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211.
T. Tsuchiya F. Yamaguchi I. Morimoto T. Nakajima T. Kumagai 《Applied Physics A: Materials Science & Processing》2010,98(4):745-749
A tin-doped indium oxide (ITO) film on a SiO2 substrate was prepared by photo-irradiation of spin-coated nanoparticles using a Xe excimer lamp and a KrF excimer laser.
The effects of the excimer lamp and the excimer laser on the resistivity, mobility, and carrier concentration of the film
were investigated. To better understand how to control the microstructure of the film, we investigated the effect of thickness
on the resistivity of a film prepared by the two-step process, and found that the resistivity was higher in a thicker film.
Using two-step irradiation plus one-step KrF irradiation in N2 at room temperature, we produced an ITO film with lowest resistivity of any in this study. The electrical resistivity of
this film was 5.94×10−4 Ω cm. On the other hand, when using a simple thermal process, the resistivity of a film sintered at 500°C in N2 was 4.10×10−3 Ω cm. The differences in resistivity are discussed on the basis of the microstructure of the films using atomic force microscopy
and Hall measurements. 相似文献
212.
Tetsuo Tsuchiya Akio Watanabe Tomohiko Nakajima Toshiya Kumagai 《Applied Physics A: Materials Science & Processing》2010,101(4):681-684
Europium-doped yttrium oxide (Y2O3:Eu) thin films were successfully deposited on quartz and ITO/glass substrates by excimer-laser-assisted metal organic deposition
(ELAMOD) at low temperatures. The effects of laser wavelength and thermal temperature on the films’ crystallinity and photoluminescence
properties were investigated. Films irradiated by an ArF laser at 80 mJ/cm2 and 400–500°C were highly crystallized compared with those prepared by thermal MOD. In contrast, when the film was irradiated
by a KrF laser at 500°C, no crystalline Y2O3:Eu was formed. The Y2O3:Eu film irradiated by the ArF laser at 80 mJ/cm2 and 500°C showed typical PL spectra of Eu3+ ions with cubic symmetry and a 5D0→7F2 transition at ∼612 nm. The PL intensity at 612 nm was much higher for the film prepared with ELAMOD than for that prepared
by the thermal-assisted process, and the photoemission intensity of the film prepared with ELAMOD strongly depended on the
substrate material. 相似文献
213.
[reaction: see text] This paper describes the selective formation of a cyclic tetramer from a readily synthesized metalloporphyrin with two self-complementary quadruple hydrogen-bonding units. The extremely strong quadruple hydrogen-bonding unit, 2-ureido-4[1H]-pyrimidinone, enabled the formation of a stable cyclic tetramer based on a tetraphenylporphyrin derivative over a wide concentration range. This hydrogen-bonded tetramer is a new functional unit for use in a higher-ordered architecture of a supramolecular porphyrin assembly. 相似文献
214.
Successive differential and integral sorptions of water vapor into the polyelectrolyte complex of poly (sty renesulfonic acid) / poly(4-vinyl-N-ethylpyridinum bromide) have been measured; films of stoichiometric (1/1 molar ratio) and nonstoichiometric (2/1 molar ratio) complex were employed in the experiments. Sorption isotherms have been also determined by using the values obtained from integral sorption experiments. The sorption data have suggested the following. (i) The rearrangement of polymer chains plays a relatively unimportant role in sorption of water. (ii) The relaxation motion of network chains is suppressed. (iii) The change of morphological structure caused by vapor sorption is obscure. (iv) The ionic character of the 1/1 complex is higher than that of 2/1 complex. (v) A small amount of water can be dispersed on specific polymer sites, but the sorption of a large amount of water is accompanied by an expansion of network structure. Points (i)-(v) have been consistently interpreted on the basis of the network structure and ionic character of this complex. 相似文献
215.
N. Nakajima 《Journal of Macromolecular Science: Physics》2013,52(2):131-139
In our previous study on thermodynamic equilibrium at infinite dilution, chain segments at the periphery of a polymer coil were shown to be more extended than the average expansion of the coil. This is because such segments are in contact with pure solvent, whereas inside the coil there is a concentration of the segments. In a subsequent work examining the low concentration range, this excess extension of the segments was shown to diminish as the concentration was increased. Having more and more neighboring coils, the chain segments at the periphery of the coil have less and less excess extension, because the concentration difference between the inside and the outside of the coil decreases. In the present work the range below the theta temperature is examined; for polymers of finite molecular weights there are soluble ranges including partial and critical miscibility. When the limits of miscibility are approached either by lowering the temperature at a constant concentration or by increasing concentration at a constant temperature, the excess extension of the chain segments at the periphery of the coil disappears. The calculation makes use of a modified Maron theory. The required input data are intrinsic viscosity and polymer-solvent interaction parameter as a function of polymer concentration. These parameters must be known as functions of temperature and molecular weight. The example used in this work is the polystyrene-cyclohexane system. 相似文献
216.
