Abstract

Reverse electrodialysis (RED) offers a promising route to harvest osmotic energy from salinity gradients, yet practical implementation is hindered by the lack of scalable, high-performance ion-selective membranes that combine efficient ion transport with mechanical robustness and environmental sustainability. Here, we report a mixed matrix membrane composed of polyethersulfone (PES), polyvinylpyrrolidone (PVP), and lithium titanium oxide (Li₂TiO₃, LTO) that addresses these challenges through biomimetic ion transport channels. The strategic integration of LTO nanoparticles introduces ion-exchange sites and oxygen-rich PES ether linkages to create preferential cation transport pathways that mimic biological ion channels. This mixed matrix design delivers over three-fold cation conduction, a power density of 31.64 W m−2 under a 500-fold salinity, and maintains 8.93 W m−2 when tested with natural seawater and river water, positioning it among state-of-the-art polymer-based RED membranes. The facile blade-coating fabrication, environmental compatibility of constituent materials, and stable operation demonstrate the practical viability of this approach for sustainable blue energy harvesting.

Keywords

cation conduction, mixed matrix membrane, osmotic power conversion, reverse electrodialysis

Document Type

Journal Article

Date of Publication

11-15-2026

Article Number

120498

ISSN

00119164

Volume

638

Publication Title

Desalination

Publisher

Elsevier

School

Mineral Recovery Research Centre / School of Engineering

Creative Commons License

Creative Commons Attribution 4.0 License
This work is licensed under a Creative Commons Attribution 4.0 License.

Recommended Citation

Tonnah, R. K., Boroumand, Y., Razbin, M., Vahdani, M., Razmjou, A., & Asadnia, M. (2026). Lithium titanate-functionalized mixed matrix polymer membrane for high-performance osmotic energy conversion. Desalination, 638, Article 120498. https://doi.org/10.1016/j.desal.2026.120498

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Link to publisher version (DOI)

10.1016/j.desal.2026.120498