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61.
Improve the field emission uniformity of carbon nanotubes treated by ball-milling process 总被引:1,自引:0,他引:1
Carbon nanotubes (CNTs) deposited by chemical vapor deposition (CVD) were treated by ball milling. The morphologies and field emission properties of the treated CNTs depending on milling time were studied. The emission turn-on field is increased, and the field emission current density is reduced, when the milling time increased from 0.5 to 3 h. The as-deposited long CNTs were cut to short CNTs (∼1 h) and micro-particles (>1 h) with increasing of the milling time. It is found that the optimized milling time is 0.5-1 h, the treated CNTs showed excellent field emission properties, such as low turn-on field, high emission current density and uniform luminescence spots distribution. 相似文献
62.
Hydrogen, as a sustainable and clean energy, has been considered as a promising candidate to replace fossil fuels. And it is meaningful to fabricate the photocatalysts to drive photocatalytic water splitting leading to hydrogen production. Herein, a facile approach was developed by the means of the template effect of poly (ionic liquid) and self-assembly of cyanuric acid and melamine through hydrogen bonds, to obtain carbon nitride hollow microspheres with highly hierarchical porosity. The influence of poly (ionic liquid) concentration on the structure and photocatalytic activity of as-prepared carbon nitride was investigated. The optimized carbon nitride hollow microspheres possessed the multiple porous channels and improved surface area (71 m2/g) due to the decomposition of poly (ionic liquid) and cyanuric acid-melamine supramolecular aggregates. Moreover, the as-prepared carbon nitride hollow microspheres exhibited a remarkable catalytic activity in the photocatalytic hydrogen evolution reaction under visible light irradiation. Especially, the sample CN-0.02 exhibits the highest hydrogen evolution rate (90.1 μmol h−1). The outstanding photocatalytic activity is attributed to the high specific surface area, broad light absorption range and fast separation rate of photogenerated electron–hole pairs. This novel method opens up a new way toward the development of highly-active photocatalysts for water splitting. 相似文献
63.
In this paper, a novel TiO2 nanosheets assembled double‐wall hollow sphere (DHS)has been prepared successfully via hydrothermal treatment of SiO2@TiO2 with the assistant of CTAB.The prepared samples are characterized with transmission electron microscopy (TEM), scanning electron microscopy (SEM), electron spin resonance (ESR), X‐ray diffraction (XRD) and X‐ray photoelectron spectra (XPS), etc.Results show that redeposited silica species play a key role in the formation of the double‐wall structure. The as‐synthesized DHS nanostructure exhibits a large surface area (417.6 m2 g‐1) and excellent mechanical strength. Furthermore, after decoration of Ag and calcination treatment, the double‐shelled TiO2/Ag heterostructures show an enhanced photocatalytic performance in the degradation of RhB under UV or visible light irradiations for the following reasons: the surface plasmon resonance effect of Ag, strong interaction between Ag and TiO2 nanosheets, large surface area, excellent adsorption capacityand unique double‐wall structure. On the basis of the experimental results, a possible mechanism for pollutantdegradation under visual light irradiation has been proposed. 相似文献
64.
Guodong Tang Rongqing Li Shanshan Kou Tingling Tang Yu Zhang Yiwei Wang 《Optics and Spectroscopy》2014,116(2):263-273
Ruthenium polypyridined-derivative complexes are used in dye-sensitized solar cell [DSSC] as a light to current conversion sensitizer. In order to lower the cost of the DSSC the normal transition metals were used to replace the noble metal ruthenium, and some compounds [ML2L′] (M = Pt, Fe, Ni, Zn; L = isonicotinic acid, L′ = maleonitriledithiolate, I = PtL2L′, II = FeL2L′, III = NiL2L′, IV = ZnL2L′) were selected as the replacement. The geometries, electronic structures and optical absorption spectra of these compounds have been studied by using density functional theory (DFT) calculation at the B3LYP/LANL2DZ, B3P86/LANL2DZ, B3LYP/GEN level of theory. All the geometric parameters are close to the experimental values. The HOMOs are mainly on the maleonitriledithiolate groups mixed with fewer characters of the metal atom, the LUMOs are mainly on the two pyridine ligands. This means that the electron transition is attributed to the LLCT. The maximum absorptions of complexes are found to be at 351 nm, 806 nm for compound I, and 542 nm for compound II. The maximum absorptions of complexes are found to be at 884 nm for compound III, and 560 nm for compound IV. This means that those compounds may be as a suitable sensitizer for solar energy conversion applications. 相似文献
65.
Wanping Zhang Liaoyuan Zhang Dan Zhu Yiwei Wu Yubo Qin Wenhua Ou 《Journal of Dispersion Science and Technology》2013,34(11):1637-1644
AbstractThe aim of this work was to study the encapsulation properties of polyols-in-oil-in-water (P/O/W) multiple emulsions for Vitamin C (Vc). The influence of formulation factors, including the concentration of lipophilic emulsifier, hydrophilic emulsifier, salt and glycerol had been investigated. The results indicated that the encapsulation stability could be improved by increasing the lipophilic emulsifier concentration which could strengthen the interfacial film. In contrast, the excess of hydrophilic emulsifier destabilized the emulsion. The presence of glycerol in the outer aqueous phase accelerated the phase transfer, thus reduced the encapsulation rate. The addition of salt in inner polyols phase had little effect on encapsulation rate while markedly affected the morphology and stability of this system. P/O/W multiple emulsions showed better encapsulation stability than the W/O/W multiple emulsions as the former’s encapsulation rate could remain more than 75% after 2?weeks while the latter only remained less than 60%. Meanwhile, the P/O/W emulsions exhibited higher storage modulus (G’), bigger loss modulus (G’’) and broaden linear viscoelastic regions than W/O/W emulsions. 相似文献
66.
