| 1. |
- Ablikim, M., et al.
(författare)
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Measurements of (XcJ)-> K+K-K+K- decays
- 2006
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Ingår i: Physics Letters B. - : Elsevier BV. - 0370-2693 .- 1873-2445. ; 642:3, s. 197-202
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Tidskriftsartikel (refereegranskat)abstract
- Using 14M psi(2S) events taken with the BESII detector, chi(cJ) -> 2(K+K-) decays are studied. For the four-kaon final state, the branching fractions are B(chi(c0,1,2) ->.2(K+K-)) = (3.48 +/- 0.23 +/- 0.47) x 10(-3), (0.70 +/- 0.13 +/- 0.10) x 10(-3), and (2.17 +/- 0.20 +/- 0.31) x 10(-3). For the phi K+K- final state, the branching fractions, which are measured for the first time, are B(chi(c0,1,2) -> phi K+K-) = (1.03 +/- 0.22 +/- 0.15) x 10(-3), (0.46 +/- 0.16 +/- 0.06) x 10(-3), and (1.67 +/- 0.26 +/- 0.24) x 10(-4). For the phi phi final state, B(chi(c0,2) -> phi phi) = (0.94 +/- 0.21 +/- 0.13) x 10(-3) and (1.70 +/- 0.30 +/- 0.25) x 10(-3).
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| 2. |
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| 3. |
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| 4. |
- Kerzenmacher, T., et al.
(författare)
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Validation of NO2 and NO from the Atmospheric Chemistry Experiment (ACE)
- 2008
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Ingår i: Atmospheric Chemistry and Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 8:19, s. 5801--5841-
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Tidskriftsartikel (refereegranskat)abstract
- Vertical profiles of NO2 and NO have been obtained from solar occultation measurements by the Atmospheric Chemistry Experiment (ACE), using an infrared Fourier Transform Spectrometer (ACE-FTS) and (for NO2) an ultraviolet-visible-near-infrared spectrometer, MAESTRO (Measurement of Aerosol Extinction in the Stratosphere and Troposphere Retrieved by Occultation). In this paper, the quality of the ACE-FTS version 2.2 NO2 and NO and the MAESTRO version 1.2 NO2 data are assessed using other solar occultation measurements (HALOE, SAGE II, SAGE III, POAM III, SCIAMACHY), stellar occultation measurements (GOMOS), limb measurements (MIPAS, OSIRIS), nadir measurements (SCIAMACHY), balloon-borne measurements (SPIRALE, SAOZ) and ground-based measurements (UV-VIS, FTIR). Time differences between the comparison measurements were reduced using either a tight coincidence criterion, or where possible, chemical box models. ACE-FTS NO2 and NO and the MAESTRO NO2 are generally consistent with the correlative data. The ACE-FTS and MAESTRO NO2 volume mixing ratio (VMR) profiles agree with the profiles from other satellite data sets to within about 20% between 25 and 40 km, with the exception of MIPAS ESA (for ACE-FTS) and SAGE II (for ACE-FTS (sunrise) and MAESTRO) and suggest a negative bias between 23 and 40 km of about 10%. MAESTRO reports larger VMR values than the ACE-FTS. In comparisons with HALOE, ACE-FTS NO VMRs typically (on average) agree to ±8% from 22 to 64 km and to +10% from 93 to 105 km, with maxima of 21% and 36%, respectively. Partial column comparisons for NO2 show that there is quite good agreement between the ACE instruments and the FTIRs, with a mean difference of +7.3% for ACE-FTS and +12.8% for MAESTRO.
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| 5. |
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| 6. |
- Chen, X. Y., et al.
