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Title: Hole‐Transfer Dependence on Blend Morphology and Energy Level Alignment in Polymer: ITIC Photovoltaic Materials

Abstract

Abstract Bulk‐heterojunction organic photovoltaic materials containing nonfullerene acceptors (NFAs) have seen remarkable advances in the past year, finally surpassing fullerenes in performance. Indeed, acceptors based on indacenodithiophene (IDT) have become synonymous with high power conversion efficiencies (PCEs). Nevertheless, NFAs have yet to achieve fill factors (FFs) comparable to those of the highest‐performing fullerene‐based materials. To address this seeming anomaly, this study examines a high efficiency IDT‐based acceptor, ITIC , paired with three donor polymers known to achieve high FFs with fullerenes, PTPD3T , PBTI3T , and PBTSA3T . Excellent PCEs up to 8.43% are achieved from PTPD3T:ITIC blends, reflecting good charge transport, optimal morphology, and efficient ITIC to PTPD3T hole‐transfer, as observed by femtosecond transient absorption spectroscopy. Hole‐transfer is observed from ITIC to PBTI3T and PBTSA3T , but less efficiently, reflecting measurably inferior morphology and nonoptimal energy level alignment, resulting in PCEs of 5.34% and 4.65%, respectively. This work demonstrates the importance of proper morphology and kinetics of ITIC → donor polymer hole‐transfer in boosting the performance of polymer: ITIC photovoltaic bulk heterojunction blends.

Authors:
 [1];  [1];  [1];  [1];  [1];  [1];  [1];  [1];  [2];  [1]; ORCiD logo [1];  [3]; ORCiD logo [1]
  1. Department of Chemistry and the Materials Research Center and Argonne‐Northwestern Solar Energy Research Center Northwestern University 2145 Sheridan Road Evanston IL 60208 USA
  2. Chemical Sciences and Engineering Division Argonne National Laboratory 9700 South Cass Avenue Lemont IL 60439 USA
  3. Department of Materials Science and Engineering and the Materials Research Center and Argonne‐Northwestern Solar Energy Research Center Northwestern University 2145 Sheridan Road Evanston IL 60208 USA
Publication Date:
Sponsoring Org.:
USDOE
OSTI Identifier:
1411256
Grant/Contract Number:  
DE‐SC0001059; DE‐AC02‐06CH11357
Resource Type:
Publisher's Accepted Manuscript
Journal Name:
Advanced Materials
Additional Journal Information:
Journal Name: Advanced Materials Journal Volume: 30 Journal Issue: 3; Journal ID: ISSN 0935-9648
Publisher:
Wiley Blackwell (John Wiley & Sons)
Country of Publication:
Germany
Language:
English

Citation Formats

Eastham, Nicholas D., Logsdon, Jenna L., Manley, Eric F., Aldrich, Thomas J., Leonardi, Matthew J., Wang, Gang, Powers‐Riggs, Natalia E., Young, Ryan M., Chen, Lin X., Wasielewski, Michael R., Melkonyan, Ferdinand S., Chang, Robert P. H., and Marks, Tobin J. Hole‐Transfer Dependence on Blend Morphology and Energy Level Alignment in Polymer: ITIC Photovoltaic Materials. Germany: N. p., 2017. Web. doi:10.1002/adma.201704263.
Eastham, Nicholas D., Logsdon, Jenna L., Manley, Eric F., Aldrich, Thomas J., Leonardi, Matthew J., Wang, Gang, Powers‐Riggs, Natalia E., Young, Ryan M., Chen, Lin X., Wasielewski, Michael R., Melkonyan, Ferdinand S., Chang, Robert P. H., & Marks, Tobin J. Hole‐Transfer Dependence on Blend Morphology and Energy Level Alignment in Polymer: ITIC Photovoltaic Materials. Germany. https://doi.org/10.1002/adma.201704263
Eastham, Nicholas D., Logsdon, Jenna L., Manley, Eric F., Aldrich, Thomas J., Leonardi, Matthew J., Wang, Gang, Powers‐Riggs, Natalia E., Young, Ryan M., Chen, Lin X., Wasielewski, Michael R., Melkonyan, Ferdinand S., Chang, Robert P. H., and Marks, Tobin J. Mon . "Hole‐Transfer Dependence on Blend Morphology and Energy Level Alignment in Polymer: ITIC Photovoltaic Materials". Germany. https://doi.org/10.1002/adma.201704263.
@article{osti_1411256,
title = {Hole‐Transfer Dependence on Blend Morphology and Energy Level Alignment in Polymer: ITIC Photovoltaic Materials},
author = {Eastham, Nicholas D. and Logsdon, Jenna L. and Manley, Eric F. and Aldrich, Thomas J. and Leonardi, Matthew J. and Wang, Gang and Powers‐Riggs, Natalia E. and Young, Ryan M. and Chen, Lin X. and Wasielewski, Michael R. and Melkonyan, Ferdinand S. and Chang, Robert P. H. and Marks, Tobin J.},
abstractNote = {Abstract Bulk‐heterojunction organic photovoltaic materials containing nonfullerene acceptors (NFAs) have seen remarkable advances in the past year, finally surpassing fullerenes in performance. Indeed, acceptors based on indacenodithiophene (IDT) have become synonymous with high power conversion efficiencies (PCEs). Nevertheless, NFAs have yet to achieve fill factors (FFs) comparable to those of the highest‐performing fullerene‐based materials. To address this seeming anomaly, this study examines a high efficiency IDT‐based acceptor, ITIC , paired with three donor polymers known to achieve high FFs with fullerenes, PTPD3T , PBTI3T , and PBTSA3T . Excellent PCEs up to 8.43% are achieved from PTPD3T:ITIC blends, reflecting good charge transport, optimal morphology, and efficient ITIC to PTPD3T hole‐transfer, as observed by femtosecond transient absorption spectroscopy. Hole‐transfer is observed from ITIC to PBTI3T and PBTSA3T , but less efficiently, reflecting measurably inferior morphology and nonoptimal energy level alignment, resulting in PCEs of 5.34% and 4.65%, respectively. This work demonstrates the importance of proper morphology and kinetics of ITIC → donor polymer hole‐transfer in boosting the performance of polymer: ITIC photovoltaic bulk heterojunction blends.},
doi = {10.1002/adma.201704263},
journal = {Advanced Materials},
number = 3,
volume = 30,
place = {Germany},
year = {Mon Dec 04 00:00:00 EST 2017},
month = {Mon Dec 04 00:00:00 EST 2017}
}

Journal Article:
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https://doi.org/10.1002/adma.201704263

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