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71.
We give the first existence and regularity results on the cheapest way to enclose and separate planar regions of prescribed
areas, where cost is given by a general norm ϕ, thus generalizing the Wulff shape for enclosing a single region. As an example,
we classify the cheapest way to enclose and separate two planar regions of prescribed areas for the ℓ1 norm (“Manhattan metric”) into three distinct types, according to the relative size of the prescribed areas. 相似文献
72.
Customized photorefractive quantum-well devices have been developed for real-time video acquisition of coherence-gated, three-dimensional images in turbid media. Large-field-of-view holographic imaging with direct video capture is now possible. We have evaluated the role of intensity-limited device performance in Fourier-plane and image-plane holography in such devices and, using near-infrared light, have imaged through turbid phantoms of 13 mean free paths' scattering depth with 50-microm transverse and 60-microm depth resolution. 相似文献
73.
It is well-known, both theoretically and experimentally, that alloying MgH(2) with transition elements can significantly improve the thermodynamic and kinetic properties for H(2) desorption, as well as the H(2) intake by Mg bulk. Here, we present a density functional theory investigation of hydrogen dissociation and surface diffusion over a Ni-doped surface and compare the findings to previously investigated Ti-doped Mg(0001) and pure Mg(0001) surfaces. Our results show that the energy barrier for hydrogen dissociation on the pure Mg(0001) surface is high, while it is small/null when NiTi are added to the surface as dopants. We find that the binding energy of the two H atoms near the dissociation site is high on Ti, effectively impeding diffusion away from the Ti site. By contrast, we find that on Ni, the energy barrier for diffusion is much reduced. Therefore, although both Ti and Ni promote H(2) dissociation, only Ni appears to be a good catalyst for Mg hydrogenation, allowing diffusion away from the catalytic sites. Experimental results corroborate these theoretical findings, i.e., faster hydrogenation of the Ni-doped Mg sample as opposed to the reference Mg- or Ti-doped Mg. 相似文献
74.
75.
A. Kuhn I. J. Blewett D. P. Hand P. French M. Richmond J. D. C. Jones 《Optics and Lasers in Engineering》2000,34(4-6):273-288
This paper investigates the extension of optical fibre beam delivery to high-brightness applications, in particular laser percussion drilling, where both a good beam quality and high peak power are required. Beam quality preservation through a number of optical fibres is studied both experimentally and by using a ray propagation model. It is determined that in order to achieve the beam quality required for percussion drilling (M2<30) the largest fibre which can be used is 400 μm diameter. The laser-induced damage threshold is measured for a number of 400 μm fibres, and a CO2 laser-annealing technique is shown to increase the damage threshold by a factor of 10, allowing 28 J, 1 ms pulses to be transmitted. 相似文献
76.
João Lagarto Jonathan D. Hares Christopher Dunsby Paul M. W. French 《Journal of fluorescence》2017,27(5):1643-1654
Autofluorescence lifetime measurements, which can provide label-free readouts in biological tissues, contrasting e.g. different types and states of tissue matrix components and different cellular metabolites, may have significant clinical potential for diagnosis and to provide surgical guidance. However, the cost of the instrumentation typically used currently presents a barrier to wider implementation. We describe a low-cost single point time-resolved autofluorescence instrument, exploiting modulated laser diodes for excitation and FPGA-based circuitry for detection, together with a custom constant fraction discriminator. Its temporal accuracy is compared against a “gold-standard” instrument incorporating commercial TCSPC circuitry by resolving the fluorescence decays of reference fluorophores presenting single and double exponential decay profiles. To illustrate the potential to read out intrinsic contrast in tissue, we present preliminary measurements of autofluorescence lifetime measurements of biological tissues ex vivo. We believe that the lower cost of this instrument could enhance the potential of autofluorescence lifetime metrology for clinical deployment and commercial development. 相似文献
77.
