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  • 1
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The effect of gas adjacent to the sample surface on the photo-acoustic displacement (PAD) measurement was studied by using an extremely sensitive laser interferometric probe with a sensitivity of 0.1 picometers. For silicon, the PAD signal measured at atmospheric pressure increased about 18% as compared to the signal obtained in vacuum, and varied by less than 0.7% for a change in pressure of 5% around 1 atm. It is shown, by a simple theoretical model, that the variation of the PAD is caused by a change in refractive index of the gas and the real PAD can be accurately obtained by correcting this effect.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 73 (1993), S. 2859-2865 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Electrochemical, optical, and magnetic properties in poly(3-phenylthiophene), as a function of doping and electronic states, are discussed in detail. The band gap of poly(3-phenylthiophene) was evaluated to be 2.0 eV, and similar to that of polythiophene. The evolution of localized states is evidenced by the spectral change with electrochemical doping. The spin density evaluated from the susceptibility was consistent with the polaron density assumed to be formed by a very small quantity of dopants. These results are interpreted in terms of the polaron and bipolaron models. The electronic band structure of poly(3-phenylthiophene) was determined. The top of the valence band of poly(3-phenylthiophene) is located at a higher energy state than that of polythiophene by about 0.1 eV and it became clear that the dopant in poly(3-phenylthiophene) is relatively stable compared with that in polythiophene. Successful n-type doping in poly(3-phenylthiophene) was also confirmed.
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 8584-8591 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The electrochemical, optical, and magnetic properties in poly(2,5-thienylene vinylene), PTV, in comparison with those of polythiophene, PT, during electrochemical p-type doping have been investigated by cyclic voltammetry, optical absorption spectrum, and electron spin resonance (ESR) measurements. The evolution of localized states is evidenced by the spectral change associating with doping. In the lightly doped state only two absorption peaks originating from the transitions between two gap states and the valence band appear within the gap region at about 0.6 and 1.2 eV. The spin susceptibility increased by about 1 order of magnitude from 3.7×10−7 to 2.6×10−6 emu/mol upon doping up to a dopant concentration of about 2.8 mol %. With further increasing dopants concentration, the spin susceptibility decreases slightly. The spin density evaluated from the susceptibility was inconsistent with the polaron density assumed to be formed by dopants of 2.8 mol %. Namely, even at lightly doped state, the newly developed species turn into p-type spinless bipolarons. The band gap of PTV was evaluated to be about 1.8 eV and smaller than that of PT by about 0.3 eV. This result can be interpreted in terms of a conformation change in the molecular structure, such as a change in the torsion angle between neighboring thiophene rings. The electronic band structure of PTV was determined. The bipolaron states in PTV appears in the band gap: about 0.6 eV below and above the conduction and the valence band, respectively. The bottom of the conduction band of PTV is in almost the same position as that of PT and successful n-type doping in PTV is expected.
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  • 4
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Subsurface lattice defects in silicon induced by ion implantation were studied by the use of the photo-acoustic displacement (PAD) method based on the sensitive measurements of the surface displacement due to the absorption of laser-light energy. A definite correlation between PAD and displaced atoms density (DAD) was found because PAD reflects the change in thermal conductivity associated with the net amount of displaced atoms in the crystal lattice beneath the surface. According to the linear dependence of 1/PAD on DAD, defects below a DAD of 1014/cm2 (corresponding to implant doses of 2×1011, 8×1010, and 6×1010 ions/cm2 for 100 keV B+, P+, and As+, respectively) were concluded to be point defects. After the DAD reached 1014/cm2, the PAD showed a gentle increase, and this can be attributed to the growth of point-defect clusters. A marked dependence of the PAD on the DAD was not observed beyond a DAD of 1016/cm2. In this region, the presence of an amorphous layer was observed by cross-sectional transmission electron microscopy. Annealing behavior due to low-temperature heating was studied by the change in temperature dependence curves of the PAD, and the results reflected the characteristics of the defects described above.
