is a direct evidence of photosynthetic life if it is detected (Kiang et al 2007). Red edge is a sharp change in reflectance spectra of vegetation in NIR region (about 700-750 nm). The sign of red edge is observed by Earthshine or remote sensing (Wolstencroft & Raven 2002, Woolf et al 2002). But, why around 700-750 nm? The photosynthetic organisms on Earth have evolved to optimize the sunlight condition. However, if we consider about photosynthetic organism on extrasolar planets, they should have developed to utilize the spectra of its principal star. Thus, it is not strange even if it shows different vegetation spectra. In this study, we focused on the light absorption mechanism of photosynthetic organisms on Earth and investigated the fundamental properties of the light harvesting mechanisms, which is the first stage for the light absorption. Light harvesting complexes contain photosynthetic pigments like chlorophylls. Effective light absorption and the energy transfer are accomplished by the electronic excitations of collective photosynthetic pigments. In order to investigate this mechanism, we constructed an energy transfer model by using a dipole-dipole approximation for the interactions between electronic excitations. Transition moments and transition energies of each pigment are calculated at the time-dependent density functional theory (TDDFT) level (Marques & Gross 2004). Quantum dynamics simulation for the excitation energy transfer was calculated by the Liouvelle's equation. We adopted the model to purple bacteria, which has been studied experimentally and known to absorb lower energy. It is meaningful to focus on the mechanism of this bacteria, since in the future mission, M planets will become a important target. We calculated the oscillator strengths in one light harvesting complex and confirmed the validity by comparing to the experimental data. This complex is made of an inner and an outer ring. The

  7. Long-range energy transfer in self-assembled quantum dot-DNA cascades

    NASA Astrophysics Data System (ADS)

    Goodman, Samuel M.; Siu, Albert; Singh, Vivek; Nagpal, Prashant

    2015-11-01

    The size-dependent energy bandgaps of semiconductor nanocrystals or quantum dots (QDs) can be utilized in converting broadband incident radiation efficiently into electric current by cascade energy transfer (ET) between layers of different sized quantum dots, followed by charge dissociation and transport in the bottom layer. Self-assembling such cascade structures with angstrom-scale spatial precision is important for building realistic devices, and DNA-based QD self-assembly can provide an important alternative. Here we show long-range Dexter energy transfer in QD-DNA self-assembled single constructs and ensemble devices. Using photoluminescence, scanning tunneling spectroscopy, current-sensing AFM measurements in single QD-DNA cascade constructs, and temperature-dependent ensemble devices using TiO2 nanotubes, we show that Dexter energy transfer, likely mediated by the exciton-shelves formed in these QD-DNA self-assembled structures, can be used for efficient transport of energy across QD-DNA thin films.The size-dependent energy bandgaps of semiconductor nanocrystals or quantum dots (QDs) can be utilized in converting broadband incident radiation efficiently into electric current by cascade energy transfer (ET) between layers of different sized quantum dots, followed by charge dissociation and transport in the bottom layer. Self-assembling such cascade structures with angstrom-scale spatial precision is important for building realistic devices, and DNA-based QD self-assembly can provide an important alternative. Here we show long-range Dexter energy transfer in QD-DNA self-assembled single constructs and ensemble devices. Using photoluminescence, scanning tunneling spectroscopy, current-sensing AFM measurements in single QD-DNA cascade constructs, and temperature-dependent ensemble devices using TiO2 nanotubes, we show that Dexter energy transfer, likely mediated by the exciton-shelves formed in these QD-DNA self-assembled structures, can be used for efficient

  8. Incorporating the Delphi Technique to investigate renewable energy technology transfer in Saudi Arabia

    NASA Astrophysics Data System (ADS)

    Al-Otaibi, Nasir K.

    Saudi Arabia is a major oil-producing nation facing a rapidly-growing population, high unemployment, climate change, and the depletion of its natural resources, potentially including its oil supply. Technology transfer is regarded as a means to diversify countries' economies beyond their natural resources. This dissertation examined the opportunities and barriers to utilizing technology transfer successfully to build renewable energy resources in Saudi Arabia to diversify the economy beyond oil production. Examples of other developing countries that have successfully used technology transfer to transform their economies are explored, including Japan, Malayasia, and the United Arab Emirates. Brazil is presented as a detailed case study to illustrate its transition to an economy based to a much greater degree than before on renewable energy. Following a pilot study, the Delphi Method was used in this research to gather the opinions of a panel of technology transfer experts consisting of 10 heterogeneous members of different institutions in the Kingdom of Saudi Arabia, including aviation, telecommunication, oil industry, education, health systems, and military and governmental organizations. In three rounds of questioning, the experts identified Education, Dependence on Oil, and Manpower as the 3 most significant factors influencing the potential for success of renewable energy technology transfer for Saudi Arabia. Political factors were also rated toward the "Very Important" end of a Likert scale and were discussed as they impact Education, Oil Dependence, and Manpower. The experts' opinions are presented and interpreted. They form the basis for recommended future research and discussion of how in light of its political system and its dependence on oil, Saudi Arabia can realistically move forward on renewable energy technology transfer and secure its economic future.

  9. Proceedings of the First National Workshop on Energy Efficiency Education Through Technology Transfer.

    ERIC Educational Resources Information Center

    Cohen, Karen C., Ed.

    This publication contains the proceedings from a workshop held in Washington, D.C. in December, 1977. The purpose of the conference was to examine project PROCEED (Program for Continuing Engineering Education) as an innovative approach to technology transfer in energy efficiency education and the potential relationships of the project with the…

  10. Controlling energy transfer in ytterbium complexes: oxygen dependent lanthanide luminescence and singlet oxygen formation.

    PubMed

    Watkis, Andrew; Hueting, Rebekka; Sørensen, Thomas Just; Tropiano, Manuel; Faulkner, Stephen

    2015-11-01

    Pyrene-appended ytterbium complexes have been prepared using Ugi reactions to vary the chromophore-lanthanide separation. Formation of the ytterbium(iii) excited state is sensitised via both the singlet and triplet excited states of the chromophore. Energy transfer from the latter is relatively slow, and gives rise to oxygen-dependent luminescence. PMID:26346499

  11. 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

  12. Luminescence resonance energy transfer from an upconverting nanoparticle to a fluorescent phycobiliprotein

    NASA Astrophysics Data System (ADS)

    Vetrone, Fiorenzo; Naccache, Rafik; Morgan, Christopher G.; Capobianco, John A.

    2010-07-01

    Water dispersible upconverting polyethylenimine (PEI)-capped NaYF4 nanoparticles co-doped with trivalent erbium (Er3+) and ytterbium (Yb3+) were prepared via solvothermal synthesis with an 18 nm average particle diameter. These upconverting nanoparticles can be used to sensitize a light-harvesting phycobiliprotein (R-Phycoerythrin) via luminescence resonance energy transfer (LRET).

  13. Excited-state dynamics in rigid media: evidence for long-range energy transfer.

    PubMed

    Ito, Akitaka; Stewart, David J; Knight, Troy E; Fang, Zhen; Brennaman, M Kyle; Meyer, Thomas J

    2013-03-28

    In semirigid PEG-DMA550 films with the added anthracene derivatives PEG-An and Acr-An, energy transfer quenching of the metal-to-ligand charge transfer excited state Ru(bpy)3(2+)* to give -(3)An occurs by both rapid, static, and slow, diffusional quenching processes. The appearance of -(3)An was verified by transient absorption measurements. The kinetics of the two quenching processes have been analyzed by a Stern-Volmer kinetic analysis. The data for static quenching are consistent with energy transfer quenching with a distance dependence consistent with Dexter (exchange) energy transfer. On the basis of this analysis Bohr radii were found to be 26 and 11 Å for PEG-An and Acr-An, respectively. Evidence for triplet-triplet annihilation between triplet anthracene excited states in the films was obtained from the concentration dependences of excited-state decay. These results provide evidence for long-range energy migration between derivatized anthracenes in rigid, cross-linked PEG-DMA550 films. PMID:23458318

