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151.
Yang VX Munce N Pekar J Gordon ML Lo S Marcon NE Wilson BC Vitkin IA 《Optics letters》2004,29(15):1754-1756
High-resolution optical coherence tomography demands a large detector bandwidth and a high numerical aperture for real-time imaging, which is difficult to achieve over a large imaging depth. To resolve these conflicting requirements we propose a novel multifocus fiber-based optical coherence tomography system with a micromachined array tip. We demonstrate the fabrication of a prototype four-channel tip that maintains a 9-14-microm spot diameter with more than 500 microm of imaging depth. Images of a resolution target and a human tooth were obtained with this tip by use of a four-channel cascaded Michelson fiber-optic interferometer, scanned simultaneously at 8 kHz with geometric power distribution across the four channels. 相似文献
152.
An analytical potential energy curve is developed from high quality ab initio calculations for the He+Li- interaction. The HeLi- electrostatic complex is found to have an Re of 18.5 bohrs and a De of 0.974 cm(-1). Numerical solution of the rovibrational Schr?dinger equation with this potential indicates two bound levels, (v,J)=(0,0) and (0,1), for all naturally occurring isotopologs (i.e., 4He7Li-, 4He6Li-, 3He7Li-, and 3He6Li-). For the common isotopolog, 4He7Li-, a D0 of 0.207 cm(-1) and an R0 of 26.5 bohrs is determined. 相似文献
153.
Auger rates are calculated for CdSe colloidal quantum dots using atomistic empirical pseudopotential wave functions. We predict the dependence of Auger electron cooling on size, on correlation effects (included via configuration interaction), and on the presence of a spectator exciton. Auger multiexciton recombination rates are predicted for biexcitons as well as for triexcitons. The results agree quantitatively with recent measurements and offer new predictions. 相似文献
154.
Gavrishchaka VV Ganguli GI Scales WA Slinker SP Chaston CC McFadden JP Ergun RE Carlson CW 《Physical review letters》2000,85(20):4285-4288
Linear theory analysis and particle-in-cell simulations show that a spatial transverse gradient in the ion drift parallel to the magnetic field, dV(di)/dx=Omega(i), where Omega(i) is the ion cyclotron frequency, can generate a broadband multimode spectrum extending from omegaOmega(i). Nonlinearly, these waves lead to multiscale spatially coherent structures, substantial cross-field transport, ion energization, and phase-space diffusion. Large spikes are formed in the parallel electric field time series. These signatures are similar to the Fast Auroral Snapshot satellite observations in the upward current region. 相似文献
155.
In this paper we study the L p ? L r boundedness of the extension operators associated with paraboloids in ${{\mathbb F}_{q}^{d}}In this paper we study the L
p
− L
r
boundedness of the extension operators associated with paraboloids in
\mathbb Fqd{{\mathbb F}_{q}^{d}} , where
\mathbbFq{\mathbb{F}_{q}} is a finite field of q elements. In even dimensions d ≥ 4, we estimate the number of additive quadruples in the subset E of the paraboloids, that is the number of quadruples (x,y,z,w) ? E4{(x,y,z,w) \in E^4} with x + y = z+w. As a result, in higher even dimensions, we obtain the sharp range of exponents p for which the extension operator is bounded, independently of q, from L
p
to L
4 in the case when −1 is a square number in
\mathbbFq{\mathbb{F}_{q}} . Using the sharp L
p
−L
4 result, we improve upon the range of exponents r, for which the L
2 − L
r
estimate holds, obtained by Mockenhaupt and Tao (Duke Math 121:35–74, 2004) in even dimensions d ≥ 4. In addition, assuming that −1 is not a square number in
\mathbbFq{\mathbb{F}_{q}}, we extend their work done in three dimension to specific odd dimensions d ≥ 7. The discrete Fourier analytic machinery and Gauss sum estimates make an important role in the proof. 相似文献
156.
Hetherington NB Kulak AN Sheard K Meldrum FC 《Langmuir : the ACS journal of surfaces and colloids》2006,22(5):1955-1958
Single crystals of calcite with regular patterned surfaces comprising close-packed arrays of hemispherical cavities or domes were produced by crystallization on colloidal monolayers or PDMS replicas of these monolayers, respectively. Perfect replication of the substrate topography was achieved for all colloidal particles, irrespective of their size and surface chemistry when the substrate geometry permitted unrestricted ion flow to the growing crystal. This work demonstrates that crystallization within a mould provides a very general route to producing single crystals with curved surfaces and unusual morphologies and that such patterning can be applied from the micro- to the nanoscale. 相似文献
157.
Deering AL Van Lue SM Kandel SA 《Langmuir : the ACS journal of surfaces and colloids》2005,21(23):10260-10263
Scanning tunneling microscopy was used to characterize self-assembled monolayers (SAMs) of octanethiol on Au(111), created using vapor deposition at elevated temperatures and ambient pressure. Monolayers contained large, close-packed ( radical3 x radical3)R30 degrees domains with sizes considerably larger than those typically formed from conventional solution-phase preparation and with crystallographically straight domain boundaries. New striped surface phases were also observed, including a 13 x radical3 phase with a density that was 69% of the close-packed density; these striped phases appeared topographically higher in STM images than close-packed monolayers. 相似文献
158.
