TY - GEN A1 - Ahrendt, H. A1 - Gesatzke, Roger A1 - Hahn, G. A1 - Herrmann, P. A1 - Julien, H. A1 - Karger, R. A1 - Kaufmann, M. A1 - Krebs, H.-J. A1 - Lucht, J. A1 - Müller, A. A1 - Müller, R. A1 - Vetter, B. T1 - Überdruckmessgeräte nach DIN EN 837 - Auswahl und Anwendung KW - Druckmessgerät KW - Sicherheit PY - 2007 SN - 978-3-410-16626-9 IS - 1. Auflage SP - 1 EP - 89 PB - Beuth CY - Berlin AN - OPUS4-15994 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schönhals, Andreas A1 - Rittig, F. A1 - Kärger, J. T1 - Self-diffusion of poly(propylene glycol) in nanoporous glasses studied by pulsed field gradient NMR: A study of molecular dynamics and surface interactions N2 - Pulsed field gradient NMR is applied to investigate the self-diffusion of poly(proypylene glycol) in nanoporous glasses (nominal pore sizes of 2.5–7.5 nm). In general, the diffusion is slowed down by the confinement compared to the bulk. For native pore surfaces covered by hydroxyl groups the spin echo attenuation Ψ displays a bimodal behavior versus q2t (q-norm of a generalized scattering vector). This was explained assuming spatial regions of different diffusivities in a two-phase model. The slow component is assigned to segments forming a surface layer close to the pore walls in which the segments have a lower mobility than those located in the center of the pores. By variation of observation time it was concluded that time constant for the dynamic exchange of segments between these two regions is around 100 ms at room temperature. For silanized pores, the bimodal behavior in the spin echo attenuation Ψ shows a stretched exponential decay versus q2t. The estimated diffusion coefficients decrease strongly with decreasing pore size. The temperature dependence of the diffusion coefficient can be approximated by an Arrhenius law where the activation energy increases with decreasing pore size. The observed pore size dependence for the diffusion of poly(propylene glycol) in silanized nanoporous glasses can be discussed assuming interaction and confining size effects. KW - Glass KW - Molecular dynamics method KW - Nanoporous materials KW - Polymers KW - Self-diffusion KW - Spin echo (NMR) PY - 2010 DO - https://doi.org/10.1063/1.3479905 SN - 0021-9606 SN - 1089-7690 VL - 133 IS - 9 SP - 094903-1 - 094903-7 PB - American Institute of Physics CY - Melville, NY AN - OPUS4-22000 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Pallasch, Sebastian M. A1 - Bhosale, Manik A1 - Smales, Glen J. A1 - Schmidt, Caroline A1 - Riedel, Sibylle A1 - Zhao-Karger, Zhirong A1 - Esser, Birgit A1 - Dumele, Oliver T1 - Porous Azatruxene Covalent Organic Frameworks for Anion Insertion in Battery Cells N2 - Covalent organic frameworks (COFs) containing well-defined redox-active groups have become competitive materials for next-generation batteries. Although high potentials and rate performance can be expected, only a few examples of p-type COFs have been reported for charge storage to date with even fewer examples on the use of COFs in multivalent ion batteries. Herein, we report the synthesis of a p-type highly porous and crystalline azatruxene-based COF and its application as a positive electrode material in Li- and Mg-based batteries. When this material is used in Li-based half cells as a COF/carbon nanotube (CNT) electrode, a discharge potential of 3.9 V is obtained with discharge capacities of up to 70 mAh g−1 at a 2 C rate. In Mg batteries using a tetrakis(hexafluoroisopropyloxy)borate electrolyte, cycling proceeds with an averge discharge voltage of 2.9 V. Even at a fast current rate of 5 C, the capacity retention amounts to 84% over 1000 cycles. KW - COFs PY - 2024 DO - https://doi.org/10.1021/jacs.4c04044 VL - 146 IS - 25 SP - 17318 EP - 17324 PB - Journal of the American Chemical Society AN - OPUS4-60419 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -