<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang H</submitter><funding>National Research Foundation</funding><pagination>eaao6657</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5775028</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>4(1)</volume><pubmed_abstract>Constructing atomically dispersed platinum (Pt) electrocatalysts is essential to build high-performance and cost-effective electrochemical water-splitting systems. We present a novel strategy to realize the traction and stabilization of isolated Pt atoms in the nitrogen-containing porous carbon matrix (Pt@PCM). In comparison with the commercial Pt/C catalyst (20 weight %), the as-prepared Pt@PCM catalyst exhibits significantly boosted mass activity (up to 25 times) for hydrogen evolution reaction. Results of extended x-ray absorption fine structure investigation and density functional theory calculation suggest that the active sites are associated with the lattice-confined Pt centers and the activated carbon (C)/nitrogen (N) atoms at the adjacency of the isolated Pt centers. This strategy may provide insights into constructing highly efficient single-atom catalysts for different energy-related applications.</pubmed_abstract><journal>Science advances</journal><pubmed_title>Dynamic traction of lattice-confined platinum atoms into mesoporous carbon matrix for hydrogen evolution reaction.</pubmed_title><pmcid>PMC5775028</pmcid><funding_grant_id>NRF Singapore - NRF-NRFI2016-04</funding_grant_id><funding_grant_id>award362696</funding_grant_id><pubmed_authors>An P</pubmed_authors><pubmed_authors>Lou XWD</pubmed_authors><pubmed_authors>Guan BY</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Dong J</pubmed_authors><pubmed_authors>Zhou W</pubmed_authors><pubmed_authors>Zhang P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dynamic traction of lattice-confined platinum atoms into mesoporous carbon matrix for hydrogen evolution reaction.</name><description>Constructing atomically dispersed platinum (Pt) electrocatalysts is essential to build high-performance and cost-effective electrochemical water-splitting systems. We present a novel strategy to realize the traction and stabilization of isolated Pt atoms in the nitrogen-containing porous carbon matrix (Pt@PCM). In comparison with the commercial Pt/C catalyst (20 weight %), the as-prepared Pt@PCM catalyst exhibits significantly boosted mass activity (up to 25 times) for hydrogen evolution reaction. Results of extended x-ray absorption fine structure investigation and density functional theory calculation suggest that the active sites are associated with the lattice-confined Pt centers and the activated carbon (C)/nitrogen (N) atoms at the adjacency of the isolated Pt centers. This strategy may provide insights into constructing highly efficient single-atom catalysts for different energy-related applications.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jan</publication><modification>2025-04-26T01:33:32.163Z</modification><creation>2019-03-26T22:58:55Z</creation></dates><accession>S-EPMC5775028</accession><cross_references><pubmed>29372181</pubmed><doi>10.1126/sciadv.aao6657</doi></cross_references></HashMap>