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961.
B. M. Forster J. M. Bailey G. A. Beer J. L. Beveridge J. H. Brewer W. N. Hardy T. M. Huber K. R. Kendall A. R. Kunselman J. A. Macdonald G. M. Marshall G. R. Mason A. Olin M. Senba J. B. Warren 《Hyperfine Interactions》1991,65(1-4):1007-1013
Muonic hydrogen isotopes (μ− p, μ− d, and μ−t) are simple quantum mechanical systems ideally suited for studies of numerous fundamental phenomena in electroweak and strong
interactions as well as in applied areas such as muon chemistry or muon catalyzed fusion.
Emission of muonic hydrogen isotopes into vacuum helps to overcome the limitations which are normally imposed on conventional
investigations with gaseous and liquid targets. A proof of principle experiment for this new technique was performed at TRIUMF
last year. Negative muons with 30 MeV/c momentum were stopped in a thin film of solid hydrogen and produced very low energy μ−d in vacuum. The distribution center of the normal velocity components of emitted μ−d atoms was measured to be ∼1 cm/μs. The yield of μ−d in vacuum is an increasing function of H2 film thickness δ up to a value of δ≥1 mm. 相似文献
962.
R. Kadono R. F. Kiefl J. H. Brewer G. M. Luke T. Pfiz T. M. Riseman B. J. Sternlieb 《Hyperfine Interactions》1991,64(1-4):635-640
The diffusion rate of muonium in the III–V compound semiconductor GaAs has been determined from measurements of muon spinT
1 relaxation induced by motion in the presence of nuclear hyperfine interactions. It is shown for the first time in a semiconductor
that (a) there is a crossover of the transport mechanism at about 90 K from stochastic to zero-phonon hopping, as evidenced
by a steep rise in the hop rate at lower temperatures, and that (b) the muonium diffuses at the hop rate of 1010 s−1 (corresponding diffusion constantD≈10−6 cm2s−1) at lower temperatures as well as at room temperature. 相似文献
963.
Hyperfine Interactions - Sm2(Co1?x Fe x )17 alloys form the basis of a new class of permanent magnets. We have investigated these materials with57Fe Mössbauer spectroscopy. Alloys... 相似文献
964.
New ferroelectric side-chain liquid-crystalline polymers, a copolymer and a homopolymer, with siloxane backbone and a triaromatic mesogen as the side group have been synthesized. The materials exhibit a chiral smectic C phase over a large temperature range extending to room temperature. They possess high values of spontaneous polarization: 105 nC cm-2 for the homopolymer and 180 nC cm-2 for the copolymer. The electro-optic switching time in the chiral smectic C phase is extremely fast (150 μs). In the smectic A phase, an electroclinic effect with switching times less than 100 μs and with field induced tilt angles of 18° is observed. 相似文献
965.
Mary F. Wheeler J. R. Whiteman 《Numerical Methods for Partial Differential Equations》1994,10(3):271-294
Superconvergent error estimates in l2(H1) and l∞(H1) norms are derived for recovered gradients of finite difference in time/piecewise linear Galerkin approximations in space for linear and quasinonlinear parabolic problems in two space dimensions. The analysis extends previous results for elliptic problems to the parabolic context, and covers problems in regions with nonsmooth boundaries under certain assumptions on the regularity of the solutions. © 1994 John Wiley & Sons, Inc. 相似文献
966.
Lu KangAlison R. Keimowitz Michaeleen R. MunrowStewart E. Novick 《Journal of Molecular Spectroscopy》2002,213(2):122-129
The rotational spectra of the argon acetone weakly bound complex was studied by pulsed jet Fabry-Perot Fourier transform microwave spectroscopy. Over 500 transitions of the complex were measured between 5.5 and 26 GHz from J=2-1 to J=12-11. The two methyl groups undergo hindered internal rotation resulting in four or five internal rotation states. The microwave transitions are within these states, resulting in a splitting of each rotational transition into four and sometimes five distinct transitions. The three-fold barrier to internal rotation is determined to be 260 cm−1, 2% less than the 266 cm−1 barrier in acetone itself. The structure of the complex has the argon atom above the heavy atom plane of the acetone, 3.52 Å from the CO bond and approximately in the Cs plane, which is perpendicular to the CCC plane of acetone. 相似文献
967.
R. Klein R. Grieser L. Hoog G. Huber I. Klaft P. Merz T. Kühl S. Schröder M. Grieser D. Habs W. Petrich D. Schwalm 《Zeitschrift für Physik A Hadrons and Nuclei》1992,342(4):455-461
We have performed for the first time precision spectroscopy on a coasting fast7Li+ ion beam in a storage ring. The ion beam moving with 6.4% speed of light was first electron cooled and then merged with two counterpropagating laser beams acting on two different hyperfine transitions sharing a common upper level (λ-system). One laser was frequency locked to thea 3 127J2 hfs frequency component established as a secondary frequency standard at 514 nm. The second laser was tuned over theλ-resonance, which was recorded relative to127J2 hfs components. This experiment is sensitive to the time dilation in fast moving frames and will lead to new limits for the verification of special relatively. The present status of the experiment and perspectives in accuracy are discussed. 相似文献
968.
Optical methods are described for determining the parameters of semiconducting quantum dots synthesized in a glassy borosilicate
matrix. The limitations of these methods and the magnitudes of their errors are analyzed. The parameters of CdSxSe1−x
nanocrystals in the commercial glasses KS-10, OS-12, Corning 2–61, and other experimental samples are determined.
Fiz. Tverd. Tela (St. Petersburg) 39, 1865–1870 (October 1997) 相似文献
969.
P. R. Hageman J. te Nijenhuis M. J. Anders L. J. Giling 《Journal of Crystal Growth》1997,170(1-4):270-275
Doping studies of the incorporation behaviour of three different dopants (Zn, In and Si) versus the misorientation of the (100) surface during MOVPE growth of GaAs have been carried out with diethylzinc, trimethylindium and disilane as precursors. The incorporation of the dopants has been studied as function of the input mole fraction dopant, growth temperature, degree and direction of misorientation. In order to explain the results we discuss the BCF theory and the nature of the steps as function of above mentioned parameters. It appears that the BCF theory alone cannot explain the results, a counteracting mechanism has been introduced based on preferential arsenic desorption from the step edges. 相似文献
970.