Cation disorder dominates the defect chemistry of high-voltage LiMn_1.5Ni_0.5O₄ (LMNO) spinel cathodes

High-voltage spinel LiMn1.5Ni0.5O4 (LMNO) can exist in a Mn/Ni ordered P4(3)32 or disordered Fd3m arrangement with a majority of literature studies reporting improved electrochemical performance for the disordered phase. Through modifying synthesis conditions, the Mn/Ni ordering can be tuned, however oxygen and Mn3+ stoichiometries are also affected, making it difficult to decouple these responses and optimise performance. Here, we investigate all intrinsic defects in P4(3)32 LMNO under various growth conditions, using density functional theory (DFT) calculations. We find that the majority of defects are deep and associated with small polarons (Mn3+, Mn2+ and Ni3+) formation. The tendency for cation disorder can be explained by the low formation energy of the antisite defects and their stoichiometric complexes. The intrinsic Fermi level of LMNO varies from moderately n-type under oxygen-poor conditions to weakly p-type under oxygen-rich conditions. Our work explains experimental observations (e.g. the Mn/Ni disorder) and provides guidelines for defect-controlled synthesis.