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841.
A novel circular Haar wavelet (CHW), which is obtained by a radially distributed polarization state, is proposed. Optical wavelet transforms using the proposed CHW are implemented by computer simulations. The proposed CHW is shown to have remarkable features: (1) it is useful for detecting outlines of input images; (2) one polarization component is available for extracting an edge feature along a required direction; and (3) unlike the previously proposed CHW (Z. He and S. Sato: Opt. Lett. 19 (1994) 686), this one can be applied to a multi-resolution edge extraction (Y. Sheng, D. Roberge and H. H. Szu: Opt. Eng. 31 (1992) 1840). 相似文献
842.
Stretched silver island multilayers have been investigated for patterned optical polarizers for the wavelength of 800 nm. Submicrometer-thick optical polarizing films are fabricated by stretching periodic multilayers consisting of silver island layers and Pyrex layers at the temperature of 660°C. As the optical anisotropy of the optical polarizing film is lost by heating at a temperature higher than the stretching temperature, the fine non-polarizing areas can be deliberately and easily formed on the optical polarizing film by laser irradiation with high power density. We have successfully formed various non-polarizing areas on the optical polarizing film with a 1 W-class carbon dioxide laser. The demonstrated fabricating techniques of deliberately patterned optical polarizing films should be useful for novel optical computing and sensing devices. 相似文献
843.
A. Schenck N.K. Sato G. Solt D. Andreica F.N. Gygax M. Pinkpank A. Amato 《The European Physical Journal B - Condensed Matter and Complex Systems》2000,13(2):245-256
We report on transverse field (TF) Muon Spin Rotation (μSR) measurements on a single crystal of the hexagonal heavy fermion
superconductor UNi2Al3 between 5 K and 300 K. From the measured muon Knight shift (KS) in the easy (
a
,
b
)-plane and along the c-axis we extracted the local magnetic susceptibility tensor [0pt] , which arises from the nearest U-neighbors. By comparison with the bulk susceptibility [0pt] it is found that [0pt] and [0pt] agree well above 150 K but deviate considerably in the basal plane below 150 K, due to the disturbance introduced by the
. We succeed in reproducing both [0pt] and [0pt] on the basis of a crystalline electric field (CEF)-approach assuming U to be in the tetravalent state. The disturbance introduced by the affects the CEF-Hamiltonian in an expected manner, suggesting strongly that a CEF-picture implying a rather local 5
f-electron wave function is indeed valid. Reanalyzing older data on UPd2Al3 we arrive at the same conclusion. A necessary condition for extracting the local susceptibility was the knowledge of the
-site, this information was derived from the analysis of the TF-relaxation rates. At low temperatures we found about 30% of
the implanted at the d-site and none at this site above 200 K. The majority fraction was found to be in a tunneling state over six m (or k)-sites around the b-site. No long range diffusion was seen up to room temperature.
Received 20 April 1999 相似文献
844.
The effects of the direction of transition dipole moment on polarization-dependent phase-conjugate (PC) reflectivity by degenerate four-wave mixing in a saturable-dye-doped film are theoretically investigated. On the basis of a four-energy-level model for the saturable dyes, the pump-intensity dependence of the PC reflectivity is calculated for the two cases of a probe wave being polarized either parallel or perpendicular to pump waves, when the transition dipole moment associated with excited-state absorption tilts from that associated with ground-state one. For the parallel polarization, in the case of two transition dipole moments having different directions, a dip appears in the PC reflectivity curve near a resonant frequency on account of the characteristics of nonlinear absorption, whereas it disappears when the frequency of light is off resonance due to the influence of nonlinear refractive index. 相似文献
845.
P. Vonlanthen J.L. Gavilano B. Ambrosini H.R. Ott Y. Aoki H. Sugawara H. Sato 《The European Physical Journal B - Condensed Matter and Complex Systems》1999,9(1):15-20
We report the results of 69Ga- and 71Ga-NMR measurements on NdGa2 at temperatures between 0.1 and and in applied magnetic fields between zero and 74 kOe. NdGa2 orders antiferromagnetically below and undergoes several metamagnetic transitions in external magnetic fields. In zero applied magnetic field and below the temperature dependence of the spin-lattice relaxation rate T1
-1
(
T
) shows a large linear-in-T term, about two orders of magnitude higher than for the reference compound LaGa2. This strong enhancement confirms the presence of low-energy excitations in the antiferromagnetic phase of NdGa2 as was previously indicated by specific heat data. Above , T1
-1
(
T
) is dominated by an exponential term, which we associate with excitations between the lowest energy levels of the f-electron system. The separation of these energy levels is determined by exchange, crystal-field and Zeeman interactions.
Received 3 September 1998 and Received in final form 3 November 1998 相似文献
846.
