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1.
J. M. Ballingall P. Ho J. Mazurowski L. Lester K. C. Hwang J. Sutliff S. Gupta J. Whitaker 《Journal of Electronic Materials》1993,22(12):1471-1475
InxGa1−xAs (x=0.25–0.35) grown at low temperature on GaAs by molecular beam epitaxy is characterized by Hall effect, transmission
electron microscopy, and ultrafast optical testing. As with low temperature (LT) GaAs, the resistivity is generally higher
after a brief anneal at 600°C. High-resolution transmission electron microscopy shows all the as-grown epilayers to be heavily
dislocated due to the large lattice mismatch (2–3%). When the layers are annealed, in addition to the dislocations, precipitates
are also generally observed. As with LT-GaAs, the lifetime shortens as growth temperature is reduced through the range 300–120°C;
also, the lifetime in LT-InxGa1−xAs is generally shorter in as-grown samples relative to annealed samples. Metal-semiconductor-metal photodetectors fabricated
on the material exhibit response times of 1–2 picoseconds, comparable to results reported on GaAs grown at low temperature,
and the fastest ever reported in the wavelength range of 1.0–1.3 μm. 相似文献
2.
Scot Lester 《电子设计技术》2006,13(11):109-109,112
降压型SMPS(开关电源)能有效地将未稳压的电源转换为稳定的输出电压。但是.输出端会出现由开关而产生的有害纹波和输入瞬变。如将有噪声的电源加在RF功率放大器上.则会在广播频谱中注入寄生信号或调制噪声。模拟系统工程师与RF系统工程师都青睐传统的低噪声电源设计.它包括一个变压器、整流器和滤波器.后面是一个线性稳压器。一只低压差线性稳压器的低输出噪声和高PSRR(电源抑制比)可以确保干净的电源.不会造成对功率放大器输出的干扰。 相似文献
3.
L.F. Lester W.J. Schaff S.D. Offsey L.F. Eastman 《Photonics Technology Letters, IEEE》1991,3(5):403-405
Graded-index separate-confinement heterostructure (GRINSCH) strained-layer lasers with five In/sub 0.3/Ga/sub 0.7/As quantum wells have been fabricated with cavity lengths from 50 to 400 mu m using chemically assisted ion-beam etching (CAIBE) to form the laser mirrors. The dry-etching process is thermally assisted, which gives a reproducible etching rate. A minimum threshold-current value is observed at a cavity length of 50 mu m, showing that the multiquantum-well design is optimum for short-cavity lasers. A relaxation oscillation frequency of 10 GHz and a -3 dB bandwidth of 15 GHz have been measured on a 200*10 mu m mesa-structure device.<> 相似文献
4.
The ab initio molecular fragment approach is applied to a characterization study of the ground state of the zwitterion of glycine. Included among the properties studied are the — conformational energy surface, the electronic structure, and the magnitude and direction of the dipole moment. The results of the present study are compared to the results of other theoretical and experimental studies.This work was supported in part by the National Science Foundation, the University of Kansas, and the Upjohn Company, Kalamazoo, Michigan 49001.NSF Trainee (1969-1972).Alfred P. Sloan Research Fellow (1971–1973). 相似文献
5.
J. D. Petke Gerald M. Maggiora‡ Lester Shipman‡ Ralph E. CHRISTOFFERSEN‡ 《Photochemistry and photobiology》1979,30(2):203-223
Abstract— Ab initio configuration interaction wavefunctions and energies are reported for the ground state and many low-lying excited singlet and triplet states of ethyl pheophorbide a (Et-Pheo a) and ethyl chlorophyllide a (Et-Chl a), and are employed in an analysis of the electronic absorption spectra of these systems. In both molecules the visible spectrum is found to consist of transitions to the two lowest-lying 1(π, π*) states, S1 and S2. The configurational compositions of S1 and S2 in both molecules are similar, and are described qualitatively in terms of a four-orbital model. The S1← S0 transition in each case is predicted to be intense, and is largely in-plane y-polarized, while the S2← S0 transition is predicted to be extremely weak and in-plane polarized. The orientation of the S2← S0 transition dipole is not conclusively established in the present calculations. The Soret band in both molecules is composed of transitions to no less than ten states (S3-S12 in Et-Chl a and S3-S7S9-S12. and S14 in Et-Pheo a), which exhibit primarily (π, π*) character. The configurational compositions of these states are generally a complex mixture of excitations from both occupied macrocyclic π molecular orbitals and occupied orbitals with electron density in the cyclopen-tanone ring and the carbomethoxy chain. No clear correspondences are evident between respective Soret states of the two systems. Transitions to these states are generally intense and display a variety of in-plane polarizations. Two additional Soret states of Et-Pheo a, S8 and S13, exhibit primarily (n. π*) character. S8 is characterized by excitations from u and non-bonding regions of the carbomethoxy chain, while S13 is described by n →π* excitations involving the nitrogen atom of ring II. No corresponding (n, π*) states were found for Et-Chl a. In both molecules the lowest two triplet states, T1 and T2, are found to lie lower in energy than S1. while T, and S1 are approximately degenerate. The configurational compositions of T1-T4 of both molecules are nearly identical, and may be described by a four-orbital model. However, the compositions of T1-T4 differ sharply from those of S1 and S2. A number of higher-lying 3(π, π*) states of both molecules (T5-T13 in Et-Chi a and T8-T9, T11-T13 in Et-Pheo a) are found to have energies similar to the singlet Soret states, relative to S0. They are characterized by a complex mixture of configurations which do not include significant contributions involving the four-orbital model. In addition, two 3(n, π*) states of Et-Pheo a, T10 and T14, are found, which are somewhat analogous to S8 and S13. Additional data presented include the charge distributions and molecular dipole moments of the S0. S1, and T1 states of both molecules, as well as energies and oscillator strengths of computed Sn←S1 and Tn←1 transitions. 相似文献
6.
