Variation of the Side Chain Branch Position Leads to Vastly Improved Molecular Weight and OPV Performance in 4,8-dialkoxybenzo[1,2-b:4,5-b′]dithiophene/2,1,3-benzothiadiazole Copolymers
Abstract
Through manipulation of the solubilizing side chains, we were able to dramatically improve the molecular weight of 4,8-dialkoxybenzo[1,2- b :4,5- b ′ ]dithiophene (BDT)/2,1,3-benzothiadiazole (BT) copolymers. When dodecyl side chains ( P1 ) are employed at the 4- and 8-positions of the BDT unit, we obtain a chloroform-soluble copolymer fraction with of 6.3 kg/mol. Surprisingly, by moving to the commonly employed 2-ethylhexyl branch ( P2 ), decreases to 3.4 kg/mol. This is despite numerous reports that this side chain increases solubility and . By moving the ethyl branch in one position relative to the polymer backbone (1-ethylhexyl, P3 ), is dramatically increased to 68.8 kg/mol. As a result of this increase, the shape of the absorption profile is dramatically altered, with = 637 nm compared with 598 nm for P1 and 579 nm for P2 . The hole mobility as determined by thin film transistor (TFT) measurements is improved from cm 2 /Vs for P1 and P2 to cm 2 /Vs for P3 , while solar cell power conversion efficiency in increased to for P3 relative to and for P1 and P2 , respectively.
- Authors:
-
- The Department of Physics and the Center for Nanotechnology and Molecular Materials, Wake Forest University, Winston-Salem, NC 27109, USA
- The Department of Chemistry, Wake Forest University, Winston-Salem, NC 27109, USA
- Publication Date:
- Sponsoring Org.:
- USDOE
- OSTI Identifier:
- 1197856
- Grant/Contract Number:
- FG02-07ER46428
- Resource Type:
- Published Article
- Journal Name:
- Journal of Nanotechnology
- Additional Journal Information:
- Journal Name: Journal of Nanotechnology Journal Volume: 2011; Journal ID: ISSN 1687-9503
- Publisher:
- Hindawi Publishing Corporation
- Country of Publication:
- United Kingdom
- Language:
- English
Citation Formats
Coffin, Robert C., MacNeill, Christopher M., Peterson, Eric D., Ward, Jeremy W., Owen, Jack W., McLellan, Claire A., Smith, Gregory M., Noftle, Ronald E., Jurchescu, Oana D., and Carroll, David L. Variation of the Side Chain Branch Position Leads to Vastly Improved Molecular Weight and OPV Performance in 4,8-dialkoxybenzo[1,2-b:4,5-b′]dithiophene/2,1,3-benzothiadiazole Copolymers. United Kingdom: N. p., 2011.
Web. doi:10.1155/2011/572329.
Coffin, Robert C., MacNeill, Christopher M., Peterson, Eric D., Ward, Jeremy W., Owen, Jack W., McLellan, Claire A., Smith, Gregory M., Noftle, Ronald E., Jurchescu, Oana D., & Carroll, David L. Variation of the Side Chain Branch Position Leads to Vastly Improved Molecular Weight and OPV Performance in 4,8-dialkoxybenzo[1,2-b:4,5-b′]dithiophene/2,1,3-benzothiadiazole Copolymers. United Kingdom. https://doi.org/10.1155/2011/572329
Coffin, Robert C., MacNeill, Christopher M., Peterson, Eric D., Ward, Jeremy W., Owen, Jack W., McLellan, Claire A., Smith, Gregory M., Noftle, Ronald E., Jurchescu, Oana D., and Carroll, David L. Sat .
"Variation of the Side Chain Branch Position Leads to Vastly Improved Molecular Weight and OPV Performance in 4,8-dialkoxybenzo[1,2-b:4,5-b′]dithiophene/2,1,3-benzothiadiazole Copolymers". United Kingdom. https://doi.org/10.1155/2011/572329.
@article{osti_1197856,
title = {Variation of the Side Chain Branch Position Leads to Vastly Improved Molecular Weight and OPV Performance in 4,8-dialkoxybenzo[1,2-b:4,5-b′]dithiophene/2,1,3-benzothiadiazole Copolymers},
author = {Coffin, Robert C. and MacNeill, Christopher M. and Peterson, Eric D. and Ward, Jeremy W. and Owen, Jack W. and McLellan, Claire A. and Smith, Gregory M. and Noftle, Ronald E. and Jurchescu, Oana D. and Carroll, David L.},
abstractNote = {Through manipulation of the solubilizing side chains, we were able to dramatically improve the molecular weight ( M w ) of 4,8-dialkoxybenzo[1,2- b :4,5- b ′ ]dithiophene (BDT)/2,1,3-benzothiadiazole (BT) copolymers. When dodecyl side chains ( P1 ) are employed at the 4- and 8-positions of the BDT unit, we obtain a chloroform-soluble copolymer fraction with M w of 6.3 kg/mol. Surprisingly, by moving to the commonly employed 2-ethylhexyl branch ( P2 ), M w decreases to 3.4 kg/mol. This is despite numerous reports that this side chain increases solubility and M w . By moving the ethyl branch in one position relative to the polymer backbone (1-ethylhexyl, P3 ), M w is dramatically increased to 68.8 kg/mol. As a result of this M w increase, the shape of the absorption profile is dramatically altered, with λ max = 637 nm compared with 598 nm for P1 and 579 nm for P2 . The hole mobility as determined by thin film transistor (TFT) measurements is improved from ~ 1 × 10 − 6 cm 2 /Vs for P1 and P2 to 7 × 10 − 4 cm 2 /Vs for P3 , while solar cell power conversion efficiency in increased to 2.91 % for P3 relative to 0.31 % and 0.19 % for P1 and P2 , respectively.},
doi = {10.1155/2011/572329},
journal = {Journal of Nanotechnology},
number = ,
volume = 2011,
place = {United Kingdom},
year = {Sat Jan 01 00:00:00 EST 2011},
month = {Sat Jan 01 00:00:00 EST 2011}
}
https://doi.org/10.1155/2011/572329
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