Lower Bounds for the Robustness of Multilevel Coherence

International Journal of Theoretical Physics - Quantum coherence, coming from quantum superposition, occupies a significant position in the field of physics. We put forward a lower bound of the...     

On the Theory of Acoustic Scanning of Damage to Underground Pipelines

Acoustical Physics - The paper studies the evolution of a pulsed signal initiated by the pushing of a cylindrical piston and propagating through a stationary fluid filling a buried pipeline with an...     

Electron energy spectrum in the field-ionized plasma

In this article, the effect of ionization on the energy spectrum of electrons within the interaction of a laser pulse with hydrogen atoms is investigated using particle-in-cell simulation codes. The results show that the behaviour of electrons' energy distribution function in the field-ionized plasma, which occurred due to the field ionization, compared with that in the pre-plasma strongly depends on the pulse shape. For short rise-time pulses (here 30 fs), due to the rapid enhancement of laser electric field, ionization occurs quickly, and as a result, there is not much difference in the electron energy in both the media. However, for pulses with rise time of 40 fs, in the pre-plasma state, the electron population reaches higher energies compared with the field-ionized plasma state. The main reason for this difference is the nonlinear wave breaking that happens earlier due to density inhomogeneity in the field-ionized plasma. On the other hand, at longer rise-time pulses (here 60 and 70 fs), electrons achieve higher energies in the field-ionized plasma than those in the case of pre-plasma. In this case, because of density fluctuations in the field-ionized plasma, the Raman backscattered radiations are seeded by a strong initial noise at the earlier times and the Mendonca condition for chaos threshold is met sooner. Therefore, the electrons gain more energy through the stochastic mechanism that is in agreement with chaotic nature of the motion.     

Phase Transitions in Frustrated ErBaCo4O7 + x (x = 0–0.06) Cobaltites at a Small Deviation from Stoichiometry

Journal of Experimental and Theoretical Physics - The structural (lattice metric) and elastic characteristics of ErBaCo4O7 + x cobaltites, which are subjected to different heat treatment and are...     

Quasi-solid state microscopic dynamics in equilibrium classical liquids: Self-consistent relaxation theory

Theoretical and Mathematical Physics - In the framework of the concept of time correlation functions, we develop a self-consistent relaxation theory of the transverse collective particle dynamics...     

Virtual Field Characterization for Ratcheting Effect Under Cyclic Loading

Experimental Mechanics - Ratcheting is an important mechanical behavior of metals and alloys, which is caused by the repeated accumulations of tensile and compressive strain in circle load....     

Nonlinear Optical Properties of Novel Metallophthalocyanines

Journal of Applied Spectroscopy - Detailed measurements of nonlinear optical properties and optical limiting for four phthalocyanine (Pc) derivatives (PcCo, PcCu, PcMn, and PcSi) are reported. The...     

配合参数对单晶炉驱动系统的影响分析

光伏产业的发展使得对硅材料的需求日益增加,同时硅单晶生产行业竞争也日趋激烈。作为生产硅单晶的重要装备,单晶炉的稳定性和可靠性关系到硅单晶生产效率的提升和成本的下降,因此其驱动系统的设计和优化成为装备制造的关键环节。本文以NVT-HG2000-V1型硅单晶生长炉的驱动系统为研究对象,用SolidWorks三维建模实现虚拟装配,采用ADAMS建立其动力学仿真模型,并对驱动系统的运动过程进行仿真模拟。采用控制变量法定量分析了铜套与升降轴的配合间隙及丝杠参数对驱动力和驱动力矩的影响规律,进而在提高硅单晶生长炉装备稳定性和可靠性方面给出合理的技术建议。结果表明,铜套与升降轴的配合间隙达到0.071 mm后能有效降低驱动系统运行所需驱动力矩,丝杠倾斜度、螺纹螺距与螺纹间摩擦系数的增大均会导致驱动系统运行所需力矩大幅增加。     

Synthesis and Structure of a New Ruthenium(II) Clathrochelate and the Use of a Highly Porous Ceramic Material with an Immobilized Complex in the Oxidative Conversion of Methane

Kinetics and Catalysis - A new ruthenium(II) cage complex with polar terminal groups in the apical substituents has been synthesized; the molecular design of the complex contributes to the...     

Key Role of a-Top CO on Terrace Sites of Metallic Pd Clusters for CO Oxidation

Pd-based catalysts are the most widely used for CO oxidation because of their outstanding catalytic activity and thermal stability. However, fundamental understanding of the detailed catalytic processes occurring on Pd-based catalysts under realistic conditions is still lacking. In this study, we investigated CO oxidation on metallic Pd clusters supported on Al₂O₃ and SiO₂. High-angle annular dark-field scanning transmission electron microscopy revealed the formation of similar-sized Pd clusters on Al₂O₃ and SiO₂. In contrast, CO chemisorption analysis indicated a gradual change in the dispersion of Pd (from 0.79 to 0.2) on Pd/Al₂O₃ and a marginal change in the dispersion (from 0.4 to 0.24) on Pd/SiO₂ as the Pd loading increased from 0.27 to 5.5 wt %; these changes were attributed to differences in the metal-support interactions. Diffuse reflectance infrared Fourier-transform spectroscopy revealed that fewer a-top CO species were present in Pd supported on Al₂O₃ than those in Pd supported on SiO₂, which is related to the morphological differences in the metallic Pd clusters on these two supports. Despite the different dispersion profiles and surface characteristics of Pd, O₂ titration demonstrated that linearly bound CO (with an infrared signal at 2090 cm⁻¹) reacted first with oxygen in the case of CO-saturated Pd on Al₂O₃ and SiO₂, which suggests that a-top CO on the terrace site plays an important role in CO oxidation. The experimental observations were corroborated by periodic density functional calculations, which confirmed that CO oxidation on the (111) terrace sites is most plausible, both kinetically and thermodynamically, compared to that on the edge or corner sites. This study will deepen the fundamental understanding of the effect of Pd clusters on CO oxidation under reaction conditions.