Kunrong Li , Shuanglai Shen , Bo Zhang , Kangli Cao , Daize Mo , Kaiwen Lin , Qing Zhang
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引用次数: 0
Abstract
Three π-conjugated donor/acceptor polyimines have been synthesized for electrochromic applications. Intramolecular hydrogen bonds between the carbamate hydrogen and the imine nitrogen on the side chains gave semi-locked planar monomer M1 and M2. Additional C-H∙∙∙N hydrogen bonds between the nitrogen on the pyrazine and the hydrogen of the azomethane resulted in a fully locked planar monomer M3. These monomers copolymerized with bis(trimethylstannyl)-2,3-dihydrothieno[3,4-b][1,4]dioxine (EDOT-Sn). Different imine acceptors can significantly affect the structures of polymers and thus their optoelectronic properties. Among them, P2 demonstrated the best electrochromic performances at a wavelength of 830 nm, including an optical contrast of 28.06 %, an ultrafast response time of 0.15 s, and a high optical stability with a reversibility of 88.54 % after 200 cycles, while the coloring efficiency was the highest at a wavelength of 592 nm (328.43 cm2 C−1). The results indicate that hydrogen-bonded π-conjugated polyimines can be promising materials for electrochromic applications.
期刊介绍:
This journal is an international medium for the rapid publication of original research papers, short communications and subject reviews dealing with research on and applications of electronic polymers and electronic molecular materials including novel carbon architectures. These functional materials have the properties of metals, semiconductors or magnets and are distinguishable from elemental and alloy/binary metals, semiconductors and magnets.