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41.
掺纳米Al2O3的纳米ZrO2(4Y)固体电解质的电性能 总被引:8,自引:1,他引:8
以纳米ZrO2(4Y)粉和纳米Al2O3粉为原料, 单轴成型, 1 200, 1 300 ℃无压烧结. 对掺不同质量分数(0.0~5.0%)Al2O3的ZrO2(4Y)烧结体, 用XRD, SEM和TEM研究了相组成和微观结构. 在不同温度下(300~1 000 ℃)测试了交流阻抗谱, 发现掺很少量的纳米Al2O3可降低ZrO2(4Y)的晶粒电阻. 但随着Al2O3掺入量的增加, 晶界电阻增大, 晶粒电阻也有所回升. 晶粒和晶界电导活化能则随Al2O3掺入量的变化不大. 对1 200 ℃,2 h烧结样品, 在1 000 ℃时, 掺0.5% Al2O3的ZrO2(4Y)样品有最大电导率, 为3.8×10-2Ω-1·cm-1. 相似文献
42.
In the process of Li+ intercalation-deintercalation, electron removal is accompanied simultaneously. Oxygen was found to compensate electron removal both in theoretical calculations and practical experiments. Chlorine addition to LiNi0.7Co0.3O2 was expected to exchange electrons in that Cl− was easier to lose electrons than O2−. LiNi0.7Co0.3O2−xClx was identified as a pure hexagonal lattice of α-NaFeO2 type by X-ray diffraction. X-ray photoelectron spectroscopy was used to analyze the influence of chlorine substitution on the oxidation state of transition-metal ions. Charge-discharge experiments and cyclic voltammetry confirmed that chlorine addition was an effective way to improve reversible capacity and structural stability in cycles. 相似文献
43.
The catalytic activities of WCI6Ph4Sn, MoCl5Ph4Sn and tetrabenzyltitanium were examined in the polymerization of acetylene. The structure, morphology and electrical conductivity of the doped and non doped polyacetylene were also studied. 相似文献
44.
Xiaohong Wang Guanzhong Lu Yun Guo Yuye Xue Liangzhu Jiang Yanglong Guo Zhigang Zhang 《Catalysis Today》2007,126(3-4):412-419
The Si-doped Ce–Zr–O solid solutions have been prepared by the reverse microemulsion method. The effects of Si and its content on the structure characters, thermal-stability and reducibility of the Ce–Zr–O solid solution have been studied by N2 adsorption, XRD, laser Raman (LR), TPR, FT-IR, NMR and XPS methods. The results indicate that, there are the bonds of Si–O–M (Ce or Zr) in the Ce–Zr–Si–O solid solutions, and the presence of Si can increase obviously the surface area, thermal-stability, crystal lattice distortion rate, and reducibility of the solid solution. The surface area of the sample with 20 wt.% Si reaches 153 m2 g−1 after being calcined at 900 °C for 6 h. The Ce–Zr–O solid solution with 5.2–10 wt.% Si shows excellent thermal-stability and reducibility. 相似文献
45.
基于分级型模数转换器AD7884对分离脱落电连接器的分离力进行测量,采用8位单片机W77E58与之接口,进行数据处理并通过485串口传输到上位机。实现了对分离脱落电连接器的分离力进行测量,系统运行稳定,且与上位机数据交互简单、可靠。 相似文献
46.
47.
The PbO2 and F−-doped PbO2 (F-PbO2) film electrodes have been prepared by an electrodeposition process onto platinum substrate. The changes of their electrochemical activity for oxygen evolution (OE) reaction with accelerated electrolysis time have been studied. The results show that the activity of the electrodes decreases with increasing electrolysis time. This can be attributed to the conductivity variations, which are caused by the decrease of the oxygen vacancy concentration in PbO2 films during OE. The mechanism of the decrease of the oxygen vacancies has been investigated. For F-PbO2 film electrodes, though its electrochemical activity is somewhat lower than that of undoped one, its activity stability is much higher in comparison with that of PbO2. The influence of F− doping on the activity of PbO2 film electrodes has been also discussed. 相似文献
48.
Effect of Acceptor and Donor Dopants on the Dielectric and Tunable Properties of Barium Strontium Titanate 总被引:1,自引:0,他引:1
Xiaofeng Liang Zhongyan Meng Wenbiao Wu 《Journal of the American Ceramic Society》2004,87(12):2218-2222
The effects of different concentrations of Mn2+ , Mg2+ , Al3+ , Fe3+ , La3+ , and Nb5+ on the dielectric and tunable properties of Ba0.6 Sr0.4 TiO3 ceramics were investigated. It was found that doping in small amounts with acceptor ions such as Mg2+ , Fe3+ , and Al3+ could meliorate the dielectric properties clearly. Decrease of dielectric loss was attributed to the formation of compensating defects originating from acceptor substitution. It was concluded that the tunability was linked to both the dielectric constant and the grain size. A higher figure of merit was obtained by doping the ceramics with smaller ions of Al and Fe, compared to Ti. 相似文献
49.
掺Tb3+钛酸铅粉末的制备和结晶行为 总被引:1,自引:0,他引:1
采用溶胶喂胶法制备了Tb^3 掺杂钛酸铅(PbTiO3,PT)超细粉末,分别用差热分析、透射电子显微镜、X射线衍射仪对其相结构、形貌特性以及晶粒粒径等进行了分析测试。结果表明:这种粉末在约600℃热处理温度下,由非晶基体转变形成钙钛矿相的过程已逐步完成,其晶粒平均尺寸约为18nm,比未掺Tb抖的PT粉末中的钙钛矿晶粒尺寸略小。形成的钙钛矿结构中,Tb^3 取代Pb^2 进入晶格位置,产生阳离子空位,诱发晶格畸变,使钙钛矿相的析晶能力比相同热处理条件下未掺杂Tb^3 的PT低。另外,掺Tb^2 的PT中钙钛矿相的晶轴比c/a比未掺Tb^3 的PT中的低,这类似于产生了赝立方结构,降低了从立方相向这种四方相转化的势垒,有效地抑制了较高温下焦绿石相的产生,使掺Tb^3 的PT中焦绿石相稳定存在的温度比未掺Tb^3 的PT中低约100℃。 相似文献
50.
Deyu Wang 《Electrochimica acta》2005,50(14):2955-2958
LiFePO4 doped by bivalent cation in Fe-sites show improved rate performance and cyclic stability. Under 10 C rate at room temperature, the capacities of LiFe0.9M0.1PO4 (M = Ni, Co, Mg) maintain at 81.7, 90.4 and 88.7 mAh/g, respectively, in comparison with 53.7 mAh/g for undoped LiFePO4 and 54.8 mAh/g for carbon-coated LiFePO4 (LiFePO4/C). The capacity retention is 95% after 100 cycles for doped samples while this value is only 70% for LiFePO4 and LiFePO4/C. Such a significant improvement in electrochemical performance should be partially related to the enhanced electronic conductivities (from 2.2 × 10−9 to <2.5 × 10−7 S cm−1) and probably the mobility of Li+ ions in the doped samples. 相似文献