Core temperature and density profile measurements in inertial confinement fusion implosions

We have measured time-integrated and time-gated electron temperature (T_e) and density (N_e) spatial profiles from indirect-drive implosions. In our experiments, we used a multiple-pinhole two-dimensional imaging spectrometer to obtain multispectral X-ray images of the imploded core. Quantitative comparisons between quasi-monochromatic images in different energy bands allowed T_e and N_e spatial profiles to be determined using two independent and validated techniques: a multi-objective search and reconstruction analysis, and an analytical analysis. We then compared the results to a simple one-dimensional (1D) mix-free hydrodynamics simulation in order to evaluate the ability of such a model to predict our experiments. Our data show spatial T_e profiles that are qualitatively consistent with the predictions of our 1D simulations, but we observe central cores that are 10–25% cooler and emit X-rays as late as 200 ps after peak compression. We infer time-gated spatial N_e profiles that are consistent with our 1D simulations near the times of peak compression, but we find significant disagreement between time-integrated data and 1D simulation predictions at large radii. Careful analysis of the time-gated and time-integrated T_e and N_e spatial profiles, together with streaked X-ray emission spectra from core and shell dopants, suggests mixing of shell material into the core is an important process that our 1D hydrodynamics simulations fail to capture, and comparison between image data and a simple analytical model suggests that 2–5 μm of the initial inner shell thickness mixes into the core during the time period of significant X-ray emission. This mix width is consistent with the predictions of a growth-factor analysis that treats instability growth seeded by capsule surface roughness, and points to the need to consider time-dependent mixing effects when interpreting T_e and N_e spatial profiles derived from multispectral X-ray image data, particularly at large radii where mixing effects will be most significant.     

含氮类金刚石薄膜的紫外辐照研究

 用射频等离子体方法在玻璃基底上制备的类金刚石（DLC）薄膜，采用离子注入法掺氮，并对掺氮DLC薄膜紫外（UV）辐照前后的性能变化进行了研究。研究结果表明：随氮离子注入剂量及UV辐照时间的增加，位于2 930cm^-1附近的SP ³C-H吸收峰明显变小，而位于1 580cm^-1附近的SP2C-H吸收峰则明显增强，薄膜的电阻率明显呈下降趋势；随UV辐照时间的增加，位于1 078cm^-1附近的Si-O-Si键数量及位于786cm^-1附近的Si-C键数量明显增加。即氮离子注入和UV辐照明显改变了DLC薄膜的结构与特性。     

2-甲氧基-4-乙酰胺基苯甲酸甲酯合成方法的改进

以ＰＡＳ－ Ｎａ 为原料，经水溶液中酰化后，再经酯化与醚化一步反应制得２－ 甲氧基－ ４ － 乙酰胺基苯甲酸甲酯，总收率８１％ 。     

Atmospheric pressure chemical vapour deposition of selenium and tellurium films by UV laser photolysis of diethyl selenium and diethyl tellurium

Excimer laser‐induced photolysis of gaseous diethyl selenium and diethyl tellurium (C₂H₅)₂M (M = Se, Te) is controlled by cleavage of both M? C bonds, it yields C₁–C₄ hydrocarbons (ethene as major product) and results in chemical vapour deposition of selenium films and nanosized tellurium powder. The selenium and tellurium properties were characterized by X‐ray photoelectron spectroscopy and Scanning electron Microscopy techniques. Copyright © 2001 John Wiley & Sons, Ltd.     

UV light‐mediated alkylation of inorganic selenium

In the presence of low molecular weight organic acids (formic, acetic, propionic and malonic), inorganic selenium(IV) is converted by UV irradiation to volatile selenium carbonyl, dimethylselenide and diethylselenide, depending on the acid used. Gas chromatography–mass spectrometry analysis of the volatile products shows that, in 0.7 M formic acid solution, approximately 60–70% (v/v) SeH₂ and 30–40% (v/v) SeCO are formed. The presence of nitrate ion appears to increase threefold the formation of SeCO while completely suppressing formation of SeH₂. Copyright © 2003 Crown in the right of Canada. Published by John Wiley & Sons, Ltd.     

