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 in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 3; no. 40; pp. 20174 - 20184 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Royal Society of Chemistry
2015
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Subjects | |
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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. |
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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 – sequence: 2 givenname: Anton surname: Li fullname: Li, Anton organization: Department of Materials Science and Engineering, University of Michigan, Ann Arbor, USA – sequence: 3 givenname: Geoffrey E. surname: Purdum fullname: Purdum, Geoffrey E. organization: Department of Chemical and Biological Engineering, Princeton University, Princeton, USA – sequence: 4 givenname: Matthew E. surname: Sykes fullname: Sykes, Matthew E. organization: Department of Materials Science and Engineering, University of Michigan, Ann Arbor, USA – sequence: 5 givenname: Bingyuan surname: Huang fullname: Huang, Bingyuan organization: Department of Materials Science and Engineering, University of Michigan, Ann Arbor, USA – sequence: 6 givenname: Edmund F. surname: Palermo fullname: Palermo, Edmund F. organization: Department of Chemistry, University of Michigan, Ann Arbor, USA – sequence: 7 givenname: Anne J. surname: McNeil fullname: McNeil, Anne J. organization: Department of Chemistry, University of Michigan, Ann Arbor, USA – sequence: 8 givenname: Max surname: Shtein fullname: Shtein, Max organization: Department of Materials Science and Engineering, University of Michigan, Ann Arbor, USA – sequence: 9 givenname: Yueh-Lin surname: Loo fullname: Loo, Yueh-Lin organization: Department of Chemical and Biological Engineering, Princeton University, Princeton, USA – sequence: 10 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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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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