Fast switching water processable electrochromic polymers
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Authors
Pengjie Shi
Chad Amb
Aubrey L Dyer
John Reynolds
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Type
Journal Article, Professional Journal
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Abstract
This paper describes the synthesis of two new blue to transmissive donor–acceptor electrochromic polymers: a polymer synthesized using an alternating copolymerization route (ECP-Blue-A) and a polymer synthesized using a random copolymerization (ECP-Blue-R) by Stille polymerization. These polymers utilize side chains with four ester groups per donor moiety, allowing organic solubility in the ester form, and water solubility upon saponification to their carboxylate salt form. We demonstrate that the saponified polymer salts of ECP-Blue-A and ECP-Blue-R (WS-ECP-Blue-A and WS-ECP-Blue-R) can be processed from aqueous solutions into thin films by spray-casting. Upon the subsequent neutralization of the thin films, the resulting polymer acid films are solvent resistant and can be electrochemically switched between their colored state and a transmissive state in a KNO3/water electrolyte solution. The polymer acids, WS-ECP-Blue-A-acid and WS-ECP-Blue-R-acid, show electrochromic contrast Δ%T of 38% at 655 nm and 39% at 555 nm for a 0.5 s switch, demonstrating the advantage of an aqueous compatible electrochrome switchable in high ionic conductivity aqueous electrolytes. The results of the electrochromic properties study indicate that these polymers are promising candidates for aqueous processable and aqueous switching electrochromic materials and devices as desired for applications where environmental impact is of importance.