TY - JOUR
T1 - Tuning the Solution Aggregate Structure of a PM7-Based Conjugated Polymer to Enable Green Solvent Processing of Organic Solar Cells
AU - Khasbaatar, Azzaya
AU - Jones, Austin L.
AU - Fernando, Pravini S.
AU - Sai, Hiroaki
AU - Zhu, Chenhui
AU - Gann, Eliot
AU - Reynolds, John R.
AU - Diao, Ying
N1 - This work was primarily supported by the Office of Naval Research under grant numbers N00014-22-1-2202 (Y.D.) and N00014-22-1-2185 (J.R.R). A.K. acknowledges the A. T. Widiger Chemical Engineering fellowship. P.F. and Y.D. acknowledge support by the NSF CAREER award under Grant No. 18-47828. This research used resources of the Advanced Light Source, a U.S. DOE Office of Science User Facility under contract no. DE-AC02-05CH11231 and the LiX beamline at National Synchrotron Light Source II, which is part of the Center for BioMolecular Structure (CBMS) primarily supported by the National Institutes of Health, the National Institute of General Medical Sciences (NIGMS) through a P30 Grant (P30GM133893), and by the DOE Office of Biological and Environmental Research (KP1605010). LiX also received additional support from NIH Grant S10 OD012331. As part of NSLS-II, a national user facility at Brookhaven National Laboratory, work performed at the CBMS is supported in part by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences Program under contract number DE-SC0012704. The research also used facilities of the Materials Research Laboratory Central Research Facilities, University of Illinois. The authors thank Dr. Lin Yang from the National Synchrotron Light Source II for support on SAXS measurements, Dr. Kathy Walsh from the Materials Research Laboratory at the University of Illinois for support on PiFM measurements, Dr. Aidan Coffey from Advanced Light Source for support on GIWAXS analysis, and Dr. Dean M. DeLongchamp from the National Institute of Standards and Technology for fruitful discussions on the interpretation of GIWAXS and RSoXS measurements.
PY - 2024/3/26
Y1 - 2024/3/26
N2 - Understanding how solvents influence the solution-state aggregation of conjugated polymers and film morphology is crucial for solution-processed organic solar cells (OSCs). Herein, using the conjugated donor polymer PM7 D2, a more processable derivative of PM7 that readily dissolves in a range of halogenated and nonhalogenated (green) solvents, we find that solvent affinity toward the polymer backbone, as opposed to the alkyl side chains, drastically tunes the polymer solution aggregate structures and the resultant blend film morphologies. Our findings reveal that using a poor side-chain solvent forms semiflexible amorphous networks with strong side-chain associations, whereas using a poor backbone solvent leads to semicrystalline fiber aggregates. On the other hand, mutual solvents, which balance the polymer backbone and side-chain solubility, result in rigid amorphous networks with weak/no side-chain interactions. Upon film deposition via blade coating, both semicrystalline fibers and flexible amorphous network aggregates of PM7 D2 yield highly crystalline films with large domains. In contrast, rigid amorphous aggregates with weak or no side-chain associations prevented excessive crystallization of PM7 D2. We found that the green solvent studied in this work (anisole) exhibits poor affinity toward the backbone but is selective to the alkyl side chains, thus forming semicrystalline fibers in solution. Consequently, PM7 D2:ITIC-4F-based OSCs cast from the green solvent only exhibit 5.8% efficiency. Interestingly, similar to using mutual solvents, utilizing hot solution processing converts the semicrystalline fibers to rigid amorphous network aggregates by increasing the backbone solubility, thereby suppressing the excessive crystallization of PM7 D2. Ultimately, the devices exhibited a significant power conversion efficiency (PCE) improvement from 5.8 to 9%, where they were fully processed and tested under ambient conditions in a glovebox-free environment (without additives).
AB - Understanding how solvents influence the solution-state aggregation of conjugated polymers and film morphology is crucial for solution-processed organic solar cells (OSCs). Herein, using the conjugated donor polymer PM7 D2, a more processable derivative of PM7 that readily dissolves in a range of halogenated and nonhalogenated (green) solvents, we find that solvent affinity toward the polymer backbone, as opposed to the alkyl side chains, drastically tunes the polymer solution aggregate structures and the resultant blend film morphologies. Our findings reveal that using a poor side-chain solvent forms semiflexible amorphous networks with strong side-chain associations, whereas using a poor backbone solvent leads to semicrystalline fiber aggregates. On the other hand, mutual solvents, which balance the polymer backbone and side-chain solubility, result in rigid amorphous networks with weak/no side-chain interactions. Upon film deposition via blade coating, both semicrystalline fibers and flexible amorphous network aggregates of PM7 D2 yield highly crystalline films with large domains. In contrast, rigid amorphous aggregates with weak or no side-chain associations prevented excessive crystallization of PM7 D2. We found that the green solvent studied in this work (anisole) exhibits poor affinity toward the backbone but is selective to the alkyl side chains, thus forming semicrystalline fibers in solution. Consequently, PM7 D2:ITIC-4F-based OSCs cast from the green solvent only exhibit 5.8% efficiency. Interestingly, similar to using mutual solvents, utilizing hot solution processing converts the semicrystalline fibers to rigid amorphous network aggregates by increasing the backbone solubility, thereby suppressing the excessive crystallization of PM7 D2. Ultimately, the devices exhibited a significant power conversion efficiency (PCE) improvement from 5.8 to 9%, where they were fully processed and tested under ambient conditions in a glovebox-free environment (without additives).
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U2 - 10.1021/acs.chemmater.3c03055
DO - 10.1021/acs.chemmater.3c03055
M3 - Article
AN - SCOPUS:85187022273
SN - 0897-4756
VL - 36
SP - 2819
EP - 2834
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 6
ER -