Probing plasma fluorinated graphene via spectromicroscopy.

Plasma fluorination of graphene is studied using a combination of spectroscopy and microscopy techniques, giving insight into the yield and fluorination mechanism for functionalization of supported graphene with both CF4 and SF6 gas precursors. Ion acceleration during fluorination is used to probe the effect on grafting functionalities. Adatom clustering, which occurs with CF4 plasma treatment, is suppressed when higher kinetic energy is supplied to the ions. During SF6 plasma functionalization, the sulfur atoms tend to bond to bare copper areas instead of affecting the graphene chemistry, except when the kinetic energy of the ions is restricted. Using scanning photoelectron microscopy, with a 100 nm spatial resolution, the chemical bonding environment is evaluated in the fluorinated carbon network at selected regions and the functionalization homogeneity is controlled in individual graphene flakes.

Transmission electron microscopy study of erbium silicide formation from Ti/Er stack for Schottky contact applications.

In this paper, we present results of transmission electron microscopy studies on erbium silicide structures fabricated under various thermal conditions. A titanium cap has been used as a protective layer against oxidation during rapid thermal annealing of an erbium layer in a temperature range of 300-700 degrees C. Both layers (200 nm Ti and 25 nm Er) were deposited by electron-beam sputtering. The investigations have shown that the transformation of the 25-nm-thick erbium into erbium silicide is completed after annealing at 500 degrees C. At higher temperatures, the formation of a titanium silicide layer above erbium silicide is observed. The lowest Schottky barrier has been measured in the sample annealed at 700 degrees C.

Age-related functional alteration of mouse liver ribosomes.

The in vitro functional capacity of the mouse liver protein synthesis machinery was studied as a function of age. Polysomes from young (one-three months old) and old (18-24 months old) C57BL/6J mice were incubated under standard conditions in a ribosome-free reticulocyte lysate containing [3H]-leucine. The incorporation of radioactivity into hot TCA-insoluble material was measured as a function of time and kinetic curves were compared. A drastic age-related decrease in the initial rate of leucine incorporation was observed when the total ribosomal fraction (containing the whole range of ribosomal aggregates including subunits and single ribosomes) was assayed. When "heavy polysomes" (fractions from which subunits and single ribosomes had been excluded) were compared, the same difference was observed. This latter result indicated that the observed alteration may be attributed to actively translating ribosomes. Results from experiments using inhibitors of initiation suggest that the observed age-related alteration can be attributed to a reduced capacity of ribosomes from older animals to sustain reinitiation.

Functional properties of rat liver protein synthesizing machinery in relation to aging.

It is well established (van Bezooijen et al., 1977a) that the protein synthesis by isolated liver parenchymal cells (ILPC) from Wag/Rij rats is dependent in a characteristic way on the age of the donor. Whereas cells of middle-aged animals exhibit a decrease in proteo-synthesis activity under in vitro incubation conditions as compared to cells of young rats, a marked increase is observed between 24 and 36 months of age. To investigate whether this overall age-related variation is directly correlated with an intrinsic change at the level of the protein synthesis apparatus of hepatic cells, we compared the size distribution and the in vitro translational activity of polysomes from four age groups. We show that both exhibit the same biphasic response to aging as does the protein synthesizing capacity of ILPC.