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Light-Induced processes in porphyrin-fullerene systems. / Konev, Alexander S.

Springer Series in Chemical Physics. Springer Nature, 2019. p. 437-451 (Springer Series in Chemical Physics; Vol. 119).

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Harvard

Konev, AS 2019, Light-Induced processes in porphyrin-fullerene systems. in Springer Series in Chemical Physics. Springer Series in Chemical Physics, vol. 119, Springer Nature, pp. 437-451. https://doi.org/10.1007/978-3-030-05974-3_22

APA

Konev, A. S. (2019). Light-Induced processes in porphyrin-fullerene systems. In Springer Series in Chemical Physics (pp. 437-451). (Springer Series in Chemical Physics; Vol. 119). Springer Nature. https://doi.org/10.1007/978-3-030-05974-3_22

Vancouver

Konev AS. Light-Induced processes in porphyrin-fullerene systems. In Springer Series in Chemical Physics. Springer Nature. 2019. p. 437-451. (Springer Series in Chemical Physics). https://doi.org/10.1007/978-3-030-05974-3_22

Author

Konev, Alexander S. / Light-Induced processes in porphyrin-fullerene systems. Springer Series in Chemical Physics. Springer Nature, 2019. pp. 437-451 (Springer Series in Chemical Physics).

BibTeX

@inbook{bd9cdfd3bdf44057bce1696f8008da93,
title = "Light-Induced processes in porphyrin-fullerene systems",
abstract = "Porphyrin-fullerene dyads are representative class of donor-acceptor molecular systems capable of undergoing photoinduced charge separation, the phenomenon that is the key process in solar energy conversion systems either in organic solar cells or photoredox catalysis. The charge-separated state generated in covalently linked dyad is a highly polarized electronically excited state. Formation of this state typically proceeds as a result of the relaxation of a locally excited state of higher energy, which is populated upon the initial excitation of the dyad. The review of computational and spectroscopic studies of the excited states in porphyrin-fullerene covalently linked dyads is given in the present chapter.",
author = "Konev, {Alexander S.}",
year = "2019",
month = jan,
day = "1",
doi = "10.1007/978-3-030-05974-3_22",
language = "English",
series = "Springer Series in Chemical Physics",
publisher = "Springer Nature",
pages = "437--451",
booktitle = "Springer Series in Chemical Physics",
address = "Germany",

}

RIS

TY - CHAP

T1 - Light-Induced processes in porphyrin-fullerene systems

AU - Konev, Alexander S.

PY - 2019/1/1

Y1 - 2019/1/1

N2 - Porphyrin-fullerene dyads are representative class of donor-acceptor molecular systems capable of undergoing photoinduced charge separation, the phenomenon that is the key process in solar energy conversion systems either in organic solar cells or photoredox catalysis. The charge-separated state generated in covalently linked dyad is a highly polarized electronically excited state. Formation of this state typically proceeds as a result of the relaxation of a locally excited state of higher energy, which is populated upon the initial excitation of the dyad. The review of computational and spectroscopic studies of the excited states in porphyrin-fullerene covalently linked dyads is given in the present chapter.

AB - Porphyrin-fullerene dyads are representative class of donor-acceptor molecular systems capable of undergoing photoinduced charge separation, the phenomenon that is the key process in solar energy conversion systems either in organic solar cells or photoredox catalysis. The charge-separated state generated in covalently linked dyad is a highly polarized electronically excited state. Formation of this state typically proceeds as a result of the relaxation of a locally excited state of higher energy, which is populated upon the initial excitation of the dyad. The review of computational and spectroscopic studies of the excited states in porphyrin-fullerene covalently linked dyads is given in the present chapter.

UR - http://www.scopus.com/inward/record.url?scp=85061045118&partnerID=8YFLogxK

UR - http://www.mendeley.com/research/lightinduced-processes-porphyrinfullerene-systems

U2 - 10.1007/978-3-030-05974-3_22

DO - 10.1007/978-3-030-05974-3_22

M3 - Chapter

AN - SCOPUS:85061045118

T3 - Springer Series in Chemical Physics

SP - 437

EP - 451

BT - Springer Series in Chemical Physics

PB - Springer Nature

ER -

ID: 39405109