Electronic band structure of a type-II ’W’ quantum well calculated by an eight-band k·p model

In this paper, we present an investigation of type-II 'W' quantum wells for the InAs/Ga_1-xIn_xSb/AlSb family, where 'W' denotes the conduction profile of the material. We focus our attention on using the eight-band k?p model to calculate the band structures within the framework of finite element method. For the sake of clarity, the simulation in this paper is simplified and based on only one period---AlSb/InAs/Ga_1-xIn_xSb/InAs/AlSb. The obtained numerical results include the energy levels and wavefunctions of carriers. We discuss the variations of the electronic properties by changing several important parameters, such as the thickness of either InAs or Ga_1-xIn_xSb layer and the alloy composition in Ga_1-xIn_xSb separately. In the last part, in order to compare the eight-band k?p model, we recalculate the conduction bands of the 'W' structure using the one-band k?p model and then discuss the difference between the two results, showing that conduction bands are strongly coupled with valence bands in the narrow band gap structure. The in-plane energy dispersions, which illustrate the suppression of the Auger recombination process, are also obtained.     

Blowup Criterion for Viscous Baratropic Flows with Vacuum States

We prove that the maximum norm of the deformation tensor of velocity gradients controls the possible breakdown of smooth(strong) solutions for the 3-dimensional (3D) barotropic compressible Navier-Stokes equations. More precisely, if a solution of the 3D barotropic compressible Navier-Stokes equations is initially regular and loses its regularity at some later time, then the loss of regularity implies the growth without bound of the deformation tensor as the critical time approaches. Our result is the same as Ponce’s criterion for 3-dimensional incompressible Euler equations (Ponce in Commun Math Phys 98:349–353, 1985). In addition, initial vacuum states are allowed in our cases.     

The Calibration Method of TOFr in the STAR Experiment

a tray of time of flight detector based on mrPc technology took part in the physics run of star both in p+p and d+au collisions in 2003. together with the information from the time Projection chamber(tPc) and the pseudo–vertex Position detector (pvPd) of the star experiment,corrections are done to calibrate the new prototype tof. the intrinsic time resolution of tofr reaches 85ps and it extends the π/K and K/p separation up to 1.6gev/c and 3.0gev/c respectively.     

二元光学元件

二元光学元件是一种新型的衍射光学元件,它对光学仪器的小型化、集成化起着很重要的作用。本文介绍了二元光学元件的概况,衍射透镜理论,二元光学元件的制造方法以及发展趋势。     

双稀土氧化物LnEuO3的Mossbauer效应研究

 本文首次利用高温高压方法合成了双稀土氧化物LaEuO₃、PrEuO₃、NdEuO₃和SmEuO₃。此外，还合成了CeEuO_3.5。X射线衍射分析表明LaEuO₃属A型（六方）结构，PrEuO₃、NdEuO₃和SmEuO₃属B型（单斜）结构，CeEuO_3.5属F型（萤石）结构。室温下用¹⁵¹Eu的21.6 eV γ射线测量了它们的Mossbauer谱，观察到了¹⁵¹Eu同质异能移位和四极劈裂强烈地依赖于Eu离子配位体体积而呈线性关系。超精细相互作用的这种体积效应，主要原因是由于Eu离子5s壳层的重叠畸变所引起。     

The time-dependent cellular response mechanism upon exposure to zinc oxide nanoparticles

Zinc oxide nanoparticle is one of the nanomaterials people engaged most in their life and its health effect has been taken into concern. In this work, A549 cell line was used as cell model, and the cytotoxicity of zinc oxide nanoparticles was revealed to be concentration-dependent. Through the measurement of cellular proteome, much more differentially expressed proteins were observed after the cells being treated for 9 h than 24 h. Also, most of these proteins expressed in the pattern which showed a significant decrease after exposure to zinc oxide nanoparticles and then an increase at 24 h. Intracellular reactive oxygen species and glutathione determination indicated that high level of oxidative stress was presented in cell after treatment with zinc oxide nanoparticles for 9 h. It can be observed from western blot analysis that the expression of NF-κB p65, PNPase, and HSP90 rose significantly after 9 h of exposure. Thus, a deduction was reached that toxicity of nanoparticles consists both of particle toxicity and ion toxicity, and a long-time treatment may conceal the toxicity induced by particles. The conclusion we made highlighted the importance of exposure time in the study of nanoparticle toxicity and would provide a new perspective for studying toxicity mechanism of nanoparticles.     

Lewis Acid Transition-Metal-Catalyzed Hydrogen Activation: Structures,Mechanisms, and Reactivities

As a new type of bifunctional catalyst, the Lewis acid transition-metal (LA-TM) catalysts have been widely applied for hydrogen activation. This study presents a mechanistic framework to understand the LA-TM-catalyzed H₂ activation through DFT studies. The mer(trans)-homolytic cleavage, the fac(cis)-homolytic cleavage, the synergetic heterolytic cleavage, and the dissociative heterolytic cleavage should be taken as general mechanisms for the field of LA-TM catalysis. Four typical LA-TM catalysts, the Z-type κ⁴-L₃B-Rh complex tri(azaindolyl)borane-Rh, the X-type κ³-L₂B-Co complex bis-phosphino-boryl (PBP)-Co, the η²-BC-type κ³-L₂B-Pd complex diphosphine-borane (DPB)-Pd, and the Z-type κ²-LB-Pt complex (boryl)iminomethane (BIM)-Pt are selected as representative models to systematically illustrate their mechanistic features and explore the influencing factors on mechanistic variations. Our results indicate that the tri(azaindolyl)borane-Rh catalyst favors the synergetic heterolytic mechanism; the PBP-Co catalyst prefers the mer(trans)-homolytic mechanism; the DPB-Pd catalyst operates through the fac(cis)-homolytic mechanism, whereas the BIM-Pt catalyst tends to undergo the dissociative heterolytic mechanism. The mechanistic variations are determined by the coordination geometry, the LA-TM bonding nature, the electronic structure of the TM center, and the flexibility or steric effect of the LA ligands. The presented mechanistic framework should provide helpful guidelines for LA-TM catalyst design and reaction developments.     

Characterization of moisture mobility and diffusion in fresh tobacco leaves during drying by the TG–NMR analysis

This paper presents the stabilization effects of inorganic filler, cerium-doped lead zirconate titanate on high-density polyethylene. The filler was loaded in two concentrations (1 and 3 wt%). The dopant contents in PbZrO₃ were 0, 0.05, 0.075, 0.1 and 0.125 mol%. The degradation of hybrid samples was accomplished by γ-irradiation at various doses up to 200 kGy. The isothermal and nonisothermal chemiluminescence (CL) and thermal analysis (TG-DSC) were applied for the thermal stability characterization of modified HDPE samples. The mechanistic considerations and radiochemical consequences caused by the variation of filler concentration and doping level are discussed. The results demonstrate that the filler acts efficiently as stabilizer at low concentration of additive when the lower filler amount is present. The start of degradation precedes melting by four processes through which the chain scission and radical oxidation represent the essential degradation stage. The filler concentration influences the degradation due to the intimate interaction between solid-state defects and free radicals. The polymer protection against oxidation is based on the scavenging of radicals by the doping elements, that is, they trap and block radicals delaying material aging. The present results open a new perspective in the quality amelioration of organic products toward high durability.