A high voltage solar cell using a donor-acceptor conjugated polymer based on pyrrolo[3,4-f]-2,1,3-benzothiadiazole-5,7-dione

作者：Li Hairong^*; Sun Shuangyong; Mhaisalkar Subodh; Zin Melvin T; Lam Yeng Ming; Grimsdale Andrew C

来源：Journal of Materials Chemistry A, 2014, 2(42): 17925-17933.

DOI：10.1039/c4ta01248h

We report an improved synthesis of the electron-accepting unit pyrrolo[3,4-f]-2,1,3-benzothiadiazole-5,7-dione (BTI) and the synthesis and characterisation of two donor-acceptor copolymers containing it: poly [6-dodecyl-4,8-bis(2-thienyl)pyrrolo[3,4-f]-2,1,3-benzothiadiazole-5,7-dione-alt-9,9-dioctyl-2,7-bis(thien-2%26apos;-yl)-9H-fluorene] (P(BTI-F)), and poly[6-dodecyl-4,8-bis(thien-2%26apos;-yl)pyrrolo[3,4-f]-2,1,3-benzothiadiazole-5,7-dione-alt-4,8-bis(octyloxy)benzo[1,2-b:4,5-b%26apos;]dithiophene] (P(BTI-B)). By the incorporation of an imide group onto a benzothiadiazole moiety, the HOMO level is lowered. To explore the effectiveness of conjugation along the polymer backbone, two electron donors: fluorene and benzobithiophene, were introduced. These represent a weak and a strong electron-donor, respectively. Both polymers have low lying HOMOs and hence are thermally stable and also result in high open-circuit voltages (V-oc) in photovoltaic applications. Compared to P(BTI-B). P(BTI-F) has a larger bandgap due to the incorporation of a weaker donor unit and thus a deeper lying HOMO level. Devices based on P(BTI-F) and [6,6]-phenyl-C-61-butyric acid methyl ester (PC61BM) can obtain a remarkably high V-oc of 1.11 V. but a PCE of only 1.61%. By contrast, polymer P(BTI-B) has stronger absorption in the longer wavelength range and can achieve a well-dispersed nanomorphology with PC61BM for efficient exciton dissociation, achieving PCE of 3.42%, with a J(sc) of 9.71 mA cm(-2), V-oc of 0.75, and FF of 0.47.

• 出版日期2014-11-14