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91.
Louguet S Kumar AC Sigaud G Duguet E Lecommandoux S Schatz C 《Journal of colloid and interface science》2011,359(2):413-422
The adsorption behavior of poly(ethylene oxide)-b-poly(L-lysine) (PEO(113)-b-PLL(10)) copolymer onto silica nanoparticles was investigated in phosphate buffer at pH 7.4 by means of dynamic light scattering, zeta potential, adsorption isotherms and microcalorimetry measurements. Both blocks have an affinity for the silica surface through hydrogen bonding (PEO and PLL) or electrostatic interactions (PLL). Competitive adsorption experiments from a mixture of PEO and PLL homopolymers evidenced greater interactions of PLL with silica while displacement experiments even revealed that free PLL chains could desorb PEO chains from the particle surface. This allowed us to better understand the adsorption mechanism of PEO-b-PLL copolymer at the silica surface. At low surface coverage, both blocks adsorbed in flat conformation leading to the flocculation of the particles as neither steric nor electrostatic forces could take place at the silica surface. The addition of a large excess of copolymer favoured the dispersion of flocs according to a presumed mechanism where PLL blocks of incoming copolymer chains preferentially adsorbed to the surface by displacing already adsorbed PEO blocks. The gradual addition of silica particles to an excess of PEO-b-PLL copolymer solution was the preferred method for particle coating as it favoured equilibrium conditions where the copolymer formed an anchor-buoy (PLL-PEO) structure with stabilizing properties at the silica-water interface. 相似文献
92.
T. Mlin F. Lelarge B. Etienne F. Laruelle 《Physica E: Low-dimensional Systems and Nanostructures》1998,2(1-4)
We report on new features in the photoluminescence excitation (PLE) spectra and PLE linear polarization spectra of GaAs/AlAs lateral superlattices grown by molecular beam epitaxy (MBE). These lines appear systematically as the tilt angle of the lateral superlattice is varied. They are identified as zone–edge excitonic transitions by comparison between experimental data and detailed numerical calculations of optical transitions including valence-band mixing and tilt effects. 相似文献
93.
94.
In this paper, we report results dealing with the effects of stoichiometry on surface properties of GaAs(001) layers grown by MBE. Three aspects of surface properties were investigated: crystallography, electronic properties and chemical reactivity. Surface crystallography was studied mainly by LEED. The reconstruction of the surface was found to be drastically dependent on the composition of the uppermost atomic layer, i.e. the surface stoichiometry. According to the arsenic surface coverage, many structures from the c(8 × 2) Ga rich to the (1 × 1) arsenic saturated surface have been observed. The influence of stoichiometry on surface electronic properties has been studied by electron loss spectroscopy (ELS) and contact potential difference (CPD) measurements. In the electron loss spectra, two peaks, at about 10.3 and 20.2 eV are very sensitive to the surface composition: they gradually disappear when the arsenic coverage increases, and consequently are associated with surface states on gallium atoms. On the other hand, the CPD measurements have shown that the variation of the work function with the arsenic surface coverage is not monotonic: in particular, an abrupt change of work function of about 300 meV occurs between the (1 × 6) and c(2 × 8) structures which are very similar as far as the arsenic surface coverage (about 0,5 and 0,6 respectively) is concerned. Therefore, it seems that the work function is strongly dependent on the atomic reconstruction occurring at the surface, and not only on its stoichiometry. The connection between stoichiometry and chemical reactivity of the surface is illustrated by the study of H2S adsorption: a large difference (factor of 103) in sticking coefficient has been found between surfaces with different arsenic coverages. 相似文献
95.
The theoretical considerations and the experimental data to calculate the activation energy of the ethylene oligomerization using a microreactor in a differential thermal analyzer are presented. 相似文献
96.
P. Etienne T. Woignier A. Alaoui J. Phalippou 《Journal of Sol-Gel Science and Technology》1997,8(1-3):801-806
The mechanical behaviour of silica aerogels in alcoholic environment has been interpreted in terms of stress corrosion in
analogy with silica glass. The chemical susceptibility factor has been determined by the dynamical method and we also measured
the Weibull’s modulus which characterizes the strength distribution. These data show a stress corrosion effect which is significant
in alcoholic atmosphere. The results could explain a possible fracture of gels during the supercritical drying treatment as
already observed. 相似文献
97.
Michel Auriel Edmond De Hoffmann Philippe Scheers Etienne Deffense 《Journal of mass spectrometry : JMS》1989,24(1):1-7
The mass spectra of some 1,3,4-substituted azetidin-2-ones are measured. Fragmentation pathways are confirmed by use of both high-resolution and mass-analysed ion kinetic energy. They are consistent with the possible [2 + 2]- cycloadditions through which the azetidin-2-ones may be synthesized. More attention has to be paid to further fragmentations of the main fragments in assessing the preferred fragmentation mode. Influence of side-chain substituents is discussed. 相似文献
98.
99.
Since the original work of Dantzig and Wolfe in 1960, the idea of decomposition has persisted as an attractive approach to large-scale linear programming. However, empirical experience reported in the literature over the years has not been encouraging enough to stimulate practical application. Recent experiments indicate that much improvement is possible through advanced implementations and careful selection of computational strategies. This paper describes such an effort based on state-of-the-art, modular linear programming software (IBM's MPSX/370). 相似文献
100.
Etienne M Grosso D Boissière C Sanchez C Walcarius A 《Chemical communications (Cambridge, England)》2005,(36):4566-4568
We provide the first electrochemical evidence of permeability changes in continuous mesoporous TiO2 thin film electrodes induced by nanocrystallisation. 相似文献