High responsivity, LWIR dots-in-a-well quantum dot infrared photodetectors

In this paper we report studies on normal incidence, InAs/In_0.15Ga_0.85As quantum dot infrared photodetectors (QDIPs) in the dots-in-a-well (DWELL) configuration. Three QDIP structures with similar dot and well dimensions were grown and devices were fabricated from each wafer. Of the three devices studied, the first served as the control, the second was grown with an additional 400 Å AlGaAs blocking layer, and the third was grown on a GaAs n+ substrate with the intention of testing a single pass geometry. Spectral measurements on all three devices show one main peak in the long-wave IR (≈8 μm). The absorption was attributed to the bound-to-bound transition between the ground state of the InAs quantum dot and the ground state of the In_0.15Ga_0.85As well. Calibrated peak responsivity and peak detectivity measurements were performed on each device at 40, 60, and 80 K. For the same temperatures, frequency response measurements from 20 Hz to 4 kHz at a bias of V_b=−1 V were also performed. The addition of the blocking layer was shown to slightly enhance responsivity, which peaked at 2.4 A/W at 77 K, V_b=−1 V and responsivity was observed to be significantly reduced in the single pass (n+ substrate) sample. The rolloff of the frequency response was observed to be heavily dependent on temperature, bias, and irradiance. The results from the characterization of each sample are reported and discussed.     

Perfect Modules

Erika Mares introduced the concepts of semi-perfectness and perfectness for projective modules, generalised the structure theorems of H. Bass and obtained results on the endomorphism rings of such modules. The present author has carried out an extensive study of endomorphism rings of various types of modules with two of his collaborators [3], [9]. In particular the concept of semi-perfectness was extended to modules not necessarily projective and results similar to those of Erika Mares obtained for quasi-projective semi-perfect modules. The object of the present paper is to extend the concept of perfectness to modules which are not necessarily projective and obtain results similar to those of Erika Mares, Roger Ware etc. concerning these modules.     

Partitioning multi-edge graphs

We introduce a new kind of graph called multi-edge graph which arises in many applications such as finite state Markov chains and broadcasting communication networks. A cluster in such a graph is a set of nodes such that for any ordered pair of nodes, there is a path of multi-edges from one to the other such that these edges remain within the same set. We give two algorithms to partition a multi-edge graph into maximal clusters. Both these algorithms are based on the depth-first search algorithm to find strongly connected components of the directed graph. We also discuss some applications of clustering in multi-edge graphs.     

Inclusive ϕ production inK − p interactions at 110 GeV/c and search for structure in φ π−

Results on inclusive ? production inK ^? p interactions at 110 GeV/c are presented. The production cross section is found to be larger than in πp andpp interactions at similar energies, suggesting OZI allowed \(s\bar s\) fusion to be the dominant mechanism in ? production. Thex distributions of ? and \(\bar K^{*0} \) are found to be similar to each other over the entirex range suggesting an overall strangeness suppression factor of 0.20±0.04 in the sea to be the dominant source of the difference in the cross section for ? and \(\bar K^{*0} \) . There is no evidence of a narrowφπ ^? state around 2.1 GeV/c² as suggested byK ⁺ experiments, but there is some excess of events in the region 1.94?1.98 GeV/c² consistent with theF-meson mass as observed ine ⁺ e ^? experiments.     

Reactions of copper acetylides. Structure of (π-C5H5)Ru(PPh3)2 (CCPh)CuCl,and new syntheses of transition metal cluster compounds

In contrast to a related iron—copper compound, the complex (π-C₅H₅)Ru(PPh₃)₂(C₂Ph)CuCl is shown to be monomeric, and contains linear dicoordinate copper(I); the reactions of this and similar complexes with metal carbonyls are sources of new mixed-metal clusters, such as (π-C₅H₅)Fe₂ Ru(C₂Ph)(CO)₆ (PPh₃).     

Synthesis of aminoquinolone derivatives

The synthesis of 3-amino-7-chloro-1-ethyl-6-fluoro-4(1H)quinolinone derivatives is described. These were investigated for their antibacterial activity.     

