{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,21]],"date-time":"2026-08-21T12:40:22Z","timestamp":1787316022810,"version":"build-2736575974"},"reference-count":44,"publisher":"Wiley","issue":"23","license":[{"start":{"date-parts":[[2026,2,20]],"date-time":"2026-02-20T00:00:00Z","timestamp":1771545600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,2,20]],"date-time":"2026-02-20T00:00:00Z","timestamp":1771545600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"funder":[{"DOI":"10.13039\/100015539","name":"Australian Government","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100015539","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001164","name":"Australian Synchrotron","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100001164","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Small"],"published-print":{"date-parts":[[2026,4]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>\n                    Covalent organic frameworks (COFs) offer ordered, nanometer\u2010scale channels with programmable chemistry and topology, making them promising membrane materials for selective ion transport. However, fabricating robust COF membranes that preserve high crystallinity remains a key challenge. Here we directly address this challenge by decoupling crystallization from membrane formation. COF membranes are first made by interfacial polymerization and subsequently healed under acid\u2010catalyzed hydrothermal conditions, which activate reversible COF linkage bond exchange and framework self\u2010correction. Using TpPa\u2010SO\n                    <jats:sub>3<\/jats:sub>\n                    H as a model, this healing process enhances the (100) x\u2010ray diffraction peak intensity by 25\u2010fold, resulting in a 375% increase in proton conductivity and enhanced monovalent cation\u2010cation selectivity. This \u201cmake\u2010then\u2010heal\u201d strategy leverages dynamic covalent chemistry to produce structurally precise, crystallinity\u2010healed COF membranes.\n                  <\/jats:p>","DOI":"10.1002\/smll.202513711","type":"journal-article","created":{"date-parts":[[2026,2,20]],"date-time":"2026-02-20T15:49:32Z","timestamp":1771602572000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Reversible Bond Dynamics Enable Crystallinity\u2010Healed COF Membranes for Selective Ion Transport"],"prefix":"10.1002","volume":"22","author":[{"given":"Wenming","family":"Zhao","sequence":"first","affiliation":[{"name":"UQ Dow Centre For Sustainable Engineering Innovation School of Chemical Engineering The University of Queensland  St Lucia Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jindi","family":"Yang","sequence":"additional","affiliation":[{"name":"UQ Dow Centre For Sustainable 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