Na2 B10 H10 exhibits exceptional superionic conductivity above ca. 360 K (e.g., ca. 0.01 S cm(-1) at 383 K) concomitant with its transition from an ordered monoclinic structure to a face-centered-cubic arrangement of orientationally disordered B10 H10 (2-) anions harboring a vacancy-rich Na(+) cation sublattice. This discovery represents a major advancement for solid-state Na(+) fast-ion conduction at technologically relevant device temperatures.
Both LiCB9H10 and NaCB9H10 exhibit liquid‐like cationic conductivities (≥0.03 S cm−1) in their disordered hexagonal phases near or at room temperature. These unprecedented conductivities and favorable stabilities enabled by the large pseudoaromatic polyhedral anions render these materials in their pristine or further modified forms as promising solid electrolytes in next‐generation, power devices.
Solid
lithium and sodium closo-polyborate-based
salts are capable of superionic conductivities surpassing even liquid
electrolytes, but often only at above-ambient temperatures where their
entropically driven disordered phases become stabilized. Here we show
by X-ray diffraction, quasielastic neutron scattering, differential
scanning calorimetry, NMR, and AC impedance measurements that by introducing
“geometric frustration” via the mixing of two different closo-polyborate anions, namely, 1-CB9H10
– and CB11H12
–, to form solid-solution anion-alloy salts of lithium or sodium,
we can successfully suppress the formation of possible ordered phases
in favor of disordered, fast-ion-conducting alloy phases over a broad
temperature range from subambient to high temperatures. This result
exemplifies an important advancement for further improving on the
remarkable conductive properties generally displayed by this class
of materials and represents a practical strategy for creating tailored,
ambient-temperature, solid, superionic conductors for a variety of
upcoming all-solid-state energy devices of the future.
To
study the reorientational motion of icosahedral [B12H12]2– anions in A2B12H12 (A = Na, K, Rb, Cs) and the translational diffusion
of Na+ cations in Na2B12H12, we have measured the 1H, 11B, and 23Na NMR spectra and spin–lattice relaxation rates in these
compounds over the temperature range of 170–580 K. For cubic
compounds K2B12H12, Rb2B12H12, and Cs2B12H12, the measured 1H and 11B spin–lattice
relaxation rates are governed by thermally activated reorientations
of the [B12H12]2– anions.
The activation energy of this reorientational motion is found to decrease
with increasing cation radius, changing from 800 meV for K2B12H12 to 549 meV for Rb2B12H12 and 427 meV for Cs2B12H12. For Na2B12H12, the first-order
transition from the low-temperature monoclinic to the high-temperature
cubic phase near 520 K is accompanied by a 2 orders of magnitude increase
in the reorientational jump rate, and the corresponding activation
energy changes from 770 meV for the low-T phase to
270 meV for the high-T phase. Measurements of the 23Na NMR spectra and spin–lattice relaxation rates show
that the transition from the low-T to the high-T phase of Na2B12H12 is
also accompanied by the onset of the fast translational diffusion
of Na+ ions. Just above the transition point, the lower
limit of the Na+ jump rate estimated from the 23Na spin–lattice relaxation data is 2 × 108 s–1, and the corresponding activation energy for
Na+ diffusion is about 410 meV.
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