Article ID Journal Published Year Pages File Type
1441847 Synthetic Metals 2012 5 Pages PDF
Abstract

A series of random low band-gap conjugated copolymers (PFO-DDSTQ) derived from 9,9-dioctylfluorene (DOF) and 6,7-dimethyl-4,9-di(selenophen-2-yl)-[1,2,5]thiadiazolo[3,4-g]quinoxaline (DDSTQ) are prepared by the palladium-catalyzed Suzuki coupling reaction. The obtained polymers are readily soluble in common organic solvents. The polymers absorb light from 300 to 880 nm with two absorbance peaks at around 370 and 740 nm. The optical band gaps of the resulting polymers with 15 or 30% narrow band-gap units in the polymer backbone calculated from the absorption onset are around 1.41 eV. The electroluminescent properties of the polymers were investigated and it was found that with 5% DDSTQ copolymerized on the main chain, the resulting polymer PFO-DDSTQ5 exhibited an exclusively near-infrared emission at 860 nm.

Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Selenophene and fluorene based narrow band gap copolymers with Eg = 1.41 eV is synthesized. ► The polymer based near infrared polymer light emitting diodes (NIPLEDs) show electroluminescence peak at 860 nm. ► The electroluminescence spectrum match telecommunications wavelength 0.8–0.9 μm. ► This is the first report about selenophene based NIPLEDs in 0.8–0.9 μm.

Related Topics
Physical Sciences and Engineering Materials Science Biomaterials
Authors
, , , , , ,