TY - JOUR
T1 - Film Formation Kinetics of Polymer Donor and Nonfullerene Acceptor Active Layers During Printing Out of 1,2,4-Trimethylbenzene in Ambient Conditions
AU - Jiang, Xinyu
AU - Grott, Sebastian
AU - Körstgens, Volker
AU - Wienhold, Kerstin S.
AU - Li, Zerui
AU - Zhang, Jinsheng
AU - Everett, Christopher R.
AU - Schwartzkopf, Matthias
AU - Roth, Stephan V.
AU - Müller-Buschbaum, Peter
N1 - Publisher Copyright:
© 2023 The Authors. Solar RRL published by Wiley-VCH GmbH.
PY - 2023/3
Y1 - 2023/3
N2 - Slot-die coating is a promising upscaling fabrication method to promote commercialization in the field of organic solar cells. Herein, the nonfullerene active layer blend of a conjugated polymer PffBT4T-2OD and a small molecule acceptor EH-IDTBR, which is printed out of the nonhalogenated solvent 1,2,4-trimethylbenzene, is studied. The film formation kinetics of the active layer PffBT4T-2OD:EH-IDTBR is probed in terms of the temporal evolutions in morphology as well as molecular conformation and aggregation as revealed by in situ grazing-incidence small angle X-ray scattering and UV–vis spectroscopy during the film printing process. A five-regime mesoscale domain growth process is observed in the active layer from the liquid state to the final dry state. The solvent evaporation-induced domain growth is accompanied with molecular stacking in a distinct J-type aggregation of the acceptor and a slight H-type aggregation of the donor molecules. The printed active layers exhibit an edge-on dominated PffBT4T-2OD and a face-on dominated EH-IDTBR crystallite structure. Compared to the neat PffBT4T-2OD and EH-IDTBR films, in the active layer, the crystallite structure deviates slightly in lattice spacing.
AB - Slot-die coating is a promising upscaling fabrication method to promote commercialization in the field of organic solar cells. Herein, the nonfullerene active layer blend of a conjugated polymer PffBT4T-2OD and a small molecule acceptor EH-IDTBR, which is printed out of the nonhalogenated solvent 1,2,4-trimethylbenzene, is studied. The film formation kinetics of the active layer PffBT4T-2OD:EH-IDTBR is probed in terms of the temporal evolutions in morphology as well as molecular conformation and aggregation as revealed by in situ grazing-incidence small angle X-ray scattering and UV–vis spectroscopy during the film printing process. A five-regime mesoscale domain growth process is observed in the active layer from the liquid state to the final dry state. The solvent evaporation-induced domain growth is accompanied with molecular stacking in a distinct J-type aggregation of the acceptor and a slight H-type aggregation of the donor molecules. The printed active layers exhibit an edge-on dominated PffBT4T-2OD and a face-on dominated EH-IDTBR crystallite structure. Compared to the neat PffBT4T-2OD and EH-IDTBR films, in the active layer, the crystallite structure deviates slightly in lattice spacing.
KW - in situ GISAXS
KW - in situ UV–vis
KW - nonfullerene acceptors
KW - printing
KW - slot-die coating
UR - http://www.scopus.com/inward/record.url?scp=85146730645&partnerID=8YFLogxK
U2 - 10.1002/solr.202201077
DO - 10.1002/solr.202201077
M3 - Article
AN - SCOPUS:85146730645
SN - 2367-198X
VL - 7
JO - Solar RRL
JF - Solar RRL
IS - 6
M1 - 2201077
ER -