TY - JOUR
T1 - Composition-Morphology Correlation in PTB7-Th/PC 71 BM Blend Films for Organic Solar Cells
AU - Song, Lin
AU - Wang, Weijia
AU - Barabino, Edoardo
AU - Yang, Dan
AU - Körstgens, Volker
AU - Zhang, Peng
AU - Roth, Stephan V.
AU - Müller-Buschbaum, Peter
N1 - Publisher Copyright:
© 2018 American Chemical Society.
PY - 2019/1/23
Y1 - 2019/1/23
N2 - From a morphological perspective, the understanding of the influence of the [6,6]-phenyl C 71 -butyric acid methyl ester (PC 71 BM) content on the morphology of the active layer is not complete in organic solar cells (OSCs) with bulk heterojunction (BHJ) configuration based on the low-bandgap polymer poly[4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b;4,5-b′]dithiophene-2,6-diyl-alt-(4-(2-ethylhexyl)-3-fluorothieno[3,4-b]thiophene-)-2-carboxylate-2-6-diyl] (PTB7-Th). In this work, we obtain the highest power conversion efficiency (PCE) of 10.5% for BHJ organic solar cells (OSCs) with a PTB7-Th/PC 71 BM weight ratio of 1:1.5. To understand the differences in PCEs caused by the PC 71 BM content, we investigate the morphology of PTB7-Th/PC 71 BM blend films in detail by determining the domain sizes, the polymer crystal structure, optical properties, and vertical composition as a function of the PC 71 BM concentration. The surface morphology is examined with atomic force microscopy, and the inner film morphology is probed with grazing incidence small-angle X-ray scattering. The PTB7-Th crystal structure is characterized with grazing incidence wide-angle X-ray scattering and UV/vis spectroscopy. X-ray reflectivity is employed to yield information about the film vertical composition. The results show that in PTB7-Th/PC 71 BM blend films, the increase of PC 71 BM content leads to an enhanced microphase separation and a decreased polymer crystallinity. Moreover, a high PC 71 BM concentration is found to decrease the polymer domain sizes and crystal sizes and to promote polymer conjugation length and formation of fullerene-rich and/or polymer-rich layers. The differences in photovoltaic performance are well explained by these findings.
AB - From a morphological perspective, the understanding of the influence of the [6,6]-phenyl C 71 -butyric acid methyl ester (PC 71 BM) content on the morphology of the active layer is not complete in organic solar cells (OSCs) with bulk heterojunction (BHJ) configuration based on the low-bandgap polymer poly[4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b;4,5-b′]dithiophene-2,6-diyl-alt-(4-(2-ethylhexyl)-3-fluorothieno[3,4-b]thiophene-)-2-carboxylate-2-6-diyl] (PTB7-Th). In this work, we obtain the highest power conversion efficiency (PCE) of 10.5% for BHJ organic solar cells (OSCs) with a PTB7-Th/PC 71 BM weight ratio of 1:1.5. To understand the differences in PCEs caused by the PC 71 BM content, we investigate the morphology of PTB7-Th/PC 71 BM blend films in detail by determining the domain sizes, the polymer crystal structure, optical properties, and vertical composition as a function of the PC 71 BM concentration. The surface morphology is examined with atomic force microscopy, and the inner film morphology is probed with grazing incidence small-angle X-ray scattering. The PTB7-Th crystal structure is characterized with grazing incidence wide-angle X-ray scattering and UV/vis spectroscopy. X-ray reflectivity is employed to yield information about the film vertical composition. The results show that in PTB7-Th/PC 71 BM blend films, the increase of PC 71 BM content leads to an enhanced microphase separation and a decreased polymer crystallinity. Moreover, a high PC 71 BM concentration is found to decrease the polymer domain sizes and crystal sizes and to promote polymer conjugation length and formation of fullerene-rich and/or polymer-rich layers. The differences in photovoltaic performance are well explained by these findings.
KW - PTB7-Th/PC BM
KW - blend ratio
KW - morphology
KW - organic photovoltaics
KW - polymer crystallization
UR - http://www.scopus.com/inward/record.url?scp=85060478929&partnerID=8YFLogxK
U2 - 10.1021/acsami.8b20316
DO - 10.1021/acsami.8b20316
M3 - Article
C2 - 30592400
AN - SCOPUS:85060478929
SN - 1944-8244
VL - 11
SP - 3125
EP - 3135
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 3
ER -