4.7 Article

Constructing ionic channels in anion exchange membrane via a Zn2+soft template: Experiment and molecular dynamics simulation

Journal

JOURNAL OF MEMBRANE SCIENCE
Volume 629, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.memsci.2021.119293

Keywords

Anion exchange membrane; Soft template; Zn2+ion; Molecular dynamics simulation; Micro-phase separation

Funding

  1. National Natural Science Foundation of China [22008021, 21776034, U1663223, 22021005]
  2. China Postdoctoral Science Foundation [2020M680039]
  3. National Key Research and Development Program of China [2019YFE0119200, 2016YFB0101203]
  4. Fundamental Research Funds for the Central Universities [DUT20LAB307, DUT21TD101]

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An effective soft-template strategy using Zn2+ metal ions to construct well-ordered ionic conductive channels in imidazolium functionalized polysulfone anion exchange membranes results in improved hydroxide conductivity and larger ionic clusters.
An effective soft-template strategy using Zn2+ metal ions is proposed to construct well-ordered ionic conductive channels in the imidazolium (Im+) functionalized polysulfone anion exchange membranes (AEMs). The divalent Zn2+ ion possesses strong electrostatic interactions to induce better microphase separation. The further removal of the sub-nanoscale water-soluble Zn2+ ions introduces free volumes to connect ionic pathways, meanwhile promotes the secondary aggregation of Im+ groups. Experiment and simulation show that Zn2+ ions organize into Zn2+ self-aggregations and interact with Im+ groups via an electrostatic anion-bridged configuration in the Zn2+ incorporated membranes, and the subsequent Zn2+ removal increases the free volume and induces the rearrangement of Im+ groups to form bigger ionic clusters (up to 7.7 nm) than those in the pristine membrane. By optimizing Zn2+ content, the induced ionic conductive channels are tailored, yielding a 50% improvement of hydroxide conductivity and achieving the top level in the previously reported polysufone-based main-chain-type AEMs. This study suggests a novel and scalable route for regulating micro-phase separations in AEMs and provides theoretical exploration for selecting effective template molecules.

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