Effect of fluorine substituents on benzothiadiazole-based D-π-A'-π-A photosensitizers for dye-sensitized solar cells.

ABSTRACT: Two D-π-A'-π-A organic dyes with triazatruxene (TAT) as the electron donor, thiophene as the π-spacer, benzoic acid as the anchor group, and benzothiadiazole (BT) or difluorobenzo[c][1,2,5]thiadiazole (DFBT) as the additional acceptor, namely LS101 and LS102, respectively, were applied to dye-sensitized solar cells (DSSCs). As fluorine substituents are usually strong electron-withdrawing groups, introducing two fluorine atoms into BT was expected to strengthen the electron-withdrawing ability of the auxiliary acceptor, resulting in DSSCs with a broader light capture region and further improved power conversion efficiency (PCE). Fluorine is the smallest electron-withdrawing group with an induction effect, but can also act as an electron-donating group owing to its conjugation effect.

SUBMITTER: Li S 

PROVIDER: S-EPMC9050066 | biostudies-literature | 2020 Mar

REPOSITORIES: biostudies-literature