TY - CONF A1 - Böttcher, Nils T1 - Kick-off LiBaTra - WP4: Safety Tests N2 - Die BAM ist Projektpartner im vom BMWE geförderten Verbundvorhaben LiBaTra („Lithium-Ionen-Batterie Transport und sichere Deaktivierung für das Recycling“). Weitere Projektpartner neben der BAM sind die Universität Braunschweig mit dem iPAT (Institut für Partikeltechnik) sowie die Firmen Siemens Energy SE sowie No Canary. Die BAM bearbeitet das Teilvorhaben „Risikobestimmung tiefenentladener Energiespeicher“ (FKZ: 03EI6145A-D). Die Präsentation gibt die wesentlichen Arbeitsinhalte des Teilvorhabens der BAM wieder. T2 - Kick-off Meeting des Verbundvorhabens LiBaTra CY - Online meeting DA - 17.02.2026 KW - Auswirkungsbetrachtungen KW - Elektrische Energiespeicher KW - Lithium-Ionen-Batterie KW - Stationäre Energiespeicher KW - Thermisches Durchgehen PY - 2026 AN - OPUS4-65657 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Pedersen, Angus A1 - Zhu, Jinjie A1 - Barrio, Jesús A1 - Parker, Joseph A1 - Hunter, Robert D. A1 - Haigh, Sarah J. A1 - Fellinger, Tim-Patrick A1 - Stephens, Ifan E. L. A1 - Titirici, Maria-Magdalena T1 - Contribution of Mg-templated porosity to activity and durability in Fe–N–C O 2 reduction catalysts N2 - Atomically dispersed Fe in N-doped carbon (Fe–N–C) catalysts are leading platinum-group-metal-free candidates for the O2 reduction reaction in proton exchange membrane fuel cells (PEMFCs). Zeolitic imidazolate framework (ZIF-8) derived Fe–N–C present the most promising performance; however, they possess a narrow distribution of small micropores, which limits active site accessibility. Here, to induce hierarchical porosity in Fe–N–C, we report a systematic study on MgCl2·6H2O-templated ZIF-8-derived Fe–N–C catalysts for the O2 reduction reaction. MgCl2·6H2O addition induced complete Zn removal, collapse of the ZIF-8 framework, and formation of large micro- and mesopores, with graphene-like structures. N content was markedly reduced, with conversion from pyridinic to pyrrolic N species. Rotating disc electrode tests showed a progressive increase in O2 reduction activity with MgCl2·6H2O, which is strongly correlated (R2 = 0.98) to the formation of large micropores and small mesopores (1–4 nm). This introduces an indirect structure–activity design principle for Fe–N–Cs. The enhanced Fe–N–C porosity also leads to increased degradation rates under accelerated stress test conditions, which we attributed to the oxidation of disordered carbon domains and active Fe loss. This study highlights a key trade-off between porosity-driven O2 reduction activity and durability in Fe–N–C catalysts. KW - Porosity KW - Single atom KW - Oxygen reduction PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-657549 DO - https://doi.org/10.1039/d5ma01488c SN - 2633-5409 SP - 1 EP - 8 PB - Royal Society of Chemistry (RSC) AN - OPUS4-65754 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ibrahim, Ahmed A. S. A1 - Bochmann, Arne A1 - Löhnert, Romy A1 - Mieller, Björn A1 - Wilde, Lutz A1 - Capraro, Beate A1 - Stelter, Michael A1 - Töpfer, Jörg T1 - Performance Enhancement of Ca3Co4O9‐based Transverse Multilayer Thermoelectric Generators for Low‐Power Applications N2 - Transverse thermoelectric generators (TTEG) enable conversion of thermal into electrical energy with perpendicular directions of the applied temperature gradient and the induced thermoelectric voltage. We report on the fabrication of transverse multilayer thermoelectric generators (TMLTEG) based on p‐type Ca3Co4O9 (CCO) ceramic tapes and printed silver which were conventionally sintered (CS) in air at 920°C or using pressure‐assisted sintering (PAS) at 920°C and 1.5 MPa. The thermoelectric performance of TMLTEGs was evaluated using analytical calculations and simulations. The transverse thermoelectric power factor and thermoelectric figure‐of‐merit of an artificial layered structure composed of CCO and silver were calculated and simulated as functions of layers tilt angle φ and metal‐to‐ceramic thickness ratio. TMLTEG devices with various CCO layer thicknesses of 150 µm, 100 µm, or 33 µm were fabricated and cofired at 920°C in air, which exhibit power outputs of 2.3 mW, 3.2 mW, and 4.1 mW at ΔT = 160 K, respectively. TMLTEGs which were cofired using PAS show a higher power density of 16.4 mW/cm3 at ΔT = 225 K. This enhancement in power (≈ 80%) is crucial for thermoelectric modules comprising multiple TMLTEG devices. The device measurements were compared with 3D simulations. KW - Ceramic multilayer KW - Thermoelectric generator KW - Pressure-assisted sintering PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-657868 DO - https://doi.org/10.1111/jace.70656 SN - 0002-7820 VL - 109 IS - 3 SP - 1 EP - 13 PB - Wiley Periodicals LLC. AN - OPUS4-65786 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -