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31.
吕功煊  李振 《分子催化》2014,(4):351-358
在强碱性溶液中低电压低电流条件下在W基底上经阳极氧化得到致密WO3层,而后在酸性条件下在WO3表面经光辅助电化学还原沉积镍,所获得的复合电极具有优异的光电化学氧化水的活性和稳定性.SEM,EDX,XPS和TEM等表征表明复合电极中具有体心立方结构的W基底经阳极氧化形成了具有单斜结构的WO3层,表面修饰的镍物种以Ni(OH)2形式存在.光电化学实验表明WO3层对可见光具有良好的光响应,表面修饰镍后,光电氧化水的起始电位显著降低,电极的稳定性也得以提高.  相似文献   
32.
Bi-substituted yttrium iron garnet (Bi-YIG, Bi1.8Y1.2Fe5O12) nanoparticles were prepared by microwave-assisted co-precipitation as well as conventional co-precipitation using ammonia aqueous solution as precipitant. The nanoparticles were characterized by thermal gravity-differential thermal analysis, X-ray powder diffraction, transmission electron microscopy, dynamic light scattering and vibrating sample magnetometer, respectively. The Faraday rotation of Bi-YIG modified PMMA slices was also investigated. Results demonstrate that the Bi-YIG nanoparticles prepared by microwave-assisted co-precipitation show smaller particle size and higher Faraday rotation than those prepared by conventional co-precipitation.  相似文献   
33.
文章描述了荧光级氧化钇中痕量稀土铈的测定方法,在溴酸钾存在下,5摩尔/升HNO_3介质中,以P507萃取微量铈,然后有机相用硝酸、过氧化氢反萃取、再将水相浓缩定容,然后以电感耦合等离子体原子发射光谱法分析。同时用铈的离子选择电极以二次标准加入法作第二种手段分析。样品溶液以乙醇预去溶方式引入等离子体,测定下限为2微克/克,方法简单、快速、准确。离子选择电极法测定铈离子下限1×10~(-5)摩尔/升,回收率为94-101%,方法简单,结果满意、价格便宜。  相似文献   
34.
Thin films of molybdenum trioxide were deposited on glass substrates employing direct current (DC) magnetron sputtering by sputtering of molybdenum at different oxygen partial pressures in the range 8 × 10−5–1 × 10−3 mbar and at a substrate temperature of 473 K. The glow discharge characteristics of magnetron cathode target of molybdenum were studied. The influence of oxygen partial pressure on the structural and optical properties of molybdenum trioxide films was investigated. The films formed at an optimum oxygen partial pressure of 2 × 10−4 mbar were polycrystalline in nature with orthorhombic α- phase and an optical band gap of 3.16 eV. The refractive index of the films formed at an oxygen partial pressure of 2 × 10−4 mbar decreased from 2.08 to 1.89 with increase of wavelength from 450 to 1,000 nm, respectively. Paper presented at the Third International Conference on Ionic Devices (ICID 2006), Chennai, Tamilnadu, India, Dec. 7–9, 2006.  相似文献   
35.
Until now, many attempts have been made to dope graphene in various ways, but each method turned out to have pros and cons. In this study, to overcome the limitations of doping methods, yttrium hypocarbide (Y2C) is investigated as one prospective material to dope graphene, using density functional theory calculations. In monolayer Y2C, the anionic electrons localized away from Y atomic layers are confirmed to contribute to occupied states near the Fermi level. Next, we investigate the electronic structure of graphene in heterojunction with Y2C. Anionic electrons of Y2C occupy the empty states of graphene in graphene/Y2C heterostructure, which makes the Dirac cone of graphene located at about 1.7 eV below the Fermi level. Such charge transfer of anionic electrons to graphene and the flatness of electric cloud of anionic electrons leads to evenly n-doped graphene in graphene/Y2C heterostructure. This suggests that Y2C is a good candidate to dope graphene.  相似文献   
36.
