Upconversion in Highly Doped Er3+-Yb3+ Fiber Pumped by Ti:Sapphire Laser at 800 nm

The up-conversion processes were investigated in highly doped Er3+-Yb3+ silica fiber pumped by CW or mode-locked Ti:Sapphire laser at 800 nm band. The mechanism is different from that at 980 nm pumped band. The pumping wavelength and power dependences of green, blue and red fluorescence emission were obtained. The up-conversion efficiencies of different doped concentration were investigated. The strong infrared emissions, which limit the efficiency of up-conversion were observed.     

Miniaturized 3-D surface profilometer using a fiber optic coupler

A 3-D surface profilometer is described which uses a simple fiber optic coupler to form a Young's double pinhole interferometer. The Young's fringes are projected onto a surface, captured by a camera and analyzed using the Fourier transform method. The phase of the fringe pattern on the object is used to reconstruct the surface profile. System analysis, results from a simulation, and preliminary experimental results are provided which indicate a system resolution on the order of a tenth of a millimeter.     

混沌Arneodo系统的输出反馈同步

对Arneodo混沌系统进行输出线性反馈同步.基于线性稳定性定理,给出了一个同步渐近稳定的充分条件,和同步渐近稳定的反馈系数的范围.对同步系统进行数值仿真,验证了方法的有效性和抗噪声能力. 关键词：     

Measurement of underground motion at the SSRF site

For the Shanghai Synchrotron Radiation Facility (SSRF) and future Shanghai Free‐Electron Laser projects, ground vibration is an important factor and, in order to attenuate it, the construction of a deep tunnel is under consideration. This paper concentrates on the investigation of ground vibration at different underground levels down to 60 m below surface, in order to understand the effect of vibration attenuation with depth. The effect of traffic is also studied using a 10 ton truck, with ground motion compared in different directions. Finally, a summary and some suggestions on these two projects are given.     

Crystal phase control in two-dimensional materials

It is the nature of crystals to exist in different polymorphs. The recent emergence of two-dimensional (2D) materials has evoked the discovery of a number of new crystal phases that are different from their bulk structures at ambient conditions, and revealed novel structure-dependent properties, which deserve in-depth understanding and further exploration. In this contribution, we review the recent development of crystal phase control in 2D materials, including group V and VI. transition metal dichalcogenides (TMDs), group IVA metal chalcogenides and noble metals. For each group of materials, we begin with introducing the various existing crystal phases and their structure-related properties, followed by a detailed discussion on factors that influence these crystal structures and thus the possible strategies for phase control. Finally, after summarizing the whole paper, we present the challenges and opportunities in this research direction.     

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.     

Asymmetric Reactions involving Lewis Base Catalyst Tethered Dearomatized Intermediates

Numerous protocols have been developed for the functionalization of aromatic substances. Among them, the strategy by which aromatic substrates are activated in situ to generate dearomatized intermediates is highly efficient but challenging, especially in the field of asymmetric catalysis. In this Concept article, the application of some well-established chiral Lewis base catalysis, including primary/secondary amines and N-heterocyclic carbenes, that can covalently form catalyst-tethered dearomatized ortho/para-quinodimethane species with diverse heteroaryl and aryl carbonyl substrates is summarized in a number of asymmetric cycloaddition and addition reactions with diverse reagents generally having electrophilic properties. As a result, a variety of enantioenriched aromatic products with higher molecular complexity are constructed effectively through a rearomatization process.