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  • 5
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 75 (1999), S. 226-228 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We have observed the electronic states at conducting polymer/conducting oxide interfaces using a low-energy photoelectron spectroscopic method. The electronic states of conducting polymer/indium tin oxide (ITO) interfaces were different from those of conducting polymer/metal interfaces. The electron transfer from a conducting polymer to ITO occurred at the interfaces, and is not related to the difference of the ionization potential between conducting polymers and ITO. Although the origin of this electron transfer is not clear at this stage, we speculate that the surface states of ITO play a major role. Moreover, the electron transfer at the interfaces is enhanced at higher temperatures. Other conducting oxides such as indium oxide (In2O3) and tin oxide (SnO2) also show a similar tendency to that of ITO. © 1999 American Institute of Physics.
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  • 6
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 63 (1993), S. 512-514 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Anisotropic optical transitions in an ordered Ga0.5In0.5P alloy semiconductor have been studied by electroreflectance (ER) polarization spectroscopy. The atomic ordering of column-III sublattices causes a splitting of the valence-band maximum into two doubly degenerated levels at k=0. The ER spectra reveal signals originated from the Γ6c-Γ4v, Γ5v and Γ6c-Γ6v transitions caused by the ordering. The [110] and [11¯0] ER signals due to the Γ6c-Γ6v transition show strong anisotropic characters of their intensity and line shape. On the other hand, the signal due to the Γ6c-Γ4v, Γ5v transition changes only in the intensity by the polarization direction. The ER intensities measured at various polarization angles follow the theoretically derived trends based on the selection rule for electronic-dipole transitions in the ordered crystal.
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  • 7
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 66 (1995), S. 1794-1796 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Photocurrent polarization properties near the band gap of long-range ordered Ga0.5In0.5P have been investigated. The linearly polarized PC spectra of the ordered Ga0.5In0.5P show an absorption anisotropy for the [110] and [11¯0] directions together with a large band-gap reduction. The anistotropy in the PC spectra is due to a crystal-field splitting at the valence-band maximum in ordered Ga0.5In0.5P. The PC edge of the [110] polarization is lower at about 10 meV than one of the [11¯0]. The polarization spectra defined by (I110−I11¯0)/(I110+I11¯0), where I110 and I11¯0 are the PC signal intensities measured at the [110] and [11¯0], respectively, show a single broad peak. The maximum polarization reaches about 50% at the energy of the transition between Γ6c and Γ4v, Γ5v. With increased sample temperature, the polarization maximum shifts to the lower energy side according to the change of the Γ6c-Γ4v,Γ5v transition energy. Even at room temperature, a clear polarization signal was observed. © 1995 American Institute of Physics.
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    Journal of Mathematical Physics 29 (1988), S. 851-860 
    ISSN: 1089-7658
    Source: AIP Digital Archive
    Topics: Mathematics , Physics
    Notes: The present paper deals with the scattering of waves in two-dimensional space by the random surface of a circular object, which is meant to be a preliminary study for treating three-dimensional scattering by a random sphere. The theory is formulated using a stochastic functional method and a group-theoretic consideration related to the rotation of the circle, in a manner analogous to the authors' previous treatment of the scattering by a planar random surface [Radio Sci. 15, 1049 (1980); J. Math. Phys. 22, 471 (1981); Radio Sci. 16, 831, 847 (1981); J. Opt. Soc. Am. A 2, 2208 (1985)]. First, the randomly scattered wave for cylindrical wave injection is given in terms of the Wiener–Hermite functional of the random field on the circle, and then the scattered field for plane-wave injection is synthesized by superposing cylindrical waves. The differential cross sections for the coherent and incoherent scattering are obtained, and a statistical version of the optical theorem is shown to hold. Some numerical calculations are made for the Mie scattering by the random circular surface with Dirichlet and Neumann conditions.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1520-6025
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
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  • 10
    ISSN: 1546-1696
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: [Auszug] An unnatural base pair of 2-amino-6-(2-thienyl)purine (denoted by s) and pyridin-2-one (denoted by y) was developed to expand the genetic code. The ribonucleoside triphosphate of y was site-specifically incorporated into RNA, opposite s in a template, by T7 RNA polymerase. This transcription was ...
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