TY - JOUR
T1 - Three new conjugated polymers based on benzo[2,1-b:3,4-b′] dithiophene
T2 - Synthesis, characterization, photoinduced charge transfer and theoretical calculation studies
AU - Chen, Shaojie
AU - Zhang, Qiuyu
AU - Zhang, Hepeng
AU - Gu, Junwei
AU - Ma, Mingliang
AU - Xin, Tiejun
AU - Zhou, Yanyang
AU - Zhou, Jian
AU - Liu, Qing
PY - 2012/8
Y1 - 2012/8
N2 - Three new conjugated polymers have been designed and synthesized via the alternate copolymerization of the electron-donating monomer benzodithiophene (BDT) and three different electron-accepting monomers: 5,8-dibromoquinoxaline, 5,8-dibromo-2,3-diphenylquinoxaline, 10,13-dibromodibenzo[a,c]phenazine. The synthesized polymers show good solubility in common organic solvents as well as broader absorptions in the visible region and narrower optical band gaps compared to homopolymers made from BDT units. It is found that the absorptions of the copolymers are red-shifted by increasing the electron-withdrawing ability of the co-monomer. In particular, the absorption edge of the P3 film extends to 778 nm, whereas that of the P1 film is only at 636 nm. Theoretical calculation studies of structure-property relations indicated that polymer chains with better coplanarity or π-π* delocalization will lead to lower band gaps. Photoinduced charge transfer (PCT) studies disclosed that exciton dissociation of photoexcited PX (X = 1, 2, 3) via electron-transfer may occur at the interface with CHL-C 60, enabling the photogeneration of electrons and holes. The P3/CHL-C 60 blended film was chosen as a representative sample to test the applicability of the polymer P3 for energy conversion, a 1.76% PCE was finally obtained.
AB - Three new conjugated polymers have been designed and synthesized via the alternate copolymerization of the electron-donating monomer benzodithiophene (BDT) and three different electron-accepting monomers: 5,8-dibromoquinoxaline, 5,8-dibromo-2,3-diphenylquinoxaline, 10,13-dibromodibenzo[a,c]phenazine. The synthesized polymers show good solubility in common organic solvents as well as broader absorptions in the visible region and narrower optical band gaps compared to homopolymers made from BDT units. It is found that the absorptions of the copolymers are red-shifted by increasing the electron-withdrawing ability of the co-monomer. In particular, the absorption edge of the P3 film extends to 778 nm, whereas that of the P1 film is only at 636 nm. Theoretical calculation studies of structure-property relations indicated that polymer chains with better coplanarity or π-π* delocalization will lead to lower band gaps. Photoinduced charge transfer (PCT) studies disclosed that exciton dissociation of photoexcited PX (X = 1, 2, 3) via electron-transfer may occur at the interface with CHL-C 60, enabling the photogeneration of electrons and holes. The P3/CHL-C 60 blended film was chosen as a representative sample to test the applicability of the polymer P3 for energy conversion, a 1.76% PCE was finally obtained.
UR - http://www.scopus.com/inward/record.url?scp=84868707758&partnerID=8YFLogxK
U2 - 10.1039/c2py20122d
DO - 10.1039/c2py20122d
M3 - 文章
AN - SCOPUS:84868707758
SN - 1759-9954
VL - 3
SP - 2244
EP - 2253
JO - Polymer Chemistry
JF - Polymer Chemistry
IS - 8
ER -