长周期光纤光栅谐振波长与曝光量的变化关系

利用波动干涉理论推导了长周期光纤光栅的光栅方程. 利用色心模型和Kramers-Kronig原理，得到了长周期光纤光栅的中心谐振波长与曝光量的变化关系的理论公式，并进行了实验研 究. 理论和实验结果都表明，长周期光纤光栅的中心谐振波长与曝光量的关系按多项e负指 数之和规律变化，其变化率受到模板占空比的控制；另外，长周期光纤光栅的中心谐振波长 与模板占空比成反比关系. 关键词： 长周期光纤光栅 谐振波长 模板占空比     

PTCR纳米陶瓷粉及其烧结体的制备

The PTCR(positive temperature coefficient of resistance) nanosized ceramic powder was prepared by Sol-Gel process and characterized by XRD, DSC, SEM and BET techniques. The results showed that the nanopowder has an average crystallite size of 35nm with sphere-shaped, whose specific surface area is 27.80m²·g^-1 and the crystal structure is abnormal cubical perovskite phase at room temperature. In addition, the nanopowder was pressed into pellets and then sintered according to improved technique which was built based on the data of thermal analysis of the PTCR green-compact to yield PTCR ceramic materials with peculiar microstructure and higher properties, which has a resistivity at room temperature of ～20Ω·cm, a temperature coefficient of resistivity of ～19%·℃^-1, a withstand voltage intensity of >160V·mm^-1 and a resistivity jump of >10⁵.     

The investigation of the stability of DNA-<Emphasis Type="Italic">b</Emphasis>-PPO vesicles formed through frame guided assembly

Frame-guided assembly is a novel assembly method which can control the shape and size of vesicles accurately. It has been reported that the DNA-b-PPO vesicles could be stable over two weeks. In this communication we have introduced restriction sites of EcoR1 in the interior DNA scaffold to the formed vesicles in order to further study their stability. Dynamic light scattering (DLS), transmission electron microscope (TEM) and fluorescence spectrum were used to characterize the digestion process. The final results revealed that the vesicles were still stable even after two weeks cultivated with EcoR1, which suggests potential in future biological applications.     

混合溶剂前体法制备纳米CuO粉体及其性能表征

Nano-CuO was prepared by heating nano-Cu₂(OH)₂CO₃ precursors in different calcination temperatures. The precursor was synthesized from water-alcohol mixed solution of Cu(Ac)₂ using mixed solution of NaOH and Na₂CO₃as precipitants. XRD, FT-IR, TEM, TG-DTA and surface area measurement techniques were used to investigate the properties of the CuO powder. The results show that the spherical, well dispersed nano-CuO powder with the average size of 15 nm and higher catalytic activity for H₂O₂ decomposition was obtained at 300 ℃. With the increasing of calcination temperature, crystal of CuO grows up, agglomeration of the powder becomes heavier and catalytic activity decreases. FT-IR patterns revealed that the vibration fine structure of Cu-O bond in nano-CuO powder disappears and main absorption is red-shifted with the average size of nano-CuO reducing.     

Pulsed-field ionization electron spectroscopy and binding energies of alkali metal-dimethyl ether and -dimethoxyethane complexes

Lithium and sodium complexes of dimethyl ether (DME) and dimethoxyethane (DXE) were produced by reactions of laser-vaporized metal atoms with organic vapors in a pulsed nozzle cluster source. The mono-ligand complexes were studied by photoionization and pulsed field ionization zero electron kinetic energy (ZEKE) spectroscopy. Vibrationally resolved ZEKE spectra were obtained for Li(DME), Na(DME) and Li(DXE) and a photoionization efficiency spectrum for Na(DXE). The ZEKE spectra were analyzed by comparing with the spectra of other metal-ether complexes and with electronic structure calculations and spectral simulations. Major vibrations measured for the M(DME) (M=Li,Na) ions were M-O and C-O stretches and M-O-C and C-O-C bends. These vibrations and additional O-Li-O and O-C-C-O bends were observed for the Li(DXE) ion. The M(DME) complexes were in C2v symmetry with the metal atom binding to oxygen, whereas Li(DXE) was in a C2 ring configuration with the Li atom attaching to both oxygen atoms. Moreover, the ionization energies of these complexes were measured from the ZEKE or photoionization spectra and bond dissociation energies were derived from a thermodynamic cycle.     

