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Precise control of the interlayer spacing of graphene oxide (GO) membranes at the sub-nanometer scale offers size-exclusion-based separation of Li+/Mg2+, a critical step towards efficient lithium resource management and energy sustainability. While previous GO-based membranes have shown high Mg2+ rejections, their performance was largely limited to static diffusion settings or diluted solutions where Donnan exclusion dominates. Here, we report a GO membrane intercalated with a uniform polyelectrolyte layer. The membrane shows substantially enhanced MgCl2 rejection over a wide concentration range, while allowing LiCl permeation under pressure-driven filtration. This enables direct lithium recovery from low-quality brines with high MgCl2 concentrations and high Mg2+/Li+ ratios. Mechanistic study reveals that the adsorption of halide counter-ions onto the charged GO channel walls narrowed the interlayer spacing and enabled size-exclusion-based ionic separation. At higher ionic concentrations, a partial exchange of these adsorbed counter-ions with those in the second hydration shell of Mg2+ allowed moderate Mg2+ permeation. We further demonstrate a streamlined GO-based membrane filtration process, which rejects 99.53% Mg2+ from a low-quality brine, effectively upgrading it towards a high-quality lithium source, and highlighting the potential of this approach for sustainable lithium production.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).
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