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  • Electronic Resource  (2)
  • 2000-2004  (2)
  • 1950-1954
  • 2002  (2)
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  • Electronic Resource  (2)
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  • 2000-2004  (2)
  • 1950-1954
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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 91 (2002), S. 451-455 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The molecular beam epitaxial growth and n type doping of Hg0.80Cd0.20Te(112)B have been investigated. The surface morphology has been determined via atomic force microscopy and is appreciably different from that of the (001) orientation; long ridges and trenches are observed whose height difference is considerably less than that of the nearly elliptically shaped mounds found in (001) alloys. The mobility has been optimized with regard to growth parameters such as the Hg/Te flux ratio resulting in a maximum value of 4.0±0.6×105 cm2/(V s) for an undoped sample at low temperatures. n type Hg0.80Cd0.20Te(112)B has been grown using iodine in the form of CdI2 as a dopant. The maximum electron concentration due to iodine doping has been determined after an Hg vacancy anneal to be 4.2±0.7×1018 cm−3. Typical mobilities at low temperatures are 4.0×104 and 1.0×105 cm2/(V s) for electron concentration levels of 1.0×1017 and 5.0×1016 cm−3, respectively. By means of secondary ion mass spectroscopy the iodine concentration has been determined and hence the degree of activation. The electron concentration is proportional to that of iodine with a 100% electrical activation for concentrations up to (approximate)1018 cm−3. At higher concentrations compensation is observed. © 2002 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 117 (2002), S. 3383-3390 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present a comparative study, down to the single-molecule level, of the linewidth and multiplet structure of the optical transitions of 2.3,8.9-dibenzanthanthrene (DBATT) in shock-frozen solutions of n-decane, n-undecane, and n-tetradecane. The n-alkane matrices show weak structural ordering and distinct incorporations of the DBATT molecules have been recognized. The order does not increase, nor does the ensemble optical linewidth decrease going from bulk to sub-volumes of less than 1 μm3. The relation between lateral position, orientation of the transition moment, and transition frequency has been investigated using single-molecule fluorescence-excitation and polarization spectroscopy. The distribution of the orientation is found not to depend on frequency and vice versa. Structural ordering on a microscopic scale is found not to be decisive as regards the linewidth and multiplet structure. © 2002 American Institute of Physics.
    Type of Medium: Electronic Resource
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