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981.
We consider site percolation on Z
d, directed edges going from any sZ
d to s+A
1,..., s+A
n, where A
1,..., A
n are the same for all sites and at least two of them are noncollinear. A site is closed if it belongs to p+Block, where p is a point in a Poisson distribution in R
dZ
d with a density and Block={sL: |s|M}+{sR
d: |s|}, where L is a linear subspace of R
d, |·| is the Euclidean norm, =max(|A
1|,..., |A
n|) and M is a parameter. We study the behavior of *, the critical value, and P
closed*, corresponding critical percentage of closed sites, when M. Denote R
d/L the factor space. Call two nonzero vectors U, V codirected if U=kV, where k>0. Theorem. If there are A
i and A
j whose projections to R
d/L are not codirected, then *1/M
dim(L) and P
closed* remains separated both from 0 and 1 when M. If projections of all A
1,..., A
n to R
d/L are codirected, then *1/M
dim(L)+1 and P
closed*1/M when M. 相似文献
982.
983.
Nanostructured perovskite-type Sr1−aCeaFeO3−x, (0?a<0.15) powders have been prepared by citrate-nitrate smoldering auto-combustion. Their phase structure and stability, surface and morphological properties, reduction behavior and interaction with oxygen have been investigated by X-ray Powder Diffraction combined with Rietveld Analysis, 57Fe Mössbauer and X-ray Photoelectron Spectroscopies, N2-adsorption method, Temperature Programmed Reduction and Oxidation experiments. Our results reveal that citrate-nitrate auto-combustion method is effective in obtaining single phase Sr1−aCeaFeO3−x. The Sr1−aCeaFeO3−x structure is cubic only for a?0.06, while for a<0.06 remains tetragonal. Moreover, for a?0.06 after semi-reductive treatment under inert gas, an expanded cubic phase is obtained instead of the brownmillerite-type structure, which is known to have ordered vacancies. Stabilization of octahedral Fe3+ by cerium doping appears to be the main factor in determining the structural properties of Sr1−aCeaFeO3−x. The highest oxygen consumption for Ce-doped SrFeO3 occurs for a=0.06. Preliminary impedance measurements show that Sr0.94Ce0.06FeO3−x has the lowest area-specific resistance. 相似文献
984.
Delong Zhang Xiaojun ChenYufang Wang Dengsong ZhuBo Wu Guoxiang Lan 《Journal of Physics and Chemistry of Solids》2002,63(2):345-358
Raman spectra of as-grown and vapor transport equilibration (VTE) treated Er:LiNbO3 crystals, which have different cut orientations (X-cut and Z-cut), different Er-doping levels (Er:(0.2, 0.4 and 2.0 mol%)LiNbO3) and different VTE durations (80, 120, 150 and 180 h), were recorded at room temperature in the wavenumber range 50-1000 cm−1 by using backward scattering geometry. The spectra were attributed on the basis of their spectral features and the previous experimental work and the most recent theoretical progress in lattice dynamics on pure LiNbO3. In comparison with the pure crystal the most remarkable effect of Er-doping on the Raman spectrum is observed for the E(TO9) mode. It does not appear at 610 cm−1 as the pure crystal, but locates at 633 cm−1. In addition, the doping also results in the lowering of the Raman phonon frequency, the broadening of the Raman linewidth and the changes of the relative Raman intensity of some peaks. The VTE treatment results in the narrowing of the linewidth, the recovery of the lowered phonon frequency and the further changes of relative Raman intensity. The narrowing of Raman linewidth indicates that the VTE processing has brought these crystals closer to stoichiometric composition. The VTE treatment has induced the formation of a precipitate ErNbO4 in the high-doped Er(2.0%):LiNbO3 crystals whether X- or Z-cut. For these precipitated crystals, besides above linewidth and phonon frequency features, they also display more significant Raman intensity changes compared with those not precipitated crystals. In addition, a slight mixing between A1(TO) and E(TO) spectra is also observed for these precipitated crystals. Above doping and VTE effects on Raman spectra were quantitatively or qualitatively correlated with the characteristics of the crystal structure and phonon vibrational system. 相似文献
985.
