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The global-in-time existence of non-negative solutions to a parabolic strongly coupled system with mixed Dirichlet–Neumann boundary conditions is shown. The system describes the time evolution of the electron and hole densities in a semiconductor when electron-hole scattering is taken into account. The parabolic equations are coupled to the Poisson equation for the electrostatic potential. Written in the quasi-Fermi potential variables, the diffusion matrix of the parabolic system contains strong cross-diffusion terms and is only positive semi-definite such that the problem is formally of degenerate type. The existence proof is based on the study of a fully discretized version of the system, using a backward Euler scheme and a Galerkin method, on estimates for the free energy, and careful weak compactness arguments. 相似文献
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Ying Lin Zhi‐Kuan Chen Teng‐Ling Ye Yan‐Feng Dai Dong‐Ge Ma Zhun Ma Qin‐De Liu Yu Chen 《Journal of polymer science. Part A, Polymer chemistry》2010,48(2):292-301
A series of conjugated blue‐light‐emitting copolymers, PTC‐1 , PTC‐2 , and PTC‐3, comprised different ratios of electron‐withdrawing segments (spirobifluorene substituted with cyanophenyl groups) and electron‐donating segments (tricarbazole‐triphenylamines), has been synthesized. The structures of these polymers were characterized and their thermal, photophysical, electrochemical, and electroluminescence properties were measured. Incorporation of rigid spirobifluorene units into the copolymers led to blue‐shifted absorption peaks in dilute toluene solution. Cyclic voltammetric measurement indicated the bandgaps of the polymers were in the range of 2.77–2.94 eV. It was found that increasing cyanophenyl‐spirobifluorene content in the polymer backbone lowered both the HOMO and LUMO energy levels of the copolymers, which was beneficial for electron injection/transporting in the polymer layer of the device. OLED device evaluation indicated that all the polymers emitted sky blue to deep blue light when the pure polymers were used as the emissive layers in the devices with a configuration of ITO/PEDOT:PSS/polymers/CsF/Ca/Al. The devices have been optimized by doping 30 wt % PBD into the polymer layers. Among the doped devices, PTC‐2 showed the best performance with the turn‐on voltage of 3.0 V, maximum brightness of 7257 cd/m2, maximum current efficiency of 1.76 cd/A, and CIE coordinates of (0.15, 0.14). © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 292–301, 2010 相似文献
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Hiroya Kitahata Kiyoharu Tadanaga Tsutomu Minami Norifumi Fujimura Taichiro Ito 《Journal of Sol-Gel Science and Technology》2000,19(1-3):589-593
Hexagonal YMnO3 has a ferroelectric property with an optimal remanent polarization along the c-axis. The c-axis oriented YMnO3 thin films with a small leakage current were prepared by the sol-gel dipping method. The c-axis orientation of the films was promoted by the addition of diethanolamine to the Mn precursor solution. A heat treatment with multiple steps led to a dense film structure with fine grains. The dense structure resulted in the decrease of the leakage current. Furthermore, when the films were heat-treated in a vacuum, the leakage current became considerably small and the ferroelectricity of the YMnO3 thin films was observed even at room temperature. 相似文献
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We propose a quasi one-dimensional quantum ring-shaped model associated with Rashba spin-orbit (SO) interaction and Aharomov-Bohm flux to study a spin-dependent quantum transport. It is a possible candidate for spintronic current modulators. By tuning SO coupling strength and Fermi energy, we find there is a broad energy range of small vanishing spin transmission in the resonance and antiresonance interferences. More interestingly, the large on/off spin-resolved polarized conductance ratios are robust even in the presence of strong random on-site Anderson-type disorder in devices, which suggests a potential application in the real system. 相似文献
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Ch. Muller D. Deleruyelle R. Müller M. Thomas A. Demolliens Ch. Turquat S. Spiga 《Solid-state electronics》2011,56(1):168-174
The present paper deals with the bipolar resistive switching of memory elements based on metal-organic complex CuTCNQ (copper-7,7’,8,8’-tetracyanoquinodimethane) nanowires grown on a dedicated HfO2 oxide switching layer. Switching characteristics are explored either at millimeter scale on pad-size devices or at nanoscale by using conductive atomic force microscopy. Whatever the investigation scales, the basic memory characteristics appear to be controlled by copper ionic transport within a switching layer. This latter corresponds to either HfO2 layer in pad-size devices or nanogap formed at nanoscale between the atomic force microscopy conductive tip and CuTCNQ surface. Depending upon the observation scale, the switching layer (either HfO2 oxide or nanogap) acts as a matrix in which copper conductive bridges are formed and dissolved thanks to redox processes controlled in alternating applied bias voltages. 相似文献
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详细介绍了基于不同种类微纳光纤的光源、光耦合器、光开关和滤波器的结构、工作过程及性能参数,总结了基于微纳光纤的光纤通信器件的研究进展情况。指出微纳光纤器件的实用化是光纤通信器件的发展方向。 相似文献