Low-Temperature Rotational Tunneling of Tetrahydroborate Anions in Lithium Benzimidazolate-Borohydride Li2(bIm)BH4

Skripov, A.V.;Dimitrievska, M.;Babanova, O.A.;Skoryunov, R.V.;Udovic, T.J.;et.al.
(2019) Journal of Physical Chemistry C — Vol. 123, n° 34, p. 20789-20799 (2019)

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Authors
  • Skripov, A.V.
    Author
  • Dimitrievska, M.
    Author
  • Babanova, O.A.
    Author
  • Skoryunov, R.V.
    Author
  • Morelle, F.UCLouvain
    Author
  • Author
  • Udovic, T.J.
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Abstract
To investigate the dynamical properties of the novel hybrid compound, lithium benzimidazolate-borohydride Li2(bIm)BH4 (where bIm denotes a benzimidazolate anion, C7N2H5 -), we have used a set of complementary techniques: neutron powder diffraction, ab initio density functional theory calculations, neutron vibrational spectroscopy, nuclear magnetic resonance, neutron spin echo, and quasi-elastic neutron scattering. Our measurements performed over the temperature range from 1.5 to 385 K have revealed the exceptionally fast low-temperature reorientational motion of BH4 - anions. This motion is facilitated by the unusual coordination of tetrahedral BH4 - anions in Li2(bIm)BH4: each anion has one of its H atoms anchored within a nearly square hollow formed by four coplanar Li+ cations, while the remaining -BH3 fragment extends into a relatively open space, being only loosely coordinated to other atoms. As a result, the energy barriers for reorientations of this fragment around the anchored B-H bond axis are very small, and at low temperatures, this motion can be described as rotational tunneling. The tunnel splitting derived from the neutron spin echo measurements at 3.6 K is 0.43(2) μeV. With increasing temperature, we have observed a gradual transition from the regime of low-temperature quantum dynamics to the regime of classical thermally activated jump reorientations. The jump rate of the uniaxial 3-fold reorientations reaches 5 × 1011 s-1 at 80 K. Nearer room temperature and above, both nuclear magnetic resonance and quasi-elastic neutron scattering measurements have revealed the second process of BH4 - reorientations characterized by the activation energy of 261 meV. This process is several orders of magnitude slower than the uniaxial 3-fold reorientations; the corresponding jump rate reaches ∼7 × 108 s-1 at 300 K. © 2019 American Chemical Society.
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Skripov, A. V., Dimitrievska, M., Babanova, O. A., Skoryunov, R. V., Soloninin, A. V., Morelle, F., Filinchuk, Y., Faraone, A., Wu, H., Zhou, W., & Udovic, T. J. (2019). Low-Temperature Rotational Tunneling of Tetrahydroborate Anions in Lithium Benzimidazolate-Borohydride Li2(bIm)BH4. Journal of Physical Chemistry C, 123(34), 20789-20799. https://doi.org/10.1021/acs.jpcc.9b06083 (Original work published 2019)