Effects of pressure and temperature on the solubility of monosodium L-glutamate monohydrate in water
Yoshihisa Suzuki Hiroshi Matsuo Yoshikata Koga Katsuya Mukae Tetsuya Kawakita Seiji Sawamura 《高压研究》2013,33(2):93-104
Abstract The solubility of monosodium L-glutamate monohydrate (MSG.H2O) in water was measured at pressures in the range of 0.10-300MPa and 298.15K. The density of MSG solution at high concentrations and heat of solution at saturated concentration were also measured at atmospheric pressure. The solubility, ms, increased with increasing pressure and the pressure coefficient, Θp, [?(? In ms,? p)T] at 0.10 MPa was (2.0 ± 0.1) × 10-10Pa-1. It agrees well with (2.1 ±0.2)× 10-10 Pa-1 thermodynamically estimated using the partial molar volume, the activity coefficient of the solute in solution, and the molar volume of the crystal. The excellent agreement at 0.10MPa gives us confidence in the solubility data at higher pressures. The heat of solution data and other pertinent values were used to calculate the temperature coefficient of solubility, ΘT [? (? In ms/?(1/T))p], by a thermodynamic equality. The resulting ΘT compares well with the data directly measured by Ogawa. 相似文献
217.
The oxidation behaviour of Ni nanoparticles at temperatures from 573 to 673 K and the formation process of hollow oxide particles were studied by transmission electron microscopy. In the course of oxidation, a single large void was observed at one site of the interface between inner Ni and outer NiO layer due to vacancy clustering, which occurs during the oxidation process resulting from the rapid outward diffusion of Ni ions through the NiO layer. This suggests that supersaturated vacancies generated at the interface migrate to the site over a long-range distance and aggregate at the site. Ni nanoparticles were fully oxidized to become hollow NiO, in which nano-holes in the form of vacancy clusters were located at the off-centred positions. The de-centring of the voids in hollow NiO is probably due to the large mobility of vacancies inside Ni during oxidation. 相似文献
218.
Strained layer quantum well semiconductor optical amplifiers: Polarization insensitive amplification
M. Joma H. Hofukawa M. Nakajima M. Kawahara T. Kamijoh 《Fiber and Integrated Optics》2013,32(4):361-364
Abstract Polarization insensitive optical amplification was demonstrated in newly developed semiconductor optical amplifiers that have strained GalnAsP quantum well structures. We tailored the active region of the quaternary strained layer quantum well structure with a small biaxially tensile strain of 0.2% in the well layers for polarization insensitive operation. 相似文献
219.
Osamu Sato Shinya Hayami Zhong-ze Gu Kazuyuki Takahashi Rie Nakajima Akira Fujishima 《Phase Transitions》2013,86(7-8):779-785
Photo-illumination effects have been measured for the compound [Co III-LS (tmpda)(3,6-DBSQ)(3,6-DBCat)]. When the aforementioned compound was illuminated at 5 K, the magnetization value increased from w eff = 1.87 to 2.03 w B . The absorption spectra after illumination show that the absorption band at around 730 nm, which is characteristic of the [Co II-HS (tmpda)(3,6-DBSQ) 2 ] state, increased in intensity and that the charge transfer band from 3,6-DBCat to 3,6-DBSQ at 2500 nm was reduced in intensity. IR spectra show that the C-O stretching peak at 1279 cm m 1 is decreased in intensity. These results confirm that a photo-induced intra-molecular electron transfer, [Co III-LS (tmpda)(3,6-DBSQ)(3,6-DBCat)] to; [Co II-HS (tmpda)(3,6-DBSQ) 2 ], was induced. The lifetime of the metastable state at 5 K was 15 min. Furthermore, it was found that reverse valence tautomerism can be induced by exciting the Co II-HS to 3,6-DBSQ charge transfer band in metastable [Co II-HS (tmpda)(3,6-DBSQ) 2 ]. 相似文献
220.
We report low-temperature specific-heat studies on the single-crystalline ternary-iron silicide superconductor Lu(2)Fe(3)Si(5) with T(c)=6.1 K down to approximately T(c)/20. We confirm a reduced normalized jump in specific heat at T(c), and find that the specific heat divided by temperature C/T shows a sudden drop at approximately T(c)/5 and goes to zero with further decreasing temperature. These results indicate the presence of two distinct superconducting gaps in Lu(2)Fe(3)Si(5), similar to the typical two-gap superconductor MgB(2). We also report Hall coefficients, band structure calculations, and the anisotropy of upper critical fields for Lu(2)Fe(3)Si(5), which support the anisotropic multiband nature and reinforce the existence of two superconducting gaps in Lu(2)Fe(3)Si(5). 相似文献