Resonant magnetopolaron effects in GaAs/AlGaAs multiple quantum well structures

A detailed experimental study of electron cyclotron resonance (CR) has been carried out at 4.2 K in three modulation-doped GaAs/Al_0.3Ga_0.7As multiple quantum well samples in fields up to 30 T. A strong avoided-level-crossing splitting of the CR energies due to resonant magnetopolaron effects is observed for all samples near the GaAs reststrahlen region. Resonant splittings in the region of AlAs-like interface phonon modes of the barriers are observed in two samples with narrower well width and smaller doping concentration. The interaction between electrons and the AlAs interface optical phonon modes has been calculated for our specific sample structures in the framework of the memory-function formalism. The calculated results are in good agreement with the experimental results, which confirms our assignment of the observed splitting near the AlAs-like phonon region is due to the resonant magnetopolaron interaction of electrons in the wells with AlAs-like interface phonons.     

The Resonant Wave Numbers of Eccentric Ring Microstrip Antennas for All Modes

The method, connected with the concentric ring microstrip antenna and based on the perturbation , for the resonant wave numbers of eccentric ring microstrip antennas for all modes is suggested. The usefulness and accuracy of the method is shown through the comparison of the calculation used here with the measurement and other method from the reference.     

Removal of recalcitrant pollutants from wastewater

Triton X-100 was oxidized in aqueous solutions with the presence of O₂ using photocatalysis and H₂O₂ addition alone or coupled. New supported TiO₂/Al₂O₃ catalysts modified with vanadium and cobalt were used. Catalysts were prepared using the classical impregnation method (CIM) and the double impregnation method (DIM). The effect of the physico-chemical properties of the catalysts on its activity were studied. The research on the interactions between the metal precursor and the titania-alumina surface by means of FT-IR/PAS (Fourier transform infrared photoacoustic spectroscopy) were also conducted.     

Adsorption of biodegradable chelating compounds on inorganic oxides

The Fourier transform infrared photoacoustic spectroscopy (FT-IR/PAS) method to characterize the interactions between selected aminopolycarboxylic acids and inorganic oxides surfaces is reviewed. In this work, the adsorption of four aminopolycarboxylates (biodegradable and with augmented biodegradability; all in the form of sodium salts), viz. ethylenediaminedisuccinic (EDDS), diethylenetriaminepentaacetic (DTPA), N-(hydroxyethyl)ethylenediaminetriacetic (HEDTA) and methylglycinediacetic (MGDA) acids on: zirconia, titania and alumina was carried out. The obtained results differ depending on the kind of aminopolycarboxylic acid used and the type of oxide support adsorbent characterized by its pH_PZC value.     

Resonant tunneling and enhanced Goos–Hänchen shift in a graphene double velocity barrier structure

Resonant transmission and Goos–Hänchen (GH) shift for Dirac fermion beams tunneling through graphene double velocity barrier structures (DVBs) are investigated theoretically. Analytical and numerical results demonstrate that strong resonant tunneling effect occurs in this structure and is highly dependent on the incident angle and the structure of velocity barriers. The resonant tunneling in graphene DVBs belongs to the Fabry–Pérot resonance and leads to oscillated conduction at wide energy range. It is also found that GH shifts in this structure can be enhanced by the resonant tunneling and multi-GH shift peaks with giant magnitudes can occur at these resonant energy positions. These special properties of GH shifts in graphene DVBs may have good application in lateral manipulation of electron beams and valley or spin beam splitter.     

Sn interaction with the CeO2(1 1 1) system: Bimetallic bonding and ceria reduction

A tin layer 0.8 nm thick was deposited onto the CeO₂(1 1 1) surface by molecular beam deposition at a temperature of 520 K. The interaction of tin with cerium oxide (ceria) was investigated by X-ray photoelectron spectroscopy (XPS), ultra-violet photoelectron spectroscopy (UPS) and resonant photoelectron spectroscopy (RPES). The strong tin-ceria interaction led to the formation of a homogeneous bulk Ce-Sn-O mixed oxide system. The bulk compound formation is accompanied by partial Ce⁴⁺ → Ce³⁺ reduction, observed as a giant 4f resonance enhancement of the Ce³⁺ species. CeO₂ and SnO₂ oxides were formed after oxygen treatment at 520 K. The study proved the existence of strong Ce-Sn interaction and charge transfer from Sn to the Ce-O complex that lead to a weakening of the cerium-oxygen bond, and consequently, to the formation of oxygen deficient active sites on the ceria surface. This behavior can be a key for understanding the higher catalytic activity of the SnO_x/CeO_x mixed oxide catalysts as compared with the individual pure oxides.     

