An iron-based fluorophosphate cathode material for K-ion batteries.

Abstract

The development of a tavorite structured K- transition metal (TM)- fluorophosphate, having earth-abundant Fe as the only TM, crystallizing in the orthorhombic crystal system and facilitating stable-cum-reversible electrochemical K-extraction/insertion, has been reported here. Synthesized using low-cost precursors, KFePO4F has also been found to be air-stable. Detailed information pertaining to the bonding/structure, including lattice site occupancy, have been obtained via diffraction, Raman spectroscopy and FTIR, with XPS and ESR revealing the oxidation states of Fe in the as-synthesized condition and upon being subjected to electrochemical potassiation/depotassiation. The electrochemical K-insertion/extraction, supported by reversible Fe-redox, leads to a reversible K-storage capacity of ~102 mAh/g (within 1.5-4.0 V), along with a 1st cycle Coulombic efficiency (CE) of ~93% (with CE >99.9% from 2nd cycle). Ex-situ X-ray diffraction, as well as operando synchrotron diffraction during galvanostatic cycling, indicates reversible changes in peak positions upon electrochemical K-extraction/insertion, with no evidence for structural change. When used as cathode material in K-ion 'full' cell (with hard carbon-based anode), a discharge capacity of ~68 mAh/g, along with capacity retention of ~70% after 50 cycles, has been obtained; which confirms that this newly-developed earth-abundant Fe-based potassium fluorophosphate can be utilized for potential application in sustainable battery chemistries, like K-ion batteries.