Meaning
Chemical dissolution of transition metal ions from the cathode material into the electrolyte, followed by their transport to the anode. This process damages the protective anode surface layer and causes rapid capacity loss. Minimizing transition metal leaching is essential to maintain the electrochemical stability of high-nickel and high-voltage lithium-ion cells.
Cathode Dissolution
High operating voltages and acid attack are the main drivers of metal extraction from the cathode lattice. During cycling, trace moisture reacts with the lithium salt to form hydrofluoric acid, which attacks the oxide surfaces. This chemical reaction leads to transition metal leaching of manganese, cobalt, and nickel ions into the electrolyte solvent.
The loss of these structural metals degrades the active cathode crystal structure, reducing its capacity to store lithium.
Anode Damage
The dissolved metal ions migrate through the separator and reach the graphite anode. Once there, they deposit on the anode surface, disrupting the solid electrolyte interphase layer and acting as catalysts for continuous electrolyte decomposition. This destruction of the passivation layer accelerates active lithium consumption and self-discharge because the cell must continuously rebuild the protective layer.
The resulting degradation from transition metal leaching is a major contributor to long-term impedance rise.
Mitigation Strategy
Cathode material suppliers apply protective surface coatings, such as metal oxides or fluorides, to shield the active material from the acid. Additionally, the use of electrolyte additives that scavenge acid or stabilize the electrode-electrolyte interface reduces the rate of metal dissolution. Specifying cells that incorporate these advanced mitigation technologies ensures longer cycle life and lower self-discharge rates in commercial applications.