ABSTRACT
The formation of Tröger's Base (TB) configuration is a useful approach to synthesize polymers of intrinsic microporosity (PIM). Herein, the V-shaped TB scaffold is incorporated to prepare electrochromic (EC) polyamide with electroactive triphenylamine (TPA) moiety. The presence of intrinsic microporosity derived from inefficient packing of TB scaffolds can facilitate the counterions diffusion between electroactive species and electrolytes. Consequently, the resulting TB-based polyamide exhibits enhanced EC behaviors, such as a lower driving potential, reduced the difference of redox potentials ΔE, and shorter switching response time compared to the corresponding EC counterpart polyamide.
Subject(s)
Nylons , Polymers , Amines , ElectrolytesABSTRACT
The electrochromic (EC) polyamides (Ether-PentiTPA1 and Ether-PentiTPA8) from the electroactive pentiptycene-derived triphenylaminediamine monomers (PentiTPA1 and PentiTPA8) were designed and prepared via polycondensation. The incorporation of rigid and contorted H-shaped pentiptycene scaffolds could restrain polymer chains from close packing and further form intrinsic microporosity in the polymer matrix which could be confirmed by the measurements of WXRD, BET, and PALS. With the existence of intrinsic microporosity, the diffusion rate of counterions between the electroactive polymer film and electrolyte can be promoted during the electrochemical procedure. Therefore, the prepared polyamide Ether-PentiTPA1 exhibits enhanced EC behaviors, such as lower driving potential (1.11 V), smaller redox potential difference ΔE (0.24 V), and shorter switching response time (3.6/5.2 s for coloring/bleaching). Consequently, the formation of intrinsic microporosity can be a useful approach for the enhancement of EC response performance.
ABSTRACT
Porous redox-active polyamide hybrid films have been successfully prepared to enhance the electrochromic (EC) properties in this report comparing with salt-caused porous films and hybrid films obtained via in situ sol-gel reaction of hydroxyl groups and zirconium dioxide (ZrO2). With the assistance of porous and hybrid structures, the diffusion rate of counterions between electrolyte and EC species could be effectively increased, and the charges could be delivered and stored between the donor-acceptor system constructed by the organic-inorganic hybrid during the electrochemical process. Furthermore, there would be a synergistic effect while combining the porous structure and hybrid system together, which can improve the EC behaviors much more obviously; that is, the enhancement of porous hybrid films is more than that of porous films and hybrid films individually. For further application, the porous hybrid films were fabricated into devices, which exhibit a lower oxidation potential (from 1.07 to 0.94 V) and shorter switching response time (from 81.3 to 9.7 s for coloring time and from 44.7 to 20.8 s for bleaching time) with good electrochemical stability. Consequently, these results indicate that the EC properties could be enhanced and improved dramatically by the facile approach of merging the porous structure and hybrid system.
ABSTRACT
Enhancing switching response capability of electrochromic (EC) polymers has been a topical issue. Herein, the H-shaped nonplanar pentiptycene scaffold is successfully introduced into the polyamide film derived from N,N'-bis(4-aminophenyl)-N,N'-di(methoxyphenyl)-1,4-phenylenediamine (TPPA), and the resulting copolymer shows enhanced EC behaviors, including lower oxidation potential and shorter switching response time, as compared to the corresponding TPPA-derived homopolymer.
