Photostability Of Ambient-Processed, Conjugated Polymer Electrochromic Devices Encapsulated By Bioderived Barrier Films

Polymer-based electrochromic devices (ECDs) are a promising technology for enabling low-voltage, disposable displays, yet are currently limited by photo-oxidative bleaching of the active materials. Here, renewable barrier films composed of cellulose and chitin are presented as an alternative to poly(ethylene terephthalate) (PET) for encapsulating ECDs. To assess barrier film effectiveness, lateral ECDs composed of poly(3,4-propylenedioxythiophene-(CH(2)OEtHx)(2)) (P-(ProDOT)) active layers were constructed and encapsulated with a multilayer barrier consisting of chitin nanofibers and cellulose nanocrystals spray cast onto a cellulose acetate substrate (oxygen transmission rate (OTR) = 29 cm(3) m(-2) day(-1)), a commercially available PET film (OTR = 8.5 cm(3) m(-2) day(-1)), and a high-performance PET-Al2O3 multilayer barrier film (OTR < 1 cm(3) m(-2) day(-1)). The photodegradation of the P(ProDOT) active layer was determined by measuring the evolution of the colorimetric contrast (Delta E*) and switching speeds as a function of light exposure (100 mW cm(-2), AM 1.5 G light). Photodegradation was found to proceed at a similar rate for all encapsulated devices (roughly 10 times more slowly than unencapsulated devices), highlighting the opportunity for replacing petroleum packaging with bioderived barrier films. Analysis of the switching kinetics, the shifts in optical absorbance, and evidence of chemical degradation indicate that both photochemical breakdown of the electrolyte and cross-linking of the P(ProDOT) active material are key drivers for loss of device performance when oxygen flux to the active material is limited. Pathways toward better understanding photodegradation are then proposed with sustainability in mind for future ECD design.