An all-conjugated gradient copolymer approach for morphological control of polymer solar cells

This work introduces fully π-conjugated gradient copolymers as promising materials to control and stabilize the nanoscale morphology of polymer:fullerene solar cells. Gradient and block sequence copolymers of 3-hexylselenophene (3HS) and 3-hexylthiophene (3HT) are utilized as the donors (D) in bulk-...

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Published inJournal of materials chemistry. A, Materials for energy and sustainability Vol. 3; no. 40; pp. 20174 - 20184
Main Authors Amonoo, Jojo A., Li, Anton, Purdum, Geoffrey E., Sykes, Matthew E., Huang, Bingyuan, Palermo, Edmund F., McNeil, Anne J., Shtein, Max, Loo, Yueh-Lin, Green, Peter F.
Format Journal Article
LanguageEnglish
Published United States Royal Society of Chemistry 2015
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Abstract This work introduces fully π-conjugated gradient copolymers as promising materials to control and stabilize the nanoscale morphology of polymer:fullerene solar cells. Gradient and block sequence copolymers of 3-hexylselenophene (3HS) and 3-hexylthiophene (3HT) are utilized as the donors (D) in bulk-heterojunction (BHJ) solar cells with phenyl-C61-butyric acid methyl ester (PCBM) as the acceptor (A). We show that for the same overall copolymer composition, the ordering of molecular constituents along the copolymer chain (copolymer sequence) significantly influences the nanoscale morphology and phase separation behavior of π-conjugated copolymer:fullerene devices. In addition, energy-filtered transmission electron microscopy (EFTEM) of the blends revealed that relative to the block copolymer:PCBM, the gradient copolymer:PCBM sample formed a more uniform, continuous and interconnected network of polymer fibrils within the acceptor-rich phase, associated with a large D/A interface. Charge extraction of photogenerated carriers by linearly increasing voltage (photo-CELIV) shows that the gradient copolymer:PCBM device possesses the highest initial carrier density, n (0) = (3.92 ± 0.3) × 10 18 cm −3 , consistent with a larger D/A interfacial area suggested by the observed morphology, albeit at the expense of increased carrier recombination rate. Accelerated degradation studies show that the gradient copolymer:PCBM system maintains the highest efficiency over prolonged heat treatment.
AbstractList This work introduces fully π-conjugated gradient copolymers as promising materials to control and stabilize the nanoscale morphology of polymer:fullerene solar cells. Gradient and block sequence copolymers of 3-hexylselenophene (3HS) and 3-hexylthiophene (3HT) are utilized as the donors (D) in bulk-heterojunction (BHJ) solar cells with phenyl-C61-butyric acid methyl ester (PCBM) as the acceptor (A). We show that for the same overall copolymer composition, the ordering of molecular constituents along the copolymer chain (copolymer sequence) significantly influences the nanoscale morphology and phase separation behavior of π-conjugated copolymer:fullerene devices. In addition, energy-filtered transmission electron microscopy (EFTEM) of the blends revealed that relative to the block copolymer:PCBM, the gradient copolymer:PCBM sample formed a more uniform, continuous and interconnected network of polymer fibrils within the acceptor-rich phase, associated with a large D/A interface. Charge extraction of photogenerated carriers by linearly increasing voltage (photo-CELIV) shows that the gradient copolymer:PCBM device possesses the highest initial carrier density, n (0) = (3.92 ± 0.3) × 10 18 cm −3 , consistent with a larger D/A interfacial area suggested by the observed morphology, albeit at the expense of increased carrier recombination rate. Accelerated degradation studies show that the gradient copolymer:PCBM system maintains the highest efficiency over prolonged heat treatment.
This work introduces fully pi -conjugated gradient copolymers as promising materials to control and stabilize the nanoscale morphology of polymer:fullerene solar cells. Gradient and block sequence copolymers of 3-hexylselenophene (3HS) and 3-hexylthiophene (3HT) are utilized as the donors (D) in bulk-heterojunction (BHJ) solar cells with phenyl-C61-butyric acid methyl ester (PCBM) as the acceptor (A). We show that for the same overall copolymer composition, the ordering of molecular constituents along the copolymer chain (copolymer sequence) significantly influences the nanoscale morphology and phase separation behavior of pi -conjugated copolymer:fullerene devices. In addition, energy-filtered transmission electron microscopy (EFTEM) of the blends revealed that relative to the block copolymer:PCBM, the gradient copolymer:PCBM sample formed a more uniform, continuous and interconnected network of polymer fibrils within the acceptor-rich phase, associated with a large D/A interface. Charge extraction of photogenerated carriers by linearly increasing voltage (photo-CELIV) shows that the gradient copolymer:PCBM device possesses the highest initial carrier density, n(0) = (3.92 plus or minus 0.3) 10 super(18) cm super(-3), consistent with a larger D/A interfacial area suggested by the observed morphology, albeit at the expense of increased carrier recombination rate. Accelerated degradation studies show that the gradient copolymer:PCBM system maintains the highest efficiency over prolonged heat treatment.
A larger interfacial area between the copolymer and fullerene is obtained with the gradient copolymer relative to the block architecture. This is correlated with two orders of magnitude higher initial carrier density.
Author Purdum, Geoffrey E.
Shtein, Max
McNeil, Anne J.
Green, Peter F.
Li, Anton
Amonoo, Jojo A.
Sykes, Matthew E.
Huang, Bingyuan
Palermo, Edmund F.
Loo, Yueh-Lin
Author_xml – sequence: 1
  givenname: Jojo A.
  surname: Amonoo
  fullname: Amonoo, Jojo A.
  organization: Applied Physics Program, University of Michigan, Ann Arbor, USA
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  givenname: Anton
  surname: Li
  fullname: Li, Anton
  organization: Department of Materials Science and Engineering, University of Michigan, Ann Arbor, USA
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  surname: Purdum
  fullname: Purdum, Geoffrey E.
  organization: Department of Chemical and Biological Engineering, Princeton University, Princeton, USA
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  givenname: Matthew E.
  surname: Sykes
  fullname: Sykes, Matthew E.
  organization: Department of Materials Science and Engineering, University of Michigan, Ann Arbor, USA
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  givenname: Bingyuan
  surname: Huang
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  organization: Department of Materials Science and Engineering, University of Michigan, Ann Arbor, USA
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  organization: Department of Chemistry, University of Michigan, Ann Arbor, USA
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  surname: Shtein
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  organization: Department of Materials Science and Engineering, University of Michigan, Ann Arbor, USA
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  organization: Department of Chemical and Biological Engineering, Princeton University, Princeton, USA
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  givenname: Peter F.
  surname: Green
  fullname: Green, Peter F.
  organization: Applied Physics Program, University of Michigan, Ann Arbor, USA, Department of Materials Science and Engineering
BackLink https://www.osti.gov/biblio/1370062$$D View this record in Osti.gov
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Snippet This work introduces fully π-conjugated gradient copolymers as promising materials to control and stabilize the nanoscale morphology of polymer:fullerene solar...
This work introduces fully pi -conjugated gradient copolymers as promising materials to control and stabilize the nanoscale morphology of polymer:fullerene...
A larger interfacial area between the copolymer and fullerene is obtained with the gradient copolymer relative to the block architecture. This is correlated...
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SourceType Open Access Repository
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StartPage 20174
SubjectTerms Block copolymers
Copolymers
Devices
Morphology
Nanostructure
Photovoltaic cells
Polymer blends
Solar cells
Title An all-conjugated gradient copolymer approach for morphological control of polymer solar cells
URI https://search.proquest.com/docview/1762078348
https://www.osti.gov/biblio/1370062
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