TY - JOUR A1 - Gong, Mengjun A1 - Mehmood, Asad A1 - de Oliveira Guilherme Buzanich, Ana A1 - Fellinger, Tim-Patrick A1 - Jackson, Colleen A1 - Cui, Junyi A1 - Drazic, Goran A1 - Kucernak, Anthony T1 - Designing Co–N/C Cathode Catalysts with Dense Atomic Cobalt Sites for Enhanced PEMFC Performance N2 - Metal-nitrogen/carbon (M-N/C) catalysts, particularly those incorporating Fe,Co, or Mn, are among the most promising non-platinum group catalysts forthe acidic oxygen reduction reaction (ORR) in fuel cells. This study reports aCo-N/C catalyst featuring high (3 wt%) cobalt content exclusively present asatomic sites. Extended X-ray absorption fine structure analysis confirms atetrapyridinic Co-N4 coordination environment in the optimized (3.0)Co-N/C𝚫catalyst. The high cobalt loading leads to a significant density ofelectrochemically accessible active sites, 3.58 × 10 19 sites g−1 , quantified viathe nitrite stripping method. The catalyst demonstrates excellent ORR activityin a rotating ring-disk electrode setup, achieving a half-wave potential (E 1/2 ) of0.76 V at a low loading of 0.2 mg cm−2 and a mass activity of 3.5 A g−1 at 0.80VRHE . Single-cell hydrogen-oxygen PEMFC tests achieve a peak power densityexceeding 1.3 W cm−2 (iR-corrected). Under hydrogen-air condition, thecatalyst delivers 0.54 A cm−2 at 0.60 V (0.39 W cm−2 ). Despite the intrinsicallyhigher turnover frequency of Fe-based sites, the optimized(3.0)Co-N/C𝚫 catalyst achieves similar fuel cell performance to that of Fe-N/C,highlighting the critical role of site density in overall activity. KW - Fuel cells KW - Single atom catalysts KW - Oxygen reduction reaction KW - Non-precious catalysts PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-644276 DO - https://doi.org/10.1002/advs.202516060 SN - 2198-3844 SP - 1 EP - 11 PB - Wiley VHC-Verlag AN - OPUS4-64427 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Menga, D. A1 - Wagner, F. E. A1 - Fellinger, Tim-Patrick T1 - Life cycle of single atom catalysts: a Mössbauer study on degradation and reactivation of tetrapyrrolic Fe–N–C powders N2 - The degradation of a single-site atomically dispersed, model Fe–N–C powder catalyst with high activity is investigated using cryo-Mössbauer spectroscopy. The results indicate a degradation initiated by an Fe2+ to Fe3+ oxidation due to coordination of oxygen to tetrapyrrolic Fe–N4 sites at atmospheric conditions (change between characteristic doublets) before iron(III) oxide is formed (sextet). Thermal reactivation can be used to restore substantial catalytic activity of aged Fe–N–C powders. KW - Single atom catalysts KW - Mössbauer study KW - Tetrapyrrolic Fe–N–C powders PY - 2023 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-589352 DO - https://doi.org/10.1039/d3mh00308f VL - 10 SP - 5577 EP - 5583 PB - Royal Society of Chemistry AN - OPUS4-58935 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Mehmood, Asad A1 - Fellinger, Tim-Patrick T1 - Porous Carbon Supported Ni and Co Single Atom Catalysts for Electrochemical Reduction of Carbon Dioxide N2 - Non-precious metal single atom catalysts (generally labelled as M/NCs where M= Co, Fe, Ni etc.) consist of active metal centres dispersed on nitrogen doped porous carbon (NC) matrix at atomic level and exhibit promising activities e. g. for electrochemical reduction of CO2, selectively forming CO. We herein use identical Mg/NCs as platform for ion-exchange reactions towards morphologically equivalent Ni/NCs and Co/NCs. The Ni/NC catalyst shows almost double the specific activity and a Faraday efficiency of >80% at a very low overpotential of U= -0.43 V (even 95% at U= -0.5 to -0.8 V) with high stability. T2 - GDCh Electrochemistry 2022 CY - Berlin, Germany DA - 27.09.2022 KW - Electrochemical CO2 conversion KW - Single atom catalysts KW - Porous Carbons PY - 2022 AN - OPUS4-61980 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -