<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pan Y</submitter><funding>Fundamental Research Funds for the Central Universities</funding><funding>Chinese Academy of Sciences</funding><funding>National Natural Science Foundation of China</funding><pagination>nwaa224</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8288370</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(1)</volume><pubmed_abstract>While the surface charge state of co-catalysts plays a critical role for boosting photocatalysis, studies on surface charge regulation via their precise structure control remain extremely rare. Herein, metal-organic framework (MOF) stabilized bimetallic Pd@Pt nanoparticles, which feature adjustable Pt coordination environment and a controlled structure from core-shell to single-atom alloy (SAA), have been fabricated. Significantly, apart from the formation of a Mott-Schottky junction in a conventional way, we elucidate that Pt surface charge regulation can be alternatively achieved by changing its coordination environment and the structure of the Pd@Pt co-catalyst, where the charge between Pd and Pt is redistributed. As a result, the optimized Pd&lt;sub>10&lt;/sub>@Pt&lt;sub>1&lt;/sub>/MOF composite, which involves an unprecedented SAA co-catalyst, exhibits exceptionally high photocatalytic hydrogen production activity, far surpassing its corresponding counterparts.</pubmed_abstract><journal>National science review</journal><pubmed_title>Precise fabrication of single-atom alloy co-catalyst with optimal charge state for enhanced photocatalysis.</pubmed_title><pmcid>PMC8288370</pmcid><funding_grant_id>21673213</funding_grant_id><funding_grant_id>21871244</funding_grant_id><funding_grant_id>21725101</funding_grant_id><pubmed_authors>Jiang HL</pubmed_authors><pubmed_authors>Yu SH</pubmed_authors><pubmed_authors>Pan Y</pubmed_authors><pubmed_authors>Qian Y</pubmed_authors><pubmed_authors>Zheng X</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Ding C</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Chu SQ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Precise fabrication of single-atom alloy co-catalyst with optimal charge state for enhanced photocatalysis.</name><description>While the surface charge state of co-catalysts plays a critical role for boosting photocatalysis, studies on surface charge regulation via their precise structure control remain extremely rare. Herein, metal-organic framework (MOF) stabilized bimetallic Pd@Pt nanoparticles, which feature adjustable Pt coordination environment and a controlled structure from core-shell to single-atom alloy (SAA), have been fabricated. Significantly, apart from the formation of a Mott-Schottky junction in a conventional way, we elucidate that Pt surface charge regulation can be alternatively achieved by changing its coordination environment and the structure of the Pd@Pt co-catalyst, where the charge between Pd and Pt is redistributed. As a result, the optimized Pd&lt;sub>10&lt;/sub>@Pt&lt;sub>1&lt;/sub>/MOF composite, which involves an unprecedented SAA co-catalyst, exhibits exceptionally high photocatalytic hydrogen production activity, far surpassing its corresponding counterparts.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jan</publication><modification>2024-10-18T18:47:26.214Z</modification><creation>2024-10-18T18:47:26.214Z</creation></dates><accession>S-EPMC8288370</accession><cross_references><pubmed>34691561</pubmed><doi>10.1093/nsr/nwaa224</doi></cross_references></HashMap>