Influence of the pi-Bridge-Fused Ring and Acceptor Unit Extension in D-pi-A-Structured Organic Dyes for Highly Efficient Dye-Sensitized Solar Cells

Abstract

Three new D-ir-A-structured organic dyes, coded as SGT-138, SGT-150, and SGT-151, with the expansion of ir- conjugation in the ir-bridge and acceptor parts have been developed to adjust HOMO/LUMO levels and to expand the light absorption range of organic dyes. Referring to the SGT-137 dye, the ir-bridge group was extended from the 4-hexyl-4H-thieno[3,2-b]indole (TI) to the 9-hexyl-9H-thieno[2 ',3 ':4,5]thieno[3,2-b]indole (TII), and the acceptor group was extended from (E)-3-(4-(benzo[c][1,2,5]-thiadiazol-4-yl)phenyl)-2-cyanoacrylic acid (BTCA) to (E)-3-(4-(benzo[c][1,2,5]thiadiazol-4-ylethynyl)phenyl)-2-cyanoacrylic acid (BTECA), where TII was introduced as a ir-bridging unit for the first time. It was determined that both extensions are promising strategies to enhance the light-harvesting ability. They present several features, such as (i) efficiently intensifying the extinction coefficient and expanding the absorption bands; (ii) exhibiting enhanced intramolecular charge transfer in comparison with the SGT-137; and (iii) being favorable to photoelectric current generation of dye-sensitized solar cells (DSSCs) with cobalt electrolytes. In particular, the ir-spacer extension from TI to TII was useful for modulating the HOMO energy levels, while the acceptor extension from BTCA to BTECA was useful for modulating the LUMO energy levels. These phenomena could be explained with the aid of density functional theory calculations. Finally, the DSSCs based on new SGT-dyes with an HC-A1 co-adsorbent presented good power conversion efficiencies as high as 11.23, 11.30, 11.05, and 10.80% for SGT-137, SGT-138, SGT-150, and SGT-151, respectively. Furthermore, it was determined that the use of the bulky co-adsorbent, HC-A1, can effectively suppress the structural relaxation of dyes in the excited state, thereby enhancing the charge injection rate of SGT-dyes. The observations in time-resolved photoluminescence were indeed consistent with the variation in the PCE, quantitatively.