(författare)
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Application of weak ferromagnetic BiFeO3 films as the photoelectrode material under visible-light irradiation
- 2007
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Ingår i: Applied Physics Letters. - : American Institute of Physics (AIP). - 0003-6951 .- 1077-3118. ; 91:2, s. 022114-
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Tidskriftsartikel (refereegranskat)abstract
- BiFeO3 films prepared by pulsed laser deposition on Pt/TiO2/SiO2/Si substrates were studied as photoelectrode for water splitting. Under visible-light irradiation, the photocurrent intensity of the polycrystalline BiFeO3 film was found to double that of the amorphous one in a three-electrode cell. The incident photon to current conversion efficiency for the polycrystalline BiFeO3 electrode was approximately 16% at 350 nm and 7% at 530 nm at 1.5 V (versus saturated calomel electrode). The ferromagnetism of the amorphous BiFeO3 film was an order of magnitude weaker than that of the polycrystalline one, supporting the "size effect" explanation for magnetic origin. (C) 2007 American Institute of Physics.
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| 7. |
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| 8. |
- Corma, Averlino, et al.
(författare)
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Synthesis and structure of polymorph B of zeolite Beta
- 2008
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Ingår i: Chemistry of Materials. - : American Chemical Society (ACS). - 0897-4756 .- 1520-5002. ; 20:9, s. 3218-3223
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Tidskriftsartikel (refereegranskat)abstract
- It was found that either polymorph B or polymorph C of zeolite beta can be obtained from the same structure directing agent: 4,4-dimethyl-4-azonia-tricyclo[5.2.2.02,6]undec-8-ene hydroxide. The synthesis occurs through a consecutive process where polymorph B is first formed and then transformed into polymorph C. It is possible to produce a zeolite highly enriched in polymorph B, provided that the transformation of this phase into polymorph C is slowed down up to the point where polymorph C is only detected at trace levels. The structure of polymorph B was determined for the first time by electron crystallography with SAED and HRTEM from areas of unfaulted polymorph B crystals.
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| 9. |
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| 10. |
- Evans, J D, et al.
(författare)
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Immune pathways and defence mechanisms in honey bees Apis mellifera.
- 2006
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Ingår i: Insect Mol Biol. - 0962-1075. ; 15:5, s. 645-56
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Tidskriftsartikel (refereegranskat)abstract
- Social insects are able to mount both group-level and individual defences against pathogens. Here we focus on individual defences, by presenting a genome-wide analysis of immunity in a social insect, the honey bee Apis mellifera. We present honey bee models for each of four signalling pathways associated with immunity, identifying plausible orthologues for nearly all predicted pathway members. When compared to the sequenced Drosophila and Anopheles genomes, honey bees possess roughly one-third as many genes in 17 gene families implicated in insect immunity. We suggest that an implied reduction in immune flexibility in bees reflects either the strength of social barriers to disease, or a tendency for bees to be attacked by a limited set of highly coevolved pathogens.
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| 11. |
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| 12. |
- Hicks, E.M., et al.
(författare)
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Controlling plasmon line shapes through diffractive coupling in linear arrays of cylindrical nanoparticles fabricated by electron beam lithography
- 2005
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Ingår i: Nano Letters. - : American Chemical Society (ACS). - 1530-6992 .- 1530-6984. ; 5:6, s. 1065-1070
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Tidskriftsartikel (refereegranskat)abstract
- The effect of diffractive coupling on the collective plasmon line shape of linear arrays of Ag nanoparticles fabricated by electron beam lithography has been investigated using Rayleigh scattering spectroscopy. The array spectra exhibit an intricate multi-peak structure, including a narrow mode that gains strength for interparticle distances that are close to the single particle resonance wavelength. A version of the discrete dipole approximation method provides an excellent qualitative description of the observed behavior.
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| 13. |
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| 14. |
- Li, Z. -L, et al.
(författare)
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Effects of electrode distances on geometric structure and electronic transport properties of molecular 4,4'-bipyridine junction
- 2006
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Ingår i: Journal of Physics: Conference Series. - : IOP Publishing. - 1742-6588 .- 1742-6596. ; 29:1, s. 110-114
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Tidskriftsartikel (refereegranskat)abstract
- Influences of electrode distances on geometric structure of molecule and on electronic transport properties of molecular junctions have been investigated by means of a generalized quantum chemical approach based on the elastic scattering Green's function method. Numerical results show that, for organic molecule 4,4'-bipyridine, the geometric structure of the molecule especially the dihedral angle between the two pyridine rings is sensitive to the distances between the two electrodes. The currents of the molecular junction are taken nonlinearly increase with the increase of the bias. Shortening the distance of the metallic electrodes will result in stronger coupling and larger conductance.
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| 15. |
- Li, Z. L., et al.
(författare)
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Electronic transport properties of molecular bipyridine junctions : Effects of isomer and contact structures
- 2006
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Ingår i: Physical Review B. Condensed Matter and Materials Physics. - 1098-0121 .- 1550-235X. ; 73:7
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Tidskriftsartikel (refereegranskat)abstract
- The effects of contact structures and isomers on the current-voltage characteristics of molecular bipyridine junctions have been investigated by means of a generalized quantum chemical approach based on the elastic scattering Green's function method. For the four isomers 4,4'-bipyridine, 2,2'-bipyridine, 2,4'-bipyridine, and 2,6'-bipyridine under investigation, the 2,4'- bipyridine junction is found to be the poorest conductor owing to its nonsymmetrical arrangement. Numerical simulations of the 4,4'-bipyridine junction show that the contact structures between molecule and metallic electrodes have a noticeable effect on the electron transport characteristics of molecular junctions. The shortening of the distance between two metallic electrodes results in a stronger coupling and lower potential barrier between them, leading to larger conductance. The external electric fields cause the charge redistribution within molecule and lead to the presence of resistivity dipoles at the molecule-metal interface, and the bias voltages are mainly dropped there. The nonlinear charge transport effect on the current and conductance of 4,4'-bipyridine molecular junctions at the lower-bias region is presented. The experimental measurement has been reproduced by the theoretical calculations for a well-defined structure.
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| 16. |
- Ma, Y., et al.
(författare)
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Theoretical studies on electronic transport properties of six-membered heterocyclic molecules
- 2006
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Ingår i: Wuli xuebao. - : Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences. - 1000-3290. ; 55:4, s. 1974-1978
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Tidskriftsartikel (refereegranskat)abstract
- By applying the elastic scattering Green's function theory in combination with the hybrid density function theory, the electronic transport properties of molecular junctions constructed by the six-membered heterocyclic molecules, pyridazine-2, 5-dithiol, pyrazine-2, 5-dithiol, and pyrimidine-2, 5-dithiol, have been studied. For the heterocyclic molecule pyridine, the influence of the terminal atoms on the current-voltage characteristics has also been obtained. We have accurately determined the coupling constant between the molecule and electrodes by using the frontier molecular orbital theory and the perturbation method. The numerical results show that pyridazine-2,5-dithiol has higher current and conductance, while the conductance of pyrimidine-2, 5-dithiol is very small when the bias voltage is lower than 4V. The conductivity of the molecule pyridine with selenium atom as the terminal atom is higher than that with oxygen atom or sulfur atom.
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| 17. |
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| 18. |
- Oleynikov, Peter, et al.
(författare)
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Structure of the pseudodecagonal Al–Co–Ni approximant PD4
- 2006
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Ingår i: Philosophical Magazine. - : Taylor and Francis. - 1478-6435 .- 1478-6443. ; 86:3-5, s. 457-462
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Tidskriftsartikel (refereegranskat)abstract
- A model for the pseudodecagonal approximant PD4 in the Al–Co–Ni system was deduced from single crystal X-ray diffraction data. The space group is Bbmm with a ?=?101.3, b ?=?32.1 and c ?=?4.1?Å. Atomic positions of 133 unique atoms in the unit cell with a reasonable geometry were found by direct methods and the difference Fourier syntheses. The obtained structure model is in good agreement with high-resolution electron microscopy images of PD4. Diffuse scattering observed along the a * direction in the hkl layers with l ?=?1/2, 3/2 etc. indicates a superstructure with a doubling of the periodicity along the c -axis and a lamellar disorder along the a -axis. If this diffuse scattering is taken into account, c ?=?8.2?Å.
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| 19. |
- Peng, Ru, 1960-, et al.
(författare)
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Determination of Grain-Orientation-Dependent Stress in Coatings
- 2005
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Ingår i: Diffusion and defect data, solid state data. Part A, Defect and diffusion forum. - 1012-0386 .- 1662-9507. ; 105, s. 107-112
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Tidskriftsartikel (refereegranskat)abstract
- Quantitative interpretations of the so-called non-linear lattice strain distributions observed in coatings and thin films are important not only for determining the macro- and micro-stress fields, but also for inferring the active mechanisms of grain interactions during various deposition processes. In this paper, we present a method, which determines simultaneously both the macro- and micro-stress fields in the coatings and thin films. This method is extended from the previous stress-orientation distribution function (SODF) analysis method, which has already been used for residual stress analysis in bulk materials subjected to rolling and fatigue deformation. The validity of analysis method is demonstrated through measurements of lattice strains by high-energy x-ray and analysis of grain-orientation-dependent stresses in a CrN coating
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| 20. |
- Reetz, Manfred T., et al.
(författare)
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Directed Evolution of an Enantioselective Epoxide Hydrolase : Uncovering the Source of Enantioselectivity at Each Evolutionary Stage
- 2009
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Ingår i: Journal of the American Chemical Society. - : ACS. - 0002-7863 .- 1520-5126. ; 131:21, s. 7334-7343
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Forskningsöversikt (refereegranskat)abstract
- Directed evolution of enzymes as enantioselective catalysts in organic chemistry is an alternative to traditional asymmetric catalysis using chiral transition-metal complexes or organocatalysts, the different approaches often being complementary. Moreover, directed evolution studies allow us to learn more about how enzymes perform mechanistically. The present study concerns a previously evolved highly enantioselective mutant of the epoxide hydrolase from Aspergillus niger in the hydrolytic kinetic resolution of racemic glycidyl phenyl ether. Kinetic data, molecular dynamics calculations, molecular modeling, inhibition experiments, and X-ray structural work for the wild-type (WT) enzyme and the best mutant reveal the basis of the large increase in enantioselectivity (E = 4.6 versus E = 115). The overall structures of the WT and the mutant are essentially identical, but dramatic differences are observed in the active site as revealed by the X-ray structures. All of the experimental and computational results support a model in which productive positioning of the preferred (S)-glycidyl phenyl ether, but not the (R)-enantiomer, forms the basis of enhanced enantioselectivity. Predictions regarding substrate scope and enantioselectivity of the best mutant are shown to be possible.
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| 21. |
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| 23. |
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| 24. |
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| 25. |
- Zou, C.-D., et al.
(författare)
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Melting temperature depression of Sn-0.4Co-0.7Cu lead-free solder nanoparticles
- 2009
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Ingår i: Soldering and Surface Mount Technology. - : Emerald. - 1758-6836 .- 0954-0911. ; 21:2, s. 9-13
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Tidskriftsartikel (refereegranskat)abstract
- Purpose - The purpose of this paper is to study the melting temperature of the nanoparticles of the new developed Sn-0.4Co-0.7Cu (wt%) lead-free solder alloy.Design/methodology/approach - Nanoparticles of Sn-0.4Co-0.7Cu lead-free solder alloy were prepared by the self-developed consumable-electrode direct current arc technique, where ultrasonic vibration was applied during the manufacturing of the particles. X-ray diffraction and field emission scanning electron microscope were employed to analyze the crystal structure and morphology of the nanopartiles, respectively. Differential scanning calorimetry was used to investigate the melting temperature of both the bulk alloy and as-prepared nanoparticles.Findings - The melting temperature of the nanoparticles was approximately 5 degrees C lower compared to that of the bulk alloy.Originality/value - As a novel developed lead-free solder alloy, the Sn-0.4Co0.7Cu (wt%) alloy provides a cost advantage compared to the extensively used Sn-Ag-Cu system. Some limitations still exist, however, mainly due to its relatively higher melting temperature compared to that of eutectic Sn-37Pb solder. In view of this situation, the attempt to lower its melting temperature has recently attracted more attention based on the knowledge that the melting temperature for pure metals is reduced when the particle size is decreased down to a few tens of nanometers.
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