聚酰胺
单体
材料科学
乙醚
聚苯胺
高分子化学
聚合物
缩聚物
反离子
化学工程
电致变色
电解质
氧化还原
电化学
有机化学
化学
电极
复合材料
聚合
物理化学
工程类
离子
冶金
作者
Min‐Hao Pai,Chien‐Chieh Hu,Wei Tan,Jye‐Shane Yang,Guey‐Sheng Liou
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2021-09-21
卷期号:10 (10): 1210-1215
被引量:12
标识
DOI:10.1021/acsmacrolett.1c00487
摘要
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.
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