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Iron oxidation to amplify the Na and Li storage capacities of nano-sized maricite NaFePO.

作者信息

Boyadzhieva Tanya, Koleva Violeta, Markov Pavel, Stoyanova Radostina

机构信息

Institute of General and Inorganic Chemistry, Bulgarian Academy of Sciences, Acad. G. Bonchev Str., Bldg. 11, 1113 Sofia, Bulgaria.

出版信息

Dalton Trans. 2021 Nov 23;50(45):16548-16561. doi: 10.1039/d1dt03318b.

DOI:10.1039/d1dt03318b
PMID:34735564
Abstract

This study reports an effective approach to improve dramatically the electrochemical performance of nanosized NaFePO with a maricite structure, which is commonly considered as electrochemically inactive due to the absence of structural channels for alkaline ion mobility. The approach is based on the complete oxidation under mild conditions ( at low temperatures around 280 °C and traces of oxygen) of the nanosized maricite phase. It is prepared by the phosphate-formate precursor method and is additionally ball-milled with a carbon additive. The oxidation of Fe proceeds at the nanoscale level within the maricite nanoparticles and causes a massive structural transformation of the maricite phase into a monoclinic NASICON phase NaFe(PO) with the preservation of the crystallinity. The oxidized maricite phase exhibits high specific capacities, cycling stability and rate capability when it is used as an electrode in both Na and Li half-cells. The effect of different sodium and lithium electrolytes on the storage performance is investigated as well. It is found that the highest specific capacity (of about 150 mA h g) is achieved in Li half-cells using the LiPF electrolyte, while in Na half-cells the electrolyte NaFSI/EC:DMC achieves a specific capacity of around 100 mA h g. The rate capability is better in Na half-cells than that in Li half-cells. The mechanism of the reversible intercalation/deintercalation of Na and Li ions is studied by XRD and TEM analyses. The results show that the maricite is an electrochemically inactive phase, but through manipulation including oxidation or amorphization it becomes an active electrode material.

摘要

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