Delineating the Effects of Transition-Metal-Ion Dissolution on Silicon Anodes in Lithium-Ion Batteries.
Rudy Martin TorresArumugam ManthiramPublished in: Small (Weinheim an der Bergstrasse, Germany) (2024)
Silicon anode is an appealing alternative to enhance the energy density of lithium-ion batteries due to its high capacity, but it suffers from severe capacity fade caused by its fast degradation. The crossover of dissolved transition-metal (TM) ions from the cathode to the anode is known to catalyze the decomposition of electrolyte on the graphite anode surface, but the relative impact of dissolved Mn 2+ versus Ni 2+ versus Co 2+ on silicon anode remains to be delineated. Since all three TM ions can dissolve from LiNi 1-x-y Mn x Co y O 2 (NMC) cathodes and migrate to the anode, here a LiFePO 4 cathode is paired with SiO x anode and assess the impact by introducing a specific amount of Mn 2+ or Ni 2+ or Co 2+ ions into the electrolyte. It is found that Mn 2+ ions cause a much larger increase in SiO x electrode thickness during cycling due to increased electrolyte decomposition and solid-electrolyte interphase (SEI) formation compared to Ni 2+ and Co 2+ ions, similar to previous findings with graphite anode. However, with a lower impedance, the SEI formed with Mn 2+ protects the Si anode from excessive degradation compared to that with Co 2+ or Ni 2+ ions. Thus, Mn 2+ ions have a less detrimental effect on Si anodes than Co 2+ or Ni 2+ ions, which is the opposite of that seen with graphite anodes.