TY - JOUR
T1 - Solvent Tuning of the Active Layer Morphology of Non-Fullerene Based Organic Solar Cells
AU - Grott, Sebastian
AU - Kotobi, Amir
AU - Reb, Lennart K.
AU - Weindl, Christian L.
AU - Guo, Renjun
AU - Yin, Shanshan
AU - Wienhold, Kerstin S.
AU - Chen, Wei
AU - Ameri, Tayebeh
AU - Schwartzkopf, Matthias
AU - Roth, Stephan V.
AU - Müller-Buschbaum, Peter
N1 - Publisher Copyright:
© 2022 The Authors. Solar RRL published by Wiley-VCH GmbH.
PY - 2022/6
Y1 - 2022/6
N2 - Non-fullerene acceptor (NFA)-based organic solar cells have made tremendous progress in recent years. For the neat NFA system PBDB-T:ITIC, the film morphology and crystallinity are tailored by the choice of the solvent used for spin coating the active layers. Three different chlorinated solvents, chlorobenzene (CB), chloroform, and dichlorobenzene, are compared and the obtained active layer morphology is correlated with the optoelectronic properties and the device performance. The small domain sizes in the case of CB are most beneficial for the device performance, whereas the largest number or size of face-on PBDB-T crystallites is not causing the highest power conversion efficiencies (PCEs). In addition, when using CB, the number of edge-on crystallites is highest and the distances between neighboring domains are small. The smoothest blend films are realized with CB, which exhibit correlated roughness with their substrates and no large aggregates have formed in these blend films. Thus, CB offers the best way to balance the aggregation and crystallization kinetics in the active layer and enables the highest PCE values.
AB - Non-fullerene acceptor (NFA)-based organic solar cells have made tremendous progress in recent years. For the neat NFA system PBDB-T:ITIC, the film morphology and crystallinity are tailored by the choice of the solvent used for spin coating the active layers. Three different chlorinated solvents, chlorobenzene (CB), chloroform, and dichlorobenzene, are compared and the obtained active layer morphology is correlated with the optoelectronic properties and the device performance. The small domain sizes in the case of CB are most beneficial for the device performance, whereas the largest number or size of face-on PBDB-T crystallites is not causing the highest power conversion efficiencies (PCEs). In addition, when using CB, the number of edge-on crystallites is highest and the distances between neighboring domains are small. The smoothest blend films are realized with CB, which exhibit correlated roughness with their substrates and no large aggregates have formed in these blend films. Thus, CB offers the best way to balance the aggregation and crystallization kinetics in the active layer and enables the highest PCE values.
KW - GISAXS
KW - morphology
KW - non-fullerene acceptors
KW - organic solar cells
KW - solvents
UR - http://www.scopus.com/inward/record.url?scp=85125108964&partnerID=8YFLogxK
U2 - 10.1002/solr.202101084
DO - 10.1002/solr.202101084
M3 - Article
AN - SCOPUS:85125108964
SN - 2367-198X
VL - 6
JO - Solar RRL
JF - Solar RRL
IS - 6
M1 - 2101084
ER -