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61.
从理论上探讨了磁阻率效应,叙述了精密角位移传感器的工作原理及结构设计。传感器的分辨率已达0.01°,通过可靠性寿命试验,传感器的失效率λ(t)<1×10-7/h。 相似文献
62.
介绍了一种数字式全定制音乐集成电路设计原理。对伪音阶发生器、节拍发生器等子电路作了较详细的叙述。采用这种原理可设计出单芯片驱动压电陶瓷和发光二极管的音乐集成电路,该电路无须外接电阻、电容,可存储数首歌曲;另外,还可设计出一种数字音频程控频率合成器,时钟为f0时,可控频率范围为f02~f02N。 相似文献
63.
64.
Lightpath (wavelength) routing in large WDM networks 总被引:11,自引:0,他引:11
Chlamtac I. Farago A. Tao Zhang 《Selected Areas in Communications, IEEE Journal on》1996,14(5):909-913
We address the problem of efficient circuit switching in wide area optical networks. The solution provided is based on finding optimal routes for lightpaths and the new concept of semilightpaths. A lightpath is a fully optical transmission path, while a semilightpath is a transmission path constructed by chaining together several lightpaths, using wavelength conversion at their junctions. A fast and practical algorithm is presented to optimally route lightpaths and semilightpaths taking into account both the cost of using the wavelengths on links and the cost of wavelength conversion. We prove that the running time of the algorithm is the best possible in the wide class of algorithms allowing linear algebraic operations on weights. This class encompasses all known related practical methods. Additionally, our method works for any physical realization of wavelength conversion, independently whether it is done via optoelectronic conversion or in a fully optical way 相似文献
65.
To incorporate an acceptor type polythiophene segment onto a supramolecular block copolymer for potential light harvesting applications, effective synthetic routes for the end‐functionalized and acceptor‐substituted polythiophenes are critical. The Ullmann coupling reaction can be utilized to obtain electron‐deficient polythiophenes and to attach terminal thiophene units that carry functional groups. In this article, the reactions involving a 2,5‐dibromothiophene monomer containing an electron‐withdrawing fluorinated ester and 5‐bromo‐2‐thiophenecarboxaldehyde (the end‐capper) were studied in detail. It was found that the Ullmann coupling reaction of the dibromide is very fast (completed in a few minutes) and the terminal bromine group does not survive long under the reaction condition. These findings lead to the development of an effective procedure for aldehyde end‐capping of electron‐deficient polythiophenes. Polymers with molecular weights around 4000 Da are routinely obtained. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 41–47, 2007 相似文献
66.
Jing Zhang Dan Shan Shaolin Mu 《Journal of polymer science. Part A, Polymer chemistry》2007,45(23):5573-5582
A copolymer, poly(aniline‐co‐o‐aminophenol), was prepared chemically by using ammonium peroxydisulfate as an oxidant. The monomer concentration ratio of o‐aminophenol to aniline strongly influences the copolymerization rate and properties of the copolymer. The optimum composition of a mixture for the chemical copolymerization consisted of 0.3 M aniline, 0.021 M o‐aminophenol, 0.42 M ammonium peroxydisulfate, and 2 M H2SO4. The result of cyclic voltammograms in a potential region of ?0.20 to 0.80 V (vs.SCE) indicates that the electrochemical activity of the copolymer prepared under the optimum condition is similar to that of polyaniline in more acid solutions. However, the copolymer still holds the good electrochemical activity until pH 11.0. Therefore, the pH dependence of the electrochemical property of the copolymer is improved, compared with poly(aniline‐co‐o‐aminophenol) prepared electrochemically, and is much better than that of polyaniline. The spectra of IR and 1H NMR confirm that o‐aminophenol units are included in the copolymer chain, which play a key role in extending the usable pH region of the copolymer. The visible spectra of the copolymers show that a high concentration ratio of o‐aminophenol to aniline in a mixture inhibits the chain growth. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 5573–5582, 2007 相似文献
67.
An improvement has been made to couple isoelectric focusing (IEF) sample injection and capillary zone electrophoresis in an untreated fused silica capillary. Electroosmotic flow is efficiently prevented by simply using a rubber block at the outlet end of the capillary during IEF sample injection. The experimental conditions that affect the concentration effect are discussed. A concentration enhancement factor of over 100-fold can be easily obtained for two model proteins: lysozyme and ribonuclease A. 相似文献
68.
本文对激光结晶a-Si∶H SOI结构砷注入和快速退火行为作了研究.a-Si∶H激光结晶有Lp-LCR,OD,FCR-2,FCR-1四个结晶区.用剖面电镜观察了结晶区的结构.扩展电阻测量表明Lp-LCR区中有两种扩散机制,即杂质在晶粒体内扩散和沿缺陷扩散.OD区中有三种扩散形式,除有上述两种以外,还有沿缺陷的扩散.首次比较了沿晶界和缺陷的扩散速度. 相似文献
69.
Koch B. Hidayat A. Hongbin Zhang Mirvoda V. Lichtinger M. Sandel D. Noe R. 《Photonics Technology Letters, IEEE》2008,20(12):961-963
We demonstrate endless polarization stabilization with a control speed of up to 9 krad/s, over random Poincare sphere trajectories. These are in total >35 Mrad long, are composed in particular of difficult-to-track circles with all radii and orientations, and thereby include all possible worst cases. The maximum polarization mismatch and relative intensity errors are 0.13 rad and 0.43%, respectively. The controller runs on a field-programmable gate array and uses a commercial multistage LiNbO3 polarization transformer as the control device. 相似文献
70.
Zhong‐Zhen Yu Mingshu Yang Qingxin Zhang Chungui Zhao Yiu‐Wing Mai 《Journal of Polymer Science.Polymer Physics》2003,41(11):1234-1243
Nylon‐66 nanocomposites were prepared by melt‐compounding nylon‐66 with an alkyl ammonium surfactant pretreated montmorillonite (MMT). The thermal stability of the organic MMT powders was measured by thermogravimetric analysis. The decomposition of the surfactant on the MMT occurred from 200 to 500 °C. The low onset decomposition temperature of the organic MMT is one shortcoming when it is used to prepare polymer nanocomposites at high melt‐compounding temperatures. To provide greater property enhancement and better thermal stability of the polymer/MMT nanocomposites, it is necessary to develop MMT modified with more thermally stable surfactants. The dispersion and spatial distribution of the organic MMT layers in the nylon‐66 matrix were characterized by X‐ray diffraction. The organic MMT layers were exfoliated but not randomly dispersed in the nylon‐66 matrix. A model was proposed to describe the spatial distribution of the organic MMT layers in an injection‐molded rectangular bar of nylon‐66/organic MMT nanocomposites. Most organic MMT layers were oriented in the injection‐molding direction. Layers near the four surfaces of the bar were parallel to their corresponding surfaces; whereas those in the bulk differed from the near‐surface layers and rotated themselves about the injection‐molding direction. The influence of the spatial distribution of the organic MMT on crystallization of nylon‐66 was also investigated. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 1234–1243, 2003 相似文献