A. Tanaka H. Sasaki K. Takahashi W. Gondo S. Suzuki S. Sato 《Journal of Physics and Chemistry of Solids》1999,60(12):719-1999
An angle-resolved photoemission study for Ag nanofilm grown on pseudomorphic metastable-fcc-phase Fe(1 0 0) has been done in order to investigate in detail the quantized electronic structures. From the low-energy electron-diffraction and angle-resolved photoemission spectra, it is found that the present Ag nanofilms were grown in the direction of [1 1 1] on pseudomorphic fcc Fe(1 0 0) substrates. The angle-resolved photoemission spectra of Ag nanofilms grown on pseudomorphic fcc Fe(1 0 0) exhibit the features derived from Shockley-type surface state and additional fine-structures derived from the quantized state of Ag sp valence electron. The experimental nanofilm-thickness dependence of binding energies of these quantized states is compared with the theoretical calculation based on the phase accumulation model, taking into account the phase shifts of electron reflection at both interfaces of the Ag nanofilm. From these results, we discuss the quantized electronic structure in Ag nanofilm grown on pseudomorphic fcc Fe(1 0 0). 相似文献
847.
T. Shimada K. Hiruma M. Shirai M. Yazawa K. Haraguchi T. Sato M. Matsui T. Katsuyama 《Superlattices and Microstructures》1998,24(6):453-458
The self-organized, position-controlled and parallel growth of GaAs and InAs nanowhiskers is successfully demonstrated by using a metal–organic chemical vapour deposition method. The growth takes place preferentially along the 111 As direction with the aid of the catalytic effect of Au nanodroplets, and not along 111 Ga or In directions. The diameter and length of the whisker can be controlled artificially down to 10 nm and to over 1 μm, respectively. Doping and composition control of p- or n-type such as GaAs–InAs heterostructure formation are possible along the length direction of the whisker by changing the source gases. In order to control the growth position of the whisker, positioning of a Au nanodroplet is essential and realized by a lithographic method. By choosing the [111]B direction to the substrate surface and normal to the patterned side edges, and by positioning the Au nanodroplet on the side wall, the positioned planar nanowhisker growth and bridging are successfully demonstrated. The growth mechanism of the nanowhiskers is revealed by the scanning and transmission electron microscope observations. Nanometer-size Au-alloy droplets play an important role in the growth of the whiskers. The whisker growth process is governed by the vapor–liquid–solid growth mechanism. 相似文献
848.
Hole transporting polymers were prepared by condensation polymerization of triphenylamine and N,N,N',N'‐tetraphenylbenzidine (TPD) having alkyl group with aldehydes in the presence of p‐toluenesulfonic acid. The obtained polymers had molecular weight higher than 10,000 and good film formation ability. It was found that the aromatic amine monomers were connected with aldehyde monomer at the p‐position of the phenyl group. TPD‐aldehyde polymers had almost the same UV absorption and redox potentials as those of TPD monomer indicating that the electronic structure of amine unit did not change by the polymerization. The hole transporting mobility was in the range of 10−3‐10−6cm2/Vs. The electroluminescent device consisting of ITO/TPD polymer/Alq/Mg‐Ag had a maximum luminance of 9000 cd/m2. 相似文献
849.
Makiko Seno Tomoya Fukui Tomohiro Hirano Tsuneyuki Sato 《Journal of polymer science. Part A, Polymer chemistry》2000,38(23):4264-4271
Polymerization of N‐(2‐phenylethoxycarbonyl)methacrylamide (PECMA) with dimethyl 2,2′‐azobisisobutyrate (MAIB) was investigated in tetrahydrofuran (THF) kinetically and by means of electron spin resonance (ESR). The overall activation energy of the polymerization was calculated to be 58 kJ/mol. The initial polymerization rate (Rp) is expressed by Rp = k[MAIB]0.3[PECMA]2.3 at 60 °C. Such unusual kinetics may be ascribable to primary radical termination and to acceleration of propagation due to monomer association. Propagating poly(PECMA) radical was observed as a 13‐line spectrum by ESR under practical polymerization conditions. ESR‐determined rate constants of propagation (kp, 4.7–10.5 L/mol s) and termination (kt, 4.6 × 104 L/ml s) at 60 °C are much lower than those of methacrylamide and methacrylate esters. The Arrhenius plots of kp and kt gave activation energies of propagation (24 kJ/mol) and termination (25 kJ/mol). The copolymerizations of PECMA with styrene (St) and acrylonitrile were examined at 60 °C in THF. Copolymerization parameters obtained for the PECMA (M1) − St(M2) system are as follows: r1 = 0.58, r2 = 0.60, Q1 = 0.73, and e1 = +0.22. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 4264–4271, 2000 相似文献
850.
p-(1-Methylcyclohexyloxy)styrene (PC6ST) was synthesized by acid catalyzed addition reaction of p-bromophenol with 1-methylcyclohexene, followed by Grignard coupling with vinyl bromide catalyzed by NiCl2(dppp). Radical polymerization of PC6ST in the presence or absence of TEMPO afforded poly(PC6ST) with narrow molecular weight distribution without the elimination of the protective group. The obtained poly(PC6ST) showed a higher deprotection ability in response to external stimulation such as an acid compared with poly(p-tert-butoxystyrene). 相似文献