Torres Rudy Martin, Manthiram Arumugam
Materials Science & Engineering Program and Texas Materials Institute, The University of Texas at Austin, Austin, TX, 78721, USA.
Small. 2024 Jul;20(27):e2309350. doi: 10.1002/smll.202309350. Epub 2024 Jan 29.
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 versus Ni versus Co on silicon anode remains to be delineated. Since all three TM ions can dissolve from LiNiMnCoO (NMC) cathodes and migrate to the anode, here a LiFePO cathode is paired with SiO anode and assess the impact by introducing a specific amount of Mn or Ni or Co ions into the electrolyte. It is found that Mn ions cause a much larger increase in SiO electrode thickness during cycling due to increased electrolyte decomposition and solid-electrolyte interphase (SEI) formation compared to Ni and Co ions, similar to previous findings with graphite anode. However, with a lower impedance, the SEI formed with Mn protects the Si anode from excessive degradation compared to that with Co or Ni ions. Thus, Mn ions have a less detrimental effect on Si anodes than Co or Ni ions, which is the opposite of that seen with graphite anodes.
硅阳极因其高容量而成为提高锂离子电池能量密度的一种有吸引力的替代方案,但它因快速降解而遭受严重的容量衰减。已知溶解的过渡金属(TM)离子从阴极交叉到阳极会催化石墨阳极表面电解质的分解,但溶解的锰、镍和钴对硅阳极的相对影响仍有待确定。由于所有这三种TM离子都可以从LiNiMnCoO(NMC)阴极溶解并迁移到阳极,因此在这里将LiFePO阴极与SiO阳极配对,并通过向电解质中引入特定量的锰、镍或钴离子来评估其影响。研究发现,与镍和钴离子相比,由于电解质分解增加和固体电解质界面(SEI)形成,锰离子在循环过程中会导致SiO电极厚度大幅增加,这与之前石墨阳极的研究结果类似。然而,与钴或镍离子形成的SEI相比,锰形成的SEI具有更低的阻抗,从而保护硅阳极免受过度降解。因此,锰离子对硅阳极的有害影响小于钴或镍离子,这与石墨阳极的情况相反。