Comparison of anion and cation dynamics in a carbon-substituted closo-hydroborate salt: 1H and 23Na NMR studies of solid-solution Na2(CB9H10)(CB11H12)

被引:13
作者
Soloninin, A., V [1 ]
Skoryunov, R., V [1 ]
Babanova, O. A. [1 ]
Skripov, A., V [1 ]
Dimitrievska, M. [2 ,3 ]
Udovic, T. J. [2 ]
机构
[1] Russian Acad Sci, Inst Met Phys, Ural Branch, Ekaterinburg 620108, Russia
[2] NIST, NIST Ctr Neutron Res, Gaithersburg, MD 20899 USA
[3] Natl Renewable Energy Lab, Golden, CO 80401 USA
基金
俄罗斯基础研究基金会;
关键词
Energy storage materials; Diffusion; Nuclear resonances; NUCLEAR-MAGNETIC-RESONANCE; SODIUM SUPERIONIC CONDUCTION; HYDROGEN DIFFUSION; MOTION; NA; REORIENTATIONS; PHASE; METAL; ORTHOPHOSPHATE; ELECTROLYTES;
D O I
10.1016/j.jallcom.2019.06.019
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The hexagonal mixed-anion solid solution Na-2(CB9H10)(CB11H12) shows the highest room-temperature ionic conductivity among all known Na-ion conductors. To study the dynamical properties of this compound, we have measured the H-1 and Na-23 nuclear magnetic resonance (NMR) spectra and spinlattice relaxation rates in Na-2(CB9H10)(CB11H12) over the temperature range of 80-435 K. It is found that the diffusive motion of Na+ ions can be described in terms of two jump processes: the fast localized motion within the pairs of tetrahedral interstitial sites of the hexagonal close-packed lattice formed by large anions and the slower jump process via octahedral sites leading to long-range diffusion. Below 350 K, the slower Na+ jump process is characterized by the activation energy of 353(11) meV. Although Na+ mobility in Na-2(CB9H10)(CB11H12) found from our NMR experiments is higher than in other ionic conductors, it appears to be an order-of-magnitude lower than that expected on the basis of the conductivity measurements. This result suggests that the complex diffusion mechanism and/or correlations between Na+ jumps should be taken into account. The measured H-1 spin-lattice relaxation rates for Na-2(CB9H10)(CB11H12) are consistent with a coexistence of at least two anion reorientational jump processes occurring at different frequency scales. Near room temperature, both reorientational processes are found to be faster than the Na+ jump process responsible for the long-range diffusion. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:247 / 253
页数:7
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