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21.
Observed first in Wilson's pioneering experiments in the cloud chamber, the sign preference has remained a mystery for more than a century. We investigate the sign preference using a quantum approach and show that this puzzling phenomenon is essentially quantum in nature. It is shown that the effect of the chemical identity of the core ion is controlled by the electronic structure of the core ion through the influence on the intermolecular bonding energies during the initial steps of cluster formation. Our results demonstrate the superiority of the quantum approach and indicate fundamental problems of conventional ion-induced nucleation theories, in which the electronic structure of the core ion is either ignored or not treated rigorously. 相似文献
22.
Christina Kjær Dr. Henriette Lissau Nina Katharina Gravesen Salinas Andreas Østergaard Madsen Dr. Mark H. Stockett Freja E. Storm Thomas Holm Hansen Prof. Jens Ulrik Andersen Prof. Bo W. Laursen Prof. Kurt V. Mikkelsen Prof. Mogens Brøndsted Nielsen Prof. Steen Brøndsted Nielsen 《Chemphyschem》2019,20(4):533-537
Being alone or together makes a difference for the photophysics of dyes but for ionic dyes it is difficult to quantify the interactions due to solvent screening and nearby counter ions. Gas-phase luminescence experiments are desirable and now possible based on recent developments in mass spectrometry. Here we present results on tailor-made rhodamine homodimers where two dye cations are separated by methylene linkers, (CH2)n. In solution the fluorescence is almost identical to that from the monomer whereas the emission from bare cation dimers redshifts with decreasing n. In the absence of screening, the electric field from the charge on one dye is strong enough to polarize the other dye, both in the ground state and in the excited state. An electrostatic model based on symmetric dye responses (equal induced-dipole moments in ground state) captures the underlying physics and demonstrates interaction even at large distances. Our results have possible implications for gas-phase Förster Resonance Energy Transfer. 相似文献
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Strain gauges are used together with the corresponding gauge factor to relate the relative electrical resistance change of the strain gauge with the strain of the underlying material. The gauge factor is found from a calibration on a stiff material - steel. Nevertheless, the gauge factor depends on the stiffness of the calibration material and ideally the calibration should be done on a similar material as tested. In practice, the gauge factor found by the strain gauge manufacturer is often used. The paper documents that even for moderately stiff materials such as glass-fibre composites a significant error is found on the strain measurements obtained by the strain gauges. This is documented both experimentally and numerically. A stiffness, also test sample and strain gauge geometry dependent correction coefficient of the gauge factor is proposed. A correction coefficient covers material stiffnesses ranging from 1 GPa to 200 GPa. 相似文献
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All-silica nanofluidic devices for DNA-analysis fabricated by imprint of sol-gel silica with silicon stamp 总被引:1,自引:0,他引:1
Mikkelsen MB Letailleur AA Søndergård E Barthel E Teisseire J Marie R Kristensen A 《Lab on a chip》2012,12(2):262-267
We present a simple and cheap method for fabrication of silica nanofluidic devices for single-molecule studies. By imprinting sol-gel materials with a multi-level stamp comprising micro- and nanofeatures, channels of different depth are produced in a single process step. Calcination of the imprinted hybrid sol-gel material produces purely inorganic silica, which has very low autofluorescence and can be fusion bonded to a glass lid. Compared to top-down processing of fused silica or silicon substrates, imprint of sol-gel silica enables fabrication of high-quality nanofluidic devices without expensive high-vacuum lithography and etching techniques. The applicability of the fabricated device for single-molecule studies is demonstrated by measuring the extension of DNA molecules of different lengths confined in the nanochannels. 相似文献
27.
We use hydrofluoric acid microdroplets to directly etch highly birefringent biconical fiber tapers from standard single-mode fibers. The fiber tapers have micrometer-sized cross sections, which are controlled by the etching condition. The characteristic teardrop cross section leads to a high group birefringence of B(G)≈0.017 and insertion losses <0.7 dB over waist lengths of about 2.1 mm. 相似文献
28.
A. Resta J. Blomquist J. Gustafson H. Karhu A. Mikkelsen E. Lundgren P. Uvdal J.N. Andersen 《Surface science》2006,600(24):5136-5141
The catalytic cracking of ethanol on clean and oxygen precovered Rh(1 1 1) surfaces has been studied by a combination of synchrotron based high-resolution core level spectroscopy and surface infrared spectroscopy. On the clean surface the decomposition of ethanol occurs without any formation of atomic oxygen. The presence of oxygen on the surface changes the reactivity significantly and acetate (CH3COO) was identified as an important surface intermediate in the ethanol oxidation. 相似文献
29.
The delay of the onset of localization and the post-necking behaviour for stretched thin sheets are determined by three-dimensional effects. Thus, a 2-D finite element analysis based on a local plasticity theory will give a physically unrealistic mesh dependent solution. This, in spite of the fact that the stress state, is essentially two-dimensional. By incorporating a length scale with relation to the thickness of the sheet, it is demonstrated how a 2-D finite element analysis based on a gradient dependent plasticity theory can give a good approximation of the post-necking behaviour. This is illustrated by numerical comparison of results from a full 3-D finite element analysis, with results from a 2-D finite element model based on a finite strain version of a gradient dependent J2-flow theory. Some numerical problems in the modeling will be discussed briefly. 相似文献
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