Ca+-叔丁胺络合物的激光诱导反应

使用反射式飞行时间质谱仪, 研究了Ca⁺-叔丁胺络合物在激光诱导下的反应. 得到了反应的光解谱和作为波长函数的光解行为光谱以及各反应通道的分支比. 反应有两个通道, Ca⁺-与分子的解离通道和生成产物Ca⁺-NH₂的反应通道, Ca⁺-是主要产物, 而且在整个激光扫描的范围都存在, 并且在530～595 nm波段是唯一的产物. 反应的光解行为光谱显示出明显的无结构的峰, 分别对应于络合物的跃迁. 结合反应通道的分支比以及量化计算, 对这些峰进行了指认, 并初步探讨了反应的动力学机理.     

Synthesis and Crystal Structur of （4,4＇-H2bipy）[CdBr4]-H2O

The title compound (4,4'-H2bipy)[CdBr4]·H2O 1 has been synthesized via hydrothermal reaction and characterized by X-ray diffraction. The crystal belongs to monoelinic,space group P21/c with a=8.260(3), b=23.926(7), c=9.774(2) (A), β=106.777(9)°,C10H12Br4CdN2O, Mr=608.26, V=1849.4(9)(A)3, Z=4, Dc=2.185 g/cm3, S=1.005, μ(MoKα)=9.814 mm-1, F(000)=1128, R=0.0646 and wR=0.0989. The crystal structure analysis of 1reveals that the title compound features an isolated structure, based on discrete 4,4'-H2bipy moieties and lattice water molecules which are linked by hydrogen bonds together with tetrahedral cadmium atoms terminally coordinated by four bromine atoms.     

Rational Construction of a N,F Co-doped Mesoporous Cobalt Phosphate with Rich-Oxygen Vacancies for Oxygen Evolution Reaction and Supercapacitors

Transition-metal phosphates have been widely applied as promising candidates for electrochemical energy storage and conversion. In this study, we report a simple method to prepare a N, F co-doped mesoporous cobalt phosphate with rich-oxygen vacancies by in-situ pyrolysis of a Co-phosphate precursor with NH₄⁺ cations and F⁻ anions. Due to this heteroatom doping, it could achieve a current density of 10 mA/cm² at lower overpotential of 276 mV and smaller Tafel slope of 57.11 mV dec⁻¹ on glassy carbon. Moreover, it could keep 92 % of initial current density for 35 h, indicating it has an excellent stability and durability. Furthermore, the optimal material applied in supercapacitor displays specific capacitance of 206.3 F g⁻¹ at 1 A ⋅ g⁻¹ and maintains cycling stability with 80 % after 3000 cycles. The excellent electrochemical properties should be attributed to N, F co-doping into this Co-based phosphate, which effectively modulates its electronic structure. In addition, its amorphous structure provides more active sites; moreover, its mesoporous structure should be beneficial to mass transfer and electrolyte diffusion.     

硅基光源的研究进展

随着人们对大容量、高速和低成本的信息传播的要求越来越迫切, 近年来硅基光电子学得以蓬勃发展, 但硅基光源一直没有得到真正的解决, 成为制约硅基光电子学发展的瓶颈. 硅的间接带隙本质给高效硅基光源的实现带来很大困难, 实用化的硅基激光是半导体科学家长期奋斗的目标. 本文分别介绍了硅基发光材料、硅基发光二极管和硅基激光的研究进展, 最后总结了目前各种硅基光源面临的问题和未来的发展方向.     

Pulsed-field ionization electron spectroscopy of group 6 metal (Cr, Mo, and W) bis(benzene) sandwich complexes

Group 6 metal bis(benzene) sandwich complexes (M-bz(2): M=Cr, Mo, and W and bz=C(6)H(6)) were produced with laser vaporization molecular beam techniques and studied by pulsed-field ionization zero electron kinetic energy spectroscopy and density functional theory calculations. Each sandwich complex is in a D(6h) eclipsed configuration with (1)A(1g) and (2)A(1g) as the neutral and cationic ground electronic states, respectively. The adiabatic ionization energies for Cr-, Mo-, and W-bz(2) are measured to be 44,081(7), 44,581(10), and 43,634(7) cm(-1), respectively. The metal-benzene stretch and benzene torsion frequencies of the ion are measured to be 264, 277, and 370 cm(-1) and 11, 21, and 45 cm(-1) for Cr-, Mo-, and W-bz(2), respectively. In addition, a C-H out-of-plane bending mode is measured to be 787 cm(-1) for the Cr(+)-bz(2) complex, while a C-C in-plane bending mode is measured to be 614 cm(-1) for the W(+)-bz(2) complex. The unusual trend in the ionization energy and metal-benzene stretch frequency indicates strong relativistic effects on tungsten binding.