Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Charge photogeneration and Recombination in Ternary Organic Photovoltaic Blend PCDTBT/PC60BM/ICBA Studied by EPR Spectroscopy. / Kulik, Leonid V.; Uvarov, Mikhail N.
в: Applied Magnetic Resonance, Том 51, № 9-10, 01.10.2020, стр. 1071-1078.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Charge photogeneration and Recombination in Ternary Organic Photovoltaic Blend PCDTBT/PC60BM/ICBA Studied by EPR Spectroscopy
AU - Kulik, Leonid V.
AU - Uvarov, Mikhail N.
PY - 2020/10/1
Y1 - 2020/10/1
N2 - Using the stationary and pulsed EPR methods, the ternary composite PCDTBT and two fullerene acceptors PCDTBT/PC60BM/ICBA 1:1:1, as well as the corresponding binary composites PCDTBT/PC60BM 1:2 and PCDTBT/ICBA 1:2, were studied at a temperature of 80 K. Modeling these spectra allows us to estimate the contributions of PC60BM and ICBA to the light-induced EPR signal of the PCDTBT/PC60BM/ICBA ternary composite as 0.7:0.3. The absence of new lines in the EPR spectrum of the ternary composite, in comparison with the corresponding binary ones, means that the mechanism of the molecular alloy of PC60BM and ICBA, as previously assumed, is not operative in this system, and the most probable scenario is the existence of two parallel heterojunctions PCDTBT/PC60BM and PCDTBT/ICBA. This conclusion is confirmed by modeling the decay curves of the light-induced EPR upon turning off the light, as well as the out-of-phase electron spin echo from the charge transfer state (the main intermediate of the photoelectric conversion) in these composites. It is noteworthy that in the ternary composite with the same fullerene acceptors, but with a different polymer donor (P3HT), the molecular alloy mechanism of two acceptors is realized (Angmo et al. in J Mater Chem C 3: 5541–5548, 2015). It is likely that the polymer donor has a decisive influence on the morphology and electron-transport properties of such ternary composites. It should be noted that the methods of light-induced EPR and out-of-phase ESE were used for the first time to study ternary donor–acceptor composites.
AB - Using the stationary and pulsed EPR methods, the ternary composite PCDTBT and two fullerene acceptors PCDTBT/PC60BM/ICBA 1:1:1, as well as the corresponding binary composites PCDTBT/PC60BM 1:2 and PCDTBT/ICBA 1:2, were studied at a temperature of 80 K. Modeling these spectra allows us to estimate the contributions of PC60BM and ICBA to the light-induced EPR signal of the PCDTBT/PC60BM/ICBA ternary composite as 0.7:0.3. The absence of new lines in the EPR spectrum of the ternary composite, in comparison with the corresponding binary ones, means that the mechanism of the molecular alloy of PC60BM and ICBA, as previously assumed, is not operative in this system, and the most probable scenario is the existence of two parallel heterojunctions PCDTBT/PC60BM and PCDTBT/ICBA. This conclusion is confirmed by modeling the decay curves of the light-induced EPR upon turning off the light, as well as the out-of-phase electron spin echo from the charge transfer state (the main intermediate of the photoelectric conversion) in these composites. It is noteworthy that in the ternary composite with the same fullerene acceptors, but with a different polymer donor (P3HT), the molecular alloy mechanism of two acceptors is realized (Angmo et al. in J Mater Chem C 3: 5541–5548, 2015). It is likely that the polymer donor has a decisive influence on the morphology and electron-transport properties of such ternary composites. It should be noted that the methods of light-induced EPR and out-of-phase ESE were used for the first time to study ternary donor–acceptor composites.
KW - ELECTRON-SPIN ECHO
KW - TRANSFER STATE
KW - P3HT/PC70BM COMPOSITE
KW - SEPARATION
KW - DYNAMICS
KW - CARRIERS
KW - PAIRS
UR - http://www.scopus.com/inward/record.url?scp=85090126857&partnerID=8YFLogxK
U2 - 10.1007/s00723-020-01258-2
DO - 10.1007/s00723-020-01258-2
M3 - Article
AN - SCOPUS:85090126857
VL - 51
SP - 1071
EP - 1078
JO - Applied Magnetic Resonance
JF - Applied Magnetic Resonance
SN - 0937-9347
IS - 9-10
ER -
ID: 25298426