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51.
All matters in the path of filaments induced by an intense femtosecond laser pulse propagating in air could be fragmented and result in the emission of characteristic fluorescence spectra from the excited fragments. The fluorescence spectra exhibit specific signatures (fingerprints) that can be used for the identification of various substances including chemical and biological species. In this paper, we present an overview of the recent progress in our laboratory concerning the “remote” sensing of chemical and biological agents/pollutants in air using filamentation-induced nonlinear fluorescence techniques.  相似文献   
52.
Our previous study presented up to 20% power conversion efficiency (PCE) enhancement of poly(3-hexylthiophene):phenyl-C61-butyric acid methyl ester (P3HT:PCBM) solar cells under the Fe3O4 nanoparticles (NPs) self-assembly (SA) effect by spin coating. Fe3O4 NPs (about 11 nm hydrodynamic diameter) form a thin layer at the top interface of the light absorbing active layer, which results in the generation of PCBM rich region improving the charge transport (Zhang et al. Sol Energ Mat Sol C 160:126–133, 2017). In order to investigate the feasibility of this Fe3O4 NPs SA effect under large-scale production condition, a smooth rod was implemented to mimic roll-to-roll coating technique and yield active layers having about the same thickness as the spin-coated ones. Small angle neutron scattering and grazing incidence X-ray diffraction were employed finding out similar morphologies of the active layers by these two coating techniques. However, rod-coated solar cell’s PCE decreases with the addition of Fe3O4 NPs compared with the one without them. This is because PCBM rich region is not created at the top interface of the active layer due to the absence of Fe3O4 NPs, which is attributed to the weak convective flow and low diffusion rate. Moreover, in the rod-coated solar cells, the presence of Fe3O4 NPs causes decrease in P3HT crystallinity, thus the charge transport and the device performance. Our study confirms the role of spin coating in the Fe3O4 NPs SA effect and enables researchers to explore this finding in other polymer nanocomposite systems.  相似文献   
53.
A water-filled impedance tube capable of improved measurement accuracy and precision is reported. The measurement instrument employs a variation of the standardized two-sensor transfer function technique. Performance improvements were achieved through minimization of elastic waveguide effects and through the use of sound-hard wall-mounted acoustic pressure sensors. Acoustic propagation inside the water-filled impedance tube was found to be well described by a plane wave model, which is a necessary condition for the technique. Measurements of the impedance of a pressure-release terminated transmission line, and the reflection coefficient from a water/air interface, were used to verify the system.  相似文献   
54.
55.
Fusion excitation functions are measured for the system 6Li + 28Si using the characteristic $ \gamma$ -ray method, encompassing both the sub-barrier and above-barrier regions, viz, E lab = 7-24 MeV. Two separate experiments were performed, one for the above-barrier region ( E lab = 11-24 MeV) and another for the below-barrier region ( E lab = 7-10 MeV). The results were compared with our previously measured fusion cross-section for the 7Li + 28Si system. We observed the enhancement of the fusion cross-section at sub-barrier regions for both 6Li and 7Li , but the yield was substantially larger for 6Li . However, for well-above-barrier regions, a similar type of suppression was identified for both the systems.  相似文献   
56.
A novel method of computing the nonlinear differential equations relating to the transient behaviour of an induction motor using a polynomial series, is presented. The stator and rotor currents and the angle of rotation are expressed as polynomial series dependent on time. These are then substituted into the differential equations of the induction motor to compute the polynomial coefficients and, consequently, the transient quantities. Since the equations are nonlinear, the computations are carried out using the step-by-step method. The stator and rotor currents, speed and torque are calculated for acceleration and braking conditions. The results are compared both analytically and experimentally.  相似文献   
57.
This paper presents a study of thermodynamic analysis of the solubility-temperature phase diagrams for solutions of calcium, strontium and barium tungstate in sodium tungstate melts in the temperature range 660 to 1200 °C. At temperatures 1000 °C and above, the solutions were ideal but below 1000 °C the solutions became non-ideal and the non-ideality increased with decreasing temperature. At any mole fraction concentration of the solute the excess free energies of mixing and the activity coefficients increased in the order CaWO4 > SrWO4 > BaWO4, whereas the excess chemical potentials decreased in the order CaWO4 < SrWO4 < BaWO4.  相似文献   
58.
D. Roy  H. Raghuvanshi 《Journal of Non》2011,357(7):1701-1704
The crystallization behavior and thermal stability of amorphous phases of Al65Cu20Ti15 alloy obtained by mechanical alloying were investigated by using in-situ X-ray diffraction and differential scanning calorimetry (DSC) under non isothermal and isothermal conditions. The result of a Kissinger analysis shows that the activation energy for crystallization is 1131 kJ/mol. The higher stability against crystallization of Al65Cu20Ti15 amorphous alloy is attributed to the stronger interaction of atoms in the Al-Cu-Ti system and formed of complicated compound like Al5CuTi2 and Al4Cu9 as primary phases. The isothermal crystallization was modeled by using the Johnson-Mehl-Avrami (JMA) equation. The Avarami exponents suggest that the isothermal crystallization is governed by a three-dimensional diffusion-controlled growth.  相似文献   
59.
The preparation and spectroscopic (1H NMR, UV and IR) characterization of three R3Sn(O2CCH2N(H)C(O)NH2) [R=Ph, c-Hex (cyclohexyl) or n-Bu] compounds are reported. A different mode of coordination is indicated for the hydantoate ligand in the R=Ph compound compared with the R=c-Hex and R=n-Bu compounds, as confirmed by a crystallographic analysis. The structure of [Ph3Sn(O2CCH2N(H)C(O)NH2)] is polymeric owing to the presence of bridging hydantoate ligands such that each ligand coordinates one tin atom, via one of the carboxylate oxygen atoms, and a symmetry-related tin atom via the carbonyl group at the other end of the molecule. The structure features distorted trigonal-bipyramidal tin atom geometries with a trans -R3SnO2 motif. The structure of [c-Hex3Sn(O2CCH2N(H)- C(O)NH2)], by contrast, is monomeric, distorted tetrahedral, as the carboxylate group is monodentate and there are no additional tin–ligand interactions. The structures are each stabilized by a number of intermolecular hydrogen bonds. Fungitoxicity and phytotoxicity studies indicate that the R=n-Bu derivative is the more active compound.  相似文献   
60.
    
Mutations in multi-domain leucine-rich repeat kinase 2 (LRRK2) have been an interest to researchers as these mutations are associated with Parkinson's disease. G2019S mutation in LRRK2 kinase domain leads to the formation of additional hydrogen bonds by S2019 which results in stabilization of the active state of the kinase, thereby increasing kinase activity. Two additional hydrogen bonds of S2019 are reported separately. Here, a mechanistic picture of the formation of additional hydrogen bonds of S2019 with Q1919 (also with E1920) is presented using ‘active’ Roco4 kinase as a homology model and its relationship with the stabilization of the ‘active’ G2019S LRRK2 kinase. A conformational flipping of residue Q1919 was found which helped to form stable hydrogen bond with S2019 and made ‘active’ state more stable in G2019S LRRK2. Two different states were found within the ‘active’ kinase with respect to the conformational change (flipping) in Q1919. Two doubly-mutated systems, G2019S/Q1919A and G2019S/E1920 K, were studied separately to check the effect of Q1919 and E1920. For both cases, the stable S2 state was not formed, leading to a decrease in kinase activity. These results indicate that both the additional hydrogen bonds of S2019 (with Q1919 and E1920) are necessary to stabilize the active G2019S LRRK2.  相似文献   
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