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991.
We establish a criterion for the existence of an invariant measure for Markov processes acting on measures defined on an arbitrary complete separable metric space. This criterion is applied to time-homogeneous Markov processes associated with a nonlinear heat equation driven by an impulsive noise.  相似文献   
992.
993.
    
Dental enamel has been widely studied by particle‐induced x‐ray emission (PIXE), but less attention was paid to its demineralization, which leads to caries formation. Using broad‐beam PIXE and µ‐PIXE, we investigated normal enamel and the in vitro formation of pre‐carious lesion in lactic acid solution, aiming also to evaluate intercusp differences within the same tooth. Broad‐beam PIXE was performed using 3.0 MeV protons, and µ‐PIXE maps of Ca, Fe and Zn were collected with 3.1 MeV protons at ~4 µm resolution. In normal enamel a differentiated Ca‐rich surface layer was observed, where Fe and Zn reached their highest levels. In deeper layers, Fe and Zn evidenced quasiperiodic patterns of maxima, possibly due to coupled diffusion‐reaction catalytic processes involved in the enamel growth. Both Fe and Zn appeared to be located in a few distinct types of pools. Near the surface, demineralization induced an increase of Fe, Cu, Zn, Sr and Pb with respect to Ca, attributed to partial hydroxyapatite dissolution and/or to chelate extraction and concentration of trace metals. Ca maps revealed limited changes in the surface layer and a massive loss in the inner enamel; here, Fe was almost depleted and Zn partially removed. The maps of Ca, Fe and Zn demonstrated major intercusp variations in both normal and altered enamel. Thus, broad‐beam PIXE and µ‐PIXE, which do not require (semi)thin sectioning of the tooth as the conventional methods, provide compositional and structural insight of normal dental enamel, of its intercusp variability and of the alterations produced by in vitro demineralization, largely not accessible to the current techniques, and highly relevant for understanding the incipient caries formation. Copyright © 2008 John Wiley & Sons, Ltd.  相似文献   
994.
995.
996.
    
We report the preliminary results on simple one‐step chemical synthesis of exfoliated graphite and other carbon‐related nanostructures via a novel combustion synthesis route. We found previously that different solid carbonates could be decomposed to elements upon reducing in solid phase by using a strong reducers and the produced carbon vapors instantly condense towards 1‐D nanocarbons. Here such combustion processing is extended towards the direct heterogeneous, efficient, and autothermic high‐pressure reduction of gaseous carbon oxides (CO2 and CO) to elements using the following reducers: Li, Mg, Ca, B, Ti, Zr, and Al. The solid products (layered graphite and nanocarbides) were chemically purified and characterized using XRD, SEM, and Raman spectroscopy.

  相似文献   

997.
    
The catalytic activity in the formic acid (HCOOH) electrooxidation reaction of the Pd multiwall carbon nanotubes (MWCNTs) supported catalyst, prepared by a microwave‐assisted polyol method, treated under different gas atmospheres, and temperatures (200 and 300 °C), was investigated. Their respective catalysts surface characterization proceeded in UHV using the electron spectroscopy methods. Content of constituents, i.e., Pd nanoparticles, C and O, was examined quantitatively. Content of Pd phases and chemical forms of C atoms was analyzed assuming respective binding energy (BE) values to Pd 3d and C 1s X‐ray photoelectron spectra (XPS) spectra fitted to Gaussian–Lorentzian components. Surface structure was examined from the 3D nanostructure analysis by quantitative analysis of surfaces by electron spectroscopy (QUASES). Catalytic activity of Pd/MWCNTs after various surface treatments was attributed to different surface content and forms of Pd nanoparticles, and PdOx/C overlayer morphology, coverage, and thickness.  相似文献   
998.
    
We report on the experimental and theoretical studies of the flexible organometallic complex Cp2Mo(dmit) which often exhibits a folding in the solid state. Raman spectra of charge‐transfer salts formed by Cp2Mo(dmit) with various anions (Br, BF4, PF6, SbF6, ReO(dmit)2, TCNQF4) were measured at room temperature using red (632.8 nm) and near‐infrared (780 nm) excitations. The influence of the folding of the MoS2C2 metallacycle in [Cp2Mo(dmit)]+• cation on the Raman spectra was investigated. Due to folding of [Cp2Mo(dmit)]+•, the bands related to the CC and some C S stretching vibrations shift toward lower wavenumbers by about 0.5–0.6 cm−1deg−1. The bond lengths, charge distribution on atoms, highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energies, and dipole moments for neutral and ionized complex with various folding angles were calculated by density functional theory (DFT) methods. Additionally, the normal vibrational modes and theoretical Raman spectra were calculated and compared with experimental data. Our results indicate that vibrational spectroscopy can be applied for investigation of complex deformations in the solid state. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   
999.
    
It is known that palladium‐based catalysts are initially very active in direct formic acid oxidation but they suffer from fast deactivation caused by a strongly adsorbed CO intermediate. Reactivation of the catalysts involving application of anodic potential may cause palladium dissolution. The aim of the present study is to increase the stability and performance of palladium‐based catalysts in direct formic acid fuel cells (DFAFCs). Preparation and characterization of palladium/multiwalled carbon nanotubes (Pd/MWCNTs) and towards formic acid oxidation via different treatments are described. The catalysts were characterized by thermogravimetric analysis (TGA), X‐ray diffraction (XRD), transmission electron microscopy (TEM) and cyclic voltammetry (CV). It was shown that the Pd and Pd–Au MWCNTs supported catalysts after reduction in H2–Ar at 200 °C (R200 treatment) were highly active in formic acid electro‐oxidation, whereas the catalysts after heating in argon at 250 °C (C250 treatment) were inactive. The catalysts after hydrogen treatment have smaller metal particles and better contact with MWCNTs support. CV, simulating reactivation of the catalysts, showed that the Pd catalyst suffers from severe Pd dissolution, whereas for the Pd–Au selective leaching of Pd is considerably slower.  相似文献   
1000.
    
In this paper, a vertical distribution of 137Cs in agricultural soil was investigated. 137Cs is an anthropogenic radioisotope which is strongly adsorbed in soil and can be used to study soil erosion. This paper presents some preliminary results of measurements of activity of 137Cs in soil in Bia?a and Odonów areas. In both areas, the upper part of the soil profile was cultivated. The experimental results show that the vertical distribution of 137Cs in agricultural soil is different from the vertical distribution of 137Cs in undisturbed soil. The 137Cs is more uniformly distributed in the cultivated soil layer than in an undisturbed site. Migration of 137Cs below plough depth is limited. These data show that the depth distribution of 137Cs in soil profiles for cultivated fields should be considered for precise determination of soil erosion.  相似文献   
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