Journal
MATERIALS
Volume 13, Issue 19, Pages -Publisher
MDPI
DOI: 10.3390/ma13194388
Keywords
lithium-ion batteries; Li; and Mn-rich materials; Li2MnO3 activation at 0 ° C; stabilized cycling; decreased the voltage hysteresis; layered-to-spinel transition; bulk and surface characteristics
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Funding
- U.S. National Science Foundation [DMR-1911592]
- Synchrotron Catalysis Consortium (U.S. DOE, Office of Basic Energy Sciences) [DE-SC0012335]
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This work continues our systematic study of Li- and Mn- rich cathodes for lithium-ion batteries. We chose Li2MnO3 as a model electrode material with the aim of correlating the improved electrochemical characteristics of these cathodes initially activated at 0 degrees C with the structural evolution of Li2MnO3, oxygen loss, formation of per-oxo like species (O-2(2-)) and the surface chemistry. It was established that performing a few initial charge/discharge (activation) cycles of Li2MnO3 at 0 degrees C resulted in increased discharge capacity and higher capacity retention, and decreased and substantially stabilized the voltage hysteresis upon subsequent cycling at 30 degrees C or at 45 degrees C. In contrast to the activation of Li2MnO3 at these higher temperatures, Li2MnO3 underwent step-by-step activation at 0 degrees C, providing a stepwise traversing of the voltage plateau at >4.5 V during initial cycling. Importantly, these findings agree well with our previous studies on the activation at 0 degrees C of 0.35Li(2)MnO(3)center dot 0.65Li[Mn0.45Ni0.35Co0.20]O-2 materials. The stability of the interface developed at 0 degrees C can be ascribed to the reduced interactions of the per-oxo-like species formed and the oxygen released from Li2MnO3 with solvents in ethylene carbonate-methyl-ethyl carbonate/LiPF6 solutions. Our TEM studies revealed that typically, upon initial cycling both at 0 degrees C and 30 degrees C, Li2MnO3 underwent partial structural layered-to-spinel (Li2Mn2O4) transition.
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