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Direct Experimental Observation of In Situ Dehydrogenation of an Amine-Borane System Using Gas Electron Diffraction

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Published copy (DOI)

Author(s)

  • Aliyu Mohammad Ja'o
  • Sarah L Masters
  • Derek Alan A Wann
  • Conor D Rankine
  • João Pedro Figueira Nunes
  • Jean-Claude Guillemin

Department/unit(s)

Publication details

JournalJournal of Physical Chemistry A
DateAccepted/In press - 17 Jul 2019
DateE-pub ahead of print (current) - 17 Jul 2019
Number of pages9
Early online date17/07/19
Original languageEnglish

Abstract

In situ dehydrogenation of azetidine-BH3, which is a candidate for hydrogen storage, was observed with the parent and dehydrogenated ana-logue subjected to rigorous structural and thermochemical investigations. The structural analyses utilized gas electron diffraction supported by high-level quantum calculations, whilst the pathway for the unimolecular hydrogen release reaction in the absence and presence of BH3 as a bi-functional catalyst was predicted at CBS-QB3 level. The catalyzed dehydrogenation pathway has a barrier lower than the predicted B-N bond dissociation energy, hence favoring the dehydrogenation process over the dissociation of the complex. The predicted enthalpy of dehydrogenation at CCSD(T)/CBS level indicates mild reaction conditions would be required for the hydrogen release and that the compound is closer to thermoneutral than the linear amine boranes. The entropy and free energy change for the dehydrogenation process show that the reaction is exergonic, energetically feasible and will proceed spontaneously towards hydrogen release; all important factors for hydrogen storage.

Bibliographical note

© 2019 American Chemical Society. This is an author-produced version of the published paper. Uploaded in accordance with the publisher’s self-archiving policy. Further copying may not be permitted; contact the publisher for details.

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