4.6 Article

Electrochemical Probing of Steric, Electrostatic and Hydrophobic Interactions of Large Cations in Polymers of Intrinsic Microporosity

期刊

出版社

ELECTROCHEMICAL SOC INC
DOI: 10.1149/1945-7111/ac5303

关键词

-

资金

  1. Center for Enhanced Nanofluidic Transport, an Energy Frontier Research Center - U.S. Department of Energy, Office of Science, Basic Energy Sciences at the University of California, Irvine [DE-SC0019112]
  2. Department of Chemistry, UC Irvine

向作者/读者索取更多资源

This study investigates the application of solid state nanopores based on PIMs in ion transport and interactions. By controlling the pore structure and selecting functional groups, nanopore channels with consistent sizes can be achieved, and the interactions between ions and molecules inside the pores can be modified, opening up new avenues for water purification and energy storage.
Porous membranes have been used for many applications, including separations in biotechnology, the food industry, water purification, and even energy storage devices. The benefit of polymers of intrinsic microporosity (PIMs) is their consistently sized nanopore channels. Inherent functionalities of the PIM structure not only create these channels but are also available for further modifications that can change the interactions of ions and molecules inside of the pore. Here we design solid state nanopores on which are drop-casted two different PIMs, functionalized with either a cyano group or a carboxylic acid. Ionic transport through the membranes is investigated based on pore size and charge-charge interactions, as well as steric and hydrophobic interactions. Achieving specific ion selectivity with easily processable porous membranes opens new avenues for water purification strategies and energy storage.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据