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921.
B. Blank J. -J. Gaimard H. Geissel K. -H. Schmidt H. Stelzer K. Sümmerer D. Bazin R. Del Moral J. P. Dufour A. Fleury F. Hubert H. -G. Clerc M. Steiner 《Zeitschrift für Physik A Hadrons and Nuclei》1992,343(4):375-379
Total charge-changing cross sections have been measured for8Li on C and Pb targets, for9Li on C, Al, Cu, Sn and Pb targets, as well as for11Li on C, Sn and Pb targets at about 80 MeV/nucleon. These data are compared to measured total reaction cross sections and Glauber-type calculations using Hartree-Fock density distributions. These comparisons allow to draw conclusions on the proton density distribution of the neutronrich lithium isotopes. The results show that even for the most exotic nucleus11Li the proton distribution is only very weakly influenced by the long tail in the neutron density distribution already established in several experiments. 相似文献
922.
To assess the historical and sociological significance of the cold fusion saga, researchers need accurate information about the dates of various events associated with the saga. Based on materials in the Cornell Cold Fusion Archive, this article provides both a chronology and citations to documentary evidence for cold fusion events from 1926 to the end of 1990. 相似文献
923.
With a suitable combination of ligand-stabilised nanoparticle suspension and ionic salt solutions, it is possible to produce microcrystals that are coated with nanoparticles. The self-assembly process of coating microcrystals by gold nanoparticles (NP) is mediated by the crystal lattice. This is the so-called CLAMS process - a generic process for self-organisation of nanoparticles on the surface of crystals [M. Murugeshan, D. Cunningham, J.-L. Martnez-Albertos, R. Vrcelj, B.D. Moore, Chem. Commun. (2005) 2677]. We are exploring here the structural properties of these self-assembled structures by using different imaging techniques. 相似文献
924.
M. J. Soupioni B. D. Symeopoulos H. V. Papaefthymiou 《Journal of Radioanalytical and Nuclear Chemistry》2006,268(3):441-444
Summary Four different bottled water brands sold in Greece in the winter of 2001-2002 were analyzed for a wide range of chemical elements,
using neutron activation analysis (NAA). The elements Na and Br were determined instrumentally (INAA), whereas the other metals
and trace elements radiochemically (RNAA). The results indicated that the mean level of all the elements determined in the
samples were well within the European Union (EU) directive on drinking water and accomplish the drinking water standards of
the World Health Organisation (WHO) as well as of the Food and Drug Administration (FDA). 相似文献
925.
V.V. Glushkov S.V. Demishev M.I. Ignatov Yu.B. Paderno N.Yu. Shitsevalova O.A. Churkin N.E. Sluchanko 《Journal of solid state chemistry》2006,179(9):2871-2874
In order to reveal the nature of the ground state of archetypal intermediate-valence compound SmB6, a comprehensive study of its transport and magnetic properties was carried out on high-quality single crystals at temperatures of 1.8-300 K in magnetic fields up to 7 T. A drastic enhancement of negative magnetoresistance was observed below 14 K, with the maximum absolute value of Δρ/ρB2∼2.2×10−3 T−2 at T≈5.2 K. This effect seems to be attributable to anomalous magnetic scattering of many-body (exciton-polaronic) complexes induced by fast valence fluctuations on Sm sites. The observed anomalies of magnetotransport, thermoelectric and magnetic characteristics are discussed in terms of electron phase transition to the coherent state of interacting many-body complexes occurring at T*∼5 K. 相似文献
926.
In this paper, according to the molecular fragment principle, a series of eight ternary luminescent lanthanide complex systems were assembled, and whose compositions were determined with elemental analysis and infrared spectrum: Ln(MA)3(L)·H2O, where Ln = Sm, Eu, Tb, Dy; HMA = α‐methylacrylic acid; L = 1,10‐phenanthroline (phen), 2,2′‐bipyridine (bipy). The photophysical properties of these functional molecular systems were studied with ultraviolet‐visible absorption spectrum, and fluorescence excitation and emission spectrum. It was found that the heterocylic compounds (phen and bipy) act as the main energy donor and luminescence sensitizer for their suitable energy match and effective energy transfer to the emission energy level of Ln3+ ions. MMA ligand was only used as the terminal structural ligand to influence the luminescence. Especially terbium complex systems show the strongest luminescence for the optimum energy match and transfer between phen (bipy) and Tb3+ ion. 相似文献
927.
A new, high performance liquid chromatography method has been developed for the separation of monovinyl- and divinyl-protochlorophyllides, using commercially available, C30 reverse phase column and isocratic elution. This method can be used both for analytical applications and preparative scale purification of monovinyl- and divinyl-protochlorophyllides using the same column where submilimolar concentrations of the crude protochlorophyllide extract can be separated in one run. The purity of the obtained protochlorophyllides was demonstrated by spectroscopic methods, as well by the formation of aggregates in toluene. 相似文献
928.
929.
Electroconductivity of BaCe0.9Nd0.1O3−α was studied as a function of the composition of the H2+H2O+Ar mixture and temperature in the interval from 873 to 1173 K. It was shown that the electroconductivity was independent
of PH2 (0.97 to 0.10 atm) and PO2 (10−21 to 10−26 atm), but depended on PH2O (0.08 to 0.005 atm). A mathematical processing of the PH2O dependencies of the electroconductivity, which was performed in terms of a classical model of defect formation in high-temperature
proton-conducting solid electrolytes, yielded equilibrium constants of the reaction of water dissolution in BaCe0.9Nd0.1O3−α and mobilities of protons and oxygen ions. The temperature dependencies of these quantities were used to determine the mobility
activation energies of protons (Ea=34±7 kJ/mole) and oxygen ions (Ea=72±8 kJ/mole), and also the enthalpy (ΔH=−150±25 kJ/mole) and the entropy (ΔS=153±26 kJ/mole·K) of the reaction of water
dissolution in BaCe0.9Nd0.1O3−α. 相似文献
930.