面向先进光源的硅像素传感器保护环结构仿真研究

硅像素传感器上的保护环结构有利于提高传感器的耐高电压性能,为评估保护环结构对硅像素传感器的保护效果,仿真分析了三种保护环结构。通过计算机辅助设计技术对三种保护环结构进行二维建模,利用TACD内置的电学模型对三种保护环结构的I-V特性进行了仿真。研究结果表明,电流收集环会提高像素的耐高电压性能,同时不等间距保护环、保护环的内外等距离Al悬挂以及多个保护环结构有利于进一步提高传感器的击穿电压。     

关于环的稳定度一个注记

我们得到了环的稳定度为2或∞的一个充分条件,并进给出了SBN环的稳定度     

Extensions of quantum enveloping algebras

In this paper, we define a class of extended quantum enveloping algebras U _q (f(K, J)) and some new Hopf algebras, which are certain extensions of quantum enveloping algebras by a Hopf algebra H. This construction generalizes some well-known extensions of quantum enveloping algebras by a Hopf algebra and provides a large of new noncommutative and noncocommutative Hopf algebras.     

杂多酸引发四氢呋喃聚合反应Ⅱ.水的反应行为

前报我们对低腐蚀性非均相的磷钨杂多酸Ｈ３ＰＷ１２Ｏ４０（ＰＷ１２）引发体系进行了研究［１］,发现环氧乙烷（ＥＯ）可有效地促进ＰＷ１２引发的四氢呋喃（ＴＨＦ）聚合反应,大幅度地降低了引发剂用量,聚合物收率显著提高,并发现聚合过程中不存在链终止反应．产物...     

一种多波长窄线宽环形掺铒光纤激光器

本文提出了一种利用多个光纤光栅串接来实现环形掺铒光纤多波长,窄线宽激光器的新颖方法,并在实验中验证了这一设计的合理性,得到了稳定的双波长输出。     

Controlled ring‐opening polymerization of L‐lactide and 1,5‐dioxepan‐2‐one forming a triblock copolymer

Novel elastomeric A‐B‐A triblock copolymers were successfully synthesized in a new two‐step process: controlled ring‐opening polymerization of the cyclic ether–ester 1,5‐dioxepan‐2‐one as the amorphous middle block (B‐block) followed by addition and polymerization of the two semicrystalline L ‐lactide blocks (A‐block). A 1,1,6,6‐tetra‐n‐butyl‐1,6‐distanna‐2,5,7,10‐tetraoxacyclodecane initiator system was utilized and the reaction was performed in chloroform at 60 °C. A good control of the synthesis was obtained, resulting in well defined triblock copolymers. The molecular weight and chemical composition were easily adjusted by the monomer‐to‐initiator ratio. The triblock copolymers formed exhibited semicrystallinity up to a content of 1,5‐dioxepan‐2‐one as high as 89% as determined by differential scanning calorimetry. WAXS investigation of the triblock copolymers showed a crystal structure similar to that of the pure poly(L ‐lactide). © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 1774–1784, 2000     

Unexpected chlorine substitution by hydrogen in the reaction of 2-chloro-3-p-toluidino-N-p-tolylmaleimide with DBU: Synthesis and molecular structure of 2-p-toluidino-N-p-tolylmaleimide

The reaction of p-toluidine with 2,3-dichloromaleic anhydride in the presence of added 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) does not give the known compound 2-chloro-3-p-toluidino-N-p-tolylmaleimide (1), but rather 2-p-toluidino-N-p-tolylmaleimide (2) in low yields. Repeating this same reaction with Et₃N, pyridine, tmeda, and 4-Me₂Npyridine in place of DBU furnishes the expected product 2-chloro-3-p-toluidino-N-p-tolylmaleimide, without the presence of 2-p-toluidino-N-p-tolylmaleimide. The participation of DBU in the chlorine for hydrogen exchange reaction in compound 1 has been demonstrated from the independent thermolysis reaction of 1 with DBU in toluene, where 2 was obtained as the sole isolable product. Compound 2 was isolated and fully characterized in solution, and the molecular structure was established by X-ray diffraction analysis. 2-p-Toluidino-N-p-tolylmaleimide crystallizes in the monoclinic space C2/c, a = 33.630(5), b = 12.508(2), c = 7.381(1), = 90.668(3), V = 3104.3(8)³, Z = 8, and D _calc = 1.251 Mg/m³; R = 0.0357, R _w = 0.0896 for 2011 reflections with I > 2(I).     

Effects of Salt on the Orientational Order in Decylammonium Chloride/Ammonium Chloride/Water Systems

The effect of NH₄Cl on the temperature dependence of deuterium oxide splitting (water order) and proton line width (surfactant order) in decylammonium chloride (DACl), D₂O systems is reported. The molar ratio of DACl to D₂O was held constant at .085 and the molar ratio of NH₄Cl to D₂O was varied from .012 to .029. We find for the above concentration ranges that in the nematic range the relative temperature dependence of the D₂O splitting is little affected by changes on salt concentration. The slopes of the proton line widths as a function of temperature decrease with increasing salt concentration. The results are compared with earlier data on salt effects on order obtained with the disodium cromoglycate system.     

Topological Effects on Conductance of Nanotubes

Abstract

Electronic states in junctions of nanotubes with different circumferences are studied in an effective-mass approximation. The junction is characterized by boundary conditions which mix wave functions associated with K and K′ points. At ε=0, they decay linearly with the distance from the thicker nanotube, showing that the conductance decays with the junction length in proportion to its third power.     

X-ray diffraction structure of (5S)-3,4-dichloro-5-menthoxy-2(5H)-furanone

The structure of (5S)-3,4-dichloro-5-menthoxy-2(5H)-furanone is reported. The title compound crystallizes in the monoclinic space group P2₁: a = 6.650(2) Å, b = 8.038(3) Å, c = 14.858(8) Å, = 97.01(3), V = 788.3(6) ų, Z = 2, R = 0.0718, R _w = 0.0795 for 735 observed reflections with I > 3 (I), and the absolute configuration at C-5 of the furanone ring is shown to be (S).