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591.
Using an ordinary ceramic fabrication technique, we fabricated lead-free (1-x)(K0.5Na0.5)NbO3-xBa(Ti0.95Zr0.05)O3 ceramics with CuO sintering aid . Ba(Ti0.95Zr0.05)O3 diffuses into (K0.5Na0.5)NbO3 to form a new solid solution. The ceramics with perovskite structure possess orthorhombic phase at x≤0.04 and become tetragonal phase at x≥0.06. Both the paraelectric cubic–ferroelectric tetragonal and the ferroelectric tetragonal–ferroelectric orthorhombic phase transition temperatures decrease with increasing the concentration of Ba(Ti0.95Zr0.05)O3. The doping of CuO effectively promotes the densification of the ceramics. The coexistence of the orthorhombic and tetragonal phases at 0.04<x<0.06 and the improvement in sintering performances of the ceramics significantly enhance the piezoelectric and dielectric properties at room temperature. The ceramics with x=0.04–0.06 and y=0.75–1.50 possess excellent properties: d33=119–185 pC/N, kP=37–44%, kt=35–49%, ε=341–1129, cosδ=0.7–4.4% and Tc=312–346 °C. PACS 77.65.-j; 77.84.Dy; 77.84.-s  相似文献   
592.
The traditional design strategies for highly bright solid‐state luminescent materials rely on weakening the intermolecular π–π interactions, which may limit diversity when developing new materials. Herein, we propose a strategy of tuning the molecular packing mode by regioisomerization to regulate the solid‐state fluorescence. TBP‐e‐TPA with a molecular rotor in the end position of a planar core adopts a long‐range cofacial packing mode, which in the solid state is almost non‐emissive. By shifting molecular rotors to the bay position, the resultant TBP‐b‐TPA possesses a discrete cross packing mode, giving a quantum yield of 15.6±0.2 %. These results demonstrate the relationship between the solid‐state fluorescence efficiency and the molecule's packing mode. Thanks to the good photophysical properties, TBP‐b‐TPA nanoparticles were used for two‐photon deep brain imaging. This molecular design philosophy provides a new way of designing highly bright solid‐state fluorophores.  相似文献   
593.
Hydrogen-borrowing catalysis represents a powerful method for the alkylation of amine or enolate nucleophiles with non-activated alcohols. This approach relies upon a catalyst that can mediate a strategic series of redox events, enabling the formation of C−C and C−N bonds and producing water as the sole by-product. In the majority of cases these reactions have been employed to target achiral or racemic products. In contrast, the focus of this Minireview is upon hydrogen-borrowing-catalysed reactions in which the absolute stereochemical outcome of the process can be controlled. Asymmetric hydrogen-borrowing catalysis is rapidly emerging as a powerful approach for the synthesis of enantioenriched amine and carbonyl containing products and examples involving both C−N and C−C bond formation are presented. A variety of different approaches are discussed including use of chiral auxiliaries, asymmetric catalysis and enantiospecific processes.  相似文献   
594.
A nanosecond time-resolved resonance Raman (ns-TR3) spectroscopic study of the triplet state benzophenone reaction with the 2-propanol hydrogen-donor solvent and subsequent reactions is presented. The TR3 spectra show that the benzophenone triplet state (npi*) hydrogen-abstraction reaction with 2-propanol is very fast (about 10 to 20 ns) and forms a diphenylketyl radical and an associated 2-propanol radical partner. The temporal evolution of the TR3 spectra also indicates that recombination of these two radical species occurs with a time constant of about 1170 ns to produce a LAT (light absorbing transient) intermediate that is identified as the 2-[4-(hydroxylphenylmethylene)cyclohexa-2,5-dienyl]propan-2-ol (p-LAT) species. Comparison of the TR3 spectra with results obtained from density functional theory calculations for the species of interest was used to elucidate the identity, structure, properties, and major spectral features of the intermediates observed in the TR3 spectra. The structures and properties of the reaction intermediates observed (triplet benzophenone, diphenyl ketyl radical, and p-LAT) are briefly discussed.  相似文献   
595.
Abstract

The fabrication process of photonic crystal fibers based on a stack-and-draw method is presented in full detail in this article. In addition, improved techniques of photonic crystal fiber preform preparation and fabrication are highlighted. A new method of connecting a handle to a preform using only a fiber drawing tower is demonstrated, which eliminates the need for a high-temperature glass working lathe. Also, a new technique of modifying the photonic crystal fiber structural pattern by sealing air holes of the photonic crystal fiber cane is presented. Using the proposed methods, several types of photonic crystal fibers are fabricated, which suggests potential for rapid photonic crystal fibers fabrication in laboratories equipped with and limited to only a fiber drawing tower.  相似文献   
596.
