Modulating Surface Oxygen Coordination to Achieve Suppressed Phase Transitions and Enhanced Cyclic Stability in Na0.67Mn0.5Fe0.5O2 Cathodes for High-Energy and Low-Cost Na-Ion Batteries
Kang Wu, Peilin Ran, Lunhua He, Zhigang Zhang, Enyue Zhao* and Zhongnian Yang*,
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引用次数: 0
Abstract
The layered iron manganese oxide cathodes accompanied by anionic redox reaction (ARR) activity show large promise of high-energy and economical sodium-ion batteries. However, the adverse surface oxygen lattice evolution caused by irreversible ARR tends to lead to poor cyclic stability and severe voltage decay, which limits its commercial application. In this work, using Na0.67Mn0.5Fe0.5O2 (NMFO) as the model compound, an optimization strategy by modulating surface oxygen coordination through a simultaneous surface Li doping and Li3PO4 coating is proposed to achieve both triggered and reversible ARR processes. As revealed by neutron diffraction techniques and transmission electron microscopy tests, Li ions and Li3PO4 are successfully doped and coated on the surface of the NMFO cathode, respectively. The optimized cathode expectedly shows not only enhanced specific capacity but also improved cyclic stability. The excellent electrochemical properties are ascribed to the suppressed detrimental P2–O2 phase transition, enhanced ARR reversibility, and improved thermal structural stability. More broadly, this work demonstrates the feasibility of modulating surface oxygen coordination to activate and stabilize the ARR ion-storage process.
期刊介绍:
Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.