Low-temperature processable organic semiconductors offer intriguing prospects for inexpensive, flexible, large-area applications, such as displays, radio-frequency identification tags, circuits, and sensors. For organic thin-film transistor (OTFT) applications, n-type organic semiconductors with pe
Synthesis and Absorption Spectra of n-Type Conjugated Polymers Based on Perylene Diimide
✍ Scribed by Lijun Huo; Yi Zhou; Yongfang Li
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 205 KB
- Volume
- 29
- Category
- Article
- ISSN
- 1022-1336
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Two novel n‐type conjugated polymers based on perylene diimide (PDI), poly(PDI‐vinylene) (PDIV), and poly(PDI‐thienylene) (PDITh), have been designed and synthesized by the Stille coupling reaction. In comparison with the PDI monomer (compound M1), PDIV and PDITh films show a significantly broad absorption band from 380 to 720 nm, and a narrower bandgap of ≈1.71 and 1.74 eV, respectively. Cyclic voltammograms of the two polymers display a couple of reversible reduction/re‐oxidation (n‐doping/dedoping) peaks. The onset reduction (n‐doping) potentials of PDIV and PDITh are at −0.62 V and −0.66 V versus Ag/Ag^+^ respectively, which correspond to the electron affinities (EAs) of 4.09 eV for PDIV and 4.05 eV for PDITh. The EA values of the two polymers are the highest among the n‐type conjugated polymers reported to date. The results indicate that PDIV and PDITh could be used as polymer acceptors in all polymer solar cells.
magnified image
📜 SIMILAR VOLUMES
## Abstract 1,8‐Diethynylcarbazole‐based conjugated polymers were synthesized by the acetylenic oxidative coupling reaction or Pd‐catalyzed Sonogashira reaction of the newly designed 3,6‐dialkylated 1,8‐diethynylcarbazole monomers. In particular, the Sonogashira polycondensation was effective for t
## Abstract High‐molecular weight polymers, namely poly(__N__,__N__‐diallyl‐__N__‐methylammonium trifluoroacetate) and poly(__N__,__N__‐diallyl‐__N__‐methylamine), were prepared by radical polymerization of __N__,__N__‐diallyl‐__N__‐methylamine in aqueous solution in the presence of an equimolar am
The feasibility of synthesizing high-molecular-weight amino acid based bioanalogous polymers (AABBPs)-poly(urethane amide)s (PUA) -via polycondensation (PC) of dip-nitrophenyl ester of N,~-(trimethylenedioxydicarbonyl)bis(L-phenylalanine) (3) with diamines or their derivatives under mild conditions