The participant Coster–Kronig preceded Auger transition in the resonant L2,3-M2,3V Auger electron spectrum of Ti metal

The L_2,3-M_2,3V resonant Auger electron spectroscopy (RAES) spectrum of Ti metal measured by Le Fêvre et al. [P. Le Fêvre, J. Danger, H. Magnan, D. Chandesris, J. Jupille, S. Bourgeois, M.-A. Arrio, R. Gotter, A. Verdini, A. Morgante, Phys. Rev. B69 (2004) 155421] is analyzed in the light of relaxation and decay of the resonantly excited L_2,3-hole states. The relaxation time of the resonantly excited L_2,3-hole state to the fully relaxed (screened) one is much shorter than the L_2,3-hole Auger decay time, whereas the participant Coster–Kronig (CK) decay time of the resonantly excited L₂-hole state to the fully relaxed L₃-hole state at the L₂ resonance is as short as the relaxation time of the resonantly excited L₂-hole state to the fully relaxed one. The excited electron is predominantly either rapidly decoupled from the L_2,3-hole decay or annihilated by the participant CK decay. Thus, near the L_2,3 edges the L_2,3-M_2,3V RAES spectral peak appears at constant kinetic energy. The L_2,3-M_2,3V RAES spectrum shows a normal L_2,3-M_2,3V Auger decay profile not modulated by the density of empty d states probed by the resonant excitation. Not only the relaxation time but also the participant CK decay time depends on photon energy because they depend on the density of empty d states probed by the resonant excitation. As a result, the L_2,3 X-ray absorption spectroscopy spectral line broadening depends on photon energy.     

反馈调制型同轴虚阴极振荡器

 对反馈调制型同轴虚阴极振荡器进行了理论分析和数值模拟研究,结果表明:该器件通过增加同轴谐振腔结构并引入反馈可以对入射电子束形成明显的调制效果,从而使得器件具有高束波转化效率和频率单一稳定的特性;同时输出微波的频率被器件结构中的同轴谐振腔锁定,调节腔参数可以在一定范围内对输出微波频率进行调谐;在二极管电压约为600 kV,电子束功率26.2 GW条件下,可以得到平均功率3.6 GW的微波输出,转换效率达到13.7%,主频为5.5 GHz,模式为TM₀₂模。     

基于快速扫描光学延迟线谐振扫描的相位调制方法

提出利用快速扫描光学延迟线(Rapid Scanning Optical Delay Line,RSOD)作为光学相干层析成像(Optical Coherence Tomography,OCT)系统的相位调制器,并采用正弦驱动方式(谐振扫描)来提高扫描频率,进而实现高频相位调制的方法.介绍了基于RSOD相位调制器的干涉信号包络解调方法,分析了大振镜低频率线性驱动、小振镜高频线性驱动和大振镜高速正弦驱动三种实施方案对OCT性能的影响,并针对谐振扫描方案中轴向扫描的非线性提出了图像畸变定量校正的方法.结果表明:RSOD大振镜谐振扫描的模式能够兼顾系统成像速度、成像范围以及系统信噪比的要求,是一种行之有效的相位调制方法.     

Splitting of coupled bright solitons in two-component Bose-Einstein condensates under parametric perturbation

We analyze the dynamics of bright-bright solitons in two-component Bose-Einstein condensates (BECs) subject to parametric perturbations using the variational approach and direct numerical simulations. The system is described by a vector nonlinear Schrödinger equation (NLSE) appropriate to coupled multi-component BECs. A periodic variation of the inter-component coupling coefficient is used to explore nonlinear resonances and splitting of the coupled bright solitons. The analytical predictions are confirmed by direct numerical simulations of the vector NLSE.