<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang Z</submitter><funding>National Natural Science Foundation of China</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>3734</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6700197</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(1)</volume><pubmed_abstract>Single-atom metal catalysts have sparked tremendous attention, but direct transformation of cheap and easily obtainable bulk metal oxide into single atoms is still a great challenge. Here we report a facile and versatile gas-transport strategy to synthesize isolated single-atom copper sites (Cu ISAS/NC) catalyst at gram levels. Commercial copper (I) oxide powder is sublimated as mobile vapor at nearly melting temperature (1500 K) and subsequently can be trapped and reduced by the defect-rich nitrogen-doped carbon (NC), forming the isolated copper sites catalyst. Strikingly, this thermally stable Cu ISAS/NC, which is obtained above 1270 K, delivers excellent oxygen reduction performance possessing a recorded half-wave potential of 0.92 V vs RHE among other Cu-based electrocatalysts. By varying metal oxide precursors, we demonstrate the universal synthesis of different metal single atoms anchored on NC materials (M ISAS/NC, where M refers to Mo and Sn). This strategy is readily scalable and the as-prepared sintering-resistant M ISAS/NC catalysts hold great potential in high-temperature applications.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Directly transforming copper (I) oxide bulk into isolated single-atom copper sites catalyst through gas-transport approach.</pubmed_title><pmcid>PMC6700197</pmcid><funding_grant_id>21802132</funding_grant_id><funding_grant_id>21522107, 21671180</funding_grant_id><pubmed_authors>Yang Z</pubmed_authors><pubmed_authors>Zhao C</pubmed_authors><pubmed_authors>Xu Q</pubmed_authors><pubmed_authors>Chen W</pubmed_authors><pubmed_authors>Qu Y</pubmed_authors><pubmed_authors>Zhou F</pubmed_authors><pubmed_authors>Chen B</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors><pubmed_authors>Duan X</pubmed_authors><pubmed_authors>Wu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Directly transforming copper (I) oxide bulk into isolated single-atom copper sites catalyst through gas-transport approach.</name><description>Single-atom metal catalysts have sparked tremendous attention, but direct transformation of cheap and easily obtainable bulk metal oxide into single atoms is still a great challenge. Here we report a facile and versatile gas-transport strategy to synthesize isolated single-atom copper sites (Cu ISAS/NC) catalyst at gram levels. Commercial copper (I) oxide powder is sublimated as mobile vapor at nearly melting temperature (1500 K) and subsequently can be trapped and reduced by the defect-rich nitrogen-doped carbon (NC), forming the isolated copper sites catalyst. Strikingly, this thermally stable Cu ISAS/NC, which is obtained above 1270 K, delivers excellent oxygen reduction performance possessing a recorded half-wave potential of 0.92 V vs RHE among other Cu-based electrocatalysts. By varying metal oxide precursors, we demonstrate the universal synthesis of different metal single atoms anchored on NC materials (M ISAS/NC, where M refers to Mo and Sn). This strategy is readily scalable and the as-prepared sintering-resistant M ISAS/NC catalysts hold great potential in high-temperature applications.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Aug</publication><modification>2024-10-18T14:46:34.579Z</modification><creation>2019-08-26T07:03:53Z</creation></dates><accession>S-EPMC6700197</accession><cross_references><pubmed>31427572</pubmed><doi>10.1038/s41467-019-11796-4</doi></cross_references></HashMap>