<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zheng M</submitter><funding>National Natural Science Foundation of China</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>1619</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12905375</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(1)</volume><pubmed_abstract>The co-contamination of arsenite (As&lt;sup>III&lt;/sup>) and cadmium (Cd&lt;sup>2+&lt;/sup>) poses a significant challenge in environmental remediation due to their divergent chemical speciation and transformation pathways. Here, a redox-active layered double oxide (MgMn-LDO) is designed, and achieves adsorption capacities of 821.7 mg g&lt;sup>‒1&lt;/sup> for As&lt;sup>III&lt;/sup> and 1895.6 mg g&lt;sup>‒1&lt;/sup> for Cd&lt;sup>2+&lt;/sup> in their coexisting system, presenting a state-of-the-art performance. Unexpectedly, the co-adsorption system not only enhances individual adsorption capacities but also accelerates the adsorption rate by 181‒fold compared to single-component systems. The LDO undergoes a four-stage spatiotemporally ordered topological transformation, which effectively decouples the oxidation of As&lt;sup>I</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Spatiotemporally ordered topological transformation in layered double hydroxides enables synergistic mineralization of As&amp;lt;sup&amp;gt;III&amp;lt;/sup&amp;gt;/Cd&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt;.</pubmed_title><pmcid>PMC12905375</pmcid><funding_grant_id>22478027, 22438007, 22288102</funding_grant_id><pubmed_authors>Xu SM</pubmed_authors><pubmed_authors>Cao X</pubmed_authors><pubmed_authors>Zheng M</pubmed_authors><pubmed_authors>Chen W</pubmed_authors><pubmed_authors>Du H</pubmed_authors><pubmed_authors>Shi W</pubmed_authors><pubmed_authors>Shao M</pubmed_authors><pubmed_authors>Kong X</pubmed_authors><pubmed_authors>Duan X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Spatiotemporally ordered topological transformation in layered double hydroxides enables synergistic mineralization of As&amp;lt;sup&amp;gt;III&amp;lt;/sup&amp;gt;/Cd&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt;.</name><description>The co-contamination of arsenite (As&lt;sup>III&lt;/sup>) and cadmium (Cd&lt;sup>2+&lt;/sup>) poses a significant challenge in environmental remediation due to their divergent chemical speciation and transformation pathways. Here, a redox-active layered double oxide (MgMn-LDO) is designed, and achieves adsorption capacities of 821.7 mg g&lt;sup>‒1&lt;/sup> for As&lt;sup>III&lt;/sup> and 1895.6 mg g&lt;sup>‒1&lt;/sup> for Cd&lt;sup>2+&lt;/sup> in their coexisting system, presenting a state-of-the-art performance. Unexpectedly, the co-adsorption system not only enhances individual adsorption capacities but also accelerates the adsorption rate by 181‒fold compared to single-component systems. The LDO undergoes a four-stage spatiotemporally ordered topological transformation, which effectively decouples the oxidation of As&lt;sup>I</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-07-15T22:21:52.822Z</modification><creation>2026-07-09T10:20:40.956Z</creation></dates><accession>S-EPMC12905375</accession><cross_references><pubmed>41545423</pubmed><doi>10.1038/s41467-026-68326-2</doi></cross_references></HashMap>