Ultrafast Energy And Electron Transfer In Conjugated Oligomer-Fullerene Molecules
Abstract The intramolecular photoinduced energy and electron transfer within a fullereneoligothiophene-fullerene triad with nine thiophene units ($ C_{60} $-9T-$ C_{60} $) and an oligo( p-phenylene vinylene)-fullerene dyad with four phenyl groups (OPV4-$ C_{60} $) is investigated with femtosecond pu...
Ausführliche Beschreibung
Autor*in: |
van Hal, P. A. [verfasserIn] Janssen, R. A. J. [verfasserIn] Lanzani, G. [verfasserIn] Cerullo, G. [verfasserIn] Zavelani-Rossi, M. [verfasserIn] De Silvestri, S. [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2000 |
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Übergeordnetes Werk: |
Enthalten in: MRS online proceedings library - Warrendale, Pa. : MRS, 1998, 665(2000), 1 vom: Dez. |
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Übergeordnetes Werk: |
volume:665 ; year:2000 ; number:1 ; month:12 |
Links: |
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DOI / URN: |
10.1557/PROC-665-C7.3 |
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520 | |a Abstract The intramolecular photoinduced energy and electron transfer within a fullereneoligothiophene-fullerene triad with nine thiophene units ($ C_{60} $-9T-$ C_{60} $) and an oligo( p-phenylene vinylene)-fullerene dyad with four phenyl groups (OPV4-$ C_{60} $) is investigated with femtosecond pump-probe spectroscopy with sub-10 fs and 200 fs time resolution in solvents of different polarity. Photoexcitation of the π-conjugated oligomer moiety in the triad and dyad results in an ultrafast singlet-energy transfer reaction to create the fullerene singlet-excited state with a time constant of 150-190 fs, irrespective of the polarity of the medium. In a polar solvent, intramolecular electron transfer occurs from the oligomer moiety to the $ C_{60} $ moiety with a time constant of 10-13 ps as a secondary reaction, subsequent to the ultrafast singlet-energy transfer. The charge-separated state has a lifetime of 50-80 ps and recombines to the ground state. | ||
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10.1557/PROC-665-C7.3 doi (DE-627)SPR042790794 (DE-599)SPRPROC-665-C7.3-e (SPR)PROC-665-C7.3-e DE-627 ger DE-627 rakwb eng 670 ASE van Hal, P. A. verfasserin aut Ultrafast Energy And Electron Transfer In Conjugated Oligomer-Fullerene Molecules 2000 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The intramolecular photoinduced energy and electron transfer within a fullereneoligothiophene-fullerene triad with nine thiophene units ($ C_{60} $-9T-$ C_{60} $) and an oligo( p-phenylene vinylene)-fullerene dyad with four phenyl groups (OPV4-$ C_{60} $) is investigated with femtosecond pump-probe spectroscopy with sub-10 fs and 200 fs time resolution in solvents of different polarity. Photoexcitation of the π-conjugated oligomer moiety in the triad and dyad results in an ultrafast singlet-energy transfer reaction to create the fullerene singlet-excited state with a time constant of 150-190 fs, irrespective of the polarity of the medium. In a polar solvent, intramolecular electron transfer occurs from the oligomer moiety to the $ C_{60} $ moiety with a time constant of 10-13 ps as a secondary reaction, subsequent to the ultrafast singlet-energy transfer. The charge-separated state has a lifetime of 50-80 ps and recombines to the ground state. Janssen, R. A. J. verfasserin aut Lanzani, G. verfasserin aut Cerullo, G. verfasserin aut Zavelani-Rossi, M. verfasserin aut De Silvestri, S. verfasserin aut Enthalten in MRS online proceedings library Warrendale, Pa. : MRS, 1998 665(2000), 1 vom: Dez. (DE-627)57782046X (DE-600)2451008-7 1946-4274 nnns volume:665 year:2000 number:1 month:12 https://dx.doi.org/10.1557/PROC-665-C7.3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_2005 AR 665 2000 1 12 |
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10.1557/PROC-665-C7.3 doi (DE-627)SPR042790794 (DE-599)SPRPROC-665-C7.3-e (SPR)PROC-665-C7.3-e DE-627 ger DE-627 rakwb eng 670 ASE van Hal, P. A. verfasserin aut Ultrafast Energy And Electron Transfer In Conjugated Oligomer-Fullerene Molecules 2000 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The intramolecular photoinduced energy and electron transfer within a fullereneoligothiophene-fullerene triad with nine thiophene units ($ C_{60} $-9T-$ C_{60} $) and an oligo( p-phenylene vinylene)-fullerene dyad with four phenyl groups (OPV4-$ C_{60} $) is investigated with femtosecond pump-probe spectroscopy with sub-10 fs and 200 fs time resolution in solvents of different polarity. Photoexcitation of the π-conjugated oligomer moiety in the triad and dyad results in an ultrafast singlet-energy transfer reaction to create the fullerene singlet-excited state with a time constant of 150-190 fs, irrespective of the polarity