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排序方式: 共有7329条查询结果,搜索用时 31 毫秒
41.
42.
T. D. Dzhafarov S. S. Yesilkaya N. Yilmaz Canli M. Caliskan 《Solar Energy Materials & Solar Cells》2005,85(3):371-383
The effective diffusion coefficients of Cu for thermal and photodiffusion in the CdTe films have been estimated from resistivity versus duration of thermal or photoannealing curves. In the temperature range 60–200°C the effective coefficient of thermal diffusion (Dt) and photodiffusion (Dph) are described as Dt=7.3×10−7exp(−0.33/kT) and Dph=4.7×10−8exp(−0.20/kT).It is found that the diffusion doping of CdTe thin films by Cu at 400°C results in a sharp decrease of resistivity up to 7 orders of magnitude of p-type material, depending on thickness of Cu film. The comparative study of performance of CdTe(Cu)/CdS and CdTe/CdS cells has been studied. It is shown that the diffusion doping of CdTe film by Cu increases efficiency of CdTe(Cu)/CdS cells from 0.9% to 6.8%. The degradation of photovoltaic parameters of CdTe(Cu)/CdS cell, during testing under forward and reverse bias at room temperature, proceeds at a larger rate than those of CdTe/CdS cell without Cu. The degradation of performance of CdTe(Cu)/CdS cells is tentatively assigned to electrodiffusion of Cu in CdTe, resulting in redistribution of concentration of Cu-related centers in CdTe film and heterojunction region. 相似文献
43.
分析了钼精矿Cu、Pb含量高的主要原因 ,通过实施一系列措施 ,达到了降低钼精矿中Cu、Pb含量的目的 相似文献
44.
Benedetto Bozzini Bertrand Busson Claudio Mele Abderrahmane Tadjeddine 《Journal of Applied Electrochemistry》2008,38(7):897-906
We report on potential-dependent in situ SFG and DFG spectroscopy carried out at Au(111), Au(210), polycrystalline Au, Au–Cu
and Au–Ag–Cu electrodes in contact with aqueous solutions containing CN− and 4-cyanopyridine (4CP). Spectroelectrochemical work was complemented by cyclic voltammetry. The chief stress has been
placed on systematising and quantifying the interaction between 4CP and CN− and the attending effects on the vibrational and electronic structures of the interface. The voltammetric behaviour of the
investigated electrodes, modified by the addition of 4CP to the CN− electrolyte, denote changes in the CN− adsorption characteristics and effects of the adsorbed CN− layer on the electrodic reactivity of 4CP. The differences among the investigated electrodes can be explained in terms of
their respective degrees of atomic packing or with alloying effects on the stability of adsorbed CN−. The potential-dependent spectra have been analysed quantitatively with a model for the second order non linear susceptibility
accounting for vibrational and electronic effects. The spectral changes induced by addition of 4CP denote interaction of the
aromatic with the electrode through the CN− monolayer. The non-resonant contribution yields information on the effects of 4CP on the fine structure of the bound electron
density of states. 相似文献
45.
Gerda C. Glaeser 《Thin solid films》2007,515(15):5964-5967
Fluorescent photon down conversion for the improvement of the blue response of ZnO/CdS/Cu(In,Ga)Se2 heterojunction solar cells and modules is investigated. Fluorescent dyes of the series Lumogen® F are analyzed by optical transmission and reflection as well as by photoluminescence measurements. A spectral transfer matrix formalism is introduced that allows to predict the suitability of a luminescent dye as a down-converter for a given solar cell from its absorption/emission properties. We find that Lumogen® F Violet 570 and Lumogen® F Yellow 083 as well as a combination of both yields improvements for Cu(In,Ga)Se2 solar modules. Particularly, we find that the short circuit current density of a Cu(In,Ga)Se2 mini-module is improved by 1.5 mA cm− 2 when applying a varnish with a combination of Lumogen® F Violet and Yellow. About 0.5 mA cm− 2 of this improvement is due to a reduced overall reflectance and an improvement of 1 mA cm− 2 results from the frequency conversion by the dyes. 相似文献
46.
