RESUMEN
Cation doping is an effective strategy for improving the cyclability of layered oxide cathode materials through suppression of phase transitions in the high voltage region. In this study, Mg and Sc are chosen as dopants in P2-Na0.67Ni0.33Mn0.67O2, and both have found to positively impact the cycling stability, but influence the high voltage regime in different ways. Through a combination of synchrotron-based methods and theoretical calculations it is shown that it is more than just suppression of the P2 to O2 phase transition that is critical for promoting the favorable properties, and that the interplay between Ni and O activity is also a critical aspect that dictates the performance. With Mg doping, the Ni activity can be enhanced while simultaneously suppressing the O activity. This is surprising because it is in contrast to what has been reported in other Mn-based layered oxides where Mg is known to trigger oxygen redox. This contradiction is addressed by proposing a competing mechanism between Ni and Mg that impacts differences in O activity in Na0.67MgxNi0.33- xMn0.67O2 (x < 0 < 0.33). These findings provide a new direction in understanding the effects of cation doping on the electrochemical behavior of layered oxides.
RESUMEN
A new in situ magic angle spinning (MAS) 7Li nuclear magnetic resonance (NMR) strategy allowing for the observation of a full lithium-ion cell is introduced. Increased spectral resolution is achieved through a novel jelly roll cell design, which allowed these studies to be performed for the first time under MAS conditions (MAS rate 10 kHz). The state of charge, metallic lithium plating and solid-electrolyte interface (SEI) formation was captured for the first charge/discharge cycle of a full electrochemical cell (LiCoO2/graphite). This strategy can be used to monitor both anode and cathode electrodes concurrently, which is valuable for tracking the lithium distribution in a full cell in real time and may also enable identification of causes of capacity loss that are not readily available from bulk electrochemical analyses, or other post-mortem strategies.
