• Medientyp: E-Artikel
  • Titel: An organic proton cage that is ultra-resistant to hydroxide-promoted degradation
  • Beteiligte: Radford, Chase L.; Saatkamp, Torben; Bennet, Andrew J.; Holdcroft, Steven
  • Erschienen: Springer Science and Business Media LLC, 2024
  • Erschienen in: Nature Communications, 15 (2024) 1
  • Sprache: Englisch
  • DOI: 10.1038/s41467-024-47809-0
  • ISSN: 2041-1723
  • Entstehung:
  • Anmerkungen:
  • Beschreibung: <jats:title>Abstract</jats:title><jats:p>Alkaline polymer membrane electrochemical energy conversion devices offer the prospect of using non-platinum group catalysts. However, their cationic functionalities are currently not sufficiently stable for vapor-phase applications, such as fuel cells. Herein, we report 1,6-diazabicyclo[4.4.4]tetradecan-1,6-ium (in-DBD), a cationic proton cage, that is orders of magnitude more resistant to hydroxide-promoted degradation than state-of-the-art organic cations under ultra-dry conditions and elevated temperature, and the first organic cation-hydroxide to persist at critically low hydration levels ( &lt; 10% RH at 80 °C). This high stability against hydroxide-promoted degradation is due to the unique combination of endohedral protection and intra-bridgehead hydrogen bonding that prevents the removal of the inter-cavity proton and lowers the susceptibility to Hofmann elimination. We anticipate this discovery will facilitate a step-change in the advancement of materials and electrochemical devices utilizing anion-exchange membranes based on in-DBD that will enable stable operation under extreme alkaline conditions.</jats:p>
  • Zugangsstatus: Freier Zugang