Affiliation:
1. Environmental Molecular Sciences Laboratory Pacific Northwest National Laboratory 902 Battelle Boulevard Richland WA 99354 USA
2. Chemical Sciences and Engineering Division Argonne National Laboratory 9700 South Cass Avenue Lemont IL 60439 USA
Abstract
AbstractSpinel‐structured LiNixMn2−xO4(LNMO), with low‐cost earth‐abundant constituents, is a promising high‐voltage cathode material for lithium‐ion batteries. Even though extensive electrochemical investigations have been conducted on these materials, few studies have explored correlations between their loss in performance and associated changes in microstructure. Here, down to the atomic scale, the structural evolution of these materials is investigated upon the progressive cycling of lithium‐ion cells. Transgranular cracking is revealed to be a key feature during cycling; this cracking is initiated at the particle surface and leads to the penetration of electrolytes along the crack path, thereby increasing particle exposure to the electrolyte. The lattice structure on the crack surface shows spatial variances, featuring a top layer of rock‐salt, a sublayer of a Mn3O4‐like arrangement, and then a mixed‐cation region adjacent to the bulk lattice. The transgranular cracking, along with the emergence of local lattice distortion, becomes more evident with extended cycling. Further, phase transformation at primary particle surfaces and void formation through vacancy condensation is found in the cycled samples. All these features collectively contribute to the performance degradation of the battery cells during electrochemical cycling.
Funder
Office of Energy Efficiency and Renewable Energy
Subject
Biomaterials,Biotechnology,General Materials Science,General Chemistry
Cited by
3 articles.
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