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  • Online Resource  (3)
  • AIP Publishing  (3)
  • 1
    In: Journal of Applied Physics, AIP Publishing, Vol. 94, No. 3 ( 2003-08-01), p. 1428-1435
    Abstract: The behavior of the densities of Si, SiF, and SiF2 radicals and SiF4 molecule were investigated for variations in electron density at pressure of 40 mTorr in a very high frequency (VHF) 60 MHz capacitively coupled plasma employing SiF4 gas. The SiF4 molecule was measured by infrared diode laser absorption spectroscopy, the SiF2 and SiF radicals were measured by laser-induced fluorescence, the Si atom was measured by ultraviolet absorption spectroscopy, and the F atom was measured by actinometric optical emission spectroscopy. The SiF4 density decreased with an increase in electron density, and the dissociation ratio of SiF4 was saturated to about 63% at electron densities of above 8.7×1010 cm−3. The SiF2 density decreased due to electron impact dissociation, whereas the F, Si, and SiF densities increased with an increase in electron density above 1.2×1011 cm−3. The total Si density was estimated to be of the order of 1010–1011 cm−3. Furthermore, the spatial distributions of SiF, SiF2, and SiF4 densities were investigated. They were almost flat inside the plasma region, but the SiF and SiF2 radicals decreased gradually outside the plasma region, and the SiF4 molecule increased. The behavior of the Si, SiF, and SiF2 radicals was in good agreement with the emission intensity of rare gases injected as trace gases. The kinetics of the species in VHF 60 MHz SiF4 plasma was clarified on the basis of the densities of the species and electrons measured. These experimental results are useful in predicting the radical densities of VHF SiF4 plasma using simulation.
    Type of Medium: Online Resource
    ISSN: 0021-8979 , 1089-7550
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2003
    detail.hit.zdb_id: 220641-9
    detail.hit.zdb_id: 3112-4
    detail.hit.zdb_id: 1476463-5
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  • 2
    In: Journal of Applied Physics, AIP Publishing, Vol. 99, No. 9 ( 2006-05-01)
    Abstract: We have investigated in situ the hybridization and denaturation of DNA in aqueous solution using infrared absorption spectroscopy (IRAS) in the multiple internal reflection (MIR) geometry. We demonstrate that conformational changes of DNA strands due to hybridization (binding of two complementary single-stranded DNAs) and denaturation (separation of double helix at elevated temperatures) are reflected in the infrared absorption spectra in the frequency region where vibrational modes of the bases of DNA appear. Comparison with results of ab initio cluster calculation shows that hybridization produces the specific CO carbonyl stretching vibration modes in the hydrogen-bonded base pairs. The ratio of absorbance of the CO stretching peak at 1690cm−1 to the absorbance at 1660cm−1 provides a definitive metric for determining DNA hybridization. We also reveal that the CO stretching vibration modes of the bases of a single strand is strongly influenced by the surrounding water molecules that may interact with the CO groups of the bases. The present results suggest that MIR-IRAS is applicable to label-free, high-sensitive biosensors that provide insight about the gene expression and a variety of biological interactions such as DNA-protein interactions.
    Type of Medium: Online Resource
    ISSN: 0021-8979 , 1089-7550
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2006
    detail.hit.zdb_id: 220641-9
    detail.hit.zdb_id: 3112-4
    detail.hit.zdb_id: 1476463-5
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  • 3
    In: Applied Physics Letters, AIP Publishing, Vol. 86, No. 5 ( 2005-01-31), p. 053902-
    Type of Medium: Online Resource
    ISSN: 0003-6951 , 1077-3118
    RVK:
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2005
    detail.hit.zdb_id: 211245-0
    detail.hit.zdb_id: 1469436-0
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