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991.
A representation of the CD 0(K)-space is given in [1, 2] for a compact Hausdorff space K without isolated points. We generalize this to an arbitrary countably compact space K without any assumption on isolated points. 相似文献
992.
993.
V. S. Zuev 《Journal of Russian Laser Research》2005,26(5):347-362
We have considered evanescent plane waves in structures with a layer of a substance with ε, μ < 0 and with a layer of a well-reflecting
metal, ε < 0, μ ≥ 1. Waves with increased amplitude as compared with the initial wave have been found to occur, due to which
evanescent waves with wave number as in the initial wave but with increased amplitude arise behind these layers. A composite
material with ε, μ < 0 at optical frequencies are proposed. Surface waves on a metal layer are considered in detail. It is
shown that surface waves with a sufficiently arbitrary wave number can be excited. It is also shown that, on very thin layers,
surface waves with wave number exceeding ten times that of a homogeneous plane wave in vacuum can be excited. Propagation
losses are calculated. For a silver layer, the wave path can be from 30 up to 100 wavelengths. Practical use in developing
techniques for optical transformations of short-wave surface waves in 2D space, similar to those in 3D space, are pointed
out. 相似文献
994.
We investigated site specific reactivity of the α-Cu-Al(17 at.%)(1 0 0) alloy surface versus that of Al and Cu by measuring neutralisation of Li+ ions. Experiments show that Li+ neutralisation on the α-CuAl(1 0 0) alloy surface does not occur efficiently on Al and is somewhat more efficient on Cu as compared to a pure Cu sample, indicating depletion of electron density on Al and transfer to neighboring Cu. It can thus be concluded that Cu sites in presence of Al are more reactive in the sense that processes involving electron capture from the surface would proceed more efficiently on these. 相似文献
995.
996.
Patrik Vrábel 《Journal of luminescence》2006,118(2):283-292
Capillary electrophoresis with laser-induced fluorescence detection (CELIF) is a powerful tool for separation and sensitive determination of fluorescent species. Biologically active compounds, such as amino acids, peptides and proteins may exhibit native fluorescence, which is however often low and/or an expensive laser is required for excitation in UV. Therefore, labelling of the analytes with a fluorescent dye is usually necessary.In this work, a home-built CELIF instrument with diode pumped frequency-doubled continuous wave Nd:YAG excitation laser with feedback power regulation (532 nm) was constructed. The suitability of this type of laser for LIF detection in a separation method was found excellent. A limit of detection (LOD) (S/N=3) of 2×10−13 mol/l was achieved with rhodamine B, which is comparable to those obtained using similar instruments with Ar+ laser [Y.F. Cheng, N.J. Dovichi, Science 242 (1988) 562, E.S. Yeung et al., J. Chromatogr. 608 (1992) 73]. LOD of a protein derivatized according to modified procedures [M.J. Little et al., Anal. Chim. Acta 339 (1997) 279, A. Chersi et al., Biochim. Biophys. Acta 1336 (1997) 83] was determined. Detection of the derivatives was found to be limited by insufficient reaction recovery at low analyte concentration, chemical noise, separation efficiency and quality of the derivatizing reagent rather than by the detector performance. As a consequence, a huge gap between the detection ability of CELIF instruments and LOD determined in real samples is revealed. 相似文献
997.
Anders Björn 《Potential Analysis》2007,27(4):381-387
We characterize regular boundary points for p-harmonic functions using weak barriers. We use this to obtain some consequences on boundary regularity. The results also
hold for -harmonic functions under the usual assumptions on , and for Cheeger p-harmonic functions in metric spaces.
相似文献
998.
Let be a -group with generator , and let be a local -semigroup commuting with . Then the operators , , form a local -semigroup. It is proved that if is injective and is the generator of , then is closable and is the generator of . Also proved are a characterization theorem for local -semigroups with not necessarily injective and a theorem about solvability of the abstract inhomogeneous Cauchy problem:
999.
n-Si(1 1 1) crystalline electrode was modified by carboxyl acid groups and sulfonic groups. The flat band potential (Ufb), relation between flat band potential and the carbon numbers to the modified samples and relation between photocurrent density and potential of the modified electrodes were studied. ATR-IR spectra and XPS analysis show that the organic compounds were connected to n-Si(1 1 1) wafer by SiC bond. Calculation indicates that the surface modification ratio increased with the carbon number of organic groups decreased. Mott-Schottky plots gives the flat band potential of the samples to shift to negative positions with the carbon number decreased in both of the two different systems and the flat band potential of the sample with the group of (CH2)3SO3H reaches to −0.82 V, which is more negative than reported, and the flat band potential of all the samples in this paper are more negative than the sample with methyl group [B. Ashish, N.S. Lewis, J. Phys. Chem. B 102 (1998) 1067; S. Takabayashi, M. Ohashi, K. Mashima, Y. Liu, S. Yamazaki, Y. Nakato, Langmuir 21 (2005) 8832]. The photocurrent and photovoltage of the modifications are stable enough under solar illumination for a long time. 相似文献
1000.
Chemisorption of 1,1-dichloroethene (Cl2CCH2) to a Si(1 1 1)-7 × 7 surface was studied by means of X-ray photoelectron spectroscopy using synchrotron radiation, recording chlorine 2p and carbon 1s spectra. For carbon 1s, spectral assignment of the chemisorbed species is based on quantum chemical calculations of chemical shifts in model compounds.The results confirm the identity of covalently bonded 1-chlorovinyl (-CClCH2) and vinylidene (CCH2) adspecies. Upon chemisorption at room temperature it was found that about one-third of the molecules break one C-Cl bond while about two-thirds of the adsorbates break two C-Cl bonds. We do not, however, find evidence for isomerization of CCH2 to di-bonded vinylene (-CHCH-). 相似文献