of the medium. In a polar solvent, intramolecular electron transfer occurs from the oligomer moiety to the $ C_{60} $ moiety with a time constant of 10-13 ps as a secondary reaction, subsequent to the ultrafast singlet-energy transfer. The charge-separated state has a lifetime of 50-80 ps and recombines to the ground state. Janssen, R. A. J. verfasserin aut Lanzani, G. verfasserin aut Cerullo, G. verfasserin aut Zavelani-Rossi, M. verfasserin aut De Silvestri, S. verfasserin aut Enthalten in MRS online proceedings library Warrendale, Pa. : MRS, 1998 665(2000), 1 vom: Dez. (DE-627)57782046X (DE-600)2451008-7 1946-4274 nnns volume:665 year:2000 number:1 month:12 https://dx.doi.org/10.1557/PROC-665-C7.3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_2005 AR 665 2000 1 12 |
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10.1557/PROC-665-C7.3 doi (DE-627)SPR042790794 (DE-599)SPRPROC-665-C7.3-e (SPR)PROC-665-C7.3-e DE-627 ger DE-627 rakwb eng 670 ASE van Hal, P. A. verfasserin aut Ultrafast Energy And Electron Transfer In Conjugated Oligomer-Fullerene Molecules 2000 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The intramolecular photoinduced energy and electron transfer within a fullereneoligothiophene-fullerene triad with nine thiophene units ($ C_{60} $-9T-$ C_{60} $) and an oligo( p-phenylene vinylene)-fullerene dyad with four phenyl groups (OPV4-$ C_{60} $) is investigated with femtosecond pump-probe spectroscopy with sub-10 fs and 200 fs time resolution in solvents of different polarity. Photoexcitation of the π-conjugated oligomer moiety in the triad and dyad results in an ultrafast singlet-energy transfer reaction to create the fullerene singlet-excited state with a time constant of 150-190 fs, irrespective of the polarity of the medium. In a polar solvent, intramolecular electron transfer occurs from the oligomer moiety to the $ C_{60} $ moiety with a time constant of 10-13 ps as a secondary reaction, subsequent to the ultrafast singlet-energy transfer. The charge-separated state has a lifetime of 50-80 ps and recombines to the ground state. Janssen, R. A. J. verfasserin aut Lanzani, G. verfasserin aut Cerullo, G. verfasserin aut Zavelani-Rossi, M. verfasserin aut De Silvestri, S. verfasserin aut Enthalten in MRS online proceedings library Warrendale, Pa. : MRS, 1998 665(2000), 1 vom: Dez. (DE-627)57782046X (DE-600)2451008-7 1946-4274 nnns volume:665 year:2000 number:1 month:12 https://dx.doi.org/10.1557/PROC-665-C7.3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_2005 AR 665 2000 1 12 |
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10.1557/PROC-665-C7.3 doi (DE-627)SPR042790794 (DE-599)SPRPROC-665-C7.3-e (SPR)PROC-665-C7.3-e DE-627 ger DE-627 rakwb eng 670 ASE van Hal, P. A. verfasserin aut Ultrafast Energy And Electron Transfer In Conjugated Oligomer-Fullerene Molecules 2000 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The intramolecular photoinduced energy and electron transfer within a fullereneoligothiophene-fullerene triad with nine thiophene units ($ C_{60} $-9T-$ C_{60} $) and an oligo( p-phenylene vinylene)-fullerene dyad with four phenyl groups (OPV4-$ C_{60} $) is investigated with femtosecond pump-probe spectroscopy with sub-10 fs and 200 fs time resolution in solvents of different polarity. Photoexcitation of the π-conjugated oligomer moiety in the triad and dyad results in an ultrafast singlet-energy transfer reaction to create the fullerene singlet-excited state with a time constant of 150-190 fs, irrespective of the polarity of the medium. In a polar solvent, intramolecular electron transfer occurs from the oligomer moiety to the $ C_{60} $ moiety with a time constant of 10-13 ps as a secondary reaction, subsequent to the ultrafast singlet-energy transfer. The charge-separated state has a lifetime of 50-80 ps and recombines to the ground state. Janssen, R. A. J. verfasserin aut Lanzani, G. verfasserin aut Cerullo, G. verfasserin aut Zavelani-Rossi, M. verfasserin aut De Silvestri, S. verfasserin aut Enthalten in MRS online proceedings library Warrendale, Pa. : MRS, 1998 665(2000), 1 vom: Dez. (DE-627)57782046X (DE-600)2451008-7 1946-4274 nnns volume:665 year:2000 number:1 month:12 https://dx.doi.org/10.1557/PROC-665-C7.3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_2005 AR 665 2000 1 12 |
