<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kc BR</submitter><funding>Basic Energy Sciences</funding><pagination>165-172</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12933503</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>4(2)</volume><pubmed_abstract>Herein, we introduce a straightforward synthesis approach for highly active dendritic multimetallic high-entropy alloy (DMHEA@PtIrPdAgRu) nanoparticles with sufficient entropic mixing, featuring uniform distribution of five noble group metals (Pt, Ir, Pd, Ag, and Ru) via a block copolymer-mediated one-pot solvothermal reduction method for oxygen evolution reaction (OER). In this synthesis, &lt;i>N&lt;/i>,&lt;i>N&lt;/i>-dimethylformamide (DMF) is used as a reductant as well as solvent and core-shell-corona-type (poly-(styrene)-&lt;i>block&lt;/i>-poly-(vinylpyridine)-&lt;i>block&lt;/i>-poly-(ethylene oxide)) (PS-PVP-PEO) block copolymer as a structure directing agent. The cooperative effect between the copolymer architecture and the reducing environment of DMF promoted a confined nucleation mechanism for forming a single-phase dendritic structure HEA with high compositional uniformity, thereby mitigating phase segregation, a common challenge in the synthesis of multimetallic nanoparticles. This prepared DMHEA@PtIrPdAgRu catalyst exhibits a low overpotential of 490 mV to attain a high current density of 100 mA cm&lt;sup>-2&lt;/sup> with a Tafel slope of 442 mV dec&lt;sup>-1&lt;/sup> for oxygen evolution. The superior OER performance is attributed to the synergistic cooperation among its active and coordinated metal centers as well as the incorporation of corrosion-resistant metal like platinum.</pubmed_abstract><journal>Precision chemistry</journal><pubmed_title>Facile One-Pot Block Copolymer-Mediated Solvothermal Approach for Synthesis of High-Entropy Alloy with Enhanced OER Activity.</pubmed_title><pmcid>PMC12933503</pmcid><funding_grant_id>DE-SC0023415</funding_grant_id><pubmed_authors>Kc BR</pubmed_authors><pubmed_authors>Bastakoti BP</pubmed_authors><pubmed_authors>Yusa SI</pubmed_authors></additional><is_claimable>false</is_claimable><name>Facile One-Pot Block Copolymer-Mediated Solvothermal Approach for Synthesis of High-Entropy Alloy with Enhanced OER Activity.</name><description>Herein, we introduce a straightforward synthesis approach for highly active dendritic multimetallic high-entropy alloy (DMHEA@PtIrPdAgRu) nanoparticles with sufficient entropic mixing, featuring uniform distribution of five noble group metals (Pt, Ir, Pd, Ag, and Ru) via a block copolymer-mediated one-pot solvothermal reduction method for oxygen evolution reaction (OER). In this synthesis, &lt;i>N&lt;/i>,&lt;i>N&lt;/i>-dimethylformamide (DMF) is used as a reductant as well as solvent and core-shell-corona-type (poly-(styrene)-&lt;i>block&lt;/i>-poly-(vinylpyridine)-&lt;i>block&lt;/i>-poly-(ethylene oxide)) (PS-PVP-PEO) block copolymer as a structure directing agent. The cooperative effect between the copolymer architecture and the reducing environment of DMF promoted a confined nucleation mechanism for forming a single-phase dendritic structure HEA with high compositional uniformity, thereby mitigating phase segregation, a common challenge in the synthesis of multimetallic nanoparticles. This prepared DMHEA@PtIrPdAgRu catalyst exhibits a low overpotential of 490 mV to attain a high current density of 100 mA cm&lt;sup>-2&lt;/sup> with a Tafel slope of 442 mV dec&lt;sup>-1&lt;/sup> for oxygen evolution. The superior OER performance is attributed to the synergistic cooperation among its active and coordinated metal centers as well as the incorporation of corrosion-resistant metal like platinum.</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-16T22:58:23.328Z</modification><creation>2026-07-12T03:09:36.216Z</creation></dates><accession>S-EPMC12933503</accession><cross_references><pubmed>41756613</pubmed><doi>10.1021/prechem.5c00094</doi></cross_references></HashMap>