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51.
This Letter reports on the acceleration of the rate of formation of the boron–oxygen defect in p‐type Czochralski silicon with illumination intensities in excess of 2.1 × 1017 photons/cm2/s. It is observed that increased light intensities greatly enhance the rate of defect formation, without increasing the saturation concentration of the defect. These results suggest a dependence of the defect formation rate upon the total majority carrier concentration. Finally, a method using temperatures up to 475 K and an illumination intensity of 1.68 × 1019 photons/cm2/s is shown to result in near‐complete defect formation within seconds. (© 2015 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim) 相似文献
52.
Uwe Gaitzsch Hansjörg KlaußStefan Roth Ludwig Schultz 《Journal of magnetism and magnetic materials》2012,324(4):430-433
A 5M Ni-Mn-Ga single crystal was investigated, supplied by Adaptamat Ltd, Finland. Especially low temperature magnetic actuation as well as cyclic tensile-compression tests revealed promising properties, which provide useful insights for training concepts in polycrystalline materials. Successive compressions lead to a significant reduction of the twinning stress by a factor of two. 相似文献
53.
R.B. Gangineni J.W. Kim K. NenkovL. Schultz 《Journal of magnetism and magnetic materials》2012,324(6):1153-1156
The spin-polarised transport in ferromagnetic polycrystalline La0.7(Sr,Ca)0.3MnO3 films on piezoelectric substrate has been investigated. The systematic study involved in finding the effect of in-situ strain on extrinsic electrical transport of various thick polycrystalline La0.7(Sr,Ca)0.3MnO3 thin films. The in-situ strain in the manganite polycrystalline thin film is achieved by applying an electric field to the piezoelectric substrate 0.72 Pb(Mg1/3Nb2/3)O3-0.28 PbTiO3 (PMN-PT). A reversible strain of about 0.11% is acquired with an application of 10 kV/cm to the piezoelectric substrate. A typical drop in resistance at low magnetic fields has been found in all the polycrystalline manganite films. The effect of reversible strain versus the resultant strain gauges was discussed in all the polycrystalline films. At low temperatures, the effect of strain on low-field magnetoresistance and high-field magnetoresistance was found to be negligible. Further, the results are compared with the transport in manganite films deposited on step edge junctions. 相似文献
54.
55.
A. Chaudhuri C. Andreoiu M. Brodeur T. Brunner U. Chowdhury S. Ettenauer A. T. Gallant A. Grossheim G. Gwinner R. Klawitter A. A. Kwiatkowski K. G. Leach A. Lennarz D. Lunney T. D. Macdonald R. Ringle B. E. Schultz V. V. Simon M. C. Simon J. Dilling 《Applied physics. B, Lasers and optics》2014,114(1-2):99-105
The introduction of Paul traps, in particular linear radio-frequency quadrupoles in the early 2000s, has revolutionized the use of ion traps for probing the properties of radioactive nuclides. It opened the path to trapping all available nuclides, independent of their chemical properties. We present an overview of direct mass measurements of short-lived nuclides using TITAN, a Penning trap mass spectrometer facility particularly suitable for precision measurements of ms-half-life nuclides. 相似文献
56.
Optimization of the irradiation power in chemical exchange dependent saturation transfer experiments
Sun PZ van Zijl PC Zhou J 《Journal of magnetic resonance (San Diego, Calif. : 1997)》2005,175(2):193-200
In chemical exchange dependent saturation transfer imaging experiments, exchangeable solute protons are saturated and the transfer of saturation to water is subsequently detected. When the applied irradiation power is comparable to the resonance frequency difference between the water protons and saturated solute protons, the proton transfer (PT) efficiency is reduced due to concomitant direct saturation effects. In this study, the PT process is modeled using a two-pool system. An empirical general proton transfer ratio (PTR) equation for arbitrary RF irradiation power is derived, and its optimal power to maximize the PTR is analyzed. The results are confirmed experimentally on 4.7 T using a poly-L-lysine solution. The theory provides a useful tool for optimizing the irradiation power of the PT sequences in the presence of direct saturation effects. 相似文献
57.
Dellago C Geissler PL Chandler D Hutter J Parrinello M 《Physical review letters》2002,89(19):199601; author reply 199602
58.
Tahmid I. Mizan Phillip E. Savage Robert M. Ziff 《Journal of computational chemistry》1996,17(15):1757-1770
This study investigates the differences between the predictions of various properties of rigid and flexible simple point charge water models at supercritical conditions. Molecular dynamics simulations were conducted for supercritical water in a temperature range of 773–1073 K and densities in the range 115–659 kg/m3. We present thermodynamic data, pair correlation functions, self-diffusivity, power spectra, dielectric constants, and variaous measures of hydrogen bonding at different state conditions. The flexible water model performs better in predicting the pressures along the supercritical isotherms simulated. Agreement between experimental and calculated dielectric constants is superior for the flexible water model, particularly at high densities. The flexible model exhibits a greater degree of hydrogen bonding and more persistent hydrogen bonds than does the rigid model. The structural features of supercritical water at high densities are identical for the two water models. At low densities, however, the flexible potential exhibits pair correlation functions with enhanced peaks. Inclusion of flexibility in the potential model does not result in a significant shift in the position of the rotational/librational peak in the power spectrum. The self-diffusivities obtained from the simulations are within the accuracy of the experimental values for both the rigid and flexible models. On balance the inclusion of flexibility improves agreement with the properties of real supercritical water while incurring little or no additional computational burden. © 1996 by John Wiley & Sons, Inc. 相似文献
59.
Andr Bnard Suresh G. Advani Jerold M. Schultz 《Journal of Polymer Science.Polymer Physics》1996,34(3):471-483
Solidification of semicrystalline materials often occurs in significantly undercooled melts. The crystal growth process in such melts is convoluted due to the fact that the interface between the solid and liquid domains of the microscopic crystals is at an unknown temperature. However, it is possible to let the temperature of this interface be unspecified and solve the problem with a semianalytical method if the growth velocity is prescribed. Solutions for the temperature profiles in both solid and liquid phases are presented in this work, along with the interface temperature, for phase change processes controlled by the kinetics of crystallization rather than diffusion processes, which is typical for polymers. The method is used for one-dimensional problems in cartesian, cylindrical, and spherical geometries that correspond to commonly found microstructures. It is found that the temperature of the interface is significantly below the equilibrium melting point and a quasi steady-state regime is reached rapidly. Comparison with the classical Neumann's solution shows that the temperature profiles are similar but the position of the interface differs considerably. © 1996 John Wiley & Sons, Inc. 相似文献
60.
Third-order nonlinear optical susceptibility, χ(3) of symmetrically octa-substituted metal-free phthalocyanine thin films measured by the third-harmonic generation technique are reported. The metal-free phthalocyanine has been found to show a χ(3) (−3ω; ω,ω, ω) value as large as 7.73×10−12 esu at 1.80 μm. The figure of merit, χ(3)/α, was estimated to be 4.17×1017 esu cm at 1.05 μm and 6.97×1016 esu cm at 1.65 μm. Both linear and third-order optical properties of liquid-crystalline metal-free phthalocyanines are discussed 相似文献