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In the present investigation, Cu0.5Ni0.5 nanoparticles were synthesized using high energy ball milling of a mixture of Cu2O, NiO, and graphite powders. The mixture of powders was milled up to 50 h. The 30 h milled sample was heat treated at various temperatures for 1 h in a vacuum tube furnace. The effects of milling time and heat treatment temperature on the powder particle characteristics were studied employing X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), differential thermal analysis (DTA), and vibrating sample magnetometer (VSM) techniques. XRD results indicated incomplete formation of Cu0.5Ni0.5 after 30 h of milling. Further heat treatment at 500 °C led to the formation of a single phase Cu0.5Ni0.5 powder. FESEM and TEM images of the heat treated sample showed spherical Cu0.5Ni0.5 nanoparticles with a mean particle size of 15 nm. Magnetic properties data measured by VSM of the above sample are correlated well with the XRD results. Coercivity and saturation magnetization have been approximately achieved at 25 Oe and 18 emu/g, respectively.  相似文献   
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Stretchable electronics outperform existing rigid and bulky electronics and benefit a wide range of species, including humans, machines, and robots, whose activities are associated with large mechanical deformation and strain. Due to the nonstretchable nature of most electronic materials, in particular semiconductors, stretchable electronics are mostly realized through the strategies of architectural engineering to accommodate mechanical stretching rather than imposing strain into the materials directly. On the other hand, recent development of stretchable electronics by creating them entirely from stretchable elastomeric electronic materials, i.e., rubbery electronics, suggests a feasible a venue. Rubbery electronics have gained increasing interest due to the unique advantages that they and their associated manufacturing technologies have offered. This work reviews the recent progress in developing rubbery electronics, including the crucial stretchable elastomeric materials of rubbery conductors, rubbery semiconductors, and rubbery dielectrics. Thereafter, various rubbery electronics such as rubbery transistors, integrated electronics, rubbery optoelectronic devices, and rubbery sensors are discussed.  相似文献   
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In this research, carbon nanotube (CNT)-modified plasmonic silver-strontium titanate (Ag@ SrTiO3) nanocomposites for the degradation of the organic dye were prepared by the sol-gel method. The characterization of all products was carried out using the X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), N2 adsorption-desorption test (BET), field emission-scanning electron microscopy (FESEM), transmission electron microscopy (TEM), UV–visible diffuse reflectance spectroscopy (DRS), photoluminescence (PL) spectroscopy, electrochemical impedance spectroscopy (EIS), and transient photocurrent (TPC) studies. It was found that the incorporation of Ag in and introducing CNT into the SrTiO3 nanoparticles reduced the crystallite size to 21 nm and the band gap energy to 2.7 eV. The Reduced PL peak intensity, increased photocurrent value, and reduced charge transfer resistance approved that the Ag@SrTiO3@CNT nanocomposite had a greater charge transfer efficiency than other samples. The optimal dosage of the photocatalyst, for the complete degradation of 5 ppm of the methylene blue (MB) solution after 30 min of the visible light irradiation, was decided as 0.5 g/L. Besides, in the experimental environment, the Ag@SrTiO3@CNT sample illustrated the most significant photocatalytic performance of the degradation of methyl orange (MO) and Rhodamine B (RhB) dyes. The detailed mechanism and kinetics of the degradation procedure were clarified. Finally, the prepared system displayed increased stability and reusability in the entire cyclic degradation experiment.  相似文献   
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The paper reports on the design and construction of a Paul ion trap as an ion source by using an impact electron ionization technique. Ions are produced in the trap and confined for the specific time which is then extracted and detected by a Faraday cup. Especial electronic configurations are employed between the end caps, ring electrodes, electron gun and a negative voltage for the detector. This configuration allows a constant low level of pure ion source between the pulsed confined ion sources. The present experimental results are based on the production and confinement of Argon ions with good stability and repeatability, but in principle, the technique can be used for various Argon like ions.  相似文献   
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Considering the high surface defects of polycrystalline perovskite, chemical passivation is effective in reducing defects-associated carrier losses. However, challenges remain in promoting passivation effects without compromising the carrier-extraction yield at the perovskite interfaces. In this work, interlayer molecules functionalized with different side groups are rationally designed to investigate the correlation between defect-passivation strength and interfacial carrier dynamics.  It is revealed that Cl-grafted molecules impose destructive effects on the perovskite structure due to its lower electronegativity and mismatched spatial configuration. The introduction of cyanide (CN) as a side group in molecules also leads to perovskite deformation and unfavorable hole collection. After the molecular optimization, the incorporation of carbonyl (C═O) as the side group (TPA─O) simultaneously promotes the carrier-collection yield as well as sufficient defect passivation. As a consequence, the devices based on TPA─O yield a champion PCE of 23.25%, along with remarkable stability by remaining above 88.5% of initial performance after 2544 h storage in the air. Furthermore, this interlayer based on TAP─O enables flexible devices to achieve a high efficiency of 21.81% and promising mechanical stability. This work paves the way for further improving the performance of perovskite solar cells.  相似文献   
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Engineered nanoparticles are increasingly being considered for use as biosensors, imaging agents and drug delivery vehicles. Their versatility in design and applications make them an attractive proposition for new biological and biomedical approaches. Despite the remarkable speed of development in nanoscience, relatively little is known about the interaction of nanoscale objects with living systems. In a biological fluid, proteins associate with nanoparticles, and the amount and the presentation of the proteins on their surface could lead to a different in vivo response than an uncoated particle. Here, in addition to protein adsorption, we are going to introduce concept of cell "vision", which would be recognized as another crucial factor that should be considered for the safe design of any type of nanoparticles that will be used in specific biomedical applications. The impact of exactly the same nanoparticles on various cells is significantly different and could not be assumed for other cells; the possible mechanisms that justify this cellular response relate to the numerous detoxification strategies that any particular cell can utilize in response to nanoparticles. The uptake and defence mechanism could be considerably different according to the cell type. Thus, what the cell "sees", when it is faced with nanoparticles, is most likely dependent on the cell type.  相似文献   
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