TY - JOUR
T1 - Regioregular and Random Difluorobenzothiadiazole Electron Donor-Acceptor Polymer Semiconductors for Thin-Film Transistors and Polymer Solar Cells
AU - Deng, Ping
AU - Wu, Bo
AU - Lei, Yanlian
AU - Cao, Huanyang
AU - ONG, Beng
N1 - This work was financially supported by a Strategic Development Fund (SDF13-0531-A02) of HK Baptist University, Hung Hin Shiu Charitable Foundation, and Shenzhen Science and Technology Innovation Grant (KQTD20140630110339343).
PY - 2016/4/26
Y1 - 2016/4/26
N2 - Random and regioregular electron donor-acceptor (D-A) polymers comprising of 3,6-bis(3-octyltridecyl)thieno[3,2-b]thiophene donor and 5,6-difluorobenzo[c][1,2,5]thiadiazole acceptor moieties were synthesized to study the effects of both structural regioregularity and molecular weight on their performance in organic thin-film transistors (OTFTs) and bulk-heterojunction (BHJ) polymer solar cells (PSCs). All the polymers displayed similar molecular orbital energy levels regardless of their structures and molecular weights (MWs). The regioregular D-A polymers exhibited higher molecular orders than their random counterparts, and the degrees in molecular ordering improved with increased MW, leading to higher charge transport capability. However, undesirably high MW led to limited polymer solubility and thus fabrication difficulties resulting in poorer device performance. A reasonably high power conversion efficiency of about 7.6% was provided by the new regioregular D-A polymer semiconductor of mid-MW properties with excellent solution processability and molecular self-assembly efficiency.
AB - Random and regioregular electron donor-acceptor (D-A) polymers comprising of 3,6-bis(3-octyltridecyl)thieno[3,2-b]thiophene donor and 5,6-difluorobenzo[c][1,2,5]thiadiazole acceptor moieties were synthesized to study the effects of both structural regioregularity and molecular weight on their performance in organic thin-film transistors (OTFTs) and bulk-heterojunction (BHJ) polymer solar cells (PSCs). All the polymers displayed similar molecular orbital energy levels regardless of their structures and molecular weights (MWs). The regioregular D-A polymers exhibited higher molecular orders than their random counterparts, and the degrees in molecular ordering improved with increased MW, leading to higher charge transport capability. However, undesirably high MW led to limited polymer solubility and thus fabrication difficulties resulting in poorer device performance. A reasonably high power conversion efficiency of about 7.6% was provided by the new regioregular D-A polymer semiconductor of mid-MW properties with excellent solution processability and molecular self-assembly efficiency.
UR - http://www.scopus.com/inward/record.url?scp=84964739565&partnerID=8YFLogxK
U2 - 10.1021/acs.macromol.5b02754
DO - 10.1021/acs.macromol.5b02754
M3 - Journal article
AN - SCOPUS:84964739565
SN - 0024-9297
VL - 49
SP - 2541
EP - 2548
JO - Macromolecules
JF - Macromolecules
IS - 7
ER -