Abstract
Summary Transition metal oxide catalysts with high oxygen reduction activity and durability are highly desirable for use in fuel cells and metal-air batteries. Herein we report, for the first time, the oxygen reduction activity of hollow porous spinel AB 2 O 4 microspheres, where A = Zn 2+ and B = Mn 3+ and/or Co 3+ (i.e., ZnMn x Co 2−x O 4 ). Among them, ZnMnCoO 4 ( x = 1) microspheres exhibit the best oxygen reduction activity with a half-wave-potential only 50 mV lower than that of the Pt/C counterpart and an excellent durability in the alkaline solution. Importantly, the electronic transition of Co 3+ ions from low-spin state in commercial Co 3 O 4 catalyst to a mixed high-spin and low-spin state in ZnMnCoO 4 catalyst was found to weaken the Co 3+ -OH bond and facilitate the O 2− /OH − displacement. The density functional theory calculation substantiated that ZnMnCoO 4 displayed a more favorable binding energy with O 2 and oxygenated species, thereby enabling the fast reaction kinetics in the oxygen reduction reaction process.
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