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  • 1
    Call number: 21/SR 93.0335(88,II)
    In: KTB-Report
    Type of Medium: Series available for loan
    Pages: 518 S.
    Series Statement: KTB-Report 88,II
    Location: Reading room
    Branch Library: GFZ Library
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  • 2
    Call number: 21/SR 93.0335(91,4)
    In: KTB-Report
    Type of Medium: Monograph available for loan
    Pages: VI, 213 S.
    ISBN: 3928559036
    Series Statement: KTB-Report 91,4
    Location: Reading room
    Branch Library: GFZ Library
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  • 3
    Call number: 21/SR 93.0335(90,5)
    In: KTB-Report
    Type of Medium: Series available for loan
    Pages: 547 S.
    Series Statement: KTB-Report 90,5
    Location: Reading room
    Branch Library: GFZ Library
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  • 4
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 88 (2000), S. 537-543 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Cationic silicon clusters, containing up to ten silicon atoms, have been measured by mass spectrometry in an argon/hydrogen/silane expanding thermal plasma. A quasi-one-dimensional model, based on the idea that the clustering process initiated by argon or hydrogen ions depends on the path length of the plasma in the deposition chamber and on silane density, is presented. The chemistry is described by ion–molecule reactions between the formed clusters and silane and by dissociative recombination. The model is able to reproduce fairly well the experimental data for various plasma conditions. It is shown that reaction rates for the clustering process do not strongly depend on the number of silicon atoms in the cluster. This result is in contrast with rates published in the previous literature. For the conditions investigated, the consumption of silane by cationic cluster formation is not significant. The contribution of neutral clusters is investigated and recombination proves to be an important process. © 2000 American Institute of Physics.
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  • 5
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 89 (2001), S. 2404-2413 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The properties of hydrogenated amorphous silicon (a-Si:H) deposited at very high growth rates (6–80 nm/s) by means of a remote Ar–H2–SiH4 plasma have been investigated as a function of the H2 flow in the Ar–H2 operated plasma source. Both the structural and optoelectronic properties of the films improve with increasing H2 flow, and a-Si:H suitable for the application in solar cells has been obtained at deposition rates of 10 nm/s for high H2 flows and a substrate temperature of 400 °C. The "optimized" material has a hole drift mobility which is about a factor of 10 higher than for standard a-Si:H. The electron drift mobility, however, is slightly lower than for standard a-Si:H. Furthermore, preliminary results on solar cells with intrinsic a-Si:H deposited at 7 nm/s are presented. Relating the film properties to the SiH4 dissociation reactions reveals that optimum film quality is obtained for conditions where H from the plasma source governs SiH4 dissociation and where SiH3 contributes dominantly to film growth. Conditions where ion-induced dissociation reactions of SiH4 prevail and where the contribution of SiH3 to film growth is much smaller lead to inferior film properties. A large contribution of very reactive (poly)silane radicals is suggested as the reason for this inferior film quality. Furthermore, a comparison with film properties and process conditions of other a-Si:H deposition techniques is presented. © 2001 American Institute of Physics.
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  • 6
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 87 (2000), S. 3313-3320 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The surface reaction probability β in a remote Ar–H2–SiH4 plasma used for high growth rate deposition of hydrogenated amorphous silicon (a-Si:H) has been investigated by a technique proposed by D. A. Doughty et al. [J. Appl. Phys. 67, 6220 (1990)]. Reactive species from the plasma are trapped in a well, created by two substrates with a small slit in the upper substrate. The distribution of amount of film deposited on both substrates yields information on the compound value of the surface reaction probability, which depends on the species entering the well. The surface reaction probability decreases from a value within the range of 0.45–0.50 in a highly dissociated plasma to 0.33±0.05 in a plasma with ∼12% SiH4 depletion. This corresponds to a shift from a plasma with a significant production of silane radicals with a high (surface) reactivity (SiHx,x〈3) to a plasma where SiH3 is dominant. This has also been corroborated by Monte Carlo simulations. The decrease in surface reaction probability is in line with an improving a-Si:H film quality. Furthermore, the influence of the substrate temperature has been investigated. © 2000 American Institute of Physics.
