EAST快速极紫外光谱仪绝对强度的原位标定

磁约束等离子体中杂质(特别是高Z杂质)的存在将大大增强等离子体辐射功率损失，破坏等离子体的约束性能。杂质行为的定量研究首先要求对杂质测量的光谱诊断系统进行绝对强度标定，获得灵敏度响应曲线。介绍了EAST托卡马克上的快速极紫外光谱仪系统绝对强度的原位标定方法。在波长范围20～150Å内，通过对比极紫外(EUV)波段连续轫致辐射强度的计算值和测量值得到光谱仪的绝对强度标定。在此过程中，首先由(523±1) nm范围内可见连续轫致辐射强度的绝对测量值计算出有效电荷数Z_eff，进而结合电子温度和密度分布计算EUV波段连续轫致辐射强度；EUV波段连续轫致辐射强度的测量值即为不同波长处探测器的连续本底计数扣除背景噪声计数值。对于较长波段范围130～280Å，通过对比等离子体中类锂杂质离子(Fe23+，Cr21+，Ar15+)和类钠杂质离子(Mo31+，Fe15+)发出的共振谱线对(跃迁分别为1s22s 2S_1/2-1s22p 2P_{1/2, 3/2}及2p63s 2S_1/2-2p63p 2P_{1/2, 3/2})强度比的理论和实验值进行相对强度标定。其中共振谱线对强度比的理论值由辐射碰撞模型计算得到，模型中处在各个能级的离子数主要由电子碰撞激发，去激发以及辐射衰变三个过程决定。两种方法相结合，实现了光谱仪20～280Å范围的绝对强度标定。考虑轫致辐射、电子温度及电子密度的测量误差，绝对标定误差约为30%。在绝对标定的基础上，我们对杂质特征谱线强度进行绝对测量，并将测量结果与杂质输运程序结合ADAS(Atomic Data and Analysis Structure)原子数据库计算得到的模拟值进行比较，进而估算等离子体中的杂质浓度。     

Dimerization by Hetero Diels-Alder Reaction of Methyl 4,6-O-Benzylidene-3-Deoxy-3-C-Methylene-α-D-Erythro-Hexopyranosid-2-Ulose

Abstract

The dimerization by hetero Diels-Alder reaction of methyl 4,6-O-benzylidene-3-deoxy-3-C-methylene-α-D-erythro-hexopyranosid-2-ulose was found to be regio and stereospecific. The structure of the cycloadduct was assigned from NMR spectrographic and X-ray crystallographic results. These results indicated that this cycloaddition occurred by a concerted hetero Diels-Alder reaction with inverse electron demand.     

Comparison of two types of vertically aligned ZnO NRs for highly efficient polymer solar cells

Vertically aligned ZnO nanorods (NR) are prepared by two different syntheses methods and applied on polymer solar cells (PSCs). The ZnO electrodes work as the electron transport layer with the P3HT:PCBM blend acting as the active material. Several organic blend solution conditions are optimized: concentration, solvent, and deposition speed. The effect of different NR electrode morphologies is analyzed on the solar cell performance and characterized by current–voltage curves and IPCE analyses. The photovoltaic performance of the solar cells was observed to be influenced by many factors, among them infiltration of the organic P3HT:PCBM blend within the ZnO NR layer. The infiltration of the active layer was monitored by cross section SEM and energy dispersive X-ray spectroscopy analyses. Our results show that higher power conversion efficiencies are achieved when shorter NRs lengths are applied. The best power conversion efficiency obtained was 2.0% for a 400 nm ZnO NR electrode. © 2012 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2013     

Modulating the Photochemistry of Bipyridylic Compounds by Symmetric Substitutions

A quantum electronic study of the effect of substituents on (2,2′‐bipyridyl)‐3,3′‐diol and (2,2′‐bipyridyl)‐3,3′‐diamine is presented. A large difference in the photochemical behavior between the original and the substituted selected systems is expected. For the sake of simplicity, the study is restricted to the symmetrically bi‐substituted compounds: fluorine, the more electronegative atom and thus a strong σ‐acceptor but also a weak π‐donor group, and NO₂, a strong π‐acceptor substituent. Among the large set of compounds studied, two receive special attention: 5,5′‐dinitro‐(2,2′‐bipyridyl)‐3,3′‐diamine and 6,6′‐difluoro‐(2,2′‐bipyridyl)‐3,3′‐diol. While in the former case the nitro substitution transforms (2,2′‐bipyridyl)‐3,3′‐diamine, previously suggested to behave as a photomemory material, into a simple fluorescent species, the latter substitution turns (2,2′‐bipyridyl)‐3,3′‐diol into a fresh new candidate for a photomemory device.     

Thirty years of platinum single crystal electrochemistry

The electrochemistry of platinum single crystals is historically reviewed. After a brief revision of historical results dating before the publication of the landmark experiment by J. Clavilier of the flame annealing in 1980, the controversy introduced by this experiment into the surface electrochemistry community is described. Questions about the structure and composition of the platinum surface after the flame annealing and their implications on the characteristic voltammetry of platinum single crystal electrodes were slowly answered in the years that followed the first introduction of this methodology. One of the last questions to be solved was that about the nature of the chemical species responsible for the charge transfer process that leads to the so-called unusual features in the voltammogram. This was solved with the charge displacement experiment. Nowadays, a great deal of knowledge has been gathered about the structure of the interphase between platinum electrodes and electrolytic solutions and also about the electrocatalytic behaviour of platinum surfaces. State-of-the-art information about platinum electrochemistry is provided, with emphasis on results from our group, especially those obtained with a thermodynamic analysis, involving either constant or variable temperatures and with the laser-induced temperature jump method.