The reversible persistent changes of the fill factor (FF) induced by the illumination and voltage bias along with changes in the electronic properties of the ZnO/CdS/Cu(In,Ga)Se2 photovoltaic devices have been studied. Admittance spectroscopy and capacitance–voltage characterization reveal a correlation between the FF and the space charge distribution within the absorber. Our experiments provide evidence that a major source of FF loss in efficient devices is caused by excess negative charge close to the interface. We explain the persistent changes in the net acceptor concentration in the interface region by the relaxation effects due to compensating donors—the same mechanism, which leads to metastable changes of the doping level in the bulk of the absorber. 相似文献
47.
研究了添加微量锡对铜基摩擦的摩擦性能的影响。结果表明,微量锡对摩擦系数无显著影响,但对磨损有显著影响,当锡含量为0.50%时,摩擦材料及对偶材料的磨损都较小。 相似文献
48.
Chaosuan Kanchanomai Yukio Miyashita Yoshiharu Mutoh 《Journal of Electronic Materials》2002,31(5):456-465
Low-cycle fatigue (LCF) tests on as-cast Sn-3.5Ag, Sn-3Ag-0.5Cu, Sn-3Ag-0.5Cu-1Bi, and Sn-3Ag-0.5Cu-3Bi solders was carried
out using a noncontact strain-controlled system at 20°C with a constant frequency of 0.1 Hz. The addition of Cu does not significantly
affect the fatigue life of eutectic Sn-Ag solder. However, the fatigue life was significantly reduced with the addition of
Bi. The LCF behavior of all solders followed the Coffin-Manson relationship. The fatigue life of the present solders is dominated
by the fracture ductility and can be described by the ductility-modified Coffin-Manson’s relationship. Steps at the boundaries
of dendrite phases were the initiation sites for microcracks for Sn-3.5Ag, Sn-3Ag-0.5Cu, and Sn-3Ag-0.5Cu-1Bi solders, while
for Sn-3Ag-0.5Cu-3Bi solder, cracks initiated along both the dendrite boundaries and subgrain boundaries in the dendrite phases.
The linking of these cracks and the propagation of cracks inside the specimen occurred both transgranularly through eutectic
phases and intergranularly along dendrite boundaries or subgrain boundaries. 相似文献
49.
通过对AlSn20Cu/Steel双金属板(带)复合轧制过程变形区变形规律的分析,确定了轧制过程的总变形率与各分层变形率的关系,解决了实际生产中各分层原料的厚度匹配问题。 相似文献
50.
《Calphad》2021
Sb2S3 and CuSbS2 have been proposed as alternative earth-abundant absorber materials for thin-film solar cells. However, no thermodynamic study of the S−Sb binary system and the Cu−S−Sb ternary system were investigated. In this paper, The S−Sb system and the Cu−S−Sb system are calculated utilizing the so-called CALPHAD (CALculation of PHAse Diagrams) technique. Using TEM-EDS and XRD, Cu0.9Sb1S2 is experimentally confirmed at the Cu1Sb1S2 and Sb2S3 two-phases region in the isothermal section at 673 K of the Cu−S−Sb ternary system. Given the asymmetric shape and miscibility gap of the liquidus in the S−Sb phase diagram, the associate solution model for the liquid phase is adopted. The solution phases (liquid, bcc, fcc) are treated with the Redlich–Kister equation. The compounds S3Sb2, Cu3SbS3, Cu12Sb4S13, CuSbS2, and Cu3SbS4 are described as a stoichiometric compound. A set of self-consistent thermodynamic parameters of the S−Sb binary system and the Cu−S−Sb ternary system are obtained. The calculated results are in good agreement with the experimental data. This study provides a set of reliable thermodynamic parameters to the Cu−Sb−S thermodynamic database, and a cost-effective tool to design material synthesis experiments and manufacturing processes. 相似文献