Unveiling Oxygen Redox Activity in P2-Type Na<sub><i>x</i></sub>Ni<sub>0.25</sub>Mn<sub>0.68</sub>O<sub>2</sub> High-Energy Cathode for Na-Ion Batteries
Arianna Massaro, Ana B. Muñoz‐García, Pier Paolo Prosini, Claudio Gerbaldi, Michele Pavone
Abstract
Na-ion batteries are emerging as convenient energy-storage devices for large-scale applications. Enhanced energy density and cycling stability are key in the optimization of functional cathode materials such as P2-type layered transition metal oxides. High operating voltage can be achieved by enabling anionic reactions, but irreversibility of O2-/O2n-/O2 evolution still limits this chance, leading to extra capacity at first cycle that is not fully recovered. Here, we dissect this intriguing oxygen redox activity in Mn-deficient NaxNi0.25Mn0.68O2 from first-principles, by analyzing the formation of oxygen vacancies and dioxygen complexes at different stages of sodiation. We identify low-energy intermediates that release molecular O2 at high voltage, and we show how to improve the overall cathode stability by partial substitution of Ni with Fe. These new atomistic insights on O2 formation mechanism set solid scientific foundations for inhibition and control of this process toward the rational design of new anionic redox-active cathode materials.