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71.
72.
We report on the four-peak structure observed in the region of 4f photoemission in Yb metal, using synchrotron radiation in the energy range 70–200 eV. We conclude, contrary to previous reports, that the doublet associated with surface emissions results from an intrinsic surface shift on clean regions of the surface. We also demonstrate that the observed structure is consistent with earlier XPS measurements, and we set an upper limit on the width of the bulk peaks.  相似文献   
73.
This paper presents results of a study carried out in order to assess the applicability of 32Si for groundwater dating. Measurements of 32Si in soil samples of the unsaturated zone, of drainage waters and plant material give a basis for estimating the 32Si initial concentration in groundwater. Different aquifers with groundwater of young and moderate ages have been selected for groundwater studies. For obtaining independent age information tritium was found to be a suitable reference isotope. A quantitative interpretation of the 32Si data is generally complicated by geochemical processes, preferably in the unsaturated zone. Favourable conditions concerning the use of 32Si in hydrogeology seem to exist in phreatic sandy aquifers, in limestone aquifers, and, depending on the thickness and composition of the unsaturated zone, in sandstone aquifers. Further improvements of the 32Si method needs a better understanding of the geochemical processes affecting this isotope.  相似文献   
74.
A method for resolution enhancement of a.c. polarograms (voltammograms) is presented. The method is based on deconvolution using fast Fourier transforms. Overlapped a.c. polarograms are mathematically narrowed and sharpened, retaining the peak position and linear proportionality of the sharpened peak height with concentration. The advantages and limitations of the method are demonstrated on simulated and experimental a.c. polarograms. The same approach is applicable to related techniques such as. differential pulse and square-wave polarography.  相似文献   
75.
Titrimetric determinations of arenediazonium salts can be based on ion-pair formation between the diazonium cation and tetraphenylborate. Titrations are done under cooling with ice and are followed potentiometrically with organic ion-selective electrodes comprising PVC membranes plasticized with polar solvents and coated on aluminium wires. The method was tested in determinations of arenediazonium salts derived from 20 aromatic amines, including aniline, toluidines, naphthylamines and their derivatives. Except for compounds containing hydrophylic groups such as —COOH and —OH, the potentiometric titration curves have well defined end-points. The results are reproducible, with relative standard deviations in the range 0.4–1.4% at the millimolar level. The method can be used for reliable determinations of arenediazonium salts in analytical control of azo dyestuff production.  相似文献   
76.
The previously synthesised (1–37), (38–75), (76–93), (94–104), (105–117) and (118–129) fragments of the analogue were combined making extensive use of the DCCI/HONSu method. The final coupling involved the (1–75) and (76–129) sub-fragments. Aggregation of the latter fragment caused problems in purification by routine gel filtration methods employing Enzacryl K2 or Sephadex LH60. The fully protected (1–129) product was partially purified by washing, then deprotectcd and purified by gel filtration and ion exchange chromatography. Satisfactory removal of the acetamidomethyl group used for cysteine protection could not be achieved.  相似文献   
77.
基于CPLD工作模式可调的线阵CCD驱动电路设计   总被引:3,自引:1,他引:3  
针对传统驱动电路一旦做出修改,则需对硬件或程序进行改变的缺点,以型号为TCD1707D的线阵CCD为例,介绍了一种工作模式可调的驱动方法.该方法是利用复杂可编程逻辑器件和控制外端结合,通过分别设置内外触发来实现的.在外触发模式下,利用外触发脉冲,可由用户控制CCD的曝光和信号输出时间;内触发时,可以调节CCD的积分时间和驱动频率.为提高信号输出质量,针对EMC问题给出了线阵CCD的外围驱动电路.实验结果表明,该方法调试方便、电路结构简单、集成度较高、输出信号可靠稳定、受干扰小,可配合多种用户需要,对高速精确测量及线阵推扫模式具有一定参考价值.  相似文献   
78.
Deep levels in LPE GaAs were studied in relation to growth conditions. The residual deep levels in LPE layers are hole traps 0.50 and 0.65 eV above the top of the valence band. Their concentrations are of the order of 1013 cm-3 for growth temperatures between 650 and 840°C, and increase with increasing growth temperature. The activation energy of incorporation is about 0.7 eV, which is very close to that of an arsenic vacancy. It is also noted that their concentrations near the grown surface are independent of the growth temperature. This indicates that the hole traps undergo an annealing effect after the growth period. From the experimental results for Fe and oxygen doping, each impurity acts as a deep level only when it makes a complex defect with a gallium vacancy, otherwise they are shallow levels, The distribution coefficients at 750°C are 1 × 10-7 and 1.1 × 10-5 for the deep and Fe and the shallow acceptor, respectively.  相似文献   
79.
A ferric nitrate-promoted cross-dehydrogenative coupling reaction of N-hydroxyphthalimide (NHPI) with toluene derivatives is reported. The reaction proceeded smoothly using molecular oxygen as an oxidant, providing an efficient method for the synthesis of N-hydroxyimide esters. Furthermore, a plausible mechanism was proposed.  相似文献   
80.
Owing to high modularity and synthetic tunability, metal–organic frameworks (MOFs) on textiles are poised to contribute to the development of state-of-the-art wearable systems with multifunctional performance. While these composite materials have demonstrated promising functions in sensing, filtration, detoxification, and biomedicine, their applicability in multifunctional systems is only beginning to materialize. This review highlights the multifunctionality and versatility of MOF-integrated textile systems. It summarizes the operational goals of MOF@textile composites, encompassing sensing, filtration, detoxification, drug delivery, UV protection, and photocatalysis. Building upon these recent advances, this review concludes with an outlook on emerging opportunities for the diverse applications of MOF@textile systems in the realm of smart wearables.  相似文献   
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