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121.
《Current Applied Physics》2014,14(5):744-748
Raman scattering spectroscopy has been performed on high quality Co-doped ZnO epitaxial films, which were grown on Al2O3 (0001) by oxygen-plasma assisted molecular beam epitaxy. Raman measurements revealed two local vibration modes (LVMs) at 723 and 699 cm−1 due to the substitution of Co2+ in wurtzite ZnO lattice. The LVM at 723 cm−1 is found to be an elemental sensitive vibration mode for Co substitution. The LVM at 699 cm−1 can be attributed to enrichment of Co2+ bound with oxygen vacancy, the cobalt–oxygen vacancy–cobalt complexes, in Zn1−xCoxO films associated with ferromagnetism. The intensity of LVM at 699 cm−1, as well as saturated magnetization, enhanced after the vacuum annealing and depressed after oxygen annealing. 相似文献
122.
Pure titania porous layers consisted of anatase and rutile phases, chemically and structurally suitable for catalytic applications, were grown via micro-arc oxidation (MAO). The effect of applied voltage, process time, and electrolyte concentration on surface structure, chemical composition, and especially photocatalytic activity of the layers was investigated. SEM and AFM studies revealed that pore size and surface roughness of the layers increased with the applied voltage, and the electrolyte concentration. Moreover, the photocatalytic performance of the layers synthesized at medium applied voltages was significantly higher than that of the layers produced at other voltages. About 90% of methylene blue solution was decomposed after 180 min UV-irradiation on the layers produced in an electrolyte with a concentration of 10 g l−1 at the applied voltage of 450 V. 相似文献
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124.
Tuong Lan Nguyen Masayuki Dokiya Shaorong Wang Hiroaki Tagawa Takuya Hashimoto 《Solid State Ionics》2000,130(3-4):229-241
The electrical property of (La1−xSrx)1−z(Al1−yMgy)O3−δ (LSAM; x≤0.3, y≤0.15 and z≤0.1) was measured using the DC four-probe method as a function of temperature (500–1000°C) and oxygen partial pressure (1–10−22 atm). Among LSAMs, (La0.9Sr0.1)AlO3−δ showed the highest ionic conductivity, σi=1.3×10−2 S cm−1 at 900°C. A simultaneous substitution at A and B sites or A site deficiency is expected to create larger oxygen vacancy and higher ionic conductivity. However, it showed a negative effect. The effect of the vacancy increase did not effect monotonously the ionic conductivity. It was found that the concentration of oxygen vacancy, [VO], influences not only the oxide ion conductivity, σi, but also the mobility, μv, of [VO]. These properties exhibit a maximum at around [VO]=0.05. With the increase in [VO], the activation energy, Ea, of the ionic conduction dropped from 1.8 to ca. 1.0 eV at [VO]=0.05 and became almost constant at [VO]>0.05. The dependency of the pre-exponential term, μ0v, and Ea on [VO] was analyzed and their effect on μv and σi was discussed with respect to crystal structure and defect association. It was estimated that the crystal structure mainly governs these properties. The effect of defect association could not be ignored but is considered to be a complicated correlation. 相似文献
125.
Influence of buffer layer thickness on the structure and optical properties of ZnO thin films 总被引:1,自引:0,他引:1
A series of ZnO thin films were deposited on ZnO buffer layers by DC reactive magnetron sputtering. The buffer layer thickness determination of microstructure and optical properties of ZnO films was investigated by X-ray diffraction (XRD), photoluminescence (PL), optical transmittance and absorption measurements. XRD results revealed that the stress of ZnO thin films varied with the buffer layer thickness. With the increase of buffer layer thickness, the band gap edge shifted toward longer wavelength. The near-band-edge (NBE) emission intensity of ZnO films deposited on ZnO buffer layer also varied with the increase of thickness due to the spatial confinement increasing the Coulomb interaction between electrons and holes. The PL measurement showed that the optimum thickness of the ZnO buffer layer was around 12 nm. 相似文献
126.
The oxide films formed on AISI 304L stainless steel at 300 °C in the oxidation time range between 2 and 4 h have been studied by photoelectrochemistry. Photocurrents were investigated as a function of the wavelength of the incident light and the electrode potential. The investigation allowed the determination of the semiconductive properties of the oxides. The oxide films showed n-type behaviour. A duplex structure of the oxide films has been suggested on the basis of the photocurrent spectra, with an internal oxide layer having an optical gap (Eg2 = 2.16-2.3 eV) depending on the applied potential and oxidation time, higher to that of the external oxide layer (Eg1 ≈ 1.9 eV). Significant variations in the amplitude of the photocurrent were detected as a function of the applied potential and the oxidation time. 相似文献
127.
A simple simulation scheme that simultaneously describes the growth kinetics of SiO2 films at the nanometer scale and the SiOx/Si interface dynamics (its extent, and spatial/temporal evolution) is presented. The simulation successfully applies to experimental data in the region above and below 10 nm, reproduces the Deal and Grove linear-parabolic law and the oxide growth rate enhancement in the very thin film regime (the so-called anomalous region). According to the simulation, the oxidation is governed mainly by two processes: (a) the formation of a transition suboxide layer and (b) its subsequent drift towards the silicon bulk. We found that it is the superposition of these two processes that produces the crossover from the anomalous oxidation region behavior to the linear-parabolic law. 相似文献
128.
本文描述农用薄膜中Al、Fe、Mg、Ca、Si、Cu、Ti杂质元素的发射光谱分析法,该方法直接压样于石墨电极中,简便,快速,取得了满意的结果。 相似文献
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