<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang Z</submitter><funding>DOE | SC | Basic Energy Sciences (BES)</funding><funding>DOE | Office of Energy Efficiency &amp;amp; Renewable Energy | Bioenergy Technologies Office</funding><funding>DOE | SC | Basic Energy Sciences</funding><funding>DOE | Office of Energy Efficiency &amp; Renewable Energy | Bioenergy Technologies Office (BETO)</funding><pagination>2664</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10169862</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(1)</volume><pubmed_abstract>Single atoms of platinum group metals on CeO&lt;sub>2&lt;/sub> represent a potential approach to lower precious metal requirements for automobile exhaust treatment catalysts. Here we show the dynamic evolution of two types of single-atom Pt (Pt&lt;sub>1&lt;/sub>) on CeO&lt;sub>2&lt;/sub>, i.e., adsorbed Pt&lt;sub>1&lt;/sub> in Pt/CeO&lt;sub>2&lt;/sub> and square planar Pt&lt;sub>1&lt;/sub> in Pt&lt;sub>AT&lt;/sub>CeO&lt;sub>2&lt;/sub>, fabricated at 500 °C and by atom-trapping method at 800 °C, respectively. Adsorbed Pt&lt;sub>1&lt;/sub> in Pt/CeO&lt;sub>2&lt;/sub> is mobile with the in situ formation of few-atom Pt clusters during CO oxidation, contributing to high reactivity with near-zero reaction order in CO. In contrast, square planar Pt&lt;sub>1&lt;/sub> in Pt&lt;sub>AT&lt;/sub>CeO&lt;sub>2&lt;/sub> is strongly anchored to the support during CO oxidation leading to relatively low reactivity with a positive reaction order in CO. Reduction of both Pt/CeO&lt;sub>2&lt;/sub> and Pt&lt;sub>AT&lt;/sub>CeO&lt;sub>2&lt;/sub> in CO transforms Pt&lt;sub>1&lt;/sub> to Pt nanoparticles. However, both catalysts retain the memory of their initial Pt&lt;sub>1&lt;/sub> state after reoxidative treatments, which illustrates the importance of the initial single-atom structure in practical applications.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Memory-dictated dynamics of single-atom Pt on CeO&lt;sub>2&lt;/sub> for CO oxidation.</pubmed_title><pmcid>PMC10169862</pmcid><funding_grant_id>NA</funding_grant_id><funding_grant_id>DE-FG02-05ER15712</funding_grant_id><pubmed_authors>Tian J</pubmed_authors><pubmed_authors>Lu Y</pubmed_authors><pubmed_authors>Hong J</pubmed_authors><pubmed_authors>Hoffman AS</pubmed_authors><pubmed_authors>Datye AK</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>Huang W</pubmed_authors><pubmed_authors>Jiang D</pubmed_authors><pubmed_authors>Bare SR</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Yang S</pubmed_authors><pubmed_authors>Engelhard MH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Memory-dictated dynamics of single-atom Pt on CeO&lt;sub>2&lt;/sub> for CO oxidation.</name><description>Single atoms of platinum group metals on CeO&lt;sub>2&lt;/sub> represent a potential approach to lower precious metal requirements for automobile exhaust treatment catalysts. Here we show the dynamic evolution of two types of single-atom Pt (Pt&lt;sub>1&lt;/sub>) on CeO&lt;sub>2&lt;/sub>, i.e., adsorbed Pt&lt;sub>1&lt;/sub> in Pt/CeO&lt;sub>2&lt;/sub> and square planar Pt&lt;sub>1&lt;/sub> in Pt&lt;sub>AT&lt;/sub>CeO&lt;sub>2&lt;/sub>, fabricated at 500 °C and by atom-trapping method at 800 °C, respectively. Adsorbed Pt&lt;sub>1&lt;/sub> in Pt/CeO&lt;sub>2&lt;/sub> is mobile with the in situ formation of few-atom Pt clusters during CO oxidation, contributing to high reactivity with near-zero reaction order in CO. In contrast, square planar Pt&lt;sub>1&lt;/sub> in Pt&lt;sub>AT&lt;/sub>CeO&lt;sub>2&lt;/sub> is strongly anchored to the support during CO oxidation leading to relatively low reactivity with a positive reaction order in CO. Reduction of both Pt/CeO&lt;sub>2&lt;/sub> and Pt&lt;sub>AT&lt;/sub>CeO&lt;sub>2&lt;/sub> in CO transforms Pt&lt;sub>1&lt;/sub> to Pt nanoparticles. However, both catalysts retain the memory of their initial Pt&lt;sub>1&lt;/sub> state after reoxidative treatments, which illustrates the importance of the initial single-atom structure in practical applications.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2025-04-19T06:42:47.305Z</modification><creation>2025-04-19T06:42:47.305Z</creation></dates><accession>S-EPMC10169862</accession><cross_references><pubmed>37160890</pubmed><doi>10.1038/s41467-023-37776-3</doi></cross_references></HashMap>