<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lv H</submitter><funding>National Natural Science Foundation of China</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>5665</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8476569</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(1)</volume><pubmed_abstract>Metal nanoparticles anchored on perovskite through in situ exsolution under reducing atmosphere provide catalytically active metal/oxide interfaces for CO&lt;sub>2&lt;/sub> electrolysis in solid oxide electrolysis cell. However, there are critical challenges to obtain abundant metal/oxide interfaces due to the sluggish diffusion process of dopant cations inside the bulk perovskite. Herein, we propose a strategy to promote exsolution of RuFe alloy nanoparticles on Sr&lt;sub>2&lt;/sub>Fe&lt;sub>1.4&lt;/sub>Ru&lt;sub>0.1&lt;/sub>Mo&lt;sub>0.5&lt;/sub>O&lt;sub>6-δ&lt;/sub> perovskite by enriching the active Ru underneath the perovskite surface via repeated redox manipulations. In situ scanning transmission electron microscopy demonstrates the dynamic structure evolution of Sr&lt;sub>2&lt;/sub>Fe&lt;sub>1.4&lt;/sub>Ru&lt;sub>0.1&lt;/sub>Mo&lt;sub>0.5&lt;/sub>O&lt;sub>6-δ&lt;/sub> perovskite under reducing and oxidizing atmosphere, as well as the facilitated CO&lt;sub>2&lt;/sub> adsorption at RuFe@Sr&lt;sub>2&lt;/sub>Fe&lt;sub>1.4&lt;/sub>Ru&lt;sub>0.1&lt;/sub>Mo&lt;sub>0.5&lt;/sub>O&lt;sub>6-δ&lt;/sub> interfaces. Solid oxide electrolysis cell with RuFe@Sr&lt;sub>2&lt;/sub>Fe&lt;sub>1.4&lt;/sub>Ru&lt;sub>0.1&lt;/sub>Mo&lt;sub>0.5&lt;/sub>O&lt;sub>6-δ&lt;/sub> interfaces shows over 74.6% enhancement in current density of CO&lt;sub>2&lt;/sub> electrolysis compared to that with Sr&lt;sub>2&lt;/sub>Fe&lt;sub>1.4&lt;/sub>Ru&lt;sub>0.1&lt;/sub>Mo&lt;sub>0.5&lt;/sub>O&lt;sub>6-δ&lt;/sub> counterpart as well as impressive stability for 1000 h at 1.2 V and 800 °C.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Promoting exsolution of RuFe alloy nanoparticles on Sr&lt;sub>2&lt;/sub>Fe&lt;sub>1.4&lt;/sub>Ru&lt;sub>0.1&lt;/sub>Mo&lt;sub>0.5&lt;/sub>O&lt;sub>6-δ&lt;/sub> via repeated redox manipulations for CO&lt;sub>2&lt;/sub> electrolysis.</pubmed_title><pmcid>PMC8476569</pmcid><funding_grant_id>92015302</funding_grant_id><pubmed_authors>Zeng C</pubmed_authors><pubmed_authors>Fu Q</pubmed_authors><pubmed_authors>Matsumoto H</pubmed_authors><pubmed_authors>Lv H</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Bao X</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Li R</pubmed_authors><pubmed_authors>Ta N</pubmed_authors><pubmed_authors>Lin L</pubmed_authors><pubmed_authors>Song Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Promoting exsolution of RuFe alloy nanoparticles on Sr&lt;sub>2&lt;/sub>Fe&lt;sub>1.4&lt;/sub>Ru&lt;sub>0.1&lt;/sub>Mo&lt;sub>0.5&lt;/sub>O&lt;sub>6-δ&lt;/sub> via repeated redox manipulations for CO&lt;sub>2&lt;/sub> electrolysis.</name><description>Metal nanoparticles anchored on perovskite through in situ exsolution under reducing atmosphere provide catalytically active metal/oxide interfaces for CO&lt;sub>2&lt;/sub> electrolysis in solid oxide electrolysis cell. However, there are critical challenges to obtain abundant metal/oxide interfaces due to the sluggish diffusion process of dopant cations inside the bulk perovskite. Herein, we propose a strategy to promote exsolution of RuFe alloy nanoparticles on Sr&lt;sub>2&lt;/sub>Fe&lt;sub>1.4&lt;/sub>Ru&lt;sub>0.1&lt;/sub>Mo&lt;sub>0.5&lt;/sub>O&lt;sub>6-δ&lt;/sub> perovskite by enriching the active Ru underneath the perovskite surface via repeated redox manipulations. In situ scanning transmission electron microscopy demonstrates the dynamic structure evolution of Sr&lt;sub>2&lt;/sub>Fe&lt;sub>1.4&lt;/sub>Ru&lt;sub>0.1&lt;/sub>Mo&lt;sub>0.5&lt;/sub>O&lt;sub>6-δ&lt;/sub> perovskite under reducing and oxidizing atmosphere, as well as the facilitated CO&lt;sub>2&lt;/sub> adsorption at RuFe@Sr&lt;sub>2&lt;/sub>Fe&lt;sub>1.4&lt;/sub>Ru&lt;sub>0.1&lt;/sub>Mo&lt;sub>0.5&lt;/sub>O&lt;sub>6-δ&lt;/sub> interfaces. Solid oxide electrolysis cell with RuFe@Sr&lt;sub>2&lt;/sub>Fe&lt;sub>1.4&lt;/sub>Ru&lt;sub>0.1&lt;/sub>Mo&lt;sub>0.5&lt;/sub>O&lt;sub>6-δ&lt;/sub> interfaces shows over 74.6% enhancement in current density of CO&lt;sub>2&lt;/sub> electrolysis compared to that with Sr&lt;sub>2&lt;/sub>Fe&lt;sub>1.4&lt;/sub>Ru&lt;sub>0.1&lt;/sub>Mo&lt;sub>0.5&lt;/sub>O&lt;sub>6-δ&lt;/sub> counterpart as well as impressive stability for 1000 h at 1.2 V and 800 °C.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2025-04-22T20:51:30.135Z</modification><creation>2025-04-06T03:19:07.074Z</creation></dates><accession>S-EPMC8476569</accession><cross_references><pubmed>34580312</pubmed><doi>10.1038/s41467-021-26001-8</doi></cross_references></HashMap>