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A photoinduced scattering effect in LiNbO3:Fe crystals was investigated in detail. The scattering depends substantially on illumination geometry, light beam profile, doping degree, and appears under coherent illumination only. It was shown that besides the photoinduced scattering a bleaching effect is possible. It consists in the fact that after the stage of low-scale inhomogeneity formation there occurs their effective erasure. The conditions were found out under which the bleaching effect can be observed.  相似文献   
13.
We present a general theory of adiabatic rapid passage (ARP) with intense, linearly chirped laser pulses. For pulses with a Gaussian profile and a fixed bandwidth, we derive a rigorous formula for the maximum temporal chirp rate that can be sustained by the pulse. A modified Landau-Zener formula displays clearly the relationships among the pulse parameters. This formula is used to derive the optimal conditions for efficient, robust population transfer. As illustrations of the theory, we present results for two- and four-level systems, and selective vibronic excitation in the I2 molecule. We demonstrate that population transfer with chirped pulses is more robust and more selective than population transfer with transform-limited pulses. Received 6 September 2000 and Received in final form 25 September 2000  相似文献   
14.
Low-frequency Raman spectra of a LiTaO3 ferroelectric crystal are studied in the temperature range 300–1273 K. The central peak associated with the relaxation susceptibility of the crystal lattice is recorded throughout the temperature range covered, including the temperatures both substantially lower and considerably higher than the Curie point (T c = 900 K). The critical slowing down of the relaxation response time predicted by the Ginzburg-Landau-Devonshire theory is observed in the temperature range from 0.9T c to 1.1T c . In contrast to the critical slowing down, the width of the central peak γR increases below 0.9T c and decreases above 1.1T c with increasing temperature.  相似文献   
15.
This is a continuation of our earlier investigation (Gurtuet al 1974Phys. Lett. 50 B 391) on multiparticle production in proton-nucleus collisions based on an exposure of emulsion stack to 200 GeV/c beam at the NAL. It is found that the ratioR em = 〈n s〉/〈n ch〉, where 〈n ch〉 is the charged particle multiplicity in pp-collisions, increases slowly from about 1 at 10 GeV/c to 1·6 at 68 GeV/c and attains a constant value of 1·71 ± 0·04 in the region 200 to 8000 GeV/c. Furthermore,R em = 1·71 implies an effectiveA-dependence ofR A =A 0.18,i.e., a very weak dependence. Predictions ofR em on various models are discussed and compared with the emulsion data. Data seem to favour models of hadron-nucleon collisions in which production of particles takes place through adouble step mechanism,e.g., diffractive excitation, hydrodynamical and energy flux cascade as opposed to models which envisage instantaneous production.  相似文献   
16.
Analytical and Bioanalytical Chemistry - Determination of the purity of a substance traceable to the International System of Units (SI) is important for the production of reference materials...  相似文献   
17.
The eigen frequencies of radial pulsations of neutron stars are calculated in a strong magnetic field. At low densities we use the magnetic BPS equation of state (EOS) similar to that obtained by Lai and Shapiro while at high densities the EOS obtained from the relativistic nuclear mean field theory is taken and extended to include strong magnetic field. It is found that magnetized neutron stars support higher maximum mass whereas the effect of magnetic field on radial stability for observed neutron star masses is minimal.  相似文献   
18.
For dipalmitoylphosphatidylcholine (DPPC) lipid/water bilayers, a detailed temperature dependence of the Raman scattering spectra at the spectral range of the CH 2-stretching modes was investigated. Below 150 K the ratio of intensities of the 2880 cm (-1) antisymmetric vibration line and the 2850 cm (-1) symmetric one was found to be nearly temperature-independent. Between 150 and 230 K it decreases slightly as temperature increases; and above 230 K it decreases remarkably. This decrease is accompanied with broadening of the antisymmetric line, from 4.2 cm (-1) at 100 K to 5.7 cm (-1) at 296 K. According to literature, the decrease of the antisymmetric line may be interpreted in two ways: (i) the appearance of a static conformational disorder (or of a disorder fluctuating at the time scale larger than picoseconds) and (ii) relaxation at the ps time scale, which is induced by coupling with temperature-activated librational-torsional motion of the lipid chain. Both these interpretations imply that obtained data evidence the appearance of molecular flexibility of lipids around approximately 200 K. The observed effect is to be compared with low-temperature dynamical transition found in disordered media with neutron scattering, Mossbauer absorption, molecular dynamics simulations and other techniques. This transition implies that with temperature increase harmonic atomic motions are transformed to large-amplitude anharmonic (or stochastic) ones. The characteristic times of these motions lay at the ps time scale. The closeness of the temperature of the transition and of the time scale of motions with those found in this work by Raman scattering for lipid bilayers supports the dynamic nature of the 2880 cm (-1) antisymmetric vibration line decrease (i.e., that it is induced by coupling with libration-torsion). To prove that the observed onset of flexibility is a property of a disordered state, Langmuir-Blodgett films of behenic acid were studied. These films contain, like lipids, long CH 2-tails, but, in opposite to bilayers, they have a well-ordered crystalline-like structure. The relative intensity of the antisymmetric/symmetric CH 2-stretching lines was found in these films to be temperature-independent in the whole temperature range studied, between 60 and 296 K.  相似文献   
19.
Compound [Co(NioxH)2(PPh 3)2]F is synthesized in the CoF2 · 4H2O-NioxH2-PPh 3 system (where NioxH is the 1,2-cyclohexanedione dioxime monoanion and PPh 3 is triphenylphosphine), and its structure is determined by X-ray diffraction. It is shown that the cobalt atom has the octahedral environment. Two nioxime residues that are related by the center of symmetry lie in the equatorial plane and are linked by the O-H?O hydrogen bond. The 1,6-positions of the octahedron are occupied by the phosphorus atoms of the triphenylphosphine ligands. The formation of the crystal structure of this compound is discussed.  相似文献   
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