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31.
The modulation depth,defined according to practical mod-ulation results,which changes with the microwave power and its fre-quency,is significant for systems utilizing the frequency-shift charac-teristic of the LiNbO3 waveguide Electro-Optic Intensity Modulator (EOIM).By analyzing the impedance mismatch between the micro-wave source and the EOIM,the effective voltage applied to the RF port of the EOIM is deprived frcm the microwave power and its fre-quency.Associating with analyses of the phase velocity mismatch be-tween the microwave and the optical wave,the theoretical modulation depth has been obtained,which is verified by experimental results.We provide a method to choose the appropriate modulation depth to optimize the desired sideband through proper transmission bias far the system based an the frequency-shift characteristic of the EOIM. 相似文献
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采用双坩埚提拉法(DCCZ)生长了各种不同成分的近化学计量比LiNbO3晶体, 并用腐蚀法观察了其电畴结构. 结果表明, 化学成分对未经极化处理晶体的电畴结构起决定性作用, 当Li2O 含量处于49.4mol%附近时, 晶体z面电畴呈现特殊的三次对称反畴; 当晶体中Li2O含量为49.7mol%时, 晶体为完全单畴. 本文对其形成机理进行了探讨, 认为在由顺电相向铁电相转变 时, 局部铁电畴的极性方向与该处沿z轴方向的温度梯度正负密切相关, z轴生长晶体时, 由于相变发生所处位置离生长界面的距离受LiNbO3晶体计量比影响, 所处温场固有温梯也 随之不同, 在此基础上解释了不同成分晶体的电畴结构形成原因. 最后讨论了控制铁电畴结构的工艺措施. 相似文献
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In:Ho:LiNbO3 crystals doped with various concentrations of In3+(0, 1 mol.%, 3 mol.%, 5 mol.%), fixed concentrations of Ho3+ (1 mol.%) were grown by Czochralski method. The X-ray powder diffraction, infrared and UV-visible absorption spectra were measured and modified. Judd-Ofelt approach was employed to study the effect of In doping on spectroscopic properties of Ho:LiNbO3 crystals. In concentrations in crystals were analyzed by an inductively coupled plasma optical emission spectrometry (ICP-OE/MS). For In (3 mol.%):Ho (1 mol.%):LiNbO3 crystal, the obtained intensity parameters were: Ω2=9.6563, Ω4=4.2195, Ω6=14.1526. The results showed that the Ω2 and Ω6 parameters increased with the increase of In3+ concentration. When the In doping concentration was up to 5 mol.%, Ω2 and Ω6 suddenly decreased. In2O3 incorporation had a strong effect on the radiative lifetime, but had less influence on fluorescence branching ratios. The effective distribution coefficient of In3+ in In:Ho:LiNbO3 crystals was less than 1 and increased with increasing concentration of In3+ in the melt. 相似文献
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高掺锌富锂铌酸锂体抗光损伤能力的研究 总被引:1,自引:0,他引:1
以Czochralski法生长Zn(6mol%):LiNbO3,Li/Nb=0.94,0.97,1,1.02。测试晶体的光损伤阈值。采用质子交换法制作高掺锌富锂铌酸锂晶体光波导,研究了它们的抗光损伤能力。 相似文献
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Gurpreet Singh Manish Kumar Manmohan Singh Rahul Vaish 《Journal of the American Ceramic Society》2021,104(3):1237-1246
LiNbO3 ceramic was fabricated using solid-state reaction route. Silver nanoparticles (NPs) were loaded on LiNbO3 at room temperature using silver nitrate and polyethylene glycol reagents, without the use of external heat and light energy. The X-ray diffraction showed only LiNbO3 phase in Ag-loaded LiNbO3 sample with no peak related to Ag metal due to small fraction of Ag loading. X-ray energy diffraction spectroscopy elemental color mapping confirmed the uniform loading of Ag metal on LiNbO3 particles. Ag metal was loaded in the form of NPs as visualized under transmission electron microscope. Ag NPs-loaded LiNbO3 showed enhanced absorption of visible light owing to the phenomenon of surface plasmon resonance (SPR). The loading of Ag NPs had no effect on the band gap energy of LiNbO3 ceramic. X-ray photoelectron spectroscopy technique confirmed the metallic chemical state of Ag in Ag NPs-loaded LiNbO3. Ag NPs-loaded LiNbO3 degraded 97% rhodamine-B model dye from the solution when irradiated for 240 minutes under visible light. The dye degradation follows pseudo-first-order kinetic having k-value (kinetic rate constant) of as 0.013 min−1. The •OH (hydroxyl) and (superoxide) radicals were the main active species behind the photocatalytic activity of Ag NPs-loaded LiNbO3. Thus, Ag NPs-loaded LiNbO3 could be a potential material for degrading organic dyes from water. 相似文献
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