采用溶剂热法合成了发光性能和水溶性良好的YVO4∶Eu纳米探针(YVO4∶Eu NPs).由于YVO4∶Eu NPs的激发光谱与色氨酸的吸收光谱有很大程度的重叠,二者可发生荧光内滤效应,其中色氨酸为吸光体、YVO4∶Eu NPs为荧光体,YVO4∶Eu NPs的发光被猝灭.基于此,建立了基于YVO4∶Eu NPs内滤效应测定色氨酸含量的方法.对YVO4∶Eu NPs的加入量、反应溶液pH值和反应时间进行了优化,在最佳反应条件下,本方法测定色氨酸的线性范围为4.0×10-6~4.0×10-4 mol/L,检出限为1.0 ×10-6 mol/L(3σ).采用本方法测定了酱油中色氨酸的含量,回收率为95.2%和97.3%.本方法具有简便快速、灵敏准确的特点.  相似文献   
37.
Using density functional theory methods, we have studied carbon trioxide, its adsorption and dissociation on Ag(100). In the gas phase, two isomers are found, D3h and C2v, with the latter of 2.0 kcal mol?1 lower in energy at the PW91PW91/6?31G(d) level. For CO3 on Ag(100), the calculated adsorption energy is 91.2 and 89.1 kcal mol?1 for the bi‐coord perpendicular and tri‐coord parallel structures, respectively. Upon the adsorption, 0.50 ~ 0.56 electron is transferred from silver to CO3, indicative of significant ionic characters of the adsorbate‐surface bonding. In addition, the geometry of CO3 is largely changed by its strong interaction with silver. For CO3(ad) → O(ad) + CO2(gas), the energy barrier is calculated to be 19.8 kcal mol?1 through the bi‐coord path. The process is endothermic with an enthalpy change of +17.3 ~ +26.7 kcal mol?1 and the weakly chemisorbed CO2 is identified as an intermediate on the potential energy surface. © 2009 Wiley Periodicals, Inc. Int J Quantum Chem, 2010  相似文献   
38.
Raman spectroscopic analysis is performed on WO3 nanowires at room temperature at pressures from ambient conditions to 45 GPa. Linear dependence of the first‐order Raman signal on various high‐pressure (HP) sections is observed. Upon increasing the applied pressure, the WO3 nanowires undergo four phase transitions at pressures around 1.7, 4.6, 21.5, and 26.2 GPa, which are all less than that reported for bulk WO3. When the pressure is up to 42.5 GPa, a new high‐pressure phase (HP5) appears. This phase has never been reported and is not reversible while unloading the pressure.  相似文献   
39.
A comparative study of the luminescent properties of Y2O3:Eu3+ phosphor powders and thin films sputtered from targets prepared from combustion synthesized powders is reported. Thin films of (Y0.96Eu0.04)2O3 were deposited on silicon substrates. Films deposited at 600 °C had both monoclinic and cubic phases of Y2O3, which developed to an oriented cubic phase after annealing. Films and powders showed a linear dependence of the intensity of the 5D77F2 (611 nm) transition with temperature in the range 26-660 °C with an average rate of change of 1.8×10−4 °C−1. The rate of change appears to be dependent on the Eu3+ concentration. This work shows that these thin films can be used as thermographic phosphors for remote temperature measurements.  相似文献   
40.
Tungsten trioxide, unhydrated with hexagonal structure (h-WO3), has been prepared by hydrothermal method at a temperature of 180 °C in acidified sodium tungstate solution. Thus prepared h-WO3 has been characterized by X-ray diffraction (XRD) method and using electrochemical techniques. The morphology has been examined by scanning and transmission electron microscopies (SEM and TEM) and it is consistent with existence of nanorods of 50-70 nm diameter and up to 5 μm length. Cyclic voltammetric characterization of thin films of h-WO3 nanorods has revealed reversible redox behaviour with charge-discharge cycling corresponding to the reversible lithium intercalation/deintercalation into the crystal lattice of the h-WO3 nanorods. In propylene carbonate containing LiClO4, two successive redox processes of hexagonal WO3 nanorods are observed at the scan rate of 50 mV/s. Such behaviour shall be attributed to the presence of at least two W atoms of different surroundings in the lattice structure of h-WO3 nanorods. On the other hand, in aqueous LiClO4 solution, only one redox process is observed at the scan rate of 10 mV/s. The above observations can be explained in terms of differences in the diffusion of ions inside two types of channel cavities existing in the structure of the h-WO3 nanorods. Moreover, the material can be applied as active support for the catalytic bi-metallic Pt-Ru nanoparticles during electrooxidation of ethanol in acid medium (0.5 mol dm−3 H2SO4).  相似文献   
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