阳离子聚合
质子
解吸
电导率
共价键
吸附
湿度
共价有机骨架
相对湿度
离子键合
材料科学
氢键
水蒸气
制作
纳米技术
化学
分子
化学工程
高分子化学
有机化学
工程类
物理
物理化学
热力学
离子
医学
替代医学
量子力学
病理
作者
Gobinda Das,Dhanraj B. Shinde,Amrutha Melepurakkal,Manjusha V. Shelke,Bikash Garai,Philippe Bazin,Abdelhafid Ait Blal,Farah Benyettou,Thirumurugan Prakasam,Rasha G. AbdulHalim,Fayrouz Abou Ibrahim,Sudhir Kumar Sharma,Sabu Varghese,James Weston,Ramesh Jagannathan,Matthew A. Addicoat,Felipe Gándara,Mark A. Olson,Mohamad El-Roz,Ali Trabolsi
出处
期刊:Chem
[Elsevier]
日期:2024-05-22
卷期号:10 (8): 2500-2517
被引量:2
标识
DOI:10.1016/j.chempr.2024.04.018
摘要
The development of flexible, humidity-responsive actuator materials is critical for advanced sensors and electronic systems. Current fabrication methods are complex and harsh. We present a novel approach that uses one-step synthesis at room temperature to prepare a self-standing cationic covalent organic framework (TG-DFP COF) film. Because hydrogen bonding and ionic surface coverage are present throughout the COF network, this material facilitates the rapid adsorption and desorption of water vapor, leading to an ultrafast actuating response rate of less than 1 s. At high humidity, the entrapped water molecules enhance the hydrogen-bonding interactions, leading to an impressive proton conductivity of 2.8 mS cm−1, which is among the highest reported for cationic COFs. This study demonstrates a unique 2D-ordered system that combines high proton conductivity and shape-changing ability with remarkable stability.
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