Transmission-mode GaN photocathode based on graded Al_xGa_(1-x)N buffer layer

We create a GaN photocathode based on graded Alx Ga1-x N buffer layers to overcome the influence of buffer-emission layer interface on the photoemission of transmission-mode GaN photocathodes.A gateshaped spectral response with a 260-nm starting wavelength and a 375-nm cut-off wavelength is obtained.Average quantum efficiency is 15% and short wavelength responses are almost equivalent to long wavelength ones.The fitted interface recombination velocity is 5×104 cm/s,with negligible magnitude,proving that the design of the graded buffer layers is efficient in obtaining good interface quality between the buffer and the emission layer.     

HeI photoelectron spectroscopy and theoretical study of trichloromethanesulfenyl acetate, CCl3SOC(O)CH3, and trichloromethanesulfenyl trifluoroacetate, CCl3SOC(O)CF3

Two novel species, trichloromethanesulfenyl acetate, CCl(3)SOC(O)CH(3), and trichloromethanesulfenyl trifluoroacetate, CCl(3)SOC(O)CF(3), have been generated in situ by the heterogeneous reactions between trichloromethanesulfenyl chloride, CCl(3)SCl, and corresponding silver salts, silver acetate (AgOC(O)CH(3)) and silver trifluoroacetate (AgOC(O)CF(3)), respectively. Photoelectron spectroscopy and quantum chemical calculations are performed to investigate these two molecules, together with their precursor, CCl(3)SCl. Both of these two compounds may exist in the gas phase as a mixture of gauche and trans conformations. As for the dihedral angles delta(RSOR') of the gauche conformers, 107.0 degrees and 108.5 degrees are derived by theoretical calculations (at the B3LYP/6-311+G(3df) level) for CCl(3)SOC(O)CH(3) and CCl(3)SOC(O)CF(3), respectively. The first vertical ionization energies of CCl(3)SOC(O)CH(3) and CCl(3)SOC(O)CF(3), which have been determined by photoelectron spectroscopy, are 9.67 and 10.34 eV, respectively. According to the experimental results and theoretical analysis, the first ionization energy of these two molecules both come from the ionization of the lone pair electron of S atom.     

可用于多种生物分析的高性能芯片毛细管电泳系统

本文采用激光诱导荧光的检测方法,搭建出高灵敏度的双通道共聚焦芯片毛细管电泳的检测系统。采用湿法刻蚀玻璃的方法获得了芯片管道的模具,并采用浇铸法在聚二甲基硅氧烷上获得高质量的微管道。将聚二甲基硅氧烷和石英玻璃贴合成为毛细管电泳芯片,该电泳芯片散热性能良好,可重复使用。以Cy5荧光素为样品,经实验证明该系统的检出限为17 pmol/L,并能在高达1 200 V/cm的场强下正常运行(高压电源的最高输出电压为1 200 V/cm),最高理论塔板数超过106N/m,表明该系统具有较高电泳效率。将该系统应用于氨基酸和DNA片段的分离分析,以及生物素标记的DNA与链霉亲合素的相互作用的检测,获得了较好的实验结果,说明该系统能够有效地应用于多种生物分析中。     

三维空间中带非线性阻尼项的等熵欧拉方程组轴对称解的爆破

研究了三维空间中带非线性阻尼项的可压缩等熵欧拉方程组Dirichlet初边值问题.采用泛函方法,定义几种不同的泛函,当初始速度足够大时分别得到了经典解在某一时间内必定爆破的结论.由于出现了非线性阻尼项,较之线性阻尼的情形,经典解爆破的难度随之增加.     

中红外、近红外和拉曼光谱法测定商品农药制剂中氰戊菊酯和马拉硫磷的含量

利用近红外、中红外和拉曼光谱法定量分析了商品农药制剂中有效成分氰戊菊酯和马拉硫磷的含量.采用偏最小二乘法(Partial least squares,PLS)建立氰戊菊酯和马拉硫磷的定量模型并进行了优化,用独立检验集对模型适应性进行评价.近红外和中红外法测定氰戊菊酯、马拉硫磷定量模型的相关系数分别是0.9981,0.9994和0.9946,0.9998,外部验证集标准差分别是0.082,0081和0.092,0.075,两种方法的定量效果接近;拉曼法氰戊菊酯和马拉硫磷定量模型的相关系数分别为0.9872和0.9993,外部验证集标准差分别为0.254和0.317,预测精度不及近红外和中红外法高.MIR-ATR,NIR和Raman 3种方法均能满足现场检测农药质量的需要.     

