<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kagkoura A</submitter><funding>Government of Aragon</funding><funding>EU H2020 "ESTEEM3"</funding><funding>EU H2020 “ESTEEM3”</funding><funding>Spanish MICINN</funding><funding>Graphene Flagship</funding><pagination>35</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9824367</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(1)</volume><pubmed_abstract>Easy and effective modification approaches for transition metal dichalcogenides are highly desired in order to make them active toward electrocatalysis. In this manner, we report functionalized molybdenum diselenide (MoSe&lt;sub>2&lt;/sub>) and tungsten diselenide (WSe&lt;sub>2&lt;/sub>) via metal-ligand coordination with pyridine rings for the subsequent covalent grafting of a cobalt-porphyrin. The new hybrid materials were tested towards an electrocatalytic hydrogen evolution reaction in both acidic and alkaline media and showed enhanced activity compared to intact MoSe&lt;sub>2&lt;/sub> and WSe&lt;sub>2&lt;/sub>. Hybrids exhibited lower overpotential, easier reaction kinetics, higher conductivity, and excellent stability after 10,000 ongoing cycles in acidic and alkaline electrolytes compared to MoSe&lt;sub>2&lt;/sub> and WSe&lt;sub>2&lt;/sub>. Markedly, MoSe&lt;sub>2&lt;/sub>-based hybrid material showed the best performance and marked a significantly low onset potential of -0.17 V vs RHE for acidic hydrogen evolution reaction. All in all, the ease and fast modification route provides a versatile functionalization procedure, extendable to other transition metal dichalcogenides, and can open new pathways for the realization of functional nanomaterials suitable in electrocatalysis.</pubmed_abstract><journal>Nanomaterials (Basel, Switzerland)</journal><pubmed_title>Molybdenum Diselenide and Tungsten Diselenide Interfacing Cobalt-Porphyrin for Electrocatalytic Hydrogen Evolution in Alkaline and Acidic Media.</pubmed_title><pmcid>PMC9824367</pmcid><funding_grant_id>Grant number 823717</funding_grant_id><funding_grant_id>881603</funding_grant_id><funding_grant_id>823717</funding_grant_id><funding_grant_id>PID2019-104739GB-100/AEI/10.13039/501100011033</funding_grant_id><funding_grant_id>DGA E13-20R</funding_grant_id><pubmed_authors>Kagkoura A</pubmed_authors><pubmed_authors>Stangel C</pubmed_authors><pubmed_authors>Tagmatarchis N</pubmed_authors><pubmed_authors>Arenal R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molybdenum Diselenide and Tungsten Diselenide Interfacing Cobalt-Porphyrin for Electrocatalytic Hydrogen Evolution in Alkaline and Acidic Media.</name><description>Easy and effective modification approaches for transition metal dichalcogenides are highly desired in order to make them active toward electrocatalysis. In this manner, we report functionalized molybdenum diselenide (MoSe&lt;sub>2&lt;/sub>) and tungsten diselenide (WSe&lt;sub>2&lt;/sub>) via metal-ligand coordination with pyridine rings for the subsequent covalent grafting of a cobalt-porphyrin. The new hybrid materials were tested towards an electrocatalytic hydrogen evolution reaction in both acidic and alkaline media and showed enhanced activity compared to intact MoSe&lt;sub>2&lt;/sub> and WSe&lt;sub>2&lt;/sub>. Hybrids exhibited lower overpotential, easier reaction kinetics, higher conductivity, and excellent stability after 10,000 ongoing cycles in acidic and alkaline electrolytes compared to MoSe&lt;sub>2&lt;/sub> and WSe&lt;sub>2&lt;/sub>. Markedly, MoSe&lt;sub>2&lt;/sub>-based hybrid material showed the best performance and marked a significantly low onset potential of -0.17 V vs RHE for acidic hydrogen evolution reaction. All in all, the ease and fast modification route provides a versatile functionalization procedure, extendable to other transition metal dichalcogenides, and can open new pathways for the realization of functional nanomaterials suitable in electrocatalysis.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-08-17T03:05:59.854Z</modification><creation>2025-04-04T20:33:23.113Z</creation></dates><accession>S-EPMC9824367</accession><cross_references><pubmed>36615945</pubmed><doi>10.3390/nano13010035</doi></cross_references></HashMap>