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  • 7
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 86 (1999), S. 4029-4039 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The formation of cationic silicon clusters SinHm+ by means of ion–molecule reactions in a remote Ar–H2–SiH4 plasma is studied by a combination of ion mass spectrometry and Langmuir probe measurements. The plasma, used for high growth rate deposition of hydrogenated amorphous silicon (a-Si:H), is based on SiH4 dissociation in a downstream region by a thermal plasma source created Ar–H2 plasma. The electron temperature, ion fluence, and most abundant ion emanating from this plasma source are studied as a function of H2 admixture in the source. The electron temperature obtained is in the range of 0.1–0.3 eV and is too low for electron induced ionization. The formation of silicon containing ions is therefore determined by charge transfer reactions between ions emanating from the plasma source and SiH4. While the ion fluence from the source decreases by about a factor of 40 when a considerable flow of H2 is admixed in the source, the flux of cationic silicon clusters towards the substrate depends only slightly on this H2 flow. This implies a strong dissociative recombination of silicon containing ions with electrons in the downstream region for low H2 flows and it causes the distribution of the cationic silicon clusters with respect to the silicon atoms present in the clusters to be rather independent of H2 admixture. The average cluster size increases, however, strongly with the SiH4 flow for constant plasma source properties. Moreover, it leads to a decrease of the ion beam radius and due to this, to an increase of the ion flux towards the substrate, which is positioned in the center of the beam. Assuming unity sticking probability the contribution of the cationic clusters to the total growth flux of the material is about 6% for the condition in which solar grade a-Si:H is deposited. Although the energy flux towards the film by ion bombardment is limited due to the low electron temperature, the clusters have a very compact structure and very low hydrogen content and can consequently have a considerable impact on film quality. The latter is discussed as well as possible implications for other (remote) SiH4 plasmas. © 1999 American Institute of Physics.
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Geophysical prospecting 33 (1985), S. 0 
    ISSN: 1365-2478
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Physics
    Notes: In the course of investigations concerning disposal of radioactive waste, DC-geoelectric soundings were performed in the salt mine Asse in 1982. The survey resulted in the determination of resistivities of various salt formations. A comparison of various resistivities obtained in salt formations in the mine shows that it is possible to estimate the content of free water in salt using Archie's equation.The significant result of this survey is that salt formations in the mine can be divided into two categories according to their resistivities:1. Salt with resistivity between 107 and 108Ωm (particularly Na2Sp and Na3β). The particularly pure halitic formations are to be found within this resistivity range.2. Salt with resistivity between 103 and 105Ωm (Na2Tl, K2, transition salt). The salt formations with thin layers of anhydrite and a high content of hygroscopic salts are classified in the paper.
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  • 9
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 72 (1998), S. 2397-2399 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Cationic silicon clusters SinHm+ with up to ten silicon atoms have been detected mass spectrometrically in an expanding argon–hydrogen–silane plasma used for fast deposition of amorphous hydrogenated silicon. A reaction pathway is proposed in which initial silane ions are produced by dissociative charge exchange between argon and hydrogen ions emanating from the plasma source and the admixed silane followed by chain reactions of the created ions with silane. The silicon clusters are hydrogen poor, which is ascribed to the high gas temperature as the initial argon–hydrogen plasma is thermal in origin. © 1998 American Institute of Physics.
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  • 10
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 84 (1998), S. 2426-2435 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The plasma chemistry of an argon/hydrogen expanding thermal arc plasma in interaction with silane injected downstream is analyzed using mass spectrometry. The dissociation mechanism and the consumption of silane are related to the ion and atomic hydrogen fluence emanating from the arc source. It is argued that as a function of hydrogen admixture in the arc, which has a profound decreasing effect on the ion-electron fluence emanating from the arc source, the dissociation mechanism of silane shifts from ion-electron induced dissociation towards atomic hydrogen induced dissociation. The latter case, the hydrogen abstraction of silane, leads to a dominance of the silyl (SiH3) radical whereas the ion-electron induced dissociation mechanism leads to SiHx (x〈3) radicals. In the pure argon case, the consumption of silane is high and approximately two silane molecules are consumed per argon ion-electron pair. It is shown that this is caused by consecutive reactions of radicals SiHx(x〈3) with silane. Almost independent of the plasma conditions used, approximately one H2 is produced per consumedSiH4 molecule. Disilane production is observed which roughly scales with the remaining silane density. Possible production mechanisms for both observations are discussed. © 1998 American Institute of Physics.
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