986.
B. Boffey Francisco Ramón Fernández García Gilbert Laporte Juan A. Mesa Blas Pelegrín Pelegrín 《TOP》1995,3(2):167-220
Summary Many network routing problems, particularly where the transportation of hazardous materials is involved, are multiobjective
in nature; that is, it is desired to optimise not only physical path length but other features as well. Several such problems
are defined here and a general framework for multiobjective routing problems is proposed. The notion of “efficient solution”
is defined and it is demonstrated, by means of an example, that a problem may have very many solutions which are efficient.
Next, potentially useful solution methods for multiobjective routing problems are discussed with emphasis being placed on
the use of shortest/k-shortest path techniques. Finally, some directions for possible further research are indicated.
Invited by B. Pelegrin 相似文献
987.
M. R. Koblischka S. L. Huang K. Fossheim T. H. Johansen H. Bratsberg 《Physica C: Superconductivity and its Applications》1998,300(3-4):207-211
Flux distributions of partial-melting processed Bi2Sr2CaCu2O8+δ ceramics are obtained using magneto-optic imaging. In remanent states (μ0Ha=0 T), large amounts of trapped flux are observed along (Sr,Ca)2CuOy particles embedded in the Bi2Sr2CaCu2O8+δ matrix. Despite the relatively large size of these particles (up to 30 μm), the pinning effect is similar to that of Y2BaCuO5 particles in melt-processed YBa2Cu3O7−δ. Furthermore, we discuss how the pinning capability of non-superconducting particles of different sizes and densities will show up in magneto-optic images. 相似文献
988.
989.
Welch K Mousavi S Lundberg B Strømme M 《The European physical journal. E, Soft matter》2005,18(1):105-112
A newly developed method for determining the frequency-dependent complex Young's modulus was employed to analyze the mechanical
response of compacted microcrystalline cellulose, sorbitol, ethyl cellulose and starch for frequencies up to 20 kHz. A Debye-like
relaxation was observed in all the studied pharmaceutical excipient materials and a comparison with corresponding dielectric
spectroscopy data was made. The location in frequency of the relaxation peak was shown to correlate to the measured tensile
strength of the tablets, and the relaxation was interpreted as the vibrational response of the interparticle hydrogen and
van der Waals bindings in the tablets. Further, the measured relaxation strength, holding information about the energy loss
involved in the relaxation processes, showed that the weakest material in terms of tensile strength, starch, is the material
among the four tested ones that is able to absorb the most energy within its structure when exposed to external perturbations
inducing vibrations in the studied frequency range. The results indicate that mechanical relaxation analysis performed over
relatively broad frequency ranges should be useful for predicting material properties of importance for the functionality
of a material in applications such as, e.g., drug delivery, drug storage and handling, and also for clarifying the origin of hitherto unexplained molecular processes. 相似文献
990.
We investigate the structural behavior of a poly(styrene)-block-poly(acrylic acid) diblock copolymer which forms hexagonally-packed PS cylinders (C-phase) in the melt state. The water dispersion of this structure provides hairy cylinders which comprise a PAA swollen cylindrical brush with a height h tunable via its degree of ionization and the ionic strength in the solution, and a water-free, PS cylindrical core of constant radius RC. Such system constitutes an out-of-equilibrium frustrated model system: the selective swelling of the PAA brush results in a frustration of the interface curvature, which the ratio h/RC allows to quantify. Upon heating at a temperature higher than the glass transition temperature of the PS core, the glassiness of the core is relieved and the mechanical constraints arising from the selective swelling of the structure can be relaxed: the cylinders undergo a cylinder-to-sphere transition upon annealing at high temperature, when above a frustration threshold h/RC 1.8. Thanks to a careful mapping of the transition diagram, an undulating cylindrical morphology (UC) is identified between unchanged cylinders ( h/RC
1.8) and spheres ( h/RC 2.0), which appears to result from a Rayleigh-like pearling instability of the copolymer cylinders. 相似文献