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51.
Study of solid-liquid phase diagram of LiPO3-Pb(PO3)2 binary system, in certain calcination conditions, shows the existence of several metastable phasis. When heated at a temperature of 723 K the binary mixtures lead uncompletely to a defined compound Pb2Li(PO3). On heating these ternary solid mixtures, three eutectic reactions have been observed: LiPO3+Pb(PO3)2→Liquid at a temperature of 793 K(1) LiPO3+Pb2Li(PO3)5→Liquid at a temperature of 843 K (2) Pb2Li(PO3)5+Pb(PO3)2→Liquid at a temperature of 891 K (3) The metastable liquid phase appears in the system at temperature of 793 K. DTA experiments performed on the binary LiPO3-Pb(PO3)2 mixtures, show a superposition of two diagrams. The first one is metastable and the second represents the stable equilibrium phase diagram. Measurements of liquid enthalpy of binary LiPO3-Pb(PO3)2 system at temperature of 979.65 K were reported. The corresponding values were very small and so the binary system can be considered as athermal. Assuming an ideal behaviour, the liquidus curves in the metastable diagram were calculated and the eutectic reaction (LiPO3-Pb(PO3)2→Liquid) was confirmed at 793 K. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   
52.
The electrochemical oxidation of indium metal in cells of the type leads to the formation of RInX2 compounds; if 2,2′-bipyridine is also present, the products are the adducts RInX2·bipy (R = CH3, C2H5, C6H5, C6H5CH2, C6F5; X = Cl, Br, I (not all combinations)). When R′4NX is present instead of bipy, the products are the salts R′4N[RInX3]. The electrochemical oxidation apparently proceeds via the general mechanism discussed previously. Anomalous results with CH3I or C2H5I are discussed in the light of the known solution chemistry of organoindium(III) compounds.  相似文献   
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Journal of Solid State Electrochemistry - Manganese phosphate (Mn3(PO4)2) particles decorated polyaniline (PANI) have been proposed as a promising electrode material for supercapacitors. Mn3(PO4)2...  相似文献   
55.
The Cd(3P1)- and Hg(3P1)-photosensitized emissions of some secondary and tertiary alkyl- and silylamines have been investigated under conditions of steady illumination at 493 and 298 K, respectively. The emission bands were observed at around 440 nm in the cadmium-photosensitized reactions of these amines. In contrast, no appreciable emission bands were observed in the mercury-photosensitized reactions of these amines. However, upon addition of tert-butyl alcohol to the amine-mercury system, an emission band evolved at around 350 nm in the mercury-photosensitization. The peak-wavelengths for secondary and tertiary alkyl- and silylamines are slightly shorter than the values predicted from the correlations between the peak wavelength and the first ionization energy obtained in the cadmium- and mercury-photosensitized luminescence of ammonia and primary amines. The quenching efficiencies of the cadmium and mercury resonance lines by secondary alkyl- and silylamines are higher than those by tertiary alkyl- and silylamines. These observations suggest that the steric hindrance by the alkyl and silyl groups to the approach of the nitrogen atom in the amines to excited cadmium and mercury atoms seems to be an important factor for the stabilization of the exciplexes and the quenching of the resonance lines. The behavior of silylamines is similar to that of alkylamines in cadmium- and mercury-photosensitized reactions.  相似文献   
56.
We previously reported the apparent formation of matrix adducts of 3,5-dimethoxy-4-hydroxy-cinnamic acid (sinapinic acid or SA) via covalent attachment to disulfide bond-containing proteins (HdeA, Hde, and YbgS) from bacterial cell lysates ionized by matrix-assisted laser desorption/ionization (MALDI) time-of-flight-time-of-flight tandem mass spectrometry (TOF-TOF-MS/MS) and post-source decay (PSD). We also reported the absence of adduct formation when using ??-cyano-4-hydroxycinnamic acid (CHCA) matrix. Further mass spectrometric analysis of disulfide-intact and disulfide-reduced over-expressed HdeA and HdeB proteins from lysates of gene-inserted E. coli plasmids suggests covalent attachment of SA occurs not at cysteine residues but at lysine residues. In this revised hypothesis, the attachment of SA is preceded by formation of a solid phase ammonium carboxylate salt between SA and accessible lysine residues of the protein during sample preparation under acidic conditions. Laser irradiation at 355?nm of the dried sample spot results in equilibrium retrogradation followed by nucleophilic attack by the amine group of lysine at the carbonyl group of SA and subsequent amide bond formation and loss of water. The absence of CHCA adducts suggests that the electron-withdrawing effect of the ??-cyano group of this matrix may inhibit salt formation and/or amide bond formation. This revised hypothesis is supported by dissociative loss of SA (?224?Da) and the amide-bound SA (?206?Da) from SA-adducted HdeA and HdeB ions by MS/MS (PSD). It is proposed that cleavage of the amide-bound SA from the lysine side-chain occurs via rearrangement involving a pentacyclic transition state followed by hydrogen abstraction/migration and loss of 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-ynal (?206?Da).  相似文献   
57.
We investigated the effects of boron atoms substitution on the thermal conductivity and mechanical properties of single-layer graphene using the non-equilibrium molecular dynamics (NEMD) simulations. By performing the uniaxial tension simulations, we observed that substituted boron atoms slightly decrease the elastic modulus and tensile strength of graphene. On the other hand, it was observed that only 0.75% concentration of boron atoms in graphene reduces the thermal conductivity of graphene by more than 60% and leads to vanishing chirality effect.  相似文献   
58.
The switching process in ferroelectric liquid crystal devices takes place through the formation and evolution of domains, which is modelled here using a three-variable approach. This approach includes variation of the director profile in one dimension, through the thickness of the cell. Here we discuss details of the model which are necessary in order to reproduce the domain nucleation and switching times as a function of applied voltage for both monopolar and bipolar pulses. We show that the three-variable modelling of SSFLC switching in one dimension produces excellent comparisons with experimental data for both bipolar and monopolar pulses.  相似文献   
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60.
The linear optical gain of gain-clamped quantum dash semiconductor optical amplifiers (GCSOAs) has been investigated using the rate equation model. The gain spectrum of GCSOA for different wavelength detuning and different doping has been studied. Our analysis shows that the linear gain can be increased as the laser wavelength is detuned to high wavelength where the peak of the optical gain, which is found at wavelengths below the ground state wavelength, is shifted to lower wavelength as the laser wavelength is increased. We find that doping the dashes by either N-type or P-type enhances the linear optical gain and shifts the gain peak to lower wavelength. Moreover, we found that GCSOA with lightly N-type doping demonstrates large separation between the laser and the amplifier wavelength. Also we find that small inhomogeneous line broadening enhances the linear gain peak, shifts the gain peak to wavelength lower than the GS wavelength and widens the gain spectrum.  相似文献   
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