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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 93 (1989), S. 899-904 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    European journal of soil science 54 (2003), S. 0 
    ISSN: 1365-2389
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Clay–Al hydroxide polymers (CAlHO) can bind heavy metals effectively and may play an important role in the adsorption behaviour and metal binding capacity of soils. We studied the dependence of Al loading and pH on the adsorption of Zn on Na-saturated montmorillonite–Al hydroxide polymer systems. The available binding sites on Al hydroxide polymers (AlHO) had a very strong affinity for Zn ions. Zinc binding on the clay surface became important when the binding sites on the AlHO were nearly all occupied. The pH had a very strong effect on the Zn binding. At pH 6.6 much more Zn could be adsorbed to the AlHO than at pH 5.0. The effect of the Al:clay ratio on Zn binding was influenced by pH. At pH 6.6, Zn binding to the AlHO, expressed per mole AlHO, was independent of the Al:clay ratio, whereas at pH 5.0 this relation was dependent. This is related to the constant charge of the AlHO at pH 6.6, whereas at pH 5.0 the charge decreases with increasing Al:clay ratio. If clay–Al hydroxide polymers are present in the soil their Zn binding to the AlHO will strongly influence the availability of the Zn.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    European journal of soil science 48 (1997), S. 0 
    ISSN: 1365-2389
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Citrate forms strong complexes with A1 ions and may thus influence the stability and formation of Clay-A1 hydroxide polymer systems (CAIHO). We studied the adsorption of citrate to CAIHO and the influence of citrate on the stability and formation of CAIHO at different A1:clay and A1:citrate ratios and pH values and at a total salt concentration of 0·01 M monovalent anions. The amount of citrate sorbed to the aged CAIHO was independent of the A1 fixed to the clay as A1 hydroxide polymers (AIHO) at 5 〈 pH 〈 6·6. The added citrate seemed not to sorb to the AIHO but only to the edges of the clay. As the citrate: Al ratio increased from 15–1:l at pH 6, more of the AIHO of the aged CAMO systems dissolved. The change in the CEC of the clay indicated that the nature of the remaining AIHO is independent of the amount of A1 dissolved. Citrate influenced the formation of CAIHO systems as measured at pH 6·6, to an extent which depended on the citrate: Al ratio. At a small ratio (1:5), AIHO formed and all citrate was incorporated in the AIHO, probably leading to a coprecipitate. The amount of citrate incorporated depended linearly on the amount of AIHO present. Co-precipitation of AIHO and citrate probably led to the formation of a separate phase, which was only weakly bound to the clay particles. At a large citrate: Al ratio (1:1) soluble Al-citrate complexes became dominant, and only a small part of the added A1 was present as AIHO.
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 30 (1991), S. 1709-1714 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 79 (1996), S. 393-402 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: PbZrxTi1−xO3 films have been grown heteroepitaxially onto (001)SrTiO3 and SrRuO3/(001)SrTiO3 by organometallic chemical vapor deposition. As a start, the microstructure of PbZrxTi1−xO3 films on (001)SrTiO3 was studied as a function of the zirconium fraction, x. Rutherford backscattering spectrometry, including channeling experiments, and transmission electron microscopy have shown that the microstructure is dominated by the crystal structure of the PbZrxTi1−xO3. In the case of tetragonal PbZrxTi1−xO3 the films may contain a-axis oriented regions. These regions have not been observed for films with a composition giving a rhombohedral unit cell. Despite the rather large mismatch of rhombohedral PbZrxTi1−xO3 with the (001)SrTiO3, values as low as 4% for the minimum channeling yield have been obtained. For a rhombohedral film the ferroelectric properties have been measured. To this end a single crystalline PbZr0.8Ti0.2O3 film was grown onto (001)SrTiO3 provided with a heteroepitaxial SrRuO3 electrode grown by pulsed-laser deposition. A heteroepitaxial top electrode was grown onto the PbZrxTi1−xO3 using the same technique. The channeling minimum yield of the heteroepitaxial stack was 11%. The hysteresis loop saturates already at 1 V. Endurance up to 1012 cycles was observed without severe degradation of the ferroelectric properties. