GLORIA

GEOMAR Library Ocean Research Information Access

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • AIP Publishing  (4)
  • 1
    Online Resource
    Online Resource
    AIP Publishing ; 1991
    In:  The Journal of Chemical Physics Vol. 95, No. 11 ( 1991-12-01), p. 8584-8591
    In: The Journal of Chemical Physics, AIP Publishing, Vol. 95, No. 11 ( 1991-12-01), p. 8584-8591
    Abstract: 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.
    Type of Medium: Online Resource
    ISSN: 0021-9606 , 1089-7690
    Language: English
    Publisher: AIP Publishing
    Publication Date: 1991
    detail.hit.zdb_id: 3113-6
    detail.hit.zdb_id: 1473050-9
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    Online Resource
    Online Resource
    AIP Publishing ; 1991
    In:  Journal of Applied Physics Vol. 69, No. 8 ( 1991-04-15), p. 4445-4447
    In: Journal of Applied Physics, AIP Publishing, Vol. 69, No. 8 ( 1991-04-15), p. 4445-4447
    Abstract: Soluble poly (3-alkylthiophene) can be transformed into a conducting polymer gel by using a radical initiator. The volume of the sample in chloroform shrinks drastically upon introduction of ethanol, and also by doping. The shrinkage ratio depends on the preparation conditions of the sample. The spectrum of the gel also changes reversibly as the volume varies.
    Type of Medium: Online Resource
    ISSN: 0021-8979 , 1089-7550
    Language: English
    Publisher: AIP Publishing
    Publication Date: 1991
    detail.hit.zdb_id: 220641-9
    detail.hit.zdb_id: 3112-4
    detail.hit.zdb_id: 1476463-5
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Online Resource
    Online Resource
    AIP Publishing ; 1993
    In:  Journal of Applied Physics Vol. 74, No. 4 ( 1993-08-15), p. 2860-2865
    In: Journal of Applied Physics, AIP Publishing, Vol. 74, No. 4 ( 1993-08-15), p. 2860-2865
    Abstract: Photoluminescence has been markedly quenched and photoconductivity has been enhanced by more than one order of magnitude upon introduction of several mol% of buckminsterfullerene (C60) to poly(2,5-dialkoxy-p-phenylene vinylene) (RO-PPV), especially at excitations about 2.2 eV, corresponding to the band gap energy of RO-PPV and also in bands at 1.8 and 3.5 eV, which correspond to optical excitation of C60 molecules, suggesting that photo-induced charge transfer occurs between RO-PPV and C60. On the other hand, absorption spectrum and electrical conductivity of RO-PPV have been scarcely influenced by doping of small amount of C60, suggesting that the ground state charge transfer between C60 and RO-PPV is not effective, contrary to the case of poly(3-hexylthiophene). These results are discussed by taking relative electronic energy states of RO-PPV and C60 into consideration. The photo-excited exciton-polaron (Ex-P) in RO-PPV is interpreted to migrate along about 100 monomer units along a polymer main chain in its lifetime and dissociates when encountered with C60. These unique doping characteristics of C60 in RO-PPV are not dependent on the alkyl chain length, contrary to the case of poly(3-alkylthiophene).
    Type of Medium: Online Resource
    ISSN: 0021-8979 , 1089-7550
    Language: English
    Publisher: AIP Publishing
    Publication Date: 1993
    detail.hit.zdb_id: 220641-9
    detail.hit.zdb_id: 3112-4
    detail.hit.zdb_id: 1476463-5
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    Online Resource
    Online Resource
    AIP Publishing ; 1993
    In:  Journal of Applied Physics Vol. 73, No. 6 ( 1993-03-15), p. 2859-2865
    In: Journal of Applied Physics, AIP Publishing, Vol. 73, No. 6 ( 1993-03-15), p. 2859-2865
    Abstract: 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.  
    Type of Medium: Online Resource
    ISSN: 0021-8979 , 1089-7550
    Language: English
    Publisher: AIP Publishing
    Publication Date: 1993
    detail.hit.zdb_id: 220641-9
    detail.hit.zdb_id: 3112-4
    detail.hit.zdb_id: 1476463-5
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...