<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kobayashi H</submitter><funding>Advanced Low Carbon Technology Research and Development Program</funding><funding>Japan Society for the Promotion of Science</funding><pagination>3135-3142</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9933879</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(3)</volume><pubmed_abstract>Magnesium rechargeable batteries (MRBs) promise to be the next post lithium-ion batteries that can help meet the increasing demand for high-energy, cost-effective, high-safety energy storage devices. Early prototype MRBs that use molybdenum-sulfide cathodes have low terminal voltages, requiring the development of oxide-based cathodes capable of overcoming the sulfide's low Mg&lt;sup>2+&lt;/sup> conductivity. Here, we fabricate an ultraporous (>500 m&lt;sup>2&lt;/sup> g&lt;sup>-1&lt;/sup>) and ultrasmall (&lt;2.5 nm) cubic spinel MgMn&lt;sub>2&lt;/sub>O&lt;sub>4&lt;/sub> (MMO) by a freeze-dry assisted room-temperature alcohol reduction process. While the as-fabricated MMO exhibits a discharge capacity of 160 mAh g&lt;sup>-1&lt;/sup>, the removal of its surface hydroxy groups by heat-treatment activates it without structural change, improving its discharge capacity to 270 mAh g&lt;sup>-1&lt;/sup>─the theoretical capacity at room temperature. These results are made possible by the ultraporous, ultrasmall particles that stabilize the metastable cubic spinel phase, promoting both the Mg&lt;sup>2+&lt;/sup> insertion/deintercalation in the MMO and the reversible transformation between the cubic spinel and cubic rock-salt phases.</pubmed_abstract><journal>ACS nano</journal><pubmed_title>Ultraporous, Ultrasmall MgMn&lt;sub>2&lt;/sub>O&lt;sub>4&lt;/sub> Spinel Cathode for a Room-Temperature Magnesium Rechargeable Battery.</pubmed_title><pmcid>PMC9933879</pmcid><funding_grant_id>JPMJAL1301</funding_grant_id><funding_grant_id>JP20H02436</funding_grant_id><pubmed_authors>Tominaga Y</pubmed_authors><pubmed_authors>Iimura R</pubmed_authors><pubmed_authors>Nishimura N</pubmed_authors><pubmed_authors>Watanabe H</pubmed_authors><pubmed_authors>Ichitsubo T</pubmed_authors><pubmed_authors>Kobayashi H</pubmed_authors><pubmed_authors>Fukumi Y</pubmed_authors><pubmed_authors>Imai H</pubmed_authors><pubmed_authors>Mandai T</pubmed_authors><pubmed_authors>Nakayama M</pubmed_authors><pubmed_authors>Honma I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ultraporous, Ultrasmall MgMn&lt;sub>2&lt;/sub>O&lt;sub>4&lt;/sub> Spinel Cathode for a Room-Temperature Magnesium Rechargeable Battery.</name><description>Magnesium rechargeable batteries (MRBs) promise to be the next post lithium-ion batteries that can help meet the increasing demand for high-energy, cost-effective, high-safety energy storage devices. Early prototype MRBs that use molybdenum-sulfide cathodes have low terminal voltages, requiring the development of oxide-based cathodes capable of overcoming the sulfide's low Mg&lt;sup>2+&lt;/sup> conductivity. Here, we fabricate an ultraporous (>500 m&lt;sup>2&lt;/sup> g&lt;sup>-1&lt;/sup>) and ultrasmall (&lt;2.5 nm) cubic spinel MgMn&lt;sub>2&lt;/sub>O&lt;sub>4&lt;/sub> (MMO) by a freeze-dry assisted room-temperature alcohol reduction process. While the as-fabricated MMO exhibits a discharge capacity of 160 mAh g&lt;sup>-1&lt;/sup>, the removal of its surface hydroxy groups by heat-treatment activates it without structural change, improving its discharge capacity to 270 mAh g&lt;sup>-1&lt;/sup>─the theoretical capacity at room temperature. These results are made possible by the ultraporous, ultrasmall particles that stabilize the metastable cubic spinel phase, promoting both the Mg&lt;sup>2+&lt;/sup> insertion/deintercalation in the MMO and the reversible transformation between the cubic spinel and cubic rock-salt phases.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2026-03-27T16:37:12.029Z</modification><creation>2025-04-04T10:36:11.983Z</creation></dates><accession>S-EPMC9933879</accession><cross_references><pubmed>36669094</pubmed><doi>10.1021/acsnano.2c12392</doi></cross_references></HashMap>