A computational investigation on the influence of different π spacer groups in the bithiazole-based organic dye sensitizers on the short-circuit photocurrent densities of dye-sensitized solar cells

Abstract

Abstract A series of experimentally synthesized metal free organic dyes based on the 2-Cyano-3-(5-(5′-(4-(diphenylamino)phenyl)-4,4′-dihexyl-2,2′-bithiazol-5-yl)thiophen-2-yl)acrylic acid (dye 1) were investigated, based on computational methods to shed light on how a tiny difference in π-linker of sensitizer, C C and thiophene moiety as the additional π spacer group in dyes 2 and 3 respectively, has a significant impact on the short-circuit photocurrent densities ( J SC ) in Dye-sensitized solar cells (DSSCs). Although dyes 2 and 3 have similar redshifts in comparison to dye 1 in the UV–vis absorption spectra, there is a significant difference between J SC values of these dyes resulting in different solar cell efficiency. To understand the origin of the disparity of the J SC values of these dyes, the key parameters related to the J SC of DSSCs, the electronic and optical properties as well as plausible mechanism of electron injection for these dyes were discussed. The results of electronic structures showed that the LUMO energy of adsorbed dye 3 is located in a region with higher accessible acceptor states of TiO 2 conduction band, in comparison with that of dyes 1 and 2, resulting in better electronic coupling between the LUMO of dye 3 and conduction band of TiO 2 , and therefore a higher efficiency of electron injection, which is in a good agreement with recently reported experimental values of J SC . This theoretical study is expected to be helpful for rational design of other bithiazole-based dyes to achieve higher short circuit current density.