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941.
We find further implications of the BMV conjecture, which states that for hermitian matrices B≥0 and A, the function is the Laplace transform of a positive measure supported on [0,∞].  相似文献   
942.
An alternating copolymer composed of heal‐to‐tail‐structured 3,4′‐dihexyl‐2,2′‐bithiophene (DHBT) and pyrene units [poly(DHBT‐alt‐PYR)] was synthesized using a Stille coupling reaction for use in photovoltaic devices as a p‐type donor. For the reduction of the bandgap energy of poly(DHBT‐alt‐PYR), 4,7‐bis(3′‐hexyl‐2,2′‐bithiophen‐5‐yl)benzo[c][1,2,5]thiadiazole (BHBTBT) units were introduced into the polymer. Poly(DHBT‐co‐PYR‐co‐BHBTBT)s were synthesized using the same polymerization reaction. The synthesized polymers were soluble in common organic solvents and formed smooth thin films after spin casting. The optical bandgap energies of the polymers were obtained from the onset absorption wavelengths. The measured optical bandgap energy of poly(DHBT‐alt‐PYR) was 2.47 eV. As the BHBTBT content in the ter‐polymers increased, the optical bandgap energies of the resulting polymers decreased. The bandgap energies of poly(50DHBT‐co‐40PYR‐co‐10BHBTBT) and poly(50DHBT‐co‐20PYR‐co‐30BHBTBT) were 1.84 and 1.73 eV, respectively. Photovoltaic devices were fabricated with a typical sandwich structure of ITO/PEDOT:PSS/active layer/LiF/Al using the polymers as electron donors and [6,6]‐phenyl C71‐butyric acid methyl ester as the electron acceptor. The device using poly(50DHBT‐co‐20PYR‐co‐30BHBTBT) showed the best performance among the fabricated devices, with an open‐circuit voltage, short‐circuit current, fill factor, and maximum power conversion efficiency of 0.68 V, 5.54 mA/cm2, 0.35, and 1.31%, respectively. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012  相似文献   
943.
944.
We study the effects of transverse spatial modulations in a multimode degenerate optical parametric oscillator. Intracavity photonic crystals allow us to tune the instability threshold and improve entanglement above threshold. Here we compare such results with the case in which the modulation is in the injected field profile.  相似文献   
945.
946.
This work studies the Soret and Dufour effects on the double-diffusive free convection over a downward-pointing vertical truncated cone with variable wall heat and mass fluxes in fluid-saturated porous media. A coordinate transformation is used to derive the nondimensional boundary-layer governing equations, and the obtained nonsimilar equations are then solved by the cubic spline collocation method. Results for local surface temperature and the local surface concentration are presented as functions of Soret parameters, Dufour parameters, power-law exponents, buoyancy ratios, and Lewis numbers. Results show that increasing the Dufour parameter tends to increase the local surface temperature, while it tends to decrease the local surface concentration. An increase in the Soret number leads to a decrease in the local surface temperature for buoyancy assisting flows, while it leads to an increase in the local surface temperature for buoyancy opposing flows. Increasing the Soret number tends to increase the local surface concentration. Moreover, the local surface temperature and the local surface concentration of the truncated cones with higher power-law exponents are lower than those with lower exponents.  相似文献   
947.
The paper presents a short review on the synthesis, characterisation and selected medical applications of poly(styrene/α-tert-butoxy-ω-vinylbenzyl-polyglycidol) (P(S/PGL)) microspheres. The soap-free emulsion-polymerisation of styrene and α-tert-butoxy-ω-vinylbenzyl-polyglycidol macromonomer (PGL) in water yielded core-shell microspheres with a low particle-diameter dispersity (ratio of the weight average particle diameter and the number average particle diameter). The interfacial fraction of PGL units, estimated by XPS, was in the range of 0–42 mole % depending on the concentration of the macromonomer in the polymerisation feed. The studies of adsorption of model proteins showed that the surface fraction of adsorbed protein was significantly reduced when the PGL interfacial fraction was higher than 40 mole %. The P(S/PGL) particles with covalently immobilised proteins were used for the preparation of photonic crystal assemblies suitable for applications in optical biosensors and the medical diagnostic test for the detection of Helicobacter pylori antibodies in the blood serum.  相似文献   
948.
This paper reports the fabrication and nanofiltration properties of a sol–gel derived microporous zirconia membrane. Effects of synthesis parameters, including hydrolysis time, hydrolysis temperature, hydrolysis ratio and chelating agent dopant, on the state and size of polymeric zirconia sol, were investigated. Highly reproducible and stable zirconia sol after refluxing at 40 °C for 180 min, with an average particle size of approximately 8.6 nm, was synthesized with a recipe of [Zirconium n-propoxide]: [Diethanolamine]: [1-propanol]: [H2O] being 1: 2.2: 28.7: 9.4 (in molar ratio). The sol was subsequently used for the fabrication of microporous ZrO2 membranes onto alumina supported mesoporous γ-Al2O3 layers. ZrO2 membranes with molecular weight cut-off (MWCO) of 354, 1,195, corresponding to the pore size of 0.94 and 1.75 nm, were successfully fabricated. Ionic retention properties of such ZrO2 membranes with respect to electrolyte solutions, like MgCl2, CaCl2, NaCl and Na2SO4, were also determined. Effects of parameters such as concentration of salt solutions and trans-membrane pressure on retention rates of microporous ZrO2 membranes were studied in detail. Results showed that zirconium n-propoxide derived microporous ZrO2 membranes exhibited comparatively high retention rates towards divalent ions like Mg2+ and Ca2+, while much lower retention rates were observed for mono-valent ion (Na+) in the present study, which are the characteristics of nanofiltration membranes.  相似文献   
949.
950.
Uniform spreading of oil on solid surfaces is important in many processes where proper lubrication is required and this can be controlled using surfactants. The role of oil–solid interfacial self-assembled surfactant structure (SASS) in oil spreading is examined in this study for the case of hexadecane-surfactant droplet spreading on a flat horizontal copper surface, with triphenyl phosphorothionate surfactants having varying chain lengths (0 to 9). It is shown that the frictional forces (FSASS) as determined by the SASS regulate droplet spreading rate according to surfactant chain length; surfactants with longer chains led to higher reduction in the spreading rate. The extent of such forces, FSASS, depends on the surfactant density of the evolving SASS, and specific configuration the evolving SASS exhibit as per the orientations of the surfactant chains therein. Thus, FSASS = [k1 + k2(t)] Γδ(t), where Γδ(t) is the surfactant adsorption density of SASS at time ‘t’ during evolution, and, k1 and k2(t) are the force coefficients for Γδ(t) and orientations (as a function of spreading time) of the surfactant chains respectively. As a SASS evolves/grows along with adsorption of surfactants at the spreading induced fresh interface, the k1Γδ(t) component of FSASS increases and contributes to reduction in the net spreading force (S). With a decrease in the net spreading force, the existence of a cross-over period, during which the transition of the spatial dynamics of the chains from disordered to realignment/packing induced ordered orientation occurs, has been inferred from the FSASS vs. chain length relationships. Such relationships also suggested that the rate of realignment/packing is increased progressively particularly due the realignment/packing induced decrease in the net spreading force. Therefore, the realignment process is a self-induced process, which spans a measurable period of time (several minutes), the cross-over period, during which the net spreading force decreases essentially due to such self-induced process.  相似文献   
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