  14. Array-Based Detection of Persistent Organic Pollutants via Cyclodextrin Promoted Energy Transfer

    PubMed Central

    Serio, Nicole; Moyano, Daniel F.; Rotello, Vincent M.; Levine, Mindy

    2015-01-01

    We report herein the selective array-based detection of 30 persistent organic pollutants via cyclodextrin-promoted energy transfer. The use of three fluorophores enabled the development of an array that classified 30 analytes with 100% accuracy and identified unknown analytes with 96% accuracy, as well as identifying 92% of analytes in urine. PMID:26096542

  15. 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

  16. DEVELOPMENT OF A REAL-TIME FLUORESCENCE RESONANCE ENERGY TRANSFER (FRET) PCR TO DETECT ARCOBACTER SPECIES

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A real-time PCR targeting the gyrase A subunit gene outside the quinolone resistance-determining region has been developed to detect Arcobacter species. The species identification was made by probe hybridization and melting curve analysis, using the Fluorescence Resonance Energy Transfer technology...

  17. Parity propensities in rotational energy transfer of OH X 2Pi(i) with helium

    NASA Technical Reports Server (NTRS)

    Wysong, Ingrid J.; Jeffries, Jay B.; Crosley, David R.

    1991-01-01

    Preliminary results of rotational energy transfer in ground state OH in collisions in He are reported. A surprising propensity is found: conservation of total parity is favored in collisions which change in spin-orbit component, the reversible reaction 2Pi3/2 yields 2Pi1/2. This has implications concerning the OH-He potential surface.

  18. DEVELOPMENT OF A REAL-TIME FLUORESCENCE RESONANCE ENERGY TRANSFER PCR TO DETECT ARCOBACTER SPECIES

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A real-time PCR targeting the gyrase A subunit gene outside the quinolone resistance-determining region has been developed to detect Arcobacter species. The species identification was made by probe hybridization and melting curve analysis, using Fluorescence Resonance Energy Transfer technology. D...

  19. Deep-tissue imaging of intramolecular fluorescence resonance energy-transfer parameters.

    PubMed

    Gaind, Vaibhav; Kularatne, Sumith; Low, Philip S; Webb, Kevin J

    2010-05-01

    We demonstrate the in vivo reconstruction of all fluorescence resonance energy transfer (FRET) parameters, including the nanometer donor-acceptor distance, in a mouse. The FRET chemical targets cancer cells, and on internalization, the acceptor is released, in lieu of a targeted anticancer drug in chemotherapy. Our method provides a new vehicle for studying disease by imaging FRET parameters in deep tissue. PMID:20436553

  20. Energy distribution and heat transfer mechanisms in atmospheric pressure non-equilibrium plasmas

    NASA Astrophysics Data System (ADS)

    Nozaki, Tomohiro; Miyazaki, Yu; Unno, Yasuko; Okazaki, Ken

    2001-12-01

    Energy distribution and heat transfer mechanisms in atmospheric pressure non-equilibrium plasmas were investigated extensively through energy balance analysis, emission spectroscopy of the rotational band of CH (A2Δ→X2Π), and gas chromatographic analysis. Two plasma sources were examined: methane-fed dielectric barrier discharge (DBD) and atmospheric pressure glow-discharge (APG). The DBD features filamentary microdischarges accompanied by surface discharge along a dielectric barrier. As a result, 60% of the input power was measured as heat transfer to the dielectric electrode, whereas 20% was to the metallic electrode. Consequently, feed gas average temperature was increased only by 20-40 K. On the other hand, rotational temperature of the corresponding emission region exceeded average gas temperature by 100 K. In APG, heat transfer to electrodes was dominated by formation of negative glow regardless of whether the electrode was covered by a dielectric. However, negative glow tended to be thinner and more intense when it formed on a metallic electrode, leading to slightly higher metallic heating. Rotational temperature in APG was close to average gas temperature since APG does not show radial localization of plasma. Energy efficiency for methane decomposition process to produce ethane, ethylene, and hydrogen was about 1% regardless of the plasma source. Energy distribution and heat transfer mechanisms depend strongly on the plasma spatial structure rather than flow fields or feed gas physical properties.