Ionic conductivity of molten alkali-metal carbonates A2CO3 (A = Li, Na, K, Rb, and Cs) and binary mixtures (Li1−xCsx)2CO3 and (Li1−xKx)2CO3: A molecular dynamics simulation

Based on experimental data, we optimized the potential parameters for the classical molecular dynamics simulation to reproduce the volume and ionic conductivity of the molten alkali-metal carbonates A2CO3 where A = Li, Na, K, Rb, and Cs at T/K = 1223 and ambient pressure. The force field was then ap...

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Veröffentlicht in:The Journal of chemical physics 2019-08, Vol.151 (7), p.074503-074503
Hauptverfasser: Kiyobayashi, Tetsu, Kojima, Toshikatsu, Ozaki, Hiroyuki, Kiyohara, Kenji
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Sprache:eng
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Zusammenfassung:Based on experimental data, we optimized the potential parameters for the classical molecular dynamics simulation to reproduce the volume and ionic conductivity of the molten alkali-metal carbonates A2CO3 where A = Li, Na, K, Rb, and Cs at T/K = 1223 and ambient pressure. The force field was then applied to the binary mixtures (Li1−xCsx)2CO3 and (Li1−xKx)2CO3. In (Li1−xCsx)2CO3, the diffusion coefficient DCs exceeds DLi at x > 0.6, testifying to the Chemla effect. The net ionic conductivity was broken down into the contributions from the velocity auto- and cross-correlations of each ionic species. The significant negative deviation of the real conductivity of (Li1−xCsx)2CO3 from the one estimated by the Nernst-Einstein (NE) relation is clearly explained by the contribution from the cross correlations; specifically, the cross term between Li+and CO32−, which is negative at x = 0, significantly shifts to the positive side when x increases, which is dominantly responsible for dampening the conductivity from the NE conductivity. A similar behavior was observed in (Li1−xKx)2CO3 with a less pronounced manner than in (Li1−xCsx)2CO3. These observations corroborate the precedent studies pointing to the trapping of Li+ by the anion when a lithium salt is mixed with another salt of which the cation size is greater than that of Li+.
ISSN:0021-9606
1089-7690
DOI:10.1063/1.5109912