Series of fluorinated compounds, 2-(3′,5′-difluoro-4′-alkoxybiphenyl-4-yl)-benzoxazole derivatives (nFBx), were prepared and characterised. Their phase transition behaviour was investigated by differential scanning calorimetry and polarising optical microscopy. In the case of carbon atoms in the alkoxy chain between 4 and 10, they exhibited enantiotropic mesophases with the mesophase ranges of 12–119°C and 23–152°C on heating and cooling for compounds bearing different substituents (H, CH3, Cl, and NO2). With the exception of nitro-substituted compounds, the nFBx series displayed intense photoluminescence emission at 380–385 nm in methylene chloride solution when they were excited at their absorption maxima. Compared to non-fluorinated analogues, fluorinated compounds nFBx (apart from nitro-substituted compounds) exhibited much lower melting points, but comparable or slightly narrower mesophase ranges during both heating and cooling, which were attributed to the disruption of the side-to-side intermolecular packing caused by the two lateral fluoro substituents. 相似文献
67.
Hongxin Wang Baijun Liu Mingyao Zhang Shuai Du Gaocheng Wu Yiwei Hu Jinhui Zhang Xiangchi Liu 《先进技术聚合物》2020,31(3):407-414
The increasing demand for monodispersed cross‐linked polymers in high‐quality applications requires continuous improvement in their preparation process. In this study, an appropriate amount of a chain transfer agent was added to a traditional cross‐linking system, resulting in the preparation by one‐step dispersion polymerization of cross‐linked polystyrene (PS) microspheres with a particle size of 3.867 μm and a diameter coefficient of variation of 0.011. The particles were characterized using scanning electron microscopy (SEM) and an Ubbelohde viscometer. The results show that the tertiary dodecyl mercaptan (TDDM) chain transfer during nucleation increases the oligomer concentration, promotes the aggregation of the oligomers, increases the primary particle size, and reduces the cross‐linking effect. This controls the volume of cross‐linked chains in the primary particles, thus avoiding the problem of poor dispersion of the polymer microspheres due to the introduction of divinylbenzene (DVB). This study produces a preparation method for cross‐linked microspheres. 相似文献
68.
A simple and selective method using ammonium pyrrolidinedithiocarbamate modified activated carbon (APDC-AC) as solid phase
extractant has been developed for speciation of As(III) in water samples. At pH 1.8–3.0, As(III) could be adsorbed quantitatively
by APDC-AC, and then eluted completely with 2.0 mL of 0.1 mol L−1 HNO3, while As(V) could almost not be retained at pH 1–7. Effects of acidity, sample flow rate, concentration of elution solution
and interfering ions on the recovery of As(III) have been systematically investigated. Under the optimal conditions, the adsorption
capacity of APDC-AC for As(III) is 7.3 mg g−1. The detection limit (3σ) of As(III) is 0.05 ng mL−1 for graphite furnace atomic absorption spectrometry (GFAAS) with enrichment factor of 50, and the relative standard deviation
(RSD) is 4.1% (n = 9, C = 5 ng mL−1). The method has been applied to the determination of trace As(III) in water, and the recoveries of As(III) are 100 ± 10%.
Correspondence: Yiwei Wu, Department of Chemistry and Environmental Engineering, Hubei Normal University, Huangshi 435002,
P.R. China 相似文献
69.
Yiwei Zeng Jiangang Lu Xiaohua Yan Minzhu Lin Xianren Meng Xioshan Wu Qingyun Tu Zhenjin Lin 《Hyperfine Interactions》1992,70(1-4):1219-1222
Two main superconducting phases, 1223 and 2223 in TiBaCa3Cu3O8.5 superconductor, are identified by powder x-ray analysis and57Fe Mössbauer spectroscopy analysis. The Mössbauer fitting results shown that iron atoms in the lattice substitute two inequivalent sites of copper atoms for each main phase. The temperature dependence of Mössbauer parameters are obtained, and several problems are discussed which relate to the electric charge transfer which takes place around the superconducting transition temperature, the lattice dynamics and the effect on oxygen deficiency at different temperatures. 相似文献
70.
A series of SmTiFe11?xCox compounds, where x ranges from zero to five, have been studied by57Fe Mössbauer spectroscopy, x-ray diffraction, and related magnetic measurements. Random site occupation of Co atom occurs in SmTiFe11?xCox when x>1. The Co concentration dependence of the magnetic hyperfine field for the samples, SmTiFe11?xCox, and temperature dependence of the magnetic hyperfine field for SmTiFe11 are obtained. 相似文献