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A single freeze cycle redirects iron mineral transformation
Umeå University, Faculty of Science and Technology, Department of Chemistry. College of Chemistry, Chemical Engineering and Materials Science, State Key Laboratory of Fluorine-Containing Functional Membrane Materials, Shandong Normal University, Jinan, China.
Umeå University, Faculty of Science and Technology, Department of Chemistry.
Umeå University, Faculty of Science and Technology, Department of Chemistry.
École Nationale Supérieure de Chimie de Rennes, Institut des Sciences Chimiques de Rennes, Unité Mixte de Recherche, Centre National de la Recherche Scientifique, Université de Rennes, Rennes, France.
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2026 (English)In: Science, ISSN 0036-8075, E-ISSN 1095-9203, Vol. 393, no 6807, p. 212-213Article in journal (Refereed) Published
Abstract [en]

Polycrystalline ice formation concentrates mineral nanoparticles into liquid boundaries between growing ice crystals. Here we show that minutes of freezing dictate iron mineral fate over subsequent months of aqueous aging. A single freeze–thaw cycle irreversibly aggregates ferrihydrite through converging physical and chemical mechanisms. Freeze concentration collapses electrostatic barriers while cryosuction strips hydration layers and compresses nanoparticles into micrometer-scale planar aggregates. Chemical evidence points to interfacial (hydr)oxo bridging, alongside hydrogen bonding, that resists disaggregation. These mechanisms lock nanoparticles into mesocrystal-like assemblages that retain their nanoscale identity but inhibit dissolution–reprecipitation to goethite, instead favoring solid-state transformation to hematite. Ice formation thus acts as a geochemical reactor, driving aggregation and interfacial bonding that redirect iron speciation, with broad implications for nutrient cycling and carbon preservation across the cryosphere.

Place, publisher, year, edition, pages
American Association for the Advancement of Science (AAAS), 2026. Vol. 393, no 6807, p. 212-213
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Materials Chemistry
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URN: urn:nbn:se:umu:diva-256820DOI: 10.1126/science.aee9519Scopus ID: 2-s2.0-105044384782OAI: oai:DiVA.org:umu-256820DiVA, id: diva2:2087347
Funder
Swedish Research Council, 2020-04853Swedish Research Council, 2024-04694Swedish Research Council, 2022-01246Carl Tryggers foundation , CTS 22:2326The Kempe Foundations, JCSMK 23-172The Kempe Foundations, JCSMK 25-0050Available from: 2026-07-20 Created: 2026-07-20 Last updated: 2026-07-20Bibliographically approved

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Luo, TaoChen, TaoBui Thi, Tra MyBoily, Jean-François

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