Regulating ion affinity and dehydration of metal-organic framework sub-nanochannels for high-precision ion separation

Ri-Jian Mo, Shuang Chen, Li-Qiu Huang, Xin-Lei Ding, Saima Rafique, Xing-Hua Xia () and Zhong-Qiu Li ()
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Ri-Jian Mo: Nanjing University
Shuang Chen: Nanjing University
Li-Qiu Huang: Nanjing University
Xin-Lei Ding: Nanjing University
Saima Rafique: Nanjing University
Xing-Hua Xia: Nanjing University
Zhong-Qiu Li: Nanjing University

Nature Communications, 2024, vol. 15, issue 1, 1-10

Abstract: Abstract Membrane consisting of ordered sub-nanochannels has been pursued in ion separation technology to achieve applications including desalination, environment management, and energy conversion. However, high-precision ion separation has not yet been achieved owing to the lack of deep understanding of ion transport mechanism in confined environments. Biological ion channels can conduct ions with ultrahigh permeability and selectivity, which is inseparable from the important role of channel size and “ion-channel” interaction. Here, inspired by the biological systems, we report the high-precision separation of monovalent and divalent cations in functionalized metal-organic framework (MOF) membranes (UiO-66-(X)2, X = NH2, SH, OH and OCH3). We find that the functional group (X) and size of the MOF sub-nanochannel synergistically regulate the ion binding affinity and dehydration process, which is the key in enlarging the transport activation energy difference between target and interference ions to improve the separation performance. The K+/Mg2+ selectivity of the UiO-66-(OCH3)2 membrane reaches as high as 1567.8. This work provides a gateway to the understanding of ion transport mechanism and development of high-precision ion separation membranes.

Date: 2024
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DOI: 10.1038/s41467-024-46378-6

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