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81.
The mass-transter characteristics of a two-phase system formed by mixing a fixed quantity (20 v/v%) of organic solvent with an aqueous ferricyanide electrolyte solution in an RDE system were studied. The Levich eqution, I1 = 0.62 nFACbD2/3v?1/6ω1/2, was found to be applicable to the two-phase system with only a minor modification in the angular velocity (ω) at Reynolds numbers between 3–5 × 104. The experimental results indicate that the interfacial tension is the most important variable for the two-phase system. One group of organic solvents with smaller interfacial tension, such as benzene or toluene, needs a modification of the Levich equation by replacing the observed angular velocity (ωo) with the true angular velocity (ωt) which was observed to be 1.1 times the observed angular velocity. For the other group with larger interfacial tension, such as n-hexane or cyclohexane, there is no need to modify the observed angular velocity. In other words, the Levich equation may be expressed as I1 = 0.65 nFACbD2/3v?1/6ω1/2 for two-phase solution if the interfacial tension is smaller than 37.0 dyne/cm. 相似文献
82.
The concentration fields, Nusselt number distributions along the electrode, and ratios of concentrations of electrochemically active components at the entrance into and exit out of an electrochemical cell are determined by numerical integration of the convective-diffusion equation for a broad range of rate constants of electrode reactions, Peclet numbers, and geometrical parameters of channels. Three regions of parameter values are revealed. At low reaction rates (K
l
< 0.5), mass transfer is completely determined by electrode kinetics; at high rates (K
l
> 20), it is completely determined by the diffusion in the gas phase; and in the intermediate region of values of K
l
it is necessary to allow for both the diffusion processes and the electrode reactions.Translated from Elektrokhimiya, Vol. 41, No. 3, 2005, pp. 317–324.Original Russian Text Copyright © 2005 by Ezin, Somov. 相似文献
83.
84.
Yue Shen Xiaohui Tang Yuwei Xu Haichao Liu Shitong Zhang Bing Yang Yuguang Ma 《中国化学快报》1990,30(11):1947-1950
Cyanophenyl as ancillary acceptor to modify donor-acceptor compound,plays an effective role in shifting the emission color to deep red and maintaining the luminescent efficiency. 相似文献
85.
Introduction Ionchromatography (IC)hasbeenrecognizedasausefulmethodfortheseparationofinorganicanionsandcationssinceitsintroductionbySmalletal .in 1975 .1AsignificanttrendinthedevelopmentofICmethodissearchforsensitiveanduniversaldetectionmethods .Themaindet… 相似文献
86.
Summary A flow-through two electrode wall-jet cell with a platinum measuring electrode and a cell volume of 20 nl has been designed and evaluated. It has been used to detect phenols by reversed phase liquid chromatography using short micro bore columns. The linear dynamic range between the measured current and the concentration is greater than 103 (1.5×10–7–5×10–4 mol/l) and the minimum analyzable amount was found to be 10 pg for pyrocatechol. A negligible broadening in the detector permits the use of micro columns down to 0.5 mm internal diameter, packed with 5 m particles, without any substantial distortion of eluted zones.Presented at the 14th International Symposium on Chromatography London, September, 1982 相似文献
87.
88.
E. I. Zhilyaeva S. A. Torunova R. N. Lyubovskaya R. B. Lyubovskii 《Russian Chemical Bulletin》1996,45(5):1107-1110
Radical cation salts with halide mercurate anions were obtained by the electrochemical oxidation of bis(ethylenedioxo)tetrathiafulvalene (BEDO-TTF), and their conductivity was studied. The compounds (BEDO-TTF)4Hg3X8 (X = Cl or Br), (BEDO-TTF)4Hg3.5I9, and (BEDO-TTF)2HgBr3 possess the conductivity of the metallic type down to helium temperatures.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 1167–1170, May, 1996. 相似文献
89.
The anodic reaction of Ni in an alkaline solution was studied by the tip–substrate voltammetry mode of scanning electrochemical microscopy (SECM) and cyclic voltammetry (CV). A platinum microdisc electrode was selected as the tip electrode, which functioned as a pH sensor with transient response capability. The pH value of the solution near the Ni electrode surface varied while the Ni substrate oxidation reaction occurred, and the pH variation could be detected by the tip faradic current. The cyclic voltammogram results showed that two types of hydroxides: i.e. α‐Ni(OH)2 and β‐Ni(OH)2 were formed during Ni oxidation in the lower potential region. In the proceedings of α‐Ni(OH)2 → γ‐NiOOH and β‐Ni(OH)2 → β‐NiOOH, the process of OH? concentration decrease in the solution was ahead and behind of electron transfer in the solid phase, respectively. These results indicate that the OH? adsorption process occurs as an elementary step in the former reaction and the H+ diffusion process from the inner to the outer layer of the solid phase occurs as a subsequent step in the latter reaction. The results also revealed that the oxide film on the Ni surface has a two‐layer structure. The real potential of the oxygen evolution reaction (OER) on the Ni surface with different cycles is also analyzed in the paper. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献
90.
The diffusion length of charge carriers in the active layer of a perovskite solar cell (PSC) of the structure Glass/PEDOT: PSS/CH3NH3PbI3/PC60BM/Al is modelled. It is found that the diffusion length depends on the position x in the active layer measured from the PEDOT: PSS interface, Urbach energy and temperature. By varying the voltage in the range from zero to , it is shown that the dependence of diffusion length on the position x in the active layer reduces at higher voltage. The combined influence of applied voltage and temperature on the diffusion length of charge carriers is investigated and it is found that in the low voltage range the diffusion length is temperature independent, but it becomes significantly temperature dependent at higher voltages. Also, it is found that the diffusion length decreases as the applied voltage increases and this reduction becomes much more significant at higher voltage and temperatures. The combined influence of applied voltage and Urbach energy on diffusion length of charge carriers reveals that the diffusion length decreases when both the applied voltage and Urbach energy increase. However, the reduction in the diffusion length due to the increase in Urbach energy becomes less significant at higher voltage. 相似文献