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91.
In this work we present a detailed structural of a series of B-doped hydrogenated microcrystalline silicon (μc-Si:H) films deposited by plasma-enhanced chemical vapor deposition (PECVD) and B-doped polycrystalline silicon (poly-Si) films produced by step-by-step laser crystallization process from amorphous silicon. The influence of doping on the structural properties and structural changes during the sequential crystallization processes were monitored by Raman spectroscopy. Unlike μc-Si:H films, that consist of a two-phase mixture of amorphous and ordered Si, partially crystallized sample shows a stratified structure with polycrystalline silicon layer at the top of an amorphous layer. With increasing doping concentration the LO-TO phonon line in poly-Si shift to smaller wave numbers and broadens asymmetrically. The results are discussed in terms of resonant interaction between optical phonons and direct intraband transitions known as a Fano resonance. In μc-Si:H films, on the other hand, the Fano effect is not observed. The increase of doping in μc-Si:H films suppressed the crystalline volume fraction, which leads to an amorphization in the film structure. The structural variation in both μc-Si:H and poly-Si films leads to a change in hydrogen bonding configuration. 相似文献
92.
Yahya Baykal 《Optics Communications》2007,269(1):30-38
The receiver intensity profile of an off-axis-Gaussian beam travelling in random medium is formulated. By examining the related exponential terms of this intensity expression, the rules governing the receiver plane displacements are deduced. Off-axis-Gaussian beam is characterized by introducing into a Gaussian beam, complex displacement parameters that exhibit transverse source coordinate dependent attenuation and phase shifts. Our results are applied to turbulent horizontal links. Intensity plots describing the dependence on the source and propagation parameters both on the source and the receiver planes are provided. Even though the normalized intensities of the off-axis-Gaussian beam having the same source sizes but differing displacements in x- and y-directions may look the same on the source plane, they will differentiate after propagation. The views from the progress of an off-axis-Gaussian beam along the turbulent link length show that a source displaced beam will act according to rules set by related exponential terms. An asymmetrical (ellipsoidal) off-axis-Gaussian beam will initially be converted into symmetric (circular) shape at the intermediate link lengths, then it will start to expand in the other direction, thus reverting to an ellipsoid shape whose major axis is now along the transverse coordinate opposite to that of the source plane. 相似文献
93.
94.
Tin dioxide (SnO2) nanoparticles having 3 nm size were synthesized by irradiating pure tin metal using high power Nd:YAG laser in deionized water. Formation of nano-SnO2 crystallites was confirmed by X-ray diffraction (XRD) and AFM study. UV-vis absorption spectral studies showed a peak at 240 nm. FTIR spectrum showed a band in the range of 400-700 cm−1 which was assigned to Sn-O antisymmetric vibrations. Photoluminescence spectrum of synthesized SnO2 nanoparticles showed peak corresponding to 3.175, 2.901 and 2.613 eV respectively. 相似文献
95.
96.
Y Nakai A el-Said Aboutaleb K Yamamoto S I Saleh M O Ahmed 《Chemical & pharmaceutical bulletin》1990,38(3):728-732
Inclusion complexes of clobazam with alpha-, beta-, gamma-cyclodextrins (CyDs) and heptakis(2.6-di-O-methyl)-beta-cyclodextrin (DM-beta-CyD) in aqueous solution and in the solid phase were studied by the solubility method, infrared (IR) spectroscopy, differential scanning calorimetry (DSC), and X-ray diffractometry. In addition, inclusion complex of clobazam with heptakis(2,3,6-tri-O-methyl)-beta-cyclodextrin and the solid dispersion of clobazam with methyl cellulose (MC) in a ground mixture were investigated by IR, DSC and X-ray diffractometry. It was observed that DM-beta-CyD had the highest stability constant among the four CyDs in solution. Thermal and X-ray diffraction analyses showed that clobazam molecules existed in a molecularly dispersed state in the ground mixture of CyDs. Infrared spectra showed lower frequency shifts in the case of the ground mixtures of clobazam with natural CyDs, which can be attributed to the formation of hydrogen bonds between the two carbonyl groups of clobazam and hydroxyl groups of natural CyDs. In contrast, higher frequency shifts were observed in the case of the ground mixtures of clobazam with methylated CyDs and MC and these were considered to be due to the monomolecular dispersion of clobazam in a hydrophobic environment. The mode of interaction of clobazam with DM-beta-CyD was different from that with natural CyDs in the ground mixtures. Furthermore, the crystalline inclusion complex of clobazam with DM-beta-CyD was obtained by heating of the coprecipitate in vacuo at 120 degrees C for 1 h. 相似文献
97.
Heru Kuswanto Franois Goutaland Abdennacer Yahya Aziz Boukenter Youcef Ouerdane 《Journal of Non》2001,280(1-3):277-280
The effects of heat-treatment and ultraviolet (UV) light at 325 nm on virgin and hydrogen loaded germanosilicate optical fibers have been investigated by using laser spectroscopy technique. The luminescence band around 650 nm is sensitive to heat treatment. The hydrogen reloading of the hydrogen loaded fibers subsequent to heat treatment showed a new emission band around 570 nm. The irradiated fibers have an emission band around 383 nm which was not detected in hydrogen loaded fibers. 相似文献
98.
99.
100.
Innus Mohammad JiYoung Mun Amber Onorato Martha D. Morton Abdullah I. Saleh Michael B. Smith 《Tetrahedron letters》2017,58(44):4162-4165
When compared to a long-straight chain terminal alkyne, a long chain terminal alkyne with a distal isopropyl unit (isobranched) isomerizes about two times faster when treated with strong base under identical conditions, and appears to follow pseudo first order kinetics. In both cases, equilibration to a 95–97:5–3 mixture of terminal:internal alkyne accompanies isomerization. The difference in rate may be due to an unusual folding of both long-chain alkynes, bringing the distal substituent close to the carbon-carbon-triple bond moiety. The distal isopropyl moiety may provide unanticipated steric hindrance that disrupts such folding, making the propargylic proton more available for reaction with base. 相似文献