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Playing with the Redox Potentials in Ludwigite Oxyborates: Fe3BO5 and Cu2MBO5 (M = Fe, Mn, and Cr)

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journal contribution
posted on 2018-07-11, 00:00 authored by Jonas Sottmann, Lucie Nataf, Laura Chaix, Valérie Pralong, Christine Martin
Ludwigite oxyborates with general formula M22+M′3+BO5 (where M and M′ are metals) represent an interesting class of conversion-type electrode materials for lithium-ion batteries. The homometallic Fe3BO5 shows a first lithiation capacity of 678 mA h g–1 (∼6.5 Li). Very low voltage polarizations for conversion-type reactions (300 and 440 mV) are observed for the two reversible redox couples at ∼1.3 and ∼1.8 V, which give rise to a stable capacity of 345 mA h g–1 between 0.75 and 3.0 V versus Li/Li+. Ex situ X-ray diffraction and operando X-ray absorption spectroscopy show that Fe3BO5 is almost completely converted to iron metal nanograins embedded in a lithia matrix during the initial lithiation and that subsequent cycling takes place between amorphous or nanocrystalline Fe-based phases. In Cu2MBO5 (M = Fe, Mn, and Cr), the trivalent transition metals are found to be electrochemically active in addition to copper, but at lower voltages, causing a large spread in redox potentials. When limiting the voltage range to the Cu2+/Cu0 redox couple (at ∼2.4 V), the best performance in terms of voltage polarization and reversible capacity is obtained for Cu2FeBO5. Annealing of Cu2FeBO5 in a reducing atmosphere at low temperatures (∼250 °C) is identified as a means to improve the first cycle reversibility.

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