PHOTOINACTIVATION OF CATALASE 总被引:6,自引:0,他引:6
Abstract— Inactivation of catalase with visible light (>400nm) has been studied in purified bovine liver catalase and in peroxisomal catalase in the mitochondrial fraction of rat liver. Light corresponding to that of maximal absorbance of the heme site (405 nm) was most effective in inactivation. Although photoinactivation is O2 dependent, scavengers of OH radical, 1 O2 and O− 2 did not protect against loss of activity in either system. Superoxide dismutase partially protected purified catalase added into the mitochondrial fraction system. However, complete protection of catalase was afforded by low concentrations of substrates such as formic acid or methanol which rapidly convert Compound I to Ferricatalase. 相似文献
7.
Summary A method has been developed for the direct spectrophotometric determination of gold by using the wine coloured complex formed in the interaction of gold with the Woods reagent. The colour reaction follows Beer's law and is stable. The method is sensitive, reproducible and accurate. Of the several anions and cations studied, only a few interfered seriously in the determination of gold. However, the ones that do interfere seriously can be separated by conventional methods. The mole ratio curve for the gold-Woods reagent system shows definite evidence that a 1 to 1 interaction product is produced in the reaction. As the mole ratio of the Woods reagent to gold was varied from 15 to 101, absorbance measurements indicated that reaction products lower or higher than 1 to 1 mole ratio are not formed.
Zusammenfassung Es wird eine Methode zur direkten spektrophotometrischen Goldbestimmung beschrieben, die auf der Bildung des weinrot gefärbten Komplexes mit Woods' Reagens beruht. Die Färbung ist beständig und befolgt das Beersche Gesetz. Das Verfahren ist empfindlich und liefert reproduzierbare und genaue Ergebnisse. Die wenigen Ionen, die beträchtliche Störungen verursachen, können nach üblichen Methoden abgetrennt werden. Es wurde festgestellt, daß das Molverhältnis Au: Reagens in dem gebildeten Komplex 11 beträgt.相似文献
8.
Reaction of laser-ablated Zr with CH(4) ((13)CH(4), CD(4), and CH(2)D(2)) in excess neon during condensation at 5 K forms CH(2)=ZrH(2), the simplest alkylidene hydride complex, which is identified by infrared absorptions at 1581.0, 1546.2, 757.0, and 634.5 cm(-)(1). Density functional theory electronic structure calculations using a large basis set with polarization functions predict a C(1) symmetry structure with agostic C-H- - -Zr bonding and distance of 2.300 A. Identification of the agostic CH(2)=ZrH(2) methylidene complex is confirmed by an excellent match of calculated and observed isotopic frequencies particularly for the four unique CHD=ZrHD isotopic modifications. The analogous reactions in excess argon give two persistent photoreversible matrix configurations for CH(2)=ZrH(2). Finally, methane activation by CH(2)=ZrH(2) gives the new (CH(3))(2)ZrH(2) molecule. 相似文献
9.
Fluorescence-dip infrared spectroscopy and predissociation dynamics of OH A 2Sigma+ (v = 4) radicals
Derro EL Pollack IB Dempsey LP Greenslade ME Lei Y Radenović DC Lester MI 《The Journal of chemical physics》2005,122(24):244313
Fluorescence-dip infrared spectroscopy, an UV-IR double-resonance technique, is employed to characterize the line positions, linewidths, and corresponding lifetimes of highly predissociative rovibrational levels of the excited A (2)Sigma(+) electronic state of the OH radical. Various lines of the 4 <--2 overtone transition in the excited A (2)Sigma(+) state are observed, from which the rotational, centrifugal distortion, and spin-rotation constants for the A (2)Sigma(+) (v = 4) state are determined, along with the vibrational frequency for the overtone transition. Homogeneous linewidths of 0.23-0.31 cm(-1) full width at half maximum are extracted from the line profiles, demonstrating that the N = 0 to 7 rotational levels of the OH A (2)Sigma(+) (v = 4) state undergo rapid predissociation with lifetimes of < or =23 ps. The experimental linewidths are in near quantitative agreement with first-principles theoretical predictions. 相似文献
10.
The mass spectra of aluminum isopropoxide show that polymers, [Al(OC3H7)3]x where x = 1 to 7, can be present in the vapor and are, therefore, probably present in the bulk sample. The polymeric composition of the vapor depends on the previous history of the sample. Exact mass measurements on many of the ions along with data on a number of metastable peaks support the proposed fragmentation mechanisms. Loss of 102 mass units between intense peaks in the mass range above 500 a.m.u. leads to the suggestion that the higher polymers may be used as high mass marking substances. 相似文献