Low-Threshold High-Temperature Operation of ～7.4μm Quantum Cascade Lasers

We report low-threshold high-temperature operation of 7.4#m strain-compensated InGaAs/lnAIAs quantum cascade lasers （QCLs）. For an uncoated 22-μm-wide and 2-mm-long laser, the low-threshold current densities, i.e. 0.33kA/cm^2 at 81 K in pulsed mode and 0.64kA/cm^2 at 84K in cw mode, are realized. High-temperature operation of uncoated devices, with a high value of 223K, is achieved in cw mode.     

The luminescence of CaYBO4:RE (REEu, Gd, Tb, Ce) in VUV-visible region

Phosphors CaYBO₄:RE³⁺ (RE=Eu, Gd, Tb, Ce) were synthesized with the method of solid-state reaction at high temperature, and their vacuum ultraviolet (VUV)-visible luminescent properties in VUV-visible region were studied at 20 K. In CaYBO₄, it is confirmed that there are two types of lattice sites that can be substituted by rare-earth ions. The host excitation and emission peaks of undoped CaYBO₄ are very weak, which locate at about 175 and 350-360 nm, respectively. The existence of Gd³⁺ can efficiently enhance the utilization of host absorption energy and result in a strong emission line at 314 nm. In CaYBO₄, Eu³⁺ has typical red emission with the strongest peak at 610 nm; Tb³⁺ shows characteristic green emission, of which the maximum emission peak is located at 542 nm. The charge transfer band of CaYBO₄:Eu³⁺ was observed at 228 nm; the co-doping of Gd³⁺ and Eu³⁺ can obviously sensitize the red emission of Eu³⁺. The fluorescent spectra of CaYBO₄:Ce³⁺ is very weak due to photoionization; the co-addition of Ce³⁺-Tb³⁺ can obviously quench the luminescence of Tb³⁺.     

碳纳米管束中的正电子理论

采用中性原子叠加模型和有限差分方法(SNA-FD)计算了大范围内不同管径的单壁碳纳米管束中的正电子情况，发现对于单壁碳纳米管束，正电子的主要湮没区域，湮没对象和正电子寿命随碳纳米管管径的不同而发生规律性变化.计算得到管径范围在0.8—1.6nm的碳纳米管束的正电子寿命范围为332—470ps，与实验测得的394ps符合较好.     

LC–APCI–MS Quantitative Analysis of Curcumin in Rabbit Plasma

A simple and specific liquid chromatography–atmospheric pressure chemical ionization–mass spectrometry (LC–APCI–MS) method was developed and validated for quantitative analysis of curcumin in rabbit plasma. Chromatographic separation was carried out on Zorbax SB-C18 column, acetonitrile-methanol–water used as mobile phase with gradient elution. APCI source was applied and operated in negative ion mode, and selective ion monitoring mode used to quantify curcumin. The method showed excellent intra-assay and inter-assay precision (relative standard deviations and bias <15%) for quality control (QC) samples. This method was successfully applied to a pharmacokinetic study of curcumin after intravenous administration to rabbits.     

New series of AB2‐type hyperbranched polytriazoles derived from the same polymeric intermediate: Different endcapping spacers with adjustable bulk and convenient syntheses via click chemistry under copper(I) catalysis

In this article, according to the concept of “suitable isolation group,” six new AB₂‐type polytriazoles containing azo‐chromophore moieties, derived from the same hyperbranched polymer intermediate, were successfully prepared through click reaction under copper(I) catalysis by modifying the synthetic route, in which different isolation groups in different size were introduced to the periphery of the hyperbranched polymers as end‐capping moieties. With the different end‐capping groups, these hyperbranched polymers, P1 – P6 , exhibited different solubility and processability; also, their nonlinear optical properties were modified accordingly, realizing the adjustment of the properties of hyperbranched polymers through the structural design. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

Alternating,gradient, block,and block–gradient copolymers of ethylene and norbornene by Pd–Diimine‐Catalyzed “living” copolymerization

We demonstrate, in this article, the facile synthesis of a broad class of low‐polydispersity ethylene–norbornene (E–NB) copolymers having various controllable comonomer composition distributions, including gradient, alternating, diblock, triblock, and block–gradient, through “living”/quasiliving E–NB copolymerization facilitated with a single Pd – diimine catalyst ( 1 ). This synthesis benefits from two remarkable features of catalyst 1 , its high capability in NB incorporation and high versatility in rendering E–NB “living” copolymerization at various NB feed concentrations ([NB]₀) while under an ethylene pressure of 1 atm and at 15 °C. At higher [NB]₀ values between 0.42 and 0.64 M, E–NB copolymerization with 1 renders nearly perfect alternating copolymers. At lower [NB]₀ values (0.11–0.22 M), gradient copolymers yield due to gradual reduction in NB concentration, with the starting chain end containing primarily alternating segments and the finishing end being hyperbranched polyethylene segments. Through two‐stage or three‐stage “living” copolymerization with sequential NB feeding, diblock or triblock copolymers containing gradient block(s) have been designed. This work thus greatly expands the family of E–NB copolymers. All the copolymers have controllable molecular weight and relatively low polydispersity (with polydispersity index below 1.20). Most notably, some of the gradient and block–gradient copolymers have been found to exhibit the characteristic broad glass transitions as a result of their possession of broad composition distribution. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013     

Second-order nonlinearities of lead borate glasses poled with different electrodes

The second-order nonlinearities in thermally poled lead borate glasses were studied. After poling with different electrodes, both bulk and near surface second-order nonlinearities were obtained. The second harmonic generation signal from near surface effect was two orders of magnitude larger than the bulk effect. By simulating the poling process with a multiple carrier model, we concluded that the bulk second-order nonlinearity was caused by the deficiency of Pb²⁺ in a thick layer after poling, and the near surface second-order nonlinearity was caused by the depletion of H⁺ in a thin layer when H⁺ injection from the atmosphere was blocked.     

A model for describing near-resonance oscillations in an elastic layer

One-dimensional transverse oscillations in a layer of a non-linear elastic medium are considered, when one of the boundaries is subjected to external actions, causing periodic changes in both tangential components of the velocity. In a mode close to resonance, the non-linear properties of the medium may lead to a slow change in the form of the oscillations as the number of the reflections from the layer boundaries increases. Differential equations describing this process were previously derived. The equations obtained are hyperbolic and the change in the solution may both keep the functions continuous and lead to the formation of jumps. In this paper a model of the evolution of the wave patterns is constructed as integral equations having the form of conservation laws, which determine the change in the functions describing the oscillations of the layer as “slow” time increases. The system of hyperbolic differential equations previously obtained follows from these conservation laws for continuous motions, in which one of the variables is slow time, for which one period of the actual time serves as an infinitesimal quantity, while the second variable is the real time. For the discontinuous solutions of the same integral equations, conditions on the discontinuity are obtained. An analogy is established between the solutions of the equations obtained and non-linear waves propagating in an unbounded uniform elastic medium with a certain chosen elastic potential. This analogy enable discontinuities which may be physically realised to be distinguished. The problem of steady oscillations of an elastic layer is discussed.