| 摘要： |
In this work, a new electron-rich building block, o-fluoro-p-alkoxyphenyl-substituted benzo[1,2-b:4,5-b'] dithiophene (BDT) unit, has been used to construct donor (D)-acceptor (A) conjugated copolymers with electron-deficient units 5,6-difluoro-4,7-di(4-(2-ethylhexyl)-2-thienyl)-2,1,3-benzothiadiazole (C8DTBTff) and 5,6-difluoro-4,7-di(4-hexyl-2-thienyl)-2,1,3-benzothiadiazole (C6DTBTff), named P-o-FBDTP-C8DTBTff (P2) and P-o-FBDTP-C6DTBTff (P3), respectively. The experimental results indicate that the incorporation of fluorine into the ortho-position of the alkoxyphenyl substituted BDT unit can enable its resultant polymer to efficiently tune the energy levels and improve the mobility of the derived bulk heterojunction layer, which results in a much higher power conversion efficiency (PCE) of P2 (8.10%). Moreover, replacing the 2-ethylhexyl chains on the DTBTff unit with hexyl chains can improve the planarity of the conjugated backbone of the polymer, which makes the P3/PC71BM blends exhibit higher carrier mobility than P2/PC71BM. Finally, a PCE of 9.02% for the device of P3 is obtained without any additive treatment, which is the highest value achieved for the widely reported D-A polymers with fluorine substituted BDT as the electron-donor unit in single junction polymer solar cells. |
