Abstract
We idealise dendrite growth in a ceramic electrolyte by climb of a thick edge dislocation. Growth of the dendrite occurs at constant chemical potential of Li+ at the dendrite tip: the free-energy to fracture and wedge open the electrolyte is provided by the flux of Li+ from the electrolyte into the dendrite tip. This free-energy is dependent on the Li+ overpotential at the dendrite tip and is thereby related to the imposed charging current density. The predicted critical current density agrees with measurements for Li/LLZO/Li symmetric cells: the critical current density decreases with increasing initial length of the dendrite and with increasing electrode/electrolyte interfacial ionic resistance. The simulations also reveal that a void on the cathode/electrolyte interface locally enhances the Li+ overpotential and significantly reduces the critical current density for the initiation of dendrite growth.
Original language | English |
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Article number | 227989 |
Number of pages | 13 |
Journal | Journal of Power Sources |
Volume | 456 |
Early online date | 26 Mar 2020 |
DOIs | |
Publication status | Published - 30 Apr 2020 |
Keywords
- Ceramic electrolyte
- Free-energy
- Lithium dendrite
- Solid-state battery