<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Aljabour A</submitter><funding>Austrian Science Fund FWF</funding><pagination>e202302208</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10947295</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>62(21)</volume><pubmed_abstract>As alternative energy sources are essential to reach a climate-neutral economy, hydrogen peroxide (H&lt;sub>2&lt;/sub> O&lt;sub>2&lt;/sub> ) as futuristic energy carrier gains enormous awareness. However, seeking for stable and electrochemically selective H&lt;sub>2&lt;/sub> O&lt;sub>2&lt;/sub> ORR electrocatalyst is yet a challenge, making the design of-ideally-bifunctional catalysts extremely important and outmost of interest. In this study, we explore the application of a trimetallic cobalt(II) triazole pyridine bis-[cobalt(III) corrole] complex Co&lt;sup>II&lt;/sup> TP[Co&lt;sup>III&lt;/sup> C]&lt;sub>2&lt;/sub> 3 in OER and ORR catalysis due to its remarkable physicochemical properties, fast charge transfer kinetics, electrochemical reversibility, and durability. With nearly 100 % selective catalytic activity towards the two-electron transfer generated H&lt;sub>2&lt;/sub> O&lt;sub>2&lt;/sub> , an ORR onset potential of 0.8 V vs RHE and a cycling stability of 50 000 cycles are detected. Similarly, promising results are obtained when applied in OER catalysis. A relatively low overpotential at 10 mA cm&lt;sup>-2&lt;/sup> of 412 mV, Faraday efficiency 98 % for oxygen, an outstanding Tafel slope of 64 mV dec&lt;sup>-1&lt;/sup> combined with superior stability.</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pubmed_title>A Bifunctional Electrocatalyst for OER and ORR based on a Cobalt(II) Triazole Pyridine Bis-[Cobalt(III) Corrole] Complex.</pubmed_title><pmcid>PMC10947295</pmcid><funding_grant_id>P 32045</funding_grant_id><funding_grant_id>P28167</funding_grant_id><funding_grant_id>P32045</funding_grant_id><pubmed_authors>Song L</pubmed_authors><pubmed_authors>Scharber MC</pubmed_authors><pubmed_authors>Schofberger W</pubmed_authors><pubmed_authors>Aljabour A</pubmed_authors><pubmed_authors>Offenthaler S</pubmed_authors><pubmed_authors>Awada H</pubmed_authors><pubmed_authors>Sun H</pubmed_authors><pubmed_authors>Yari F</pubmed_authors><pubmed_authors>Bechmann M</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Bifunctional Electrocatalyst for OER and ORR based on a Cobalt(II) Triazole Pyridine Bis-[Cobalt(III) Corrole] Complex.</name><description>As alternative energy sources are essential to reach a climate-neutral economy, hydrogen peroxide (H&lt;sub>2&lt;/sub> O&lt;sub>2&lt;/sub> ) as futuristic energy carrier gains enormous awareness. However, seeking for stable and electrochemically selective H&lt;sub>2&lt;/sub> O&lt;sub>2&lt;/sub> ORR electrocatalyst is yet a challenge, making the design of-ideally-bifunctional catalysts extremely important and outmost of interest. In this study, we explore the application of a trimetallic cobalt(II) triazole pyridine bis-[cobalt(III) corrole] complex Co&lt;sup>II&lt;/sup> TP[Co&lt;sup>III&lt;/sup> C]&lt;sub>2&lt;/sub> 3 in OER and ORR catalysis due to its remarkable physicochemical properties, fast charge transfer kinetics, electrochemical reversibility, and durability. With nearly 100 % selective catalytic activity towards the two-electron transfer generated H&lt;sub>2&lt;/sub> O&lt;sub>2&lt;/sub> , an ORR onset potential of 0.8 V vs RHE and a cycling stability of 50 000 cycles are detected. Similarly, promising results are obtained when applied in OER catalysis. A relatively low overpotential at 10 mA cm&lt;sup>-2&lt;/sup> of 412 mV, Faraday efficiency 98 % for oxygen, an outstanding Tafel slope of 64 mV dec&lt;sup>-1&lt;/sup> combined with superior stability.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2025-04-20T02:50:22.333Z</modification><creation>2025-02-19T03:09:37.133Z</creation></dates><accession>S-EPMC10947295</accession><cross_references><pubmed>36821699</pubmed><doi>10.1002/anie.202302208</doi></cross_references></HashMap>