Topological effects on the confinement of a moving neutral particle with an induced electric dipole moment confined to a quantum ring and a two-dimensional quantum dot (described by a hard-wall confining potential) are investigated. It is shown in this work that the spectrum of energy depends on the geometric phase obtained by Wei et al. [H. Wei, R. Han, X. Wei, Phys. Rev. Lett. 75, 2071 (1995)] and persistent currents arise from this dependence in both the quantum ring and the quantum dot. Further, the behaviour of the analogue of the Landau system for a moving electric dipole confined to a two-dimensional quantum dot is discussed, and it is shown that persistent currents are absent in this case.  相似文献   
597.
Theoretical and experimental analysis of the rewriting time of liquid crystal (LC) optical rewritable (ORW) e-paper was conducted. The equations of rewriting time of alignment molecule SD1 film with and without interaction with LC based on diffusion model were derived, which shows that the rewriting time of LC ORW e-paper could be shortened by enlarging light intensity or decreasing azimuthal anchoring energy. The rewriting time of pure SD1 films and LC ORW cells was measured under different light intensities. And LC ORW cells with different azimuthal anchoring energy were prepared for rewriting time measurement. A good agreement between experimental and theoretical results was obtained, which indicates that using larger light intensity and making LC cell with smaller azimuthal anchoring energy, ORW rewriting time could be decreased to the amount suitable for practical use.  相似文献   
598.
The ISO 25101 (International Organization for Standardization, Geneva) describes a new international standard method for the determination of perfluorooctanesulfonate (PFOS) and perfluorooctanoate (PFOA) in unfiltered samples of drinking and surface waters. The method is based on the extraction of target analytes by solid phase extraction, solvent elution, and determination by high performance liquid chromatography–tandem mass spectrometry (HPLC–MS/MS). For the determination of the performance of this method, more than 20 laboratories from 9 different countries participated in an inter-laboratory trial in 2006. In addition, inter-laboratory trials were conducted in 2008 and 2009 for the analysis of perfluoroalkylsubstances (PFASs), including PFOS and PFOA, in water samples by following the protocols of Japanese Industrial Standard (JIS). Overall, the repeatability coefficients of variation (i.e., within-laboratory precision) for PFOS and PFOA in all water samples were between 3 and 11%, showing a adequate precision of the ISO and JIS methods. The reproducibility coefficients of variation (i.e., between-laboratory precision) were found to vary within a range of 7–31% for surface water and 20–40% for wastewater. The recoveries of PFOS and PFOA, as a measure of accuracy, varied from 84 to 100% for surface water and from 84 to 100% for wastewater among the samples with acceptable criteria for internal standards recovery. The determined concentrations of PFASs in samples compared well with the “true” values. The results of the inter-laboratory trial confirmed that the analytical methods are robust and reliable and can be used as a standard method for the analysis of target compounds in water samples.  相似文献   
599.
ZK60A nanocomposite containing Al2O3 nanoparticle reinforcement (50 nm average size) was fabricated using solidification processing followed by hot extrusion. The nanocomposite exhibited similar grain size to the monolithic alloy, reasonable Al2O3 nanoparticle distribution, non-dominant (0 0 0 2) texture in the longitudinal direction, and 15% higher hardness than the monolithic alloy. Compared to the monolithic alloy (in tension), the nanocomposite exhibited lower yield strength (0.2%TYS) (−4%) and higher ultimate strength (UTS), failure strain, and work of fracture (WOF) (+13%, +170%, and +200%, respectively). Compared to the monolithic alloy (in compression), the nanocomposite exhibited lower yield strength (0.2%CYS) (−5%) and higher ultimate strength (UCS), failure strain, and WOF (+6%, +41%, and +43%, respectively). The effects of Al2O3 nanoparticle addition on the enhancement of tensile and compressive properties of ZK60A are investigated in this article.  相似文献   
600.
In recent years, a variety of effective chaos-based image cryptosystems have been proposed. One of the architectures of this kind of cryptosystems is composed of multiple rounds of substitution and diffusion. As the confusion and diffusion effects are solely contributed by the substitution and the diffusion stages, respectively, the required overall rounds of operations in achieving a certain level of security is found more than necessary. In this Letter, we suggest to introduce a certain diffusion effect in the substitution stage by simple sequential add-and-shift operations. Although this leads to a longer processing time in a single round, the overall encryption time is reduced as fewer rounds are required. Simulation results show that at a similar performance level, the proposed cryptosystem needs less than one-third the encryption time of an existing fast cryptosystem. The effective acceleration of chaos-based image cryptosystems is thus achieved.  相似文献   
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