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Spin-dependent recombination of the charge-transfer state in photovoltaic polymer/fullerene blends. / Lukina, E. A.; Reijerse, E.; Lubitz, W. et al.

In: Molecular Physics, Vol. 117, No. 19, 01.01.2019, p. 2654-2663.

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Lukina EA, Reijerse E, Lubitz W, Kulik LV. Spin-dependent recombination of the charge-transfer state in photovoltaic polymer/fullerene blends. Molecular Physics. 2019 Jan 1;117(19):2654-2663. doi: 10.1080/00268976.2018.1548713

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Lukina, E. A. ; Reijerse, E. ; Lubitz, W. et al. / Spin-dependent recombination of the charge-transfer state in photovoltaic polymer/fullerene blends. In: Molecular Physics. 2019 ; Vol. 117, No. 19. pp. 2654-2663.

BibTeX

@article{b0bd5769289a49cf8c0df2c9d8293ed0,
title = "Spin-dependent recombination of the charge-transfer state in photovoltaic polymer/fullerene blends",
abstract = "Q-band electron spin echo (ESE) spectroscopy was applied for studying the spin-dependent recombination of charge transfer (CT) states in the benchmark organic photovoltaics (OPV) blend of poly(3-hexylthiophene-2,5-diyl) and [6,6]-phenyl C61 butyric acid methyl ester (P3HT/PC60BM). Selective microwave excitation and a special protocol for ESE data treatment allowed to suppress the ESE signal of thermalised polarons and weakly coupled CT states and to address CT states with a relatively short distance between positive and negative polarons (1.5 nm < r < 2.5 nm). Inversion of the in-phase ESE signal with increase of the delay after laser flash was observed for the regioregular P3HT +/PC60BM − CT state at a temperature of 40 K. This effect is very similar to the inversion of the time resolved (TR) EPR spectrum of the same system obtained previously. Both effects can be explained by spin-dependent recombination of the CT state, with the recombination via the triplet channel proceeding much slower than via the singlet channel. For the regiorandom P3HT+/PC60BM − CT state no ESE sign inversion was observed in an analogous experiment. The result suggests the importance of CT state formation via a triplet exciton, a process which was not considered previously for the P3HT/PC60BM blend.",
keywords = "conjugated polymer, electron spin echo, fullerene PC60BM, geminate recombination, Organic photovoltaics, SELECTIVE EXCITATION, ENERGY, PULSED EPR, ECHO, SEPARATED STATE, DOUBLE-QUANTUM COHERENCE, CORRELATED RADICAL PAIRS, P3HT/PC70BM COMPOSITE, DYNAMICS, PHOTOSYNTHESIS",
author = "Lukina, {E. A.} and E. Reijerse and W. Lubitz and Kulik, {L. V.}",
year = "2019",
month = jan,
day = "1",
doi = "10.1080/00268976.2018.1548713",
language = "English",
volume = "117",
pages = "2654--2663",
journal = "Molecular Physics",
issn = "0026-8976",
publisher = "Taylor and Francis Ltd.",
number = "19",

}

RIS

TY - JOUR

T1 - Spin-dependent recombination of the charge-transfer state in photovoltaic polymer/fullerene blends

AU - Lukina, E. A.

AU - Reijerse, E.

AU - Lubitz, W.

AU - Kulik, L. V.

PY - 2019/1/1

Y1 - 2019/1/1

N2 - Q-band electron spin echo (ESE) spectroscopy was applied for studying the spin-dependent recombination of charge transfer (CT) states in the benchmark organic photovoltaics (OPV) blend of poly(3-hexylthiophene-2,5-diyl) and [6,6]-phenyl C61 butyric acid methyl ester (P3HT/PC60BM). Selective microwave excitation and a special protocol for ESE data treatment allowed to suppress the ESE signal of thermalised polarons and weakly coupled CT states and to address CT states with a relatively short distance between positive and negative polarons (1.5 nm < r < 2.5 nm). Inversion of the in-phase ESE signal with increase of the delay after laser flash was observed for the regioregular P3HT +/PC60BM − CT state at a temperature of 40 K. This effect is very similar to the inversion of the time resolved (TR) EPR spectrum of the same system obtained previously. Both effects can be explained by spin-dependent recombination of the CT state, with the recombination via the triplet channel proceeding much slower than via the singlet channel. For the regiorandom P3HT+/PC60BM − CT state no ESE sign inversion was observed in an analogous experiment. The result suggests the importance of CT state formation via a triplet exciton, a process which was not considered previously for the P3HT/PC60BM blend.

AB - Q-band electron spin echo (ESE) spectroscopy was applied for studying the spin-dependent recombination of charge transfer (CT) states in the benchmark organic photovoltaics (OPV) blend of poly(3-hexylthiophene-2,5-diyl) and [6,6]-phenyl C61 butyric acid methyl ester (P3HT/PC60BM). Selective microwave excitation and a special protocol for ESE data treatment allowed to suppress the ESE signal of thermalised polarons and weakly coupled CT states and to address CT states with a relatively short distance between positive and negative polarons (1.5 nm < r < 2.5 nm). Inversion of the in-phase ESE signal with increase of the delay after laser flash was observed for the regioregular P3HT +/PC60BM − CT state at a temperature of 40 K. This effect is very similar to the inversion of the time resolved (TR) EPR spectrum of the same system obtained previously. Both effects can be explained by spin-dependent recombination of the CT state, with the recombination via the triplet channel proceeding much slower than via the singlet channel. For the regiorandom P3HT+/PC60BM − CT state no ESE sign inversion was observed in an analogous experiment. The result suggests the importance of CT state formation via a triplet exciton, a process which was not considered previously for the P3HT/PC60BM blend.

KW - conjugated polymer

KW - electron spin echo

KW - fullerene PC60BM

KW - geminate recombination

KW - Organic photovoltaics

KW - SELECTIVE EXCITATION

KW - ENERGY

KW - PULSED EPR

KW - ECHO

KW - SEPARATED STATE

KW - DOUBLE-QUANTUM COHERENCE

KW - CORRELATED RADICAL PAIRS

KW - P3HT/PC70BM COMPOSITE

KW - DYNAMICS

KW - PHOTOSYNTHESIS

UR - http://www.scopus.com/inward/record.url?scp=85057329673&partnerID=8YFLogxK

U2 - 10.1080/00268976.2018.1548713

DO - 10.1080/00268976.2018.1548713

M3 - Article

AN - SCOPUS:85057329673

VL - 117

SP - 2654

EP - 2663

JO - Molecular Physics

JF - Molecular Physics

SN - 0026-8976

IS - 19

ER -

ID: 17565317