Extraction behavior of uranium(VI), plutonium(IV), zirconium(IV), ruthenium(III) and europium(III) with γ-pre-irradiated solutions of N,N′-methylbutyl substituted amides in n-dodecane

The extraction of plutonium(IV), uranium(VI), zirconium(IV), europium(III) and ruthenium(III) with -pre-irradiated n-dodecane solutions of methylbutyl substituted hexanamide (MBHA), octanamide (MBOA) and decanamide (MBDA) from 3.5M HNO₃ has been studied as a function of absorbed dose up to 184×10⁴ Gray. The distribution ratios (K_d) of uranium(VI) decreased gradually up to a dose of 50×10⁴ Gray and became almost constant thereafter, while ruthenium(III) and europium(III) were not extracted in the entire dose range studied. The K_d values of Pu(IV) decreased gradually up to 10×10⁴ Gray, for MBOA, and 30×10⁴ Gray for MBHA and MBDA and then increased up to a dose of 72×10⁴ Gray, indicating the synergistic effect of radiolytic products at higher doses. The extraction of zirconium(IV) was found to increase gradually up to 72×10⁴ Gray. However, the steep fall in K_d values of plutonium(IV), zirconium(IV) beyond a dose of 72×10⁴ Gray was atrributed to third phase formation. The radiolytic degradation of amides was monitored by quantitative IR spectroscopy and was found to follow the order MBOA>MBDA>MBHA at 184×10⁴ Gray having the amines and carboxylic acids as the main radiolytic products.     

o-hydroxylmethylphenylchalcogens: synthesis, intramolecular nonbonded chalcogen...OH interactions, and glutathione peroxidase-like activity

[Structure: see text]. The synthesis and characterization of a series of organochalcogen (Se, Te) compounds derived from benzyl alcohol 13 are described. The synthesis of the key precursor dichalcogenides 15, 22, and 29 was achieved by the ortho-lithiation route. Selenide 18 was obtained by the reaction of the dilithiated derivative 14 with Se(dtc)2. Oxidation of 15 and 22 with H2O2 afforded the corresponding cyclic ester derivatives 17 and 24, respectively. Oxidation of selenide 18 with H2O2 affords the spirocyclic compound 19. The presence of intramolecular interactions in dichalcogenides 15 and 22 has been proven by single-crystal X-ray studies. The cyclic compounds 17 and 19 have also been characterized by single-crystal X-ray studies. GP(X)-like antioxidant activity of selenium compounds has been evaluated by the coupled bioassay method. Density functional theory calculations at the mPW1PW91 level on ditelluride 22 have identified a fairly strong nonbonding interaction between the hydroxy oxygen and tellurium atom. The second-order perturbation energy obtained through NBO analysis conveys the involvement of n(O) --> sigma(Te-Te) orbital overlap in nonbonding interaction. Post wave function analysis with the Atoms in Molecules (AIM) method identified distinct bond critical point in 15 and 22 and also indicated that the nonbonding interaction is predominantly covalent. Comparison between diselenide 15 and ditelluride 22 using the extent of orbital interaction as well as the value of electron density at the bond critical points unequivocally established that a ditelluride could be a better acceptor in nonbonding interaction, when the hydroxy group acts as the donor.     

Isomeric ruthenium terpyridine complexes [Ru(trpy)(L)Cl]n+ containing the unsymmetrically bidentate acceptor L=3-amino-6-(3,5-dimethylpyrazol-1-yl)-1,2,4,5-tetrazine. Synthesis, structures, electrochemistry, spectroscopy and DFT calculations

The isomeric title complexes were obtained in almost equimolar ratio from the reaction of Ru(trpy)Cl3 and L. Crystal structure analyses of the perchlorate hemihydrates, electrochemical and spectroscopic (NMR, UV/VIS, EPR) studies, supported by DFT calculations, reveal distinct differences between the isomeric redox series [1]n+(tetrazine-Nt trans to Cl) and [2]n+(pyrazolyl-Np trans to Cl; n= 0, 1, 2). The latter system with the pi acceptors trpy and tetrazine in the equatorial plane and the pyrazolyl and chloride donors in the axial positions exhibits facilitated oxidation, lower energy MLCT transitions, more balanced chelate coordination, and a higher g anisotropy in the oxidised (RuIII) state. According to partially resolved EPR spectra of one-electron reduced neutral compounds and they have the unpaired electron predominantly in the tetrazine ring of L.