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851.
Geodesic convex sets, Steiner convex sets, and J-convex (alias induced path convex) sets of lexicographic products of graphs are characterized. The geodesic case in particular rectifies Theorem 3.1 in Canoy and Garces (Graphs Combin 18(4):787–793, 2002).  相似文献   
852.
Periodic, self-consistent DFT-GGA(PW91) calculations are used to study the interaction of hydrogen with different facets of seventeen transition metals—the (100) and (111) facets of face-centered cubic (fcc) metals, the (0001) facet of hexagonal-close packed (hcp) metals, and the (100) and (110) facets of body-centered cubic (bcc) metals. Calculated geometries and binding energies for surface and subsurface hydrogen are reported and are, in general, in good agreement with both previous modeling studies and experimental data. There are significant differences between the binding on the close-packed and more open (100) facets of the same metal. Geometries of subsurface hydrogen on different facets of the same metal are generally similar; however, binding energies of hydrogen in the subsurface of the different facets studied showed significant variation. Formation of surface hydrogen is exothermic with respect to gas-phase H2 on all metals studied with the exception of Ag and Au. For each metal studied, hydrogen in its preferred subsurface state is always less stable than its preferred surface state. The magnitude of the activation energy for hydrogen diffusion from the surface layer into the first subsurface layer is dominated by the difference in the thermodynamic stability of these two states. Diffusion from the first subsurface layer to one layer further into the bulk does not generally have a large thermodynamic barrier but still has a moderate kinetic barrier. Despite the proximity to the metal surface, the activation energy for hydrogen diffusion from the first to the second subsurface layer is generally similar to experimentally-determined activation energies for bulk diffusion found in the literature. There are also some significant differences in the activation energy for hydrogen diffusion into the bulk through different facets of the same metal.  相似文献   
853.
Li–Mn–O films are deposited by RF magnetron sputtering using 27.12 MHz as the excitation frequency. The sputtering rate of deposition is found to be higher than the one with conventional sputtering frequency. The rate of deposition as high as 42 Å/min has been achieved using this frequency. The X-ray diffraction patterns of films annealed in air show a gradual increase in crystallinity with the increase in annealing temperature. The electrochemical studies reveal that the films annealed at 700 °C show the best results in terms of crystallinity as well as discharge capacity. It is evident from this investigation that the higher excitation frequency magnetron discharge enhances the nucleation, and there by the rate of sputtering. This can be due to the reduced dc voltage appearing at the target surface at higher excitation frequency, which reduces the unnecessary ion bombardment of the growing film.  相似文献   
854.
In the twisted nematic liquid crystal spatial light modulators (TN-LCSLM), distortion of uniform twist and decrease in tilt angle of liquid crystal molecules on application of an electric field lead to amplitude and phase modulations of the transmitted or reflected wavefront, respectively. The amplitude and phase modulation characterization of TN-LCSLM using Jones calculi is simple and extensively used but does not give any information about important polarimetric parameters such as diattenuation and depolarizance. On the other hand, the characterization using Mueller calculi provides all information in terms of polarimetric properties such as diattenuation, retardance (birefringence) and depolarization. In this paper, polarimetric properties of the transmissive TN-LCSLM (HOLOEYE LC2002) are characterized measuring 17 different Mueller matrices at different addressed gray scale through Mueller Matrix Imaging Polarimeter (MMIP) at 530 nm wavelength. Lu-Chipman polar decomposition for Mueller matrix is utilized to separate out three independent Mueller matrices for diattenuation, depolarization and retardance as a function of addressed gray scale. Further, Mueller-Stokes combined formulation is used to examine the effect of depolarization present in the TN-LCSLM on six different states of polarization and evaluation of eigenpolarization states for the TN-LCSLM has been presented.  相似文献   
855.
Parasitic diseases are among neglected disease of human and animals, especially in tropical and sub tropical regions. In the era of artificial intelligence, the novel biosensing diagnostic platform is needed for an early control measure implementation. This goal can be successfully achieved by onsite application of electrochemical biosensors. They are being developed towards point of care diagnostics; however commercial availability is scanty. The recent developments during last one decade in terms of the electrode surface modification for rapid diagnosis of important emerging/re-emerging parasites is presented. The information would help future improvement in the electrochemical biosensing of parasites.  相似文献   
856.
857.
JPC – Journal of Planar Chromatography – Modern TLC - Two new, simple, fast, and sensitive methods, normal- and reversed-phase high-performance thin-layer chromatography (NP-HPTLC and...  相似文献   
858.
Early research in aerodynamics and biological propulsion was dramatically advanced by the analytical solutions of Theodorsen, von Kármán, Wu and others. While these classical solutions apply only to isolated swimmers, the flow interactions between multiple swimmers are relevant to many practical applications, including the schooling and flocking of animal collectives. In this work, we derive a class of solutions that describe the hydrodynamic interactions between an arbitrary number of swimmers in a two-dimensional inviscid fluid. Our approach is rooted in multiply-connected complex analysis and exploits several recent results. Specifically, the transcendental (Schottky–Klein) prime function serves as the basic building block to construct the appropriate conformal maps and leading-edge-suction functions, which allows us to solve the modified Schwarz problem that arises. As such, our solutions generalize classical thin aerofoil theory, specifically Wu's waving-plate analysis, to the case of multiple swimmers. For the case of a pair of interacting swimmers, we develop an efficient numerical implementation that allows rapid computations of the forces on each swimmer. We investigate flow-mediated equilibria and find excellent agreement between our new solutions and previously reported experimental results. Our solutions recover and unify disparate results in the literature, thereby opening the door for future studies into the interactions between multiple swimmers.  相似文献   
859.
CoS@MorphcdtH NPs and CoS@4-MPipzcdtH NPs were synthesized by precipitation method involving three mechanisms: inclusion, occlusion, and adsorption. The synthesized NPs were characterized with the help of UV-Vis spectroscopy, FESEM-EDAX, powder x-ray diffraction, TEM, ESIMS, TG/DSC analysis. The morphology of the CoS@MorphcdtH NPs and CoS@4-MPipzcdtH NPs were hexagonal and rectangular, and the particles were in the range 7–12 nm. UV–visible spectral measurements showed surface plasmon resonance at 320 nm–340 nm with band gap of 3.65 eV–3.86 eV. The catalytically active CoSNPs called were investigated for the reduction of 4-nitrophenol (4-NP) via hydrogenation using sodium borohydride (NaBH4) as a reducing agent. Both the CoS NPs successfully reduced 4-NP to 4- aminophenol (4-AP) in a short time, catalytic performances are almost unchanged for the first five cycles. Herein, we report the preparation and characterizations of efficient active CoS NPs consisting carbodithioic acid framework as a support/capping material, along with catalytic property.  相似文献   
860.
We have developed a highly efficient new method for the introduction of Lewis acidic boron centers into the side chains of organic polymers. Our methodology involves three steps: (i) the controlled polymerization of a functional monomer, (ii) the exchange of the functional group for Lewis acidic boron centers, and (iii) the fine-tuning of the Lewis acidity of the individual centers through substituent exchange reactions with nucleophiles. This approach gives access to a family of new well-defined organoboron polymers including moderately Lewis acidic poly(arylboronates) and the first examples of highly Lewis acidic fluorinated triarylborane polymers.  相似文献   
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