纳米MgTi2O5的制备

纳米ＭｇＴｉ_２Ｏ_５的制备彭子飞，冯贵武，汪国忠，田兴友，张伟，张立德（中国科学院固体物理研究所合肥２３００３１，安徽大学化学系合肥）关键词ＭｇＴｉ_２Ｏ_５，纳米材料，制备，共沉淀钛酸镁是高频低介电常数的电容陶瓷材料，以往合成ＭｇＴｉ２Ｏ５的方法都采...     

J0相干角向偏振涡旋光束的深聚焦

通过矢量德拜理论,研究了J0相干角向偏振涡旋光束深聚焦的性质。推导了在焦点区域的光强分布、光谱相干度和偏振度的表达式。数值模拟结果表明,光强分布、相干度和偏振度不仅依赖于相干长度和数值孔径最大角,而且依赖于拓扑电荷数。这种光束在焦平面还可获得非常小的焦点和焦洞。     

The effect of PbF2 content on the microstructure and upconversion luminescence of Er-doped SiO2-PbF2-PbO glass ceramics

The Er³⁺ doped transparent oxyfluoride glass ceramics were obtained by appropriate heat treatment of the precursor glasses with composition (mol%) 50SiO₂-xPbF₂-(50 − x)PbO-0.5ErF₃. The microstructure and optical properties of the glasses and glass ceramics were determined by differential scanning calorimetry (DSC), X-ray diffraction (XRD), absorption spectra and luminescence spectra. The intensity of upconversion luminescence significantly increased in glass ceramics compared to that in precursor glass. The emission bands centered around 660 nm (⁴F_9/2 → ⁴I_15/2) and 410 nm (²H_9/2 → ⁴I_15/2) were simultaneously observed in glass ceramics but cannot be seen in the corresponding precursor glass. The influence of different PbF₂ content on the microstructure and upconversion luminescence of the samples was analyzed in detail. The results indicated that with the increase of PbF₂ content, the Ω₂ was almost the same and the ratios of red to green upconversion luminescence decreased in glass ceramics.     

磁电弹性体中多条位错与Griffith裂纹

根据本征方程，研究磁电弹性体中若干平行螺型位错与Griffith裂纹的相互作用.结合Muskhelishvili方法和算子理论，得到磁电弹性体中由位错和裂纹所诱导的应力场、电场和磁场的解析解.数值算例表明：在裂纹的端点及位错点上仍然存在应力的奇异性，离位错点越远处广义力越小，结论与已有的结果相符，证明了结论的正确性.当位错点与裂纹端点距离越近时，裂纹与位错间的应力场越小，并逐渐趋近于零.     

Morphological and structural evolution of Si-Cu nanocomposites by an instantaneous vapor-liquid-solid growth and the electrochemical lithiation/delithiation performances

Journal of Solid State Electrochemistry - Polymorphic Si-Cu nanocomposites of Si@Cu3Si nanowires, Si@Cu3Si nanorods, and Si@Cu3Si(Cu) nanocapsules are synthesized via the high-energy arc-discharge...     

Atomically Dispersed Iron Regulating Electronic Structure of Iron Atom Clusters for Electrocatalytic H2O2 Production and Biomass Upgrading

The integration of highly active single atoms (SAs) and atom clusters (ACs) into an electrocatalyst is critically important for high-efficiency two-electron oxygen reduction reaction (2e⁻ ORR) to hydrogen peroxide (H₂O₂). Here we report a tandem impregnation-pyrolysis-etching strategy to fabricate the oxygen-coordinated Fe SAs and ACs anchored on bacterial cellulose-derived carbon (BCC) (FeSAs/ACs-BCC). As the electrocatalyst, FeSAs/ACs-BCC exhibits superior electrocatalytic activity and selectivity toward 2e⁻ ORR, affording an onset potential of 0.78 V (vs. RHE) and a high H₂O₂ selectivity of 96.5 % in 0.1 M KOH. In a flow cell reactor, the FeSAs/ACs-BCC also achieves high-efficiency H₂O₂ production with a yield rate of 12.51±0.18 mol g_cat⁻¹ h⁻¹ and a faradaic efficiency of 89.4 %±1.3 % at 150 mA cm⁻². Additionally, the feasibility of coupling the produced H₂O₂ and electro-Fenton process for the valorization of ethylene glycol was explored in detail. The theoretical calculations uncover that the oxygen-coordinated Fe SAs effectively regulate the electronic structure of Fe ACs which are the 2e⁻ ORR active sites, resulting in the optimal binding strength of *OOH intermediate for high-efficiency H₂O₂ production.     

Spectroscopic studies of dehydrogenation of ammonia borane in carbon cryogel

Ammonia borane (AB) is of great interest for storing hydrogen, an important issue in the growing field of hydrogen technology. The reaction pathways leading to the thermal decomposition of solid-state AB incorporated in carbon cryogels (CC) have been studied by spectroscopic methods. The time-dependent thermal decomposition was followed by in situ 11B nuclear magnetic resonance (NMR) and showed a significant increase in hydrogen release kinetics for AB in CC compared to neat AB. Both 11B NMR and Fourier transform infrared spectroscopy show a new reaction product, formed in the thermal decomposition of AB in CC scaffold (CC-AB) that is assigned to reactions with surface oxygen groups. The results indicate that incorporation of AB in CC enhances kinetics because of the reactions with residual surface-bound oxygen functional groups. The formation of new products with surface -O-B bonds is consistent with the greater reaction exothermicity observed when hydrogen is released from CC-AB materials. Scanning electron microscopy shows different morphology of AB in CC-AB nanocomposite as compared to neat AB.     

Coherent carbon cryogel-ammonia borane nanocomposites for H2 storage

Coherent carbon cryogel-ammonia borane (C-AB) nanocomposites were synthesized, and improved H2 storage properties are reported. Porous carbon cryogels were impregnated with AB in tetrahydrofuran solution at 25 degrees C under argon; 30% of the carbon cryogel pore volume was filled to produce a 24 wt % C-AB nanocomposite. Nitrogen sorption isotherms, X-ray diffraction, differential scanning calorimetry, differential thermal/thermal gravimetric analyses, mass spectrometry, and 11B NMR were used to characterize the coherent C-AB nanocomposites. Findings include a merged two-step hydrogen release reaction with an appreciable reduction in the dehydrogenation temperature to <90 degrees C as well as the suppression of borazine release. The possible nanosize effects on the H2 storage properties are discussed.     

痕量银的催化动力学光度法研究——银(Ⅰ)-乙二胺-过硫酸铵-还原型酚酞新体系

催化动力学法测定银的指示反应多为配他体取代反应与氧化还原反应,通常以后者的灵敏度较高,重现性较好,Mueller依据过硫酸钾-对氨基苯磺酸-乙二胺反应体系建立的催化动力学法,其灵敏度达1×10^-3μg/ml。