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10.1557/PROC-665-C7.3 doi (DE-627)SPR042790794 (DE-599)SPRPROC-665-C7.3-e (SPR)PROC-665-C7.3-e DE-627 ger DE-627 rakwb eng 670 ASE van Hal, P. A. verfasserin aut Ultrafast Energy And Electron Transfer In Conjugated Oligomer-Fullerene Molecules 2000 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The intramolecular photoinduced energy and electron transfer within a fullereneoligothiophene-fullerene triad with nine thiophene units ($ C_{60} $-9T-$ C_{60} $) and an oligo( p-phenylene vinylene)-fullerene dyad with four phenyl groups (OPV4-$ C_{60} $) is investigated with femtosecond pump-probe spectroscopy with sub-10 fs and 200 fs time resolution in solvents of different polarity. Photoexcitation of the π-conjugated oligomer moiety in the triad and dyad results in an ultrafast singlet-energy transfer reaction to create the fullerene singlet-excited state with a time constant of 150-190 fs, irrespective of the polarity of the medium. In a polar solvent, intramolecular electron transfer occurs from the oligomer moiety to the $ C_{60} $ moiety with a time constant of 10-13 ps as a secondary reaction, subsequent to the ultrafast singlet-energy transfer. The charge-separated state has a lifetime of 50-80 ps and recombines to the ground state. Janssen, R. A. J. verfasserin aut Lanzani, G. verfasserin aut Cerullo, G. verfasserin aut Zavelani-Rossi, M. verfasserin aut De Silvestri, S. verfasserin aut Enthalten in MRS online proceedings library Warrendale, Pa. : MRS, 1998 665(2000), 1 vom: Dez. (DE-627)57782046X (DE-600)2451008-7 1946-4274 nnns volume:665 year:2000 number:1 month:12 https://dx.doi.org/10.1557/PROC-665-C7.3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_2005 AR 665 2000 1 12 |
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Ultrafast Energy And Electron Transfer In Conjugated Oligomer-Fullerene Molecules |
abstract |
Abstract The intramolecular photoinduced energy and electron transfer within a fullereneoligothiophene-fullerene triad with nine thiophene units ($ C_{60} $-9T-$ C_{60} $) and an oligo( p-phenylene vinylene)-fullerene dyad with four phenyl groups (OPV4-$ C_{60} $) is investigated with femtosecond pump-probe spectroscopy with sub-10 fs and 200 fs time resolution in solvents of different polarity. Photoexcitation of the π-conjugated oligomer moiety in the triad and dyad results in an ultrafast singlet-energy transfer reaction to create the fullerene singlet-excited state with a time constant of 150-190 fs, irrespective of the polarity of the medium. In a polar solvent, intramolecular electron transfer occurs from the oligomer moiety to the $ C_{60} $ moiety with a time constant of 10-13 ps as a secondary reaction, subsequent to the ultrafast singlet-energy transfer. The charge-separated state has a lifetime of 50-80 ps and recombines to the ground state. |
abstractGer |
Abstract The intramolecular photoinduced energy and electron transfer within a fullereneoligothiophene-fullerene triad with nine thiophene units ($ C_{60} $-9T-$ C_{60} $) and an oligo( p-phenylene vinylene)-fullerene dyad with four phenyl groups (OPV4-$ C_{60} $) is investigated with femtosecond pump-probe spectroscopy with sub-10 fs and 200 fs time resolution in solvents of different polarity. Photoexcitation of the π-conjugated oligomer moiety in the triad and dyad results in an ultrafast singlet-energy transfer reaction to create the fullerene singlet-excited state with a time constant of 150-190 fs, irrespective of the polarity of the medium. In a polar solvent, intramolecular electron transfer occurs from the oligomer moiety to the $ C_{60} $ moiety with a time constant of 10-13 ps as a secondary reaction, subsequent to the ultrafast singlet-energy transfer. The charge-separated state has a lifetime of 50-80 ps and recombines to the ground state. |
abstract_unstemmed |
Abstract The intramolecular photoinduced energy and electron transfer within a fullereneoligothiophene-fullerene triad with nine thiophene units ($ C_{60} $-9T-$ C_{60} $) and an oligo( p-phenylene vinylene)-fullerene dyad with four phenyl groups (OPV4-$ C_{60} $) is investigated with femtosecond pump-probe spectroscopy with sub-10 fs and 200 fs time resolution in solvents of different polarity. Photoexcitation of the π-conjugated oligomer moiety in the triad and dyad results in an ultrafast singlet-energy transfer reaction to create the fullerene singlet-excited state with a time constant of 150-190 fs, irrespective of the polarity of the medium. In a polar solvent, intramolecular electron transfer occurs from the oligomer moiety to the $ C_{60} $ moiety with a time constant of 10-13 ps as a secondary reaction, subsequent to the ultrafast singlet-energy transfer. The charge-separated state has a lifetime of 50-80 ps and recombines to the ground state. |
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Janssen, R. A. J. Lanzani, G. Cerullo, G. Zavelani-Rossi, M. De Silvestri, S. |
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Janssen, R. A. J. Lanzani, G. Cerullo, G. Zavelani-Rossi, M. De Silvestri, S. |
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10.1557/PROC-665-C7.3 |
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2024-07-03T14:50:57.487Z |
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