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961.
962.
合成了金属有机框架化合物沸石咪唑框架-90(ZIF-90)溶胶和ZIF-90晶体薄膜,分别以这2种材料为基底,制备出了Ag@ZIF-90复合材料和Ag/ZIF-90自组装薄膜.通过傅里叶变换红外(FT-IR),X射线衍射(XRD),扫描电子显微镜(SEM)对产物进行表征,分析了它们的形貌和结构特征.以罗丹明6G(R 6G)作为检测分子,对所制备材料的表面增强拉曼散射(SERS)性能进行测试.结果表明制备出的Ag/ZIF-90自组装薄膜具有好的SERS性能,而ZIF-90本身的拉曼峰并不会对Ag/ZIF-90自组装薄膜的SERS检测效果产生影响.这种材料可以作为一种较好的表面增强拉曼(SERS)活性基底,在农药残留检测方面具有很好的应用前景. 相似文献
963.
Dr. Dulce M. Morales Dr. Mariya A. Kazakova Dr. Danea Medina Dr. Javier Villalobos Dr. Götz Schuck Dr. Marcel Risch Prof. Dr. Wolfgang Schuhmann 《ChemCatChem》2024,16(9):e202301174
High-performance bifunctional electrocatalysts for the oxygen reduction (ORR) and oxygen evolution reaction (OER) are essential components in energy conversion and storage technologies. Yet, their poor reversibility hinders their applicability. A highly active ORR/OER catalyst, consisting of multiwalled carbon nanotubes-supported MnFeNiOx nanoparticles, was subjected to sequences of chronoamperometric steps alternating between the ORR, the OER and highly cathodic potentials (Ec). Rotating ring disk electrode methods revealed that applying Ec leads to a small increase in the current and peroxide species yield during the ORR while enhancing substantially the OER. X-ray absorption spectroscopy showed irreversible changes in the chemical state of MnFeNiOx correlating with its catalytic properties. The complexity of changes that a composite catalyst may undergo under varying potentials, the importance of monitoring product formation, and the convenience of using dynamic electrochemical sequences for the assessment of catalyst reversibility, as well as for the activation and/or restoration of their catalytic properties, are highlighted. 相似文献
964.
In this work, we synthesized electroactive cubic Prussian blue (PB) modified single‐walled carbon nanotubes (SWNTs) nanocomposites using the mixture solution of ferric‐(III) chloride and potassium ferricyanide under ambient conditions. The successful fabrication of the PB‐SWNTs nanocomposites was confirmed by scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV‐vis absorption spectroscopy, Fourier transform infrared (FTIR) spectroscopy, and cyclic voltammetry (CV). PB nanocrystallites are observed to be finely attached on the SWNTs sidewalls in which the SWNTs not only act as a carrier of PB nanocrystallites but also as Fe(III)‐reducer. The electrochemical properties of PB‐SWNTs nanocomposites were also investigated. Using the electrodeposition technique, a thin film of PB‐SWNTs/chitosan nanocomposites was prepared onto glassy carbon electrode (GCE) for the construction of a H2O2 sensor. PB‐SWNTs/chitosan nanocomposites film shows enhanced electrocatalytic activity towards the reduction of H2O2 and the amperometric responses show a linear dependence on the concentration of H2O2 in a range of 0.5–27.5 mM and a low detection limit of 10 nM at the signal‐to‐noise ratio of 3. The time required to reach the 95% steady state response was less than 2 s. CV studies demonstrate that the modified electrode has outstanding stability. In addition, a glucose biosensor is further developed through the simple one‐step electrodeposition method. The observed wide concentration range, high stability and high reproducibility of the PB‐SWNTs/chitosan nanocomposites film make them promising for the reliable and durable detection of H2O2 and glucose. 相似文献
965.
Analysis of the differential capacity at the silver / lithium perchlorate aqueous solution interface
Maria Jurkiewicz-Herbich Magdalena Miłkowska 《Journal of Solid State Electrochemistry》2001,5(1):36-42
Analysis of the differential capacity of ideally polarized Ag electrodes without specific adsorption is presented. The capacity
was measured for three crystal faces of Ag [(111), (100) and (110)] and for polycrystalline Ag in aqueous solutions at different
concentrations of LiClO4. The inner layer contribution C
i was analysed for all the systems studied according to Grahame's concept. Moreover, using the procedure proposed by Amokrane
and Badiali, several contributions to C
i, i.e. the metal (C
m), the solvent (C
s) and dipole orientation (C
dip), were calculated. The influence of the kind of crystal face of the Ag electrode on the values of these contributions is
discussed.
Received: 21 May 1999 / Accepted: 19 November 1999 相似文献
966.
《Electroanalysis》2006,18(9):854-861
Nafion polymer coated bismuth‐film‐modified carbon film electrodes have been investigated for reducing the influence of contaminants such as surfactants in the anodic stripping voltammetry of trace metal ions. The influence of the coating on electrode response has been tested with both ex situ and in situ bismuth film deposition, with and without the polymer coating. The electrode assemblies and interfacial characteristics in the presence of the non‐ionic surfactant Triton‐X‐100 have been probed with electrochemical impedance spectroscopy. The Nafion coating successfully decreases the adsorption of Triton on the bismuth film surface, and demonstrates that this strategy allows measurement of these trace metals in environmental samples containing surfactants. 相似文献
967.
