Electron mobility and drift velocity in selectively doped InAlAs/InGaAs/InAlAs heterostructures

An increase in the electron mobility and drift velocity in high electric fields in quantum wells of selectively doped InAlAs/InGaAs/InAsAs heterostructures is obtained experimentally via controlling the composition of semiconductors forming the interface. The electron mobility at the interface in the In_0.8Ga_0.2As/In_0.7Al_0.3As metamorphic structure with a high molar fraction of In (0.7–0.8) is as high as 12.3 × 10³ cm² V⁻¹ s⁻¹ at room temperature. An increase in the electron mobility by a factor of 1.1–1.4 is attained upon the introduction of thin (1–3 nm) InAs layers into a quantum well of selectively doped In_0.53Ga_0.47As/In_0.52Al_0.48As heterostructures. A maximal drift velocity attains 2.5 × 10⁷ cm/s in electric fields of 2–5 kV/cm. The threshold field F _th for the intervalley Γ-L electron transfer (the Gunn effect) in the InGaAs quantum well is higher than in the bulk material by a factor of 2.5–3. The effect of two- to threefold decrease in the threshold field F _th in the InGaAs quantum well is established upon increasing the molar fraction of In in the InAlAs barrier, as well as upon the introduction of thin InAs inserts into the InGaAs quantum well.     

Dry sliding tribological behaviour of bilayer Cr/Cr coatings obtained in sulphate Cr(III) baths

This study was intended to investigate the properties of Cr/Cr bilayer coatings. These coatings were deposited on a copper substrate by the DC electrodeposition method from Cr(III) sulphate baths with additions of formate-urea or glycine as complexing agents. Examination of the surface morphology of Cr coatings with SEM has shown that both single and bilayer Cr coatings obtained in the Cr(III) bath with formate-urea, and those obtained in the Cr(III) bath with glycine are cracked. It has been determined that the surface microhardness (HV) of bilayer Cr coatings obtained in the Cr(III) bath with glycine is higher compared with that of single-layer Cr coatings. Wear testing of the coatings was undertaken against an Al₂O₃ ball counterface (6?mm diameter) at 1N load. The results indicate that the friction coefficients (COF) of bilayer Cr/Cr coatings obtained in the Cr(III) bath with formate-urea increased from 0.2 to 0.5 compared with that of single-layer Cr coatings, while their wear resistance deteriorated. However, bilayer Cr/Cr coatings obtained in the Cr(III) bath with glycine exhibit wear resistance close to that of single coatings with COF equal to 0.05.     

Electrons and phonons in quantum wells

The modulation of electron and polar optical phonon states in an AlGaAs/GaAs/AlGaAs quantum well (QW) with an inserted thin AlAs barrier is considered. The OW width dependence of electron-phonon scattering rates are estimated. The large contribution to the change of the electron subband population, the photovoltaic effect, and the electron mobility in the QW accounts for the resonant intersubband scattering of electrons by interface phonons. The decrease of electron mobility limited by polar optical phonon scattering with increasing carrier concentration in the QW is established. The conditions for the increase of mobility in the QW by inserting the AlAs barrier are found. Fiz. Tekh. Poluprovodn. 33, 1049–1053 (September 1999) This article was published in English in the original Russian journal. Reproduced here with stylistic changes by the Translation Editor.     

The Hansenula polymorpha PDD1 gene product,essential for the selective degradation of peroxisomes,is a homologue of Saccharomyces cerevisiae Vps34p

Via functional complementation we have isolated the Hansenula polymorpha PDD1 gene essential for selective, macroautophagic peroxisome degradation. HpPDD1 encodes a 116 kDa protein with high similarity (42% identity) to Saccharomyces cerevisiae Vps34p, which has been implicated in vacuolar protein sorting and endocytosis. Western blotting experiments revealed that HpPDD1 is expressed constitutively. In a H. polymorpha pdd1 disruption strain peroxisome degradation is fully impaired. Sequestered peroxisomes, typical for the first stage of peroxisome degradation in H. polymorpha, were never observed, suggesting that HpPdd1p plays a role in the tagging of redundant peroxisomes and/or sequestration of these organelles from the cytosol. Possibly, HpPdd1p is the functional homologue of ScVps34p, because—like S. cerevisiae vps34 mutants—H. polymorpha pdd1 mutants are temperature‐sensitive for growth and are impaired in the sorting of vacuolar carboxypeptidase Y. Moreover, HpPdd1p is associated to membranes, as was also observed for ScVps34p. Copyright © 1999 John Wiley & Sons, Ltd.     

Identification and characterization of cytosolic Hansenula polymorpha proteins belonging to the Hsp70 protein family

We have isolated two members of the Hsp70 protein family from the yeast Hansenula polymorpha using affinity chromatography. Both proteins were located in the cytoplasm. One of these, designated Hsp72, was inducible in nature (e.g. by heat shock). The second protein (designated Hsc74) was constitutively present. Peptides derived from both Hsp72 and Hsc74 showed sequence homology to the cytosolic Saccharomyces cerevisiae Hsp70s, Ssa1p and Ssa2p. The gene encoding Hsp72 (designated HSA1) was cloned, sequenced and used to construct HSA1 disruption and HSA1 overexpression strains. Comparison of the stress tolerances of these strains with those of wild-type H. polymorpha revealed that HSA1 overexpression negatively affected the tolerance of the cells to killing effects of temperature or ethanol, but enhanced the tolerance to copper and cadmium. The tolerance for other chemicals (arsenite, arsenate, H₂O₂) or to high osmolarity was unaffected by either deletion or overexpression of HSA1. The nucleotide sequence of HSA1 was submitted to the EMBL data library and given the Accession Number Z29379.     

Development of bigel based dysphagia-oriented products,structured with collagen and carnauba wax: characterisation and rheological behaviour

The aim of the study was to design composition of the bigels with required rheological properties that responds the needs of the dysphagia patients. Bigels were prepared with carnauba wax and different collagen concentrations in the hydrogel phase (40, 60%) as well as by changing oleogel to hydrogel ratio from 40:60 to 60:40. The stability, physical and rheological properties of obtained bigels were evaluated after their preparation and after 14 days storage. All obtained bigels were stable without phase separation and had a pleasant taste and good mouth-feel, exept bigels with the higher oleogel fraction. Viscosity values at 50 s⁻¹ divided formulated bigels into two groups: honey-like and spoon thick. An increase of oleogel fraction caused an increase in the consistency index and elastic modulus. Higher firmness and cohesiveness values were obtained in the samples with the higher collagen concentration. It was also obtained that all rheological parameters increased after 14 days of storage. The present work develops a novel bigel-based product with strong shear-thinning behaviour and high protein concentration (16–36%). It is believed that such product could not only ensure the safe swallowing process but also reduce the risk of malnutrition development.