An artificial sodium-selective subnanochannel

Author:

Lu Jun1ORCID,Jiang Gengping2ORCID,Zhang Huacheng3ORCID,Qian Binbin1ORCID,Zhu Haijin4ORCID,Gu Qinfen5ORCID,Yan Yuan6,Liu Jefferson Zhe6ORCID,Freeman Benny D.7ORCID,Jiang Lei1ORCID,Wang Huanting1ORCID

Affiliation:

1. Department of Chemical and Biological Engineering, Monash University, Clayton, Victoria 3800, Australia.

2. Department of Applied Physics, College of Science, Wuhan University of Science and Technology, Wuhan 430072, China.

3. Chemical and Environmental Engineering, School of Engineering, RMIT University, Melbourne, Victoria 3000, Australia.

4. Institute for Frontier Materials, Deakin University Waurn Ponds Campus, Geelong, Victoria 3216, Australia.

5. ANSTO, Australian Synchrotron, 800 Blackburn Rd., Clayton, Victoria 3168, Australia.

6. Department of Mechanical Engineering, The University of Melbourne, Parkville, Victoria 3010, Australia.

7. Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, USA.

Abstract

Single-ion selectivity with high precision has long been pursued for fundamental bioinspired engineering and applications such as in ion separation and energy conversion. However, it remains a challenge to develop artificial ion channels to achieve single-ion selectivity comparable to their biological analogs, especially for high Na + /K + selectivity. Here, we report an artificial sodium channel by subnanoconfinement of 4′-aminobenzo-15-crown-5 ethers (15C5s) into ~6-Å-sized metal-organic framework subnanochannel (MOFSNC). The resulting 15C5-MOFSNC shows an unprecedented Na + /K + selectivity of tens to 10 2 and Na + /Li + selectivity of 10 3 under multicomponent permeation conditions, comparable to biological sodium channels. A co–ion-responsive single-file transport mechanism in 15C-MOFSNC is proposed for the preferential transport of Na + over K + due to the synergetic effects of size exclusion, charge selectivity, local hydrophobicity, and preferential binding with functional groups. This study provides an alternative strategy for developing potential single-ion selective channels and membranes for many applications.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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