Effects of partial halide anion substitution on reorientational motion in NaBH4: A nuclear magnetic resonance study

JOURNAL OF ALLOYS AND COMPOUNDS

卷:636

Article

Skoryunov, R. V.¹  Babanova, O. A.¹  Soloninin, A. V.¹  Skripov, A. V.¹  Verdal, N.^2,3  Udovic, T. J.² 

[1] Russian Acad Sci, Inst Met Phys, Ural Branch, Ekaterinburg 620990, Russia

[2] NIST, NIST Ctr Neutron Res, Gaithersburg, MD 20899 USA

[3] Univ Maryland, Dept Mat Sci & Engn, College Pk, MD 20742 USA

关键词: Energy storage materials;    Diffusion;    Nuclear resonances;   

DOI  :  10.1016/j.jallcom.2015.02.194

来源: Elsevier

【 摘 要 】

To study the effects of partial halide anion substitution on the reorientational motion of [BH4] anions in NaBH4, we have measured the H-1 and B-11 NMR spectra and spin-lattice relaxation rates in the cubic solid solutions Na(BH4)(0.5)Cl-0.5 and Na(BH4)(0.5)I-0.5 over broad ranges of temperature (8-324 K) and the resonance frequency (14-90 MHz). For both solid solutions, the measured H-1 spin-lattice relaxation rates are governed by reorientations of BH4 groups, and the experimental data can be satisfactorily described by the model with a Gaussian distribution of the activation energies. The average values of the activation energies derived from the H-1 spin-lattice relaxation data are 192 +/- 7 meV for Na(BH4)(0.5)Cl-0.5 and 120 +/- 3 meV for Na(BH4)0.5I0.5. At a given temperature, the reorientational jump rates are found to increase in the order of Na(BH4)(0.5)Cl-0.5-NaBH4-Na(BH4)(0.5)I-0.5, in agreement with the quasielastic neutron scattering (QENS) results. This trend correlates with the lattice expansion reflecting the increase in the size of the corresponding anions (in the order of Cl -[BH4] -I). (C) 2015 Elsevier B.V. All rights reserved.

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