Covalent organic nanosheets with large lateral size and high aspect ratio synthesized by Langmuir-Blodgett method

Four chemically stable covalent organic nanosheets are successfully synthesized at the air-water interface with large later size and tunable hydrophobicity, with potential applications as functional coating and membrane materials.     

Synthesis,Crystal Structures,and Properties of (4,4'-Hbipy)2[Sn2(C2O4)3] and (4,4'-Hmbipy)[SnX2] (X = C2O42–, m = 2; X = Cl,m = 0; bipy = bipyridine)

Three new tin coordination compounds (4,4'-Hbipy)₂[Sn₂(C₂O₄)₃] ( 1 ), (4,4'-H₂bipy)[Sn(C₂O₄)₂] ( 2 ), and SnCl₂(4,4'-bipy) ( 3 ) were synthesized under hydro-(solvo-)thermal conditions and their crystal structures were determined by single-crystal X-ray diffraction. Compound 1 exhibits a ionic structure based on discrete [4,4'-Hbipy]⁺ cations and [Sn₂(C₂O₄)₃]^2– anions. These two units are linked via N–H ··· O hydrogen bonds to form a pseudo-one-dimensional zigzag hydrogen-bonded chain. In compound 2 , four-coordinate Sn atoms form monomeric tin dioxalato complexes, which are connected to the doubly protonated [4,4'-H₂bipy]²⁺ cations through N–H ··· O hydrogen bonded to give a one-dimensional zigzag hydrogen-bonded chain. Compound 3 forms a three-dimensional hydrogen-bonded network, in which ¹_∞[SnCl₂(4,4'-bipy)] linear chains are interconnected to each other by C–H ··· Cl hydrogen bonding. The solid-state UV/Vis/NIR diffuse reflectance spectroscopy shows that three compounds are broadband semiconductors. The thermogravimetric analysis evidences the thermal stability of the three compounds up to 175, 201, and 246 °C, respectively.     

ATTITUDE CONTROL TECHNOLOGY FOR MASS MOMENT NANO-SATELLITE IN LOW EARTH ORBIT 1)

针对气动力矩严重影响低轨纳卫星姿态控制效果的问题,创新性地提出了利用质量矩技术将气动干扰转化为控制力矩的解决方法.由于气动力矩矢量垂直于大气来流速度方向,因而采用质量矩与磁力矩相结合的方式三轴全驱动控制卫星姿态,从而避免系统欠驱动. 建立双执行机构控制方式的姿态动力学模型,并根据各干扰项的影响简化了控制方程.针对气动力不确定、星体参数误差、未知环境影响等复杂干扰,设计了针对理想控制力矩基于干扰观测器的滑模控制器. 为减小滑块附加干扰力矩,研究了理想控制力矩的最优分配策略. 最后, 为双执行机构搭建了半物理仿真平台,结果表明: 姿态机动过程中, 与滑块加速度相关的附加惯性力矩远大于其他干扰项,最优力矩分配策略能够大幅减小快时变的附加干扰, 优化效果明显; 姿态保持过程中,干扰观测器能有效观测系统慢时变干扰, 提高滑模控制律的姿态控制精度,姿态角收敛误差小于$\pm $0.1$^\circ$.最终验证了在低轨纳卫星上利用质量矩技术控制姿态的可行性.     

典型非线性光学晶体生长方法综述

非线性光学晶体具有多种生长方法,每种方法都有其独特的优势和适用的晶体,通过了解典型非线性光学晶体生长方法的特点,可以确定采用哪种方法获得高质量的晶体,达到预期的目的.本文主要对典型非线性光学晶体生长方法进行相关介绍,如水热法生长KTP晶体、水溶液法生长KDP晶体、有机溶液法生长DAST晶体、高温溶液法生长BBO、LBO、KBBF等晶体、泡生法生长CBO晶体、提拉法生长LiNbO3晶体、布里奇曼法生长CdSiP2、ZnGeP2、BaGa4 Se7等晶体,阐述典型非线性光学晶体的原料、溶液配制、温度压力的控制等实验制备条件,展示所生长出的晶体样品.通过对上述方法总结,为今后的晶体生长方法选取提供借鉴.     

Cartan型广义李超代数

设F是特征不为2的域.本文定义了F上的广义李超代数，证明了Z-阶化广义李超代数的单性准则.然后定义了有限维Cartan型广义李超代数W(n),证明了W(n)的单性.最后指出对Cartan型广义李超代数S(n)与H(n)，亦有与W(n)相似的结果.     