拖曳线列阵用光纤水听器的研究

报道了光纤水听器用于拖曳线列阵的研究结果。在保证光纤水听器声相位灵敏度的前提下, 优化设计了光纤水听器的结构,降低了光纤水听器的加速度灵敏度36dB。实验测得在20-1600Hz 频段,该光纤水听器的相位灵敏度为-162．7dB,频段内灵敏度的起伏为±0．7dB,加速度灵敏度小于-30dB。     

氧化镁用于制备氢氧化铁胶体的实验设计

Fe（OH）3胶体的制备是中学重要的课堂演示实验,由于实验过程需要加热而耗时较长。从理论与实验的角度证实了使用MgO可促进Fe3+水解形成Fe（OH）3胶体。该方法在常温下即可进行,无需加热,实验成功率高及实验现象明显,符合绿色化学理念,非常适合课堂演示实验与学生自主实验。     

Effects of Ionic Liquids on the Thermodynamics of Hydrogen Activation by Frustrated Lewis Pairs: A Density Functional Theory Study**

Nowadays, hydrogen activation by frustrated Lewis pairs (FLPs) and their applications are one of the emerging research topics in the field of catalysis. Previous studies have shown that the thermodynamics of this reaction is determined by electronic structures of FLPs and solvents. Herein, we investigated systems consisting of typical FLPs and ionic liquids (ILs), which are well known by their large number of types and excellent solvent effects. The density functional theory (DFT) calculations were performed to study the thermodynamics for H₂ activation by both inter- and intra-molecular FLPs, as well as the individual components. The results show that the computed overall Gibbs free energies in ILs are more negative than that computed in toluene. Through the thermodynamics partitioning, we find that ILs favor the H−H cleavage elemental step over the elemental steps of proton attachment, hydride attachment and zwitterionic stabilization. Moreover, the results show that these effects are strongly dependent on the type of FLPs, where intra-molecular FLPs are more affected compared to the inter-molecular FLPs.     

改性膨胀土路堤填筑含水量优化试验研究

在控制含水量的前提下,对分别掺入不同量石灰、不同量水泥改性膨胀土试件进行强度和膨胀量试验,得到不同含 水量及不同石灰(水泥)掺量对改性膨胀土强度和膨胀性的影响,通过对实验所得数据的分析,找出含水量和掺石灰(水泥)剂 量的最佳融合点,并据此对膨胀土路堤填料的改性施工提出了一些有益的建议。     

Synthesis and controlled hydrolysis of organolanthanide complexes with mono- and dianionic benzimidazole-2-thiolate ligands

Treatment of Cp(3)Er with one equivalent of benzimidazole-2-thiol (H(2)Bzimt) in THF affords the monoanionic HBzimt(-) complex Cp(2)Er(η(2)-HBzimt)(THF)(2) (1). Reaction of Cp(3)Yb with two equivalents of H(2)Bzimt gives complex CpYb(η(2)-HBzimt)(2)(THF) (2) at room temperature. Treatment of Cp(3)Ln with three equivalents of H(2)Bzimt in reflux THF affords the homoleptic Ln(η(2)-HBzimt)(3)(THF)(2) (Ln = Er (3), Y (4)). Cp(3)Ln reacts with 0.5 equivalents of H(2)Bzimt to afford the dianionic Bzimt(2-) complexes [(Cp(2)Ln)(THF)](2)(μ-Bzimt) (Ln = Yb (5), Er (6), Dy (7), Y (8)) in good yields, in which the Bzimt(2-) ligand bridges the two metals in an μ-η(2):η(2) coordination mode. Interestingly, controlled hydrolysis of complexes Cp(2)Ln(η(2)-HBzimt)(THF)(2), CpLn(η(2)-HBzimt)(2)(THF) and [(Cp(2)Ln)(THF)](2)(μ-Bzimt) produces the same tetranuclear complexes [CpLn(μ(3)-OH)(μ-η(1):η(2)-HBzimt)](4) (Ln = Yb (9), Er (10), Y (11)), indicating that the hydrolysis selectivity greatly depends on the number of coordinated cyclopentadienyl groups. All complexes were characterized by elemental analysis, spectroscopic properties and X-ray single crystal diffraction analysis.