139 research outputs found

    Observation of Metastable and Stable Energy Levels of EL2 in Semi-insulating GaAs

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    By using combination of detailed experimental studies, we identify the metastable and stable energy levels of EL2 in semi-insulating GaAs. These results are discussed in the light of the recently proposed models for stable and metastable configurations of EL2 in GaAs

    A Hybrid model for the origin of photoluminescence from Ge nanocrystals in SiO2_2 matrix

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    In spite of several articles, the origin of visible luminescence from germanium nanocrystals in SiO2_2 matrix is controversial even today. Some authors attribute the luminescence to quantum confinement of charge carriers in these nanocrystals. On the other hand, surface or defect states formed during the growth process, have also been proposed as the source of luminescence in this system. We have addressed this long standing query by simultaneous photoluminescence and Raman measurements on germanium nanocrystals embedded in SiO2_2 matrix, grown by two different techniques: (i) low energy ion-implantation and (ii) atom beam sputtering. Along with our own experimental observations, we have summarized relevant information available in the literature and proposed a \emph{Hybrid Model} to explain the visible photoluminescence from nanocrystalline germanium in SiO2_2 matrix.Comment: 23 pages, 8 figure

    Visual tool for estimating the fractal dimension of images

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    This work presents a new Visual Basic 6.0 application for estimating the fractal dimension of images, based on an optimized version of the box-counting algorithm. Following the attempt to separate the real information from noise, we considered also the family of all band-pass filters with the same band-width (specified as parameter). The fractal dimension can be thus represented as a function of the pixel color code. The program was used for the study of paintings cracks, as an additional tool which can help the critic to decide if an artistic work is original or not. In its second version, the application was extended for working also with csv files and three-dimensional images.Comment: A new version was accepted to Computer Physics Communications doi:10.1016/j.cpc.2009.12.00

    Mechanistic details of the formation and growth of nanoscale voids in Ge under extreme conditions within an ion track

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    The formation of nanoscale voids in amorphous-germanium (a-Ge), and their size and shape evolution under ultra-fast thermal spikes within an ion track of swift heavy ion, is meticulously expatiated using experimental and theoretical approaches. Two step energetic ion irradiation processes were used to fabricate novel and distinct embedded nanovoids within bulk Ge. The 'bow-tie' shape of voids formed in a single ion track tends to attain a spherical shape as the ion tracks overlap at a fluence of about 1 x 10(12) ions cm(-2). The void assumes a prolate spheroid shape with major axis along the ion trajectory at sufficiently high ion fluences. Small angle x-ray scattering can provide complementary information about the primary stage of void formation hence this technique is applied for monitoring simultaneously their formation and growth dynamics. The results are supported by the investigation of cross-sectional transmission and scanning electron micrographs. The multi-time-scale theoretical approach corroborates the experimental findings and relates the bow-tie shape void formation to density variations as a result of melting and resolidification of Ge within the region of thermal spike generated along an ion track, plus non-isotropic stresses generated towards the end of the thermal spike.Peer reviewe

    Swift Heavy Ion Induced Interface Modification in Metal/Ge Systems

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    A microscopic complex potential description of elastic, inelastic cross section in the Coulomb nuclear interference region in the 28Si on 28Si system

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    Elastic and inelastic angular distribution and excitation functions were measured for the 28Si + 28Si system in the vicinity of the Coulomb barrier. While the elastic data could be described very well by using fully microscopic complex potential, the inelastic cross sections were found to be more sensitive to small variations in the potential. In particular the Coulomb nuclear interference dip observed in the inelastic excitation functions could not be fitted satisfactorily with calculation. Inclusion of an energy dependent term of Gaussian shape to the associated matrix element with the reorientation coupling in the phenomenological calculations leads to a better fit the inelastic excitation functions. © 1998 Elsevier Science B.V

    SLC25A22 is a novel gene for migrating partial seizures in infancy

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    Objective To identify a genetic cause for migrating partial seizures in infancy (MPSI). Methods We characterized a consanguineous pedigree with MPSI and obtained DNA from affected and unaffected family members. We analyzed single nucleotide polymorphism 500K data to identify regions with evidence of linkage. We performed whole exome sequencing and analyzed homozygous variants in regions of linkage to identify a candidate gene and performed functional studies of the candidate gene SLC25A22. Results In a consanguineous pedigree with 2 individuals with MPSI, we identified 2 regions of linkage, chromosome 4p16.1-p16.3 and chromosome 11p15.4-pter. Using whole exome sequencing, we identified 8 novel homozygous variants in genes in these regions. Only 1 variant, SLC25A22 c.G328C, results in a change of a highly conserved amino acid (p.G110R) and was not present in control samples. SLC25A22 encodes a glutamate transporter with strong expression in the developing brain. We show that the specific G110R mutation, located in a transmembrane domain of the protein, disrupts mitochondrial glutamate transport. Interpretation We have shown that MPSI can be inherited and have identified a novel homozygous mutation in SLC25A22 in the affected individuals. Our data strongly suggest that SLC25A22 is responsible for MPSI, a severe condition with few known etiologies. We have demonstrated that a combination of linkage analysis and whole exome sequencing can be used for disease gene discovery. Finally, as SLC25A22 had been implicated in the distinct syndrome of neonatal epilepsy with suppression bursts on electroencephalogram, we have expanded the phenotypic spectrum associated with SLC25A22. Ann Neurol 2013;74:873-882 © 2013 American Neurological Association
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