V. A. Safonov M. A. Choba Yu. D. Seropegin E. N. Lubnin 《Russian Journal of Electrochemistry》2006,42(8):861-872
The behavior of electrodes, which are made of binary Au-Ag alloys (Ag content 1–15 at %) and renewed by mechanical cutting in aqueous solutions of sodium fluoride, is studied with the aid of cyclic voltammetry and impedance methods. It is established that, in the region of potentials corresponding to ideal polarizability, the differential capacitance of the electrical double layer rapidly changes with time elapsed after the renewal of the surface of the electrodes. The change in the capacitance is brought about by the exit of silver atoms into a surface layer. The implication is that silver is the surface-active component in these alloys. The rate of the surface segregation of silver atoms depends on the electrode potential. The segregation rate substantially increases upon going into the region that corresponds to positive charges of the silver electrode surface and to the beginning of adsorption of atomic oxygen on the electrode. Based on phenomenological models, a method for processing capacitance curves is realized, which links experimentally observed time effects to variations that occur in the surface composition, and assumptions concerning the mechanism of relaxation processes that are responsible for the observed time effects are put forth. Explicit data on the effect, which is exerted by mechanical renewal on the composition of the surface layer of Au-Ag alloys at different distances from the interface with a vacuum, are obtained with the aid of an x-ray photoelectron spectroscopy method. It is established that the surface layer (~0.5 nm) is enriched by silver atoms as compared with the alloy’s bulk. 相似文献
968.
《Electroanalysis》2006,18(9):849-853
A novel electroanalytical methodology for the sensing of anticarcinogenic catechin compounds epigallocatechin gallate (EGCG) and epigallocatechin (EGC) is presented. The protocol is based on the electrochemical oxidation of aminophenol in aqueous solutions, where the quinoneimine oxidation product chemically reacts with the EGCG or EGC compounds resulting in consumption of quinoneimine and consequently results in a reduction in the magnitude of the quinoneimine reduction wave, which is found to provide an analytical signal from which to indirectly detect EGCG and/or EGC. 相似文献
969.
Jesús Santos-Peña Patrick Soudan Carlos Otero Areán Gemma Turnes Palomino Sylvain Franger 《Journal of Solid State Electrochemistry》2006,10(1):1-9
Mesoporous iron phosphate containing CTAB as templating agent was synthesized and characterized by means of X-ray diffraction, Fourier transform infrared spectroscopy and TGA techniques. The mesoporous material shows a highly ordered structure, that collapses when submitted to extraction with acetate ions. The treatment of the exchanged samples at 573 K under nitrogen atmosphere leads to amorphous phases with an electrochemical behaviour typical of carbon-coated iron phosphate electrodes. The existence of this coating, proceeding from incomplete pyrolysis of the organic exchange agent, enhances the electronic properties of the system, as evidenced by galvanostatic experiments and impedance spectroscopy measurements. 相似文献
970.
Gregory J. Barbante Conor F. Hogan Andrew B. Hughes 《Journal of Solid State Electrochemistry》2009,13(4):599-608
The solid state electrochemistry and solid state spectroelectrochemistry of two ruthenium complexes, ruthenium tris-(4,7-diphenyl-1,10-phenanthroline)
bis-hexafluorophosphate, [Ru(dpp)3](PF6)2, and ruthenium bis-(2,2′-bipyridine)(4,6-diphenyl-2,2′-bipyridine)bis-hexafluorophosphate, [Ru(bpy)2(dpb)](PF6)2, is described. Microparticles of the material are immobilised on ITO electrodes, and stable voltammetric signals are obtained
in contact with aqueous electrolyte solution. Spectral changes monitored during a slow cyclic voltammetric scan confirm the
exhaustive oxidation of the Ru2+ species to the Ru3+ form. The derivative of the absorbance signal monitored at a single wavelength during potential cycling is morphologically
identical to a cyclic voltammogram with no background current. This technique is shown to be useful when peaks of small magnitude
are obscured by capacitive background or when peaks close to the solvent limit are obscured by solvent electrolysis current.
The technique effectively widens the electrochemical window available for voltammetric measurements. After suitable correction
of the signal, the value of the voltammetric peak height (I
p) as well as peak potential (E
p) may be obtained from the derivative absorbance signal. Chronospectrometry is demonstrated to provide the equivalent to a
chronocoulometric response, but is closer to the ideal simulated response. A facile method for simulating time or potential-dependant
spectroelectrochemical responses using commercial electrochemical simulation software is described. Absorbance transients
monitored during the electrolysis of solid particles of [Ru(dpp)3](PF6)2 show best agreement with simulated data at very short and very long timescales. This observation, in conjunction with the
observations from the potential scan experiments, suggests that the absorbance, charge, or current vs. time behaviour of the
system can be adequately described by a semi-infinite diffusional model at short experimental timescales and by a finite diffusional
model at sufficiently long timescales.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.
Dedicated to the 80th birthday of Keith B. Oldham. 相似文献