Abstract
Synthesis of robust, functional membranes is hindered by the lack of spatial control in conventional bulk-phase reactions, which offer limited regulation over network structure and nanoscale uniformity. Here we report a nanoconfinement strategy to fabricate membranes where polymerization occurs within sub-2-nm channels that act as spatially defined reaction compartments. The nanoconfined space governs nanoscale alignment and network packing, producing high-density poly(epoxy) membranes (1.51 g cm−3), 37% denser than their non-confined analogue (1.10 g cm−3) and exceeding typical polymers. The resulting materials combine high tensile strength (119.9 MPa), flexibility (100,000 bending cycles) and broad solvent resistance, unifying properties that are difficult to achieve simultaneously. We further demonstrate that producing high-density membrane matrices facilitates selective ion transport, as shown by as-fabricated positively charged poly(ammonium) membranes, which outperform state-of-the-art counterparts in terms of mechanical strength, OH⁻ conductivity and selectivity against small neutral molecules. This work demonstrates nanomaterials as spatially confined reactors to govern polymer architecture and function, while also offering fundamental insights into structure regulation under nanoconfinement.

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The data supporting the findings of this study are available within the article and its Supplementary Information. Source data are provided with this paper.
Change history
20 March 2026
A Correction to this paper has been published: https://doi.org/10.1038/s44160-026-01050-3
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Acknowledgements
This research was conducted by the ARC Centre of Excellence for Green Electrochemical Transformation of Carbon Dioxide (CE230100017)and funded by the Australian Government. X. Zhang thanks the Australian Research Council for his ARC Future Fellowship (FT210100593). This work was supported by resources provided by the Pawsey Supercomputing Research Centre with funding from the Australian Government and the Government of Western Australia. This research was undertaken with the assistance of resources and services from the National Computational Infrastructure (NCI), which is supported by the Australian Government. D.V.A. and K.S.N. acknowledge the support from the Ministry of Education (Singapore) under the Research Centre of Excellence programme (grant EDUN C-33-18-279-V12, the Institute for Functional Intelligent Materials (I-FIM)).
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Conceptualization was done by X. Zhang and Z.W. The methodology was developed by Z.W., X. Zhang, A.K.W., D.V.A. and K.S.N. Computational studies and simulations were designed and performed by Y.W., X.Y. and J.Z.L. Experiments, characterizations, data analysis and validation were carried out by Z.W., M.Y., Z.-X.L., X. Zeng, H.Z., X.L., K.S., M.T., J.Y., R.X., W.Z., K.X., Y.K., E.S., C.J. and C.Z. All authors reviewed the paper.
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Nature Synthesis thanks Xiaoqiang An, Yan Wang and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. Primary handling editor: Jet-Sing Lee, in collaboration with the Nature Synthesis team.
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Materials and methods, Supplementary Figs. 1–32, Discussion, Tables 1–5 and References.
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Robust membranes enabled by nanochannel-confined polymerization
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Computational insights into polymer configuration regulation within nanochannels
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Wang, Z., Jia, C., Wang, Y. et al. Confined polymerization in nanochannels for synthesizing functional membranes. Nat. Synth (2026). https://doi.org/10.1038/s44160-026-00991-z
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DOI: https://doi.org/10.1038/s44160-026-00991-z


