首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   9篇
  免费   0篇
化学   6篇
力学   1篇
物理学   2篇
  2016年   2篇
  2013年   1篇
  2012年   1篇
  2011年   1篇
  2010年   1篇
  2006年   1篇
  2005年   1篇
  2003年   1篇
排序方式: 共有9条查询结果,搜索用时 15 毫秒
1
1.
Monodisperse ruthenium nanoparticles were prepared by reduction of RuCl3 in 1,2-propanediol. The mean particle size was controlled by appropriate choice of the reduction temperature and the acetate ion concentration. Colloidal solutions in toluene were obtained by coating the metal particles with dodecanethiol. High-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), and X-ray absorption spectroscopy (XANES and EXAFS for the Ru K-absorption edge) were performed on particles of two different diameters, 2 and 4 nm, and in different environments, polyol/acetate or thiol. For particles stored in polyol/acetate XPS studies revealed superficial oxidation limited to one monolayer and a surface coating containing mostly acetate ions. Analysis of the EXAFS spectra showed both oxygen and ruthenium atoms around the ruthenium atoms with a Ru-Ru coordination number N smaller than the bulk value, as expected for fine particles. In the case of 2 nm acetate-capped particles N is consistent with particles made up of a metallic core and an oxidized monolayer. For 2 nm thiol-coated particles, a Ru-S bond was evidenced by XPS and XAS. For the 4 nm particles XANES and XPS studies showed that most of the ruthenium atoms are in the zerovalent state. Nevertheless, in both cases, when capped with thiol, the Ru-Ru coordination number inferred from EXAFS is much smaller than for particles of the same size stored in polyol. This is attributed to a structural disorganization of the particles by thiol chemisorption. HRTEM studies confirm the marked dependence of the structural properties of the ruthenium particles on their chemical environment; they show the acetate-coated particles to be single crystals, whereas the thiol-coated particles appear to be polycrystalline.  相似文献   
2.
The numerical predictions confirm a new classification of flow patterns of triple jet interaction. The addition of side jets increase the rate of decrease of the centreline velocity for the flow of type A and decreases in the other cases. The effect of various types of flow on the rate of decrease of the velocity, the turbulent kinetic energy and the temperature in the combined region are detailed. Several correlations are proposed.  相似文献   
3.
4.
Monodisperse ruthenium nanoparticles functionalized by electroactive oligothiophenes have been prepared and characterized. Using TEM, UV-visible and FTIR we established that the organization of these nanoparticles into nanospheres can be directly controlled via modulation of the pi-pi interaction between the organic components adsorbed on the surface. This finding also shows that the self-assembled nanoheterostructures may be switched from monodisperse nanoparticles to ordered nanospheres by tuning the pH.  相似文献   
5.
Experimental studies of the structural, magnetic and magnetocaloric properties of the three compounds Pr0.5X0.1Sr0.4MnO3 (X = Ce, Eu and Y) are reported. Our samples were synthesized using the Pechini sol–gel method. X-ray powder diffraction at room temperature indicates that our materials crystallize in the orthorhombic structure with Pbnm space group. The compounds undergo a second-order magnetic transition from paramagnetic to ferromagnetic state around their own Curie temperatures T C ~ 310, 270 and 230 K for X = Ce, Eu and Y, respectively. A considerable magnetocaloric effect (MCE) is observed around room temperature. The maximum values of magnetic entropy change ?S max are 3.54, 3.81 and 2.99 J/kgK for the samples with X = Ce, Eu and Y, respectively, when a magnetic field of 5 T was applied. The relative cooling power (RCP) values for the corresponding materials are 246.60, 261.66 and 298 J/kg. It is shown that for Pr0.5X0.1Sr0.4MnO3 the exponent n and the magnetic entropy change follow a master curve behavior. With the universal scaling curve, the experimental ?S at several temperatures and fields can be extrapolated.  相似文献   
6.
Seed husk extracts of Convolvulus tricolor L. (Convolvulaceae) afforded six compounds, identified for the first time from this plant: isorhamnetin 3-O-beta-D-galactopyranoside (1), isorhamnetin 3-O-beta-D-(6"-acetyl)-galactopyranoside (2), isorhamnetin 3-O-robinobioside (3), 3,4-di-O-caffeoylquinic acid (4), gentisic acid 5-O-glucoside (5), and scopoletin (6). Separation of compounds was carried out by CC and CPC. Structural elucidations were performed by HPLC-UV-DAD, HPLC-ESI/MS (negative mode) and NMR.  相似文献   
7.
α-[C6H4(NH3)2]2Bi2I10, which is a new material containing low-dimensional iodobismuthate anions, was synthesized and through its single crystal X-ray diffraction measurements, was proven to crystallize at room temperature in the centrosymmetric space group P21/c. It consists of a p-phenylenediammonium dication and a discrete (0-D) anion built up of edge-sharing bioctahedron. Due to the hydrogen bonds and the interatomic distances (Bi-I, I?I and π-π) changes, α-phase was transformed into the corresponding centrosymmetric β-phase, β-[C6H4(NH3)2]2Bi2I10, through a single-crystal to single-crystal transformation occurring upon cooling to −28/−26 °C. Below the transition temperature, β-[C6H4(NH3)2]2Bi2I10 crystallizes in the monoclinic system, centrosymmetric space group P21/n. Besides, the optical transmission measurements on α-[C6H4(NH3)2]2Bi2I10 thin films have revealed two absorption bands at 2.47 and 3.01 eV. Finally, two room temperature photoluminescence emissions attributed to excitons radiative recombinations confined within the bioctahedra Bi2I104−, were observed in the red spectral range at 1.9 and 2.05 eV energy.  相似文献   
8.
9.
Reduction of silver nitrate in polyol/toluene biphasic medium containing dodecanethiol led to organised silver nanowires, results of an interaction between silver nanoparticles and the layered phase AgSC12H25.  相似文献   
1
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号