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101.
102.
We report a ring-cavity thulium fiber laser mode locked with a single-wall carbon nanotube absorber used in transmission. A carboxymethyl cellulose polymer film with incorporated carbon nanotubes synthesized by the arc discharge method has an absorption coinciding with in the amplification bandwidth of a Tm-doped fiber. This laser is pumped by an erbium fiber laser at 1.57 microm wavelength and produces a 37 MHz train of mode-locked 1.32 ps pulses at 1.93 microm wavelength with an average output power of 3.4 mW.  相似文献   
103.
We continue the study of the connection between the “geometric” properties of SU ‐rank 1 structures and the properties of “generic” pairs of such structures, started in [8]. In particular, we show that the SU‐rank of the (complete) theory of generic pairs of models of an SU ‐rank 1 theory T can only take values 1 (if and only if T is trivial), 2 (if and only if T is linear) or ω, generalizing the corresponding results for a strongly minimal T in [3]. We also use pairs to derive the implication from pseudolinearity to linearity for ω ‐categorical SU ‐rank 1 structures, established in [7], from the conjecture that an ω ‐categorical supersimple theory has finite SU ‐rank, and find a condition on generic pairs, equivalent to pseudolinearity in the general case (© 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   
104.
In this paper, we present a study on two-channel multilayer mirrors which can operate at two wavelengths in Extreme Ultraviolet (EUV) spectral range. We propose a new method to design two-channel EUV multilayer mirrors with enhanced spectral selectivity. The mirror structure is a stack of two periodic multilayers separated by a buffer layer. We have defined the main parameters which allow adjustment of the distance between different order Bragg’s peak and of wavelength positions of reflectivity minima. Two mirrors have been designed and deposited for solar EUV telescope applications by using this method. The first mirror reflects Fe IX–X line (17.1 nm) and Fe XVI (33.5 nm) lines with attenuation of the He II line (30.4 nm). The second mirror reflects Fe IX–X and He II lines with attenuation of Fe XV (28.4 nm) and Fe XVI lines. Measurements with synchrotron radiation source confirm that, in both cases, for these mirrors, we are able to adjust reflectivity maxima (Bragg peak position) and minima. Such multilayers offer new possibilities for compact design of multi-wavelength EUV telescopes and/or for high spectral selectivity.  相似文献   
105.
Calcined hydrotalcite with or without added metal (Mg(Al)O, Pt/Mg(Al)O and Pt,Sn/Mg(Al)O) have been investigated with in situ X-ray photoelectron spectroscopy (XPS) during ethane dehydrogenation experiments. The temperature in the analysis chamber was 450 °C and the gas pressure was in the range 0.3-1 mbar. Depth profiling of calcined hydrotalcite and platinum catalysts under reaction, oxidation and in hydrogen-water mixture was performed by varying the photon energy, covering an analysis depth of 10-21 Å. It was observed that the Mg/Al ratio in the Mg(Al)O crystallites does not vary significantly in the analysis depth range studied. This result indicates that Mg and Al are homogeneously distributed in the Mg(Al)O crystallites. Catalytic tests have shown that the initial activity of a Pt,Sn/Mg(Al)O catalyst increases during an activation period consisting of several cycles of reduction-dehydrogenation-oxidation. The Sn/Mg ratio in a Pt,Sn/Mg(Al)O catalyst was followed during several such cycles, and was found to increase during the activation period, probably due to a process where tin spreads over the carrier material and covers an increasing fraction of the Mg(Al)O surface. The results further indicate that spreading of tin occurs under reduction conditions.A PtSn2 alloy was studied separately. The surface of the alloy was enriched in Sn during reduction and reaction conditions at 450 °C. Binding energies were determined and indicated that Sn on the particle surface is predominantly in an oxidised state under reaction conditions, while Pt and a fraction of Sn is present as a reduced Pt-Sn alloy.  相似文献   
106.
Both individual and combined effects of the horizontal and vertical variability of cumulus clouds on solar radiative transfer are investigated using a two-dimensional (x- and z-directions) cloud radar dataset. This high-resolution dataset of typical fair-weather marine cumulus is derived from ground-based cloud radar observations. The domain-averaged (along x-direction) radiative properties are computed by a Monte Carlo method. It is shown that (i) different cloud-scale resolutions can be used for accurate calculations of the mean absorption, upward and downward fluxes; (ii) the resolution effects can depend strongly on the solar zenith angle; and (iii) a few cloud statistics can be successfully applied for calculating the averaged radiative properties.  相似文献   
107.
We construct a nonvanishing inner function I in the unit ball B?Cn such that the subspace IHp(B) is not weakly dense in the Hardy space Hp(B), with 0<p<1. To cite this article: E. Doubtsov, C. R. Acad. Sci. Paris, Ser. I 334 (2002) 957–960.  相似文献   
108.
109.
A series of optically pure 3,3′-bis(RO)-MeO-BIPHEP derivatives are prepared and used in palladium catalyzed asymmetric transformations. The phosphine oxide of (±)-5 is prepared in four steps from p-methoxyphenol and resolved using the novel resolving reagent chloro(l-menthoxy)dimethylsilane. Subsequent conversions provide catalysts 8 and 9. Ligands 6, 7 and 10 are prepared in six steps from p-methoxyphenol and the phosphine oxides of 6 and 7, and 10 are resolved using di-p-toluoyl- and dibenzoyl-l-tartaric acid, respectively. (R)-3,3′-Bispivalate 8 is superior to the other catalysts in asymmetric Heck reaction with 2,3-dihydrofuran while (R)-(+)-bis(tolyloxy) 10 and (+)-(R)-sugar derivative 9 are better in the Pd-catalyzed polyene cyclization; however, the absolute sense of chirality in the product from the polyene cyclization was reversed to that obtained when (R)-(+)-BINAP and (R)-(+)-MeO-BIPHEP were used.  相似文献   
110.
Sorption of n-hexane on monodimensional pure silica SSZ-35, CIT-5, ZSM-12, and ZSM-22 zeolites with different pore dimension and on recently synthesized ITQ-29 was studied by IR spectroscopic and computational chemistry methods. Heats of sorption of n-hexane on these zeolites was determined experimentally from the temperature dependence of the intensity of IR bands of sorbed hexane as well as from theoretical calculations. Calculations have shown the different orientations of sorbed hexane molecules inside zeolite channels, which depend on the type of zeolite and loading. At high loadings, ordering of hexane inside the channels is observed due to optimization of sorbate-sorbate and sorbate-zeolite interaction energies. Such ordering is responsible for the increase of the sorption energy. A decrease of the sorption energy upon increasing the pore dimension of zeolite was observed, in agreement with results previously published in the literature. Effects of pore diameter of zeolites and ordering of molecules inside zeolite channels on the sorption energy of hexane are discussed.  相似文献   
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