Answers are grounded in this paper and cite their sources.
A facile and scalable synthetic route to a soluble dithieno[3,2- b:2′,3′- d ]thiophene (DTT) unit has been developed, which utilizes a Stille coupling reaction to efficiently synthesize the bisthienyl sulfide intermediate. This simplifies the overall DTT synthesis to only four steps with a 44% yield and facilitates its use as a donor unit in low-band-gap polymers. Solution processable alternating D-π–A-π polymers (DTTBTO and DTTDPP) have been synthesized with DTT as the donor unit and either a benzothiodiazole derivative (BTO) or fused ring 1,4-diketopyrrolo[3,4- c ]pyrrole (DPP) serving as the acceptor unit. The ability to tailor the structure of these donor–acceptor systems permits a detailed understanding of structure/property relationships for band-gap engineering, absorbance, V oc, and efficiency to be developed and applied to the design of high-performance organic solar cells.
No takes yet. Share an insight, caveat, or question.
Ku et al. (2011) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: