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91.
本文运用密度矩阵方程推导了V型三能级系统的荧光量子拍讯号强度,并对其结果进行了分析和讨论。 相似文献
92.
93.
I. Souza Azevedo E. Baggio Saitovitch M. Hücker B. Büchner H. Micklitz 《The European Physical Journal B - Condensed Matter and Complex Systems》1998,6(3):313-315
57Fe M?ssbauer effect studies of La1.65Eu0.20Sr0.15CuO4 doped with 0.5 at% 57Fe performed in the temperature region 300 K >
T
> 4.2 K give an onset temperature for magnetic ordering of K. This temperature practically is the same as that found in Nd doped La2-xSrxCuO4. It indicates that the magnetic ordering temperature in the LTT phase of rare earth (RE) doped La2-xSrxCuO4 is independent of the RE moment. The direction of the 57Fe magnetic moment in the magnetically ordered state is within the CuO2 plane, while it has been found to be parallel to the c-axis in Nd doped La2-xSrxCuO4.
Received: 23 June 1998 / Accepted: 14 July 1998 相似文献
94.
A striking size dependence of the mean-square displacement of diffusing particles in the two-dimensional lattice gas of hard squares has been observed by Monte Carlo simulation. It is shown that the size effect is due to the formation of a stable cage structure in small lattices when the particle concentration is high. The formation of cages is governed by a new type of percolation problem related to bootstrap percolation. 相似文献
95.
Shiori Hanada 《Tetrahedron letters》2006,47(35):6173-6177
Combination of commercially available platinum catalysts with siloxanes containing more than two Si-H groups is found to be an efficient catalyst system for the reduction of carboxamides to amines. In particular, facile removal of silicon and platinum residues from the product can be achieved by the use of polymethylhydrosiloxanes as reducing reagents. 相似文献
96.
Jos Vargas Carlos Ramos Roberto D. Zysler Hctor Romero 《Physica B: Condensed Matter》2002,320(1-4):178-180
Chemically prepared (CoxNi1−x)1−yBy (x=0.5, 0.75, 1; y≈0.4) amorphous fine particles were characterized by X-ray diffraction, DTA and TGA, and in situ magnetic measurement as a function of annealing temperature in an inert atmosphere. Magnetic measurement performed in as-prepared and 150°C annealed samples shows an increase of the saturation magnetization and magnetic moment after thermal treatment. Room temperature magnetization increases by factors of 3.5, 1.8, and 1.5, for x=0.5, 0.75, and 1, respectively. These measurements may indicate a local re-ordering of the amorphous phase at temperatures much lower than the full crystallization temperature. 相似文献
97.
Vlase T. Vlase G. Chiriac A. Doca N. 《Journal of Thermal Analysis and Calorimetry》2003,72(3):839-845
The thermal decomposition in non-isothermal conditions of formates, acetates, propionates and butyrates of Mn, Co, Zn, Cd,
Eu, Sm and Ni was studied. The observed compensation effect allows us to calculate the isokinetic temperature. A selective
activation mechanism was suggested. This leads to a good agreement between kinetic and spectroscopic data.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
98.
Polycrystalline perovskite La0.67Ca0.33MnO3 was synthesized by a sol–gel method. Its adiabatic temperature change ΔTad induced by a magnetic field change was measured directly. At 268 K, near its Curie temperature TC, ΔTad of La0.67Ca0.33MnO3 induced by a magnetic field change of 2.02 T reaches 2.4 K. The latent heat Q and magnetic entropy change −ΔSM induced by a magnetic field change were calculated from the temperature dependence of ΔTad and zero-field heat capacity Cp. The maximum values of Q and −ΔSM in La0.67Ca0.33MnO3 induced by a magnetic field change of 2.02 T are 1.85 J g−1 and 6.9 J kg−1 K−1, respectively. The former is larger than the phase transition latent heat of heating or cooling, which is about 1.70 J g−1. 相似文献
99.
100.
A series of molecular dynamics simulations have been performed to study the supramolecular structure of self‐assembled complexes formed by N‐dodecyltrimethylammonium cations and the synthetic polypeptide poly(α,L ‐glutamate). The influence of the type of solvent has been investigated, considering explicit environments of chloroform, water, and methanol on a stoichiometric complex containing 15 residues. In chloroform, the complex stabilizes in a regular structure: the polypeptide adopts an α‐helix conformation that is regularly surrounded by surfactant molecules to form electrostatic interactions through a multiple interaction pattern. However, this structure destabilizes in methanol and water: (a) the α‐helix unfolds in the two solvents and (b) the electrostatic links between the surfactant molecules and the polyanion are disrupted in aqueous solution, although these interactions are still preserved in methanol. The role of the solvent environment in stabilizing or destabilizing the polypeptide secondary structure, the organization of the surfactant molecules, and predominantly the surfactant–polypeptide supramolecular organization is discussed in detail. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 1122–1133, 2006 相似文献