<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hu Y</submitter><funding>Research Grants Council of Hong Kong</funding><funding>National Natural Science Foundation</funding><funding>Hong Kong Polytechnic University</funding><pagination>e2205299</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9799016</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(36)</volume><pubmed_abstract>Nearly theoretical 100% atomic utilization (supposing each atom could serve as independent sites to play a role in catalyz) of single-atom catalysts (SACs) makes it highly promising for various applications. However, for most SACs, single-atom sites are trapped in a solid carbon matrix, which makes the inner parts hardly available for reaction. Herein, a hollow N-doped carbon confined single-atom Rh (Rh-SACs/HNCR) is developed via a coordination-template method. Both aberration-corrected scanning transmission electron microscopy and energy dispersive X-ray spectroscopy mapping confirm the uniform distribution of Rh single atoms. Owning to the unique hollow structure and effective carbon confinement, excessive conversion from pyridinic/pyrrolic N to graphic N is hindered. As a proof of concept, Rh-SACs/HNCR exhibits superior activity, stability, selectivity, and anti-poisoning capability in formic acid oxidation reaction compared with the counterpart Rh/C, Pd/C, and Pt/C catalysts. This work provides a powerful strategy for synthesizing hollow carbon confined single-atom catalysts apply in various energy-related systems.</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Hollow Carbon Nanorod Confined Single Atom Rh for Direct Formic Acid Electrooxidation.</pubmed_title><pmcid>PMC9799016</pmcid><funding_grant_id>ZVRP</funding_grant_id><funding_grant_id>91963109</funding_grant_id><funding_grant_id>C5029-18E</funding_grant_id><pubmed_authors>Hu Y</pubmed_authors><pubmed_authors>Zhu Y</pubmed_authors><pubmed_authors>Guo X</pubmed_authors><pubmed_authors>Wang D</pubmed_authors><pubmed_authors>Shen T</pubmed_authors><pubmed_authors>Chen C</pubmed_authors><pubmed_authors>Yang C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hollow Carbon Nanorod Confined Single Atom Rh for Direct Formic Acid Electrooxidation.</name><description>Nearly theoretical 100% atomic utilization (supposing each atom could serve as independent sites to play a role in catalyz) of single-atom catalysts (SACs) makes it highly promising for various applications. However, for most SACs, single-atom sites are trapped in a solid carbon matrix, which makes the inner parts hardly available for reaction. Herein, a hollow N-doped carbon confined single-atom Rh (Rh-SACs/HNCR) is developed via a coordination-template method. Both aberration-corrected scanning transmission electron microscopy and energy dispersive X-ray spectroscopy mapping confirm the uniform distribution of Rh single atoms. Owning to the unique hollow structure and effective carbon confinement, excessive conversion from pyridinic/pyrrolic N to graphic N is hindered. As a proof of concept, Rh-SACs/HNCR exhibits superior activity, stability, selectivity, and anti-poisoning capability in formic acid oxidation reaction compared with the counterpart Rh/C, Pd/C, and Pt/C catalysts. This work provides a powerful strategy for synthesizing hollow carbon confined single-atom catalysts apply in various energy-related systems.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-04T21:04:58.426Z</modification><creation>2025-04-04T21:04:58.426Z</creation></dates><accession>S-EPMC9799016</accession><cross_references><pubmed>36366919</pubmed><doi>10.1002/advs.202205299</doi></cross_references></HashMap>