Origin of multiple voltage plateaus in P2-type sodium layered oxides.

Although layered transition metal (TM) oxides have attracted considerable attention for cathode materials of sodium-ion batteries, they suffer from uncontrolled multiple voltage plateaus due to local structure transformations such as TM-layer gliding and Na + /vacancy ordering upon Na + extraction and insertion. However, the intrinsic origins of these local structure transformations are not fully understood, preventing the rational design of better cathode materials. Here, we concentrate on Na + /vacancy ordering in single phase domains to reveal the underlying mechanism of multiple voltage plateaus by tracking desodiation-induced electronic structure evolutions of two typical compounds, P2-Na 0.6 [Cr 0.6 Ti 0.4 ]O 2 and P2-NaCrO 2 . During desodiation, P2-NaCrO 2 generates obvious multiple voltage plateaus, which are not observed in P2-Na 0.6 [Cr 0.6 Ti 0.4 ]O 2 due to TM disordering. A combination of first-principles desodiation calculations and electronic structure analysis reveals that charge localization accompanied by Na + migration is an intrinsic feature of multiple voltage plateaus in P2-NaCrO 2 . A correlation between charge localization and multiple voltage plateaus is established by a comparative study in which P2-Na 0.6 [Cr 0.6 Ti 0.4 ]O 2 always follows the charge transfer order from high-activity to low-activity sites. This finding reveals that disordering design of active sites to avoid charge localization in redox is of much importance for developing high-performance Na-ion cathode materials.