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51.
太阳红外光谱中蕴含着丰富的物理信息,其中CO 4.6μm波段是具有代表性的分子谱带,其形成于温度极小区附近,对研究太阳物理具有极其重要的意义。为获得CO 4.6μm波段太阳单色像,本文建立了一套全反射太阳红外成像观测系统。该系统采用定天镜跟踪引光,通过成像反射镜将太阳成像于3~5μm波段红外相机的焦平面上,该相机采用的是国产HgCdTe焦平面阵列器件。同时,为提高信噪比,提出了一种有效计算平场提取观测目标的方法,并利用该方法获得了CO 4.6μm波段的太阳单色像。  相似文献   
52.
A sol–gel method for the synthesis of nanosized powders of yttrium disilicate doped with Tb3 + is presented. The influence of grain size and annealing temperature on the structure and luminescence properties of the materials obtained has been investigated. The preparation of glass-ceramic composite has been also described. The effect of incorporating the nanocrystals into sol–gel silica glasses on their physicochemical properties has been shown and discussed. A lack of influence of the annealing above 1300°C on the lifetimes measured for the nanocrystals embedded in the glass, as compared to the Y2Si2O7:Tb3 + powders, has been observed.  相似文献   
53.
用两种方法合成长余辉发光玻璃的对比研究   总被引:5,自引:0,他引:5  
在还原性气氛下高温固相反应法(一步法)合成了长余辉发光玻璃GA;用SrAl2O4:Eu,Dy荧光粉(SAED)与玻璃粉混合高温熔融(二步法)合成了长余辉发光玻璃GB和GC,通过XRD,发光光谱和磷光衰减曲线对样品进行了表征,荧光粉SAED和玻璃GA,GB,GC的发射峰值依次是525,493。462,516nm,发光强度和余辉时间都是SAED>GC>GB>GA,玻璃的发射光谱峰随玻璃组成不同发生位移,两种发生合成的夜光玻璃发光性质存在明显的差异,同一合成方法下,玻璃基料决定着玻璃网络结构,同时也影响着夜光玻璃的发光性质。  相似文献   
54.
By using (1R,2R)-1,2-diphenylethylenediamine as a chiral molecule and 2-anthracenecarboxylic acid as a fluorescent molecule, we created a chiral supramolecular organic fluorophore having circularly polarized luminescence properties in the solid-state.  相似文献   
55.
A 2D coordination compound {[Cu2(HL)(N3)]?ClO4} ( 1 ; H3L=2,6‐bis(hydroxyethyliminoethyl)‐4‐methyl phenol) was synthesized and characterized by single‐crystal X‐ray diffraction to be a polymer in the crystalline state. Each [Cu2(HL)(N3)]+ species is connected to its adjacent unit by a bridging alkoxide oxygen atom of the ligand to form a helical propagation along the crystallographic a axis. The adjacent helical frameworks are connected by a ligand alcoholic oxygen atom along the crystallographic b axis to produce pleated 2D sheets. In solution, 1 dissociates into [Cu2(HL)2(H3L)]?2H2O ( 2 ); the monomer displays high selectivity for Zn2+ and can be used in HEPES buffer (pH 7.4) as a zinc ion selective luminescent probe for biological application. The system shows a nearly 19‐fold Zn2+‐selective chelation‐enhanced fluorescence response in the working buffer. Application of 2 to cultured living cells (B16F10 mouse melanoma and A375 human melanoma) and rat hippocampal slices was also studied by fluorescence microscopy.  相似文献   
56.
It was recently found that typical Chromatographic carrier gases such as argon or nitrogen could be used in a modified flame photometric detector for general or selective determination of eluted molecules. The detector was powered not by a flame but by a radioactively stimulated, mild discharge. The luminescence arose from the second positive system of nitrogen (in argon), and various emissions from aroyl-containing molecules (in nitrogen).This study describes experiments that take away not only the flame but also the discharge: The energy that produces the luminescence is derived solely from the beta decay of63Ni. Because of this low power input, the sensitivity of the present beta-driven photometric detector (-PD) is limited to about 25 ppm of nitrogen (in argon), and to about 5 pg/s for benzaldehyde and other well-responding aroyl compounds (in nitrogen). In accordance with mechanisms postulated earlier, other types of molecules do not produce significant responses in the absence of an electrical field.Material taken from doctoral thesis  相似文献   
57.
Summary This review highlights recent advances in the use of quantum dots (QD’s) as luminescent sensors. The bulk of the study concentrates on systems that possess organic ligands bound to the surface of QD’s. These ligands vary from low molecular weight thiols to larger molecules such as maltose binding protein. All have one thing in common: when a target analyte binds to the ligand/receptor, a perturbation of the system occurs, that registers itself as a change in the luminescence intensity of the QD. Two main mechanisms are prevalent in controlling the luminescent intensity in such systems. The first is Photoinduced Electron Transfer (PET) and the second energy transfer. This review looks at current sensors that operate by using these mechanisms. Two component systems are also investigated where a quencher is first added to a solution of the QD, followed by addition of the target analyte that interacts with the quencher to influence the luminescence intensity.  相似文献   
58.
Lutetium(III) forms an association compound with a new synthetic reagent, 1,6-bi(1-phenyl-3-methyl-5-pyrazolone-4)hexandione (BPMPHD), and cetyltrimethylammonium bromide (CTMAB). The compound enhances the natural fluorescence of BPMPHD remarkably, upon which a new fluorescence method was developed for determining lutetium in rare earth (RE) samples. The determination range was 1.80 × 10–7–8.8 × 10–6 g/ml. The determination limit was 29 ng/ml. The composition of the ion associate was [Lu(BPMPHD)2]–CTMAB+.  相似文献   
59.
Uniform and sphere-like nanoparticles of crystalline Pr3+-doped CaTiO3 have been prepared from complex polymer precursor at 600°C, in which, metal atoms are previously dispersed by citric acid in ethylene glycol solvent. The decomposition process of the precursor, crystallization, and particle sizes of CaTiO3 have been investigated by using thermal analysis, powder X-ray diffraction and transmission electron microscopy. Diffuse reflectance spectra, photoluminescence and decay curve indicate that a strong red emission located at the nearly NTCS “ideal red” site is deduced from the energy transfer from the band gap absorption to doping Pr3+ ions. The thermoluminescence curves exhibit that a potential long phosphorescent material based on Pr3+-doped CaTiO3 will be explored in future.  相似文献   
60.
针对以往电子俘获光存储材料存在的问题,利用高温固相反应发制备了一种Eu^2 掺杂的氟氧化物玻璃陶瓷,研究表明在该材料中具有光激励发光(PSL)特性,并可用于电子俘获光存储。XRD分析表明该材料含有大量的BaF2微晶。根据其与BaF2相似的发光特性,推断玻璃陶瓷的PSL有可能来源于微晶中Eu^2 的5d-4f发射。但是决定光激励发光过程中的电子(空穴)陷阱的存在方式、电子迁移途径都有待进一步探讨的问题。与传统的BaFCl:Eu相比,这种材料的光激励发光衰减速度较慢。  相似文献   
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