N. G. Semaltianos W. Perrie P. French M. Sharp G. Dearden S. Logothetidis K. G. Watkins 《Applied Physics A: Materials Science & Processing》2009,94(4):999-1009
Femtosecond laser (180 fs, 775 nm, 1 kHz) ablation characteristics of the nickel-based superalloy C263 are investigated. The
single pulse ablation threshold is measured to be 0.26±0.03 J/cm2 and the incubation parameter ξ=0.72±0.03 by also measuring the dependence of ablation threshold on the number of laser pulses.
The ablation rate exhibits two logarithmic dependencies on fluence corresponding to ablation determined by the optical penetration
depth at fluences below ∼5 J/cm2 (for single pulse) and by the electron thermal diffusion length above that fluence. The central surface morphology of ablated
craters (dimples) with laser fluence and number of laser pulses shows the development of several kinds of periodic structures
(ripples) with different periodicities as well as the formation of resolidified material and holes at the centre of the ablated
crater at high fluences. The debris produced during ablation consists of crystalline C263 oxidized nanoparticles with diameters
of ∼2–20 nm (for F=9.6 J/cm2). The mechanisms involved in femtosecond laser microprocessing of the superalloy C263 as well as in the synthesis of C263
nanoparticles are elucidated and discussed in terms of the properties of the material. 相似文献
78.
Jun Cheng P. Hu Peter Ellis Sam French Gordon Kelly C. Martin Lok 《Surface science》2009,603(17):2752-2758
Transition metals are often introduced to a catalyst as promoters to improve catalytic performance. In this work, we study the promotion effect of transition metals on Co, the preferred catalytic metal for Fischer–Tropsch synthesis because of its good compromise of activity, selectivity and stability, for ethylene chemisorption using density functional theory (DFT) calculations, aiming to provide some insight into improving the α-olefin selectivity. In order to obtain the general trend of influence on ethylene chemisorption, twelve transition metals (Zr, Mn, Re, Ru, Rh, Ir, Ni, Pd, Pt, Cu, Ag and Au) are calculated. We find that the late transition metals (e.g. Pd and Cu) can decrease ethylene chemisorption energy. These results suggest that the addition of the late transition metals may improve α-olefin selectivity. Electronic structure analyses (both charge density distributions and density of states) are also performed and the understanding of calculated results is presented. 相似文献
79.
Fourier Transform Infrared (FTIR) Spectroscopy has long been utilized as an analytical technique for qualitatively determining the presence of various different chemical bonds in gasses, liquids, solids, and on surfaces. Most recently, FTIR has been proven to be extremely useful for understanding the different types of bonding present in low dielectric constant “low-k” organosilicate materials. These low-k materials are predominantly utilized in the nanoelectronics industry as the interlayer dielectric material in advanced Cu interconnect structures. In this article, we utilize FTIR to perform a detailed analysis of the changes in chemical bonding that occur in Plasma Enhanced Chemically Vapor Deposited (PECVD) low-k a-SiC:H thin films. PECVD low-k a-SiC:H materials are equally important in advanced Cu interconnects and are utilized as both etch stop and Cu diffusion barrier layers. We specifically investigate the changes that occur in low-k a-SiC:H films as the dielectric constant and mass density of these films are decreased from > 7 to < 3 and from 2.5 to 1 g/cm3 respectively. We show that decreases in mass density and dielectric constant are accompanied by both an increase in terminal SiHx and CHx bonding and a decrease in SiC network bonding. At densities of 1.85 g/cm3, the concentration of terminal SiHx bonding peaks and subsequent hydrogen incorporation are achieved predominantly via terminal CH3 groups. Low-k a-SiC:H films with k < 3.5 and density < 1.3 g/cm3 can be achieved via incorporating larger organic phenyl groups but result in non-stoichiometric carbon rich films. Electron beam curing of these lower density a-SiC:H films results in volatilization of the phenyl groups leaving behind nanoporous regions and production of some CCC chain linkages in the network. 相似文献
80.