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 52 (1988), S. 98-100 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A pseudorandom cross-correlation technique has been used to study the thermal etching of aluminum with molecular chlorine. Time-of-flight (TOF) distributions of particles desorbing from the substrate are measured by modulating the ejected product beam. Modulation is achieved by a rotating chopping disk with slots in a pseudorandom sequence on its periphery. TOF distributions and temperature-dependent reaction product yields are measured for the products desorbing from the chlorinated aluminum substrate in the temperature range from 300 to 900 K. A reaction mechanism will be discussed in some detail.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 102 (1995), S. 2628-2635 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present near steady-state photoinduced absorption (PIA) spectroscopy and steady-state light-induced electron spin resonance (LESR) studies on photoinduced electron transfer reactions in composite films of well defined α-oligothiophenes (Tn, n=6, 7, 9, and 11) as electron donor with buckminsterfullerene (C60) and a methanofullerene derivative (1-(3-cholestanoxycarbonyl)- propyl-1-phenyl-[6.6]C61) as electron acceptors. Dispersion on a molecular level of these fullerenes in oligothiophene films causes quenching of both the photoluminescence and intersystem crossing after photoexcitation across the π–π* energy gap as a result of a fast electron transfer reaction. The PIA spectra exhibit bands due to T+•n radical cations, fullerene radical anions and electroabsorption oscillations of the π–π* band edge resulting from strong local electric fields set up by the photoinduced charges. LESR spectra give additional unambiguous evidence of the photoinduced electron transfer reaction. Using PIA and LESR, we do not observe an effect of the conjugation length of the photoinduced electron transfer reaction or on the metastability of the charge-separated state. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 1787-1798 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present studies of steady-state photoinduced absorption (PIA) spectroscopy on photoexcitations in a series of well-defined α-oligothiophene (Tn, n=6, 7, 9, and 11) films and solutions. The PIA spectra and the excited state lifetimes are consistent with the signatures of a photoexcited triplet state. The PIA spectra consist of a strong vibronically resolved subgap absorption, which is readily observed in solid-state films and in solutions at ambient and cryogenic temperatures. The transition energy is linearly dependent on the reciprocal chain length and shifts to lower energy for longer oligomers. Variation of the modulation frequency and the pump intensity under matrix-isolated conditions reveals that the photoexcitation is created via an intrachain mechanism and decays nonradiatively with monomolecular kinetics. In solid films we find a significant contribution of a bimolecular decay process to the relaxation rate.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 100 (1994), S. 8641-8645 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present spectral evidence of the efficient photogeneration of triplet-state excitations in poly(3-alkylthiophene), P3AT, solutions. The steady-state photoinduced absorption spectra display a PIA band centered at 1.50 eV which is attributed to a dipole-allowed triplet–triplet transition. Photoexcitation of P3AT solutions containing C60, results in an efficient energy transfer reaction and provides an estimate for the P3AT triplet-state energy of 1.57–1.72 eV.
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 9519-9527 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present near-steady-state photoinduced absorption (PIA) studies on photoexcited states of a series of oligothiophenes (nT, n=6,7,9,11) in solution. Photoexcitation in solution reveals efficient formation of a metastable triplet state (3nT). In addition, oligothiophene radical cations (nT+.) are formed from the singlet excited state via electron transfer to the medium in solvents of high electron affinity. The reactivity of the 3nT state towards acceptor molecules is investigated. In the presence of C60 an energy transfer reaction is observed which quenches the 3nT state and produces 3C60 via photosensitization. Addition of tetracyanoethylene (TCNE) results in quenching of the 3nT state via electron transfer and efficiently produces the corresponding nT+. radical cations, as evidenced from PIA and light-induced electron spin resonance (ESR). © 1994 American Institute of Physics.
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