TY - JOUR
T1 - Modeling of Electron-Transfer Kinetics in Magnesium Electrolytes: Influence of the Solvent on the Battery Performance
AU - Drews, Janina
AU - Jankowski, Piotr
AU - Häcker, Joachim
AU - Li, Zhenyou
AU - Danner, Timo
AU - Lastra, Juan Maria García
AU - Vegge, Tejs
AU - Wagner, Norbert
AU - Friedrich, K. Andreas
AU - Zhao-Karger, Zhirong
AU - Fichtner, Maximilian
AU - Latz, Arnulf
PY - 2021
Y1 - 2021
N2 - The performance of rechargeable magnesium batteries is strongly dependent on the choice of electrolyte. The desolvation of multivalent cations usually goes along with high energy barriers, which can have a crucial impact on the plating reaction. This can lead to significantly higher overpotentials for magnesium deposition compared to magnesium dissolution. In this work we combine experimental measurements with DFT calculations and continuum modelling to analyze Mg deposition in various solvents. Jointly, these methods provide a better understanding of the electrode reactions and especially the magnesium deposition mechanism. Thereby, a kinetic model for electrochemical reactions at metal electrodes is developed, which explicitly couples desolvation to electron transfer and, furthermore, qualitatively takes into account effects of the electrochemical double layer. The influence of different solvents on the battery performance is studied for the state-of-the-art Mg[B(hfip)4]2 salt. It becomes apparent that not necessarily a whole solvent molecule must be stripped from the solvated Mg2+ cation before the first reduction step can take place. It seems to be sufficient to have one coordination site available, so that the Mg2+ cation is able to get closer to the electrode surface. Thereby, the initial desolvation determines the deposition reaction for mono-, tri- and tetraglyme, whereas the influence of the desolvation on the plating reaction is minor for diglyme and THF. Overall, we can give a clear recommendation for diglyme to be applied as solvent in magnesium electrolytes.
AB - The performance of rechargeable magnesium batteries is strongly dependent on the choice of electrolyte. The desolvation of multivalent cations usually goes along with high energy barriers, which can have a crucial impact on the plating reaction. This can lead to significantly higher overpotentials for magnesium deposition compared to magnesium dissolution. In this work we combine experimental measurements with DFT calculations and continuum modelling to analyze Mg deposition in various solvents. Jointly, these methods provide a better understanding of the electrode reactions and especially the magnesium deposition mechanism. Thereby, a kinetic model for electrochemical reactions at metal electrodes is developed, which explicitly couples desolvation to electron transfer and, furthermore, qualitatively takes into account effects of the electrochemical double layer. The influence of different solvents on the battery performance is studied for the state-of-the-art Mg[B(hfip)4]2 salt. It becomes apparent that not necessarily a whole solvent molecule must be stripped from the solvated Mg2+ cation before the first reduction step can take place. It seems to be sufficient to have one coordination site available, so that the Mg2+ cation is able to get closer to the electrode surface. Thereby, the initial desolvation determines the deposition reaction for mono-, tri- and tetraglyme, whereas the influence of the desolvation on the plating reaction is minor for diglyme and THF. Overall, we can give a clear recommendation for diglyme to be applied as solvent in magnesium electrolytes.
KW - Computational chemistry
KW - Deposition mechanism
KW - Desolvation
KW - Kinetics
KW - Rechargable magnesium batteries
U2 - 10.1002/cssc.202101498
DO - 10.1002/cssc.202101498
M3 - Journal article
C2 - 34459116
VL - 14
SP - 4820
EP - 4835
JO - ChemSusChem (Print)
JF - ChemSusChem (Print)
SN - 1864-5631
IS - 21
ER -