Synthesis and optical properties of fluorene‐based polymers incorporating organosilicon unit

The synthesis and optical properties of polymers bearing the repeating unit of terfluorene and various organosilicon groups were investigated. Polymers with high molecular weight and good solubility could be obtained by Suzuki coupling polymerization from silylene‐containing fluorene‐based dibromo monomers and 9,9‐dihexylfluorene‐2,7‐bis(trimethyleneborate). From UV spectra of polymers bearing acyclic silylene bridge, the organosilicon units not only interrupted a π‐conjugation but also contributed to an electronic communication between connected fluorenes. The emission maximum wavelengths (ca. 400 nm) blue‐shifted when compared with that of polyfluorene (418 nm) and the fluorescence quantum yields were considerably high (>0.82) in the CHCl₃ solution. On the other hand, rather broad emission was observed at 480 nm and the fluorescence quantum yield was quite low (0.004) in the solution‐state PL spectrum of tetraphenylsilole‐containing polymer. The polymer emitted visible green light in the spin‐coated film. The fluorescence peak intensity at 486 nm gradually decreased when the film was illuminated with the UV light of 359 nm in air. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4786–4794, 2007     

Spectral features of 1,2-biradicals isomeric to C2–C4 perfluoroolefins

Absorption spectra of 1,2-biradicals were obtained by kinetic spectroscopy under adiabatic compression of mixtures of perfluoroolefins with argon.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 2048–2050, October, 1995.     

Comparative study on the optical properties and stability of linear and branched polysilanes

A typical linear polysilane—poly(methylphenyl)silane and two branched polysilanes—poly(phenyl-dimethyl)silane and poly(phenyl-methylphenyl)silane were synthesized by Wurtz reductive coupling reaction. The ultraviolet (UV) absorption and photoluminescence (PL) properties of these three polysilanes were investigated. The results, that the absorption band of the two branched polysilanes tailing to visible region and the corresponding emission peak having obvious red shift compared to the linear one, indicate that branched polysilanes have lower energy band gap. Thermogravimetric analysis (TGA) demonstrates that branched polysilanes have better thermo-stability. This conclusion has been verified by the Ozawa treatment, which provides theoretical explanation on thermo-decomposition. Besides, the results of exposing to ultraviolet reveal that branched polysilanes have better ultraviolet-resistant stability.     

Synthesis,hole mobility,and photovoltaic properties of two alternating poly[3‐(hex‐1‐enyl)thiophene‐co‐thiophene]s

Two alternating poly[3‐(hex‐1‐enyl)thiophene‐co‐thiophene]s, Pa (with 77% trans‐isomer and 23% cis‐isomer) and Pb (with 100% trans‐isomer), were synthesized by the coupling of 2,5‐dibromo‐3‐hex‐1‐enyl‐thiophene to 2,5‐bis(tributylstannyl)thiophene via a Stille reaction and compared with poly(3‐hexylthiophene‐co‐thiophene) ( P1 ) to study the effect of changing the carbon(α)–carbon(β) single bond into a carbon–carbon double bond on the properties of the polymers. From P1 to Pb and to Pa , the ultraviolet–visible absorption peaks of the polymers were slightly redshifted, and their electrochemical bandgaps decreased by 0.05–0.1 eV. X‐ray diffraction analysis indicated that Pa had a better lamellar structure than Pb . The hole mobilities of the three polymers, determined with the space‐charge‐limited current model, were 5.23 × 10^?6 ( P1 ), 2.34 × 10^?4 ( Pb ), and 7.02 × 10^?4 cm²/V s ( Pa ). The power conversion efficiencies (PCEs) of polymer solar cells based on the three polymers were 0.87 ( P1 ), 1.16 ( Pb ), and 1.70% ( Pa ). The increase in the hole mobility and PCE revealed the important effect of changing the carbon(α)–carbon(β) single bond into a carbon–carbon double bond on the properties of polythiophene derivatives containing 3‐alkylthiophene. The strategy used in this work enlarges the thinking to obtain novel, efficient donor polymers for optoelectronic applications. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 629–638, 2007