Utilizing the Mn(II) Dissolution‐Induced Vacancy for Optimum Mg 2+ Storage of Spinel Mn 3 O 4

Abstract Manganese‐based oxide can theoretically exert the multivalent advantages of an aqueous magnesium‐ion cathode due to its redox activity and abundant crystal structure. However, sluggish diffusion kinetics of Mg 2+ and Mn dissolution limit the rate performance and structure stability. Herein, we successfully utilize the notorious dissolution of Mn(II) tetrahedral site contributed vacancies for packaging optimum Mg 2+ storage of a popular spinel Mn 3 O 4 electrode. Such mechanism reverses the sluggish diffusion kinetics. Moreover, merited by the common ion effect and drug dissolution, a suitable preaddition of Mn 2+ to electrolyte inhibit Mn(III) dissolution and optimize the integrity of the spinel framework. Impressively, the cathode achieves a reversible capacity of 310 mAh g −1 and a stable cycle performance of 2000 cycles with 94.9% retention. Our research shows that reversible insertion/extraction at vacancies and effective stabilization of spinel framework is a powerful strategy to achieve Mg 2+ ion energy storage system with high rate performance and long lifespan.