Fossil fuels are expected to be the major source of energy for the next few decades. However, combustion of nonrenewable resources leads to the release of large quantities of CO2, the primary greenhouse gas. Notably, the concentration of CO2 in the atmosphere is increasing annually at an astounding rate. Electrochemical CO2 reduction (ECR) to value-added fuels and chemicals using electricity from intermittent renewable energy sources is a carbon-neutral method to alleviate anthropogenic CO2 emissions. Despite the steady progress in the selective generation of C1 products (CO and formic acid), the production of multi-carbon species still suffers from low selectivity and efficiency. As an ECR product, ethylene (C2H4) has a higher energy density than do C1 species and is an important industrial feedstock in high demand. However, the conversion of CO2 to C2H4 is plagued by low productivity and large overpotential, in addition to the severe competing hydrogen evolution reaction (HER) during the ECR. To address these issues, the design and development of advanced electrocatalysts are critical. Here, we demonstrate fine-tuning of ECR to C2H4 by taking advantage of the prominent interaction of Cu with shape-controlled CeO2 nanocrystals, that is, cubes, rods, and octahedra predominantly covered with (100), (110), and (111) surfaces, respectively. We found that the selectivity and activity of the ECR depended strongly on the exposed crystal facets of CeO2. The overall ECR Faradaic efficiency (FE) over Cu/CeO2(110) (FE ≈ 56.7%) surpassed that of both Cu/CeO2(100) (FE ≈ 51.5%) and Cu/CeO2(111) (FE ≈ 48.4%) in 0.1 mol·L-1 KHCO3 solutions with an H-type cell. This was in stark contrast to the exclusive occurrence of the HER over pure carbon paper, CeO2(100), CeO2(110), and CeO2(111). In particular, the FE toward C2H4 formation and the partial current density increased in the sequence Cu/CeO2(111) < Cu/CeO2(100) < Cu/CeO2(110) within applied bias potentials from -1.00 to -1.15 V (vs. the reversible hydrogen electrode), reaching 39.1% over Cu/CeO2(110) at a mild overpotential (1.13 V). The corresponding values for Cu/CeO2(100) and Cu/CeO2(111) were FEC2H4 ≈ 31.8% and FEC2H4 ≈ 29.6%, respectively. The C2H4 selectivity was comparable to that of many reported Cu-based electrocatalysts at similar overpotentials. Furthermore, the FE for C2H4 remained stable even after 6 h of continuous electrolysis. The superior ECR activity of Cu/CeO2(110) to yield C2H4 was attributed to the metastable (110) surface, which not only promoted the effective adsorption of CO2 but also remarkably stabilized Cu+, thereby boosting the ECR to produce C2H4. This work offers an alternative strategy to enhance the ECR efficiency by crystal facet engineering. 相似文献
159.
Yoshikazu Giga Katsuya Inui Alex Mahalov Shin’ya Matsui Jürgen Saal 《Archive for Rational Mechanics and Analysis》2007,186(2):177-224
We prove time local existence and uniqueness of solutions to a boundary layer problem in a rotating frame around the stationary
solution called the Ekman spiral. We choose initial data in the vector-valued homogeneous Besov space for 2 < p < ∞. Here the L
p
-integrability is imposed in the normal direction, while we may have no decay in tangential components, since the Besov space
contains nondecaying functions such as almost periodic functions. A crucial ingredient is theory for vector-valued homogeneous
Besov spaces. For instance we provide and apply an operator-valued bounded H
∞-calculus for the Laplacian in for a general Banach space . 相似文献
160.
Smyth TJ Ramachandran VN McGuigan A Hopps J Smyth WF 《Rapid communications in mass spectrometry : RCM》2007,21(4):557-566
Electrospray ionisation ion trap mass spectrometry (ESI-MS(n)) has been used to study the fragmentation patterns of nicotine and nine of its related compounds. From this study certain characteristic fragmentations are apparent with generally the pyrrolidine or piperidine ring being subject to chemical modifications. The structures of the product ions proposed for the ESI-MS(n) study have been supported by results from electrospray ionisation quadrupole time-of-flight mass spectrometry (ESI-QTOF-MS). Compounds with pyrrolidine and piperidine rings that possess an unsubstituted N atom have been shown to lose NH(3) at the MS(2) stage. Those compounds with N-methyl groups lose CH(3)NH(2) at the MS(2) stage. The loss of NH(3) or CH(3)NH(2) leaves the corresponding rings opened and this is followed by ring closure at the pyridine-2 carbon atom. Mono-N-oxides fragment in a similar way but the di-N-oxide can also fragment by cleavage of the bond between the pyridine and pyrrolidine rings. Cotinine also can undergo cleavage of this bond between the rings.This data therefore provides useful information on how substituents and the nature of the non-pyridine ring can affect the fragmentation patterns of nicotine and its related compounds. This information can be used in the characterisation of these compounds by liquid chromatography/electrospray ionization mass spectrometry (LC/ESI-MS) which results in the separation of nicotine and its related compounds with limits of detection (LODs) ranging from 15 to 105 ng/mL. The use of LC/ESI-MS to study nicotine-containing samples resulted in the simultaneous and unambiguous identification of seven of the compounds discussed in this paper: cotinine identified at retention time 12.5 min (with its [M+H](+) ion at m/z 177), nornicotine 16.0 min (m/z 149), anatabine 18.0 min (m/z 161), myosmine 18.5 min (m/z 147), anabasine 20.4 min (m/z 163), nicotine 22.2 min (m/z 163), and nicotyrine 31.4 min (m/z 159). For quality control of nicotine replacement therapy products, these nicotine impurities can be readily identified and determined at levels up to 0.3% for single impurities and up to 1.0% for total impurities. 相似文献