A smile insensitive method for spectral linewidth narrowing on high power laser diode arrays

To eliminate the smile effect in spectral linewidth narrowing on high power laser diode arrays, we have introduced a plane reflective mirror into a common Littrow configuration external cavity to enhance the correlation among emitters. By this way, we obtained uniform spectral distribution among emitters of a 64-elements laser diode array with 35 GHz linewidth and 41 W output laser power.     

碱蒸气激光半导体泵浦源谱宽压窄

 笑脸效应严重制约大功率半导体激光器输出谱宽压窄。为避免笑脸效应,以中心波长780 nm单宽面源大功率半导体激光器为研究对象,利用利特曼外腔结构,优化外腔参数,在激光器自由运转19 W时,获得11.5 W、外腔效率达61%的窄线宽输出。将窄线宽输出激光通过长25 cm, 80 kPa乙烷、110 ℃的铷池,96.7%的泵浦光被吸收,通过与理论模型对比,推断半导体激光器的输出谱宽为15 GHz(0.03 nm)。     

液固两相流中流体旋涡对固体粒子运动影响的数值研究

基于离散涡方法求得的非定常、不稳定流场和颗粒的Lagrangian运动方程,数值计算了四种St数下的泥沙粒子在圆柱绕流场中的运动。计算结果证明了颗粒运动与流体旋涡存在着明确的相关结构：在钝体（圆柱）表面附着泥沙,当流体流过钝体时产生具有剧烈分离的不稳定流动,带动钝体表面泥沙起浮。对于小St数（0．15～0．59）与中等St数（1．33～2．36）的泥沙颗粒被流体旋涡所带起,井被卷入流体旋涡结构内,被卷入流体旋涡结构内的泥沙颗粒在运动过程中始终分布于旋涡区,即在旋涡区聚集。     

Rb(3)Ti(3)(P(4)S(13))(PS(4))(3) and Cs(2)Ti(2)(P(2)S(8))(PS(4))(2): two polar titanium thiophosphates with complex one-dimensional tunnels

The reactions of Ti with in situ formed polythiophosphate fluxes of A(2)S(3) (A = Rb, Cs), P(2)S(5), and S at 500 degrees C result in the formation of two new quaternary titanium thiophosphates with compositions Rb(3)Ti(3)(P(4)S(13))(PS(4))(3) (1) and Cs(2)Ti(2)(P(2)S(8))(PS(4))(2) (2). Rb(3)Ti(3)(P(4)S(13))(PS(4))(3) (1) crystallizes in the chiral hexagonal space group P6(3) (No. 173) with lattice parameters a = 18.2475(9) Angstrom, c = 6.8687(3) Angstrom, V = 1980.7(2) Angstrom(3), Z = 2. Cs(2)Ti(2)(P(2)S(8))(PS(4))(2) (2) crystallizes in the noncentrosymmetric monoclinic space group Cc (No. 9) with a = 21.9709(14) Angstrom, b = 6.9093(3) Angstrom, c = 17.1489(10) Angstrom, beta = 98.79(1) degrees, V = 2572.7(2) Angstrom(3), Z = 4. In the structure of 1 TiS(6) octahedra, three [PS(4)] tetrahedra, and the hitherto unknown [P(4)S(13)](6-) anion are joined to form two different types of helical chains. These chains are connected yielding two different helical tunnels being directed along [001]. The tunnels are occupied by the Rb+ ions. The [P(4)S(13)](6-) anion is generated by three [PS(4)] tetrahedra sharing corners with one [PS(4)] group in the center of the starlike anion. The P atoms of the three [PS(4)] tetrahedra attached to the central [PS(4)] group define an equilateral triangle. The [P(4)S(13)](6-) anion may be regarded as a new member of the [P(n)S(3n+1)]((n+2)-) series. The structure of Cs(2)Ti(2)(P(2)S(8))(PS(4))(2) (2) consists of the one-dimensional polar tunnels containing the Cs(+) cations. The rare [P(2)S(8)](4-) anion which is composed of two [PS(4)] tetrahedra joined by a S(2)(2-) anion is a fundamental building unit in the structure of 2. One-dimensional undulated chains being directed along [100] are joined by [PS(4)] tetrahedra to form the three-dimensional network with polar tunnels running along [010]. The compounds are characterized with IR, Raman spectroscopy, and UV/vis diffuse reflectance spectroscopy.