# Synergistic Interfacial Design of Cation Exchange Membranes via Sequential Electro-Assembly for High-Efficiency Lithium Separation

**Authors:** Zhibo Zhang, Geting Xu, Yangbo Qiu, Junbin Liao, Tong Mu, Wanji Zhou, Yunfang Gao, Jianquan Weng, Jiangnan Shen

PMC · DOI: 10.3390/membranes16030087 · 2026-02-28

## TL;DR

A new in-situ method for making ion-exchange membranes improves lithium separation efficiency from complex salt solutions.

## Contribution

A novel electro-assembly strategy for fabricating selective membrane layers directly in electrodialysis stacks.

## Key findings

- The method achieves a Li+/Mg2+ selectivity of 107.9.
- The membrane retains a selectivity of 47 after 10 cycles in real salt lake brine.
- The fabricated membrane shows enhanced ion transport and stability.

## Abstract

The industrial application of modified ion-exchange membranes is limited by complex, discontinuous ex-situ processes. This study introduces an in-situ electro-assembly strategy that enables the direct fabrication of a selective layer within an electrodialysis stack without disassembly. By utilizing a programmed current reversal to orchestrate the sequential deposition of polyethyleneimine (PEI), glutaraldehyde cross-linking, and polystyrene sulfonate (PSS) adsorption, we achieve meticulous interfacial engineering on a commercial cation exchange membrane. Comprehensive characterization confirms the successful construction of a hydrophilic, charge-tuned multilayer, which enhances ion transport kinetics and raises the limiting current density. This method culminates in a membrane with an exceptional Li+/Mg2+ selectivity of 107.9 and robust stability, retaining a significant selectivity of 47 over 10 cycles in real salt lake brine. This synergistic integration of operational simplicity, interfacial precision, and superior performance establishes a transformative and scalable platform for manufacturing high-performance membranes for selective ion separation from complex brine sources.

## Linked entities

- **Chemicals:** glutaraldehyde (PubChem CID 3485), Li+ (PubChem CID 28486), Mg2+ (PubChem CID 888)

## Full-text entities

- **Diseases:** injury to (MESH:D014947), AEM (MESH:D015433)
- **Chemicals:** Polyamine (MESH:D011073), Carbon (MESH:D002244), PSS (MESH:C003321), aldehyde (MESH:D000447), CEM (-), -SO3- (MESH:C011118), brine (MESH:C017082), H+ (MESH:D006859), Na2SO4 (MESH:C012036), Schiff-base (MESH:D012545), poly(sodium 4-styrenesulfonate (MESH:C077114), K+ (MESH:D011188), sulfonic acid (MESH:D013451), sulfonate (MESH:D000476), platinum (MESH:D010984), imine (MESH:D007097), salt (MESH:D012492), magnesium (MESH:D008274), Na+ (MESH:D012964), N (MESH:D009584), NaCl (MESH:D012965), Water (MESH:D014867), PLi+ (MESH:C044850), Li+ (MESH:D008094), amine (MESH:D000588), GA (MESH:D005976), S (MESH:D013455)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** CEMs — Mus musculus (Mouse), Embryonic stem cell (CVCL_8949), CEM — Homo sapiens (Human), Childhood T acute lymphoblastic leukemia, Cancer cell line (CVCL_0207)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13027606/full.md

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Source: https://tomesphere.com/paper/PMC13027606