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Copper substituted lithium iron phosphate, with the olivine structure, has been synthesized hydrothermally as dark-brown single crystals with 15% of the iron sites occupied by cupric ions. Single crystal X-ray diffraction and magnetic susceptibility,combined with Li solid state NMR studies performed on powder sample, showed that 5% of the lithium ions also reside on the iron site, giving the formula Li 0.95 [(Fe 2+ ) 0.70 (Fe 3+ ) 0.10 (Cu 2+ ) 0.15 Li 0.05 )]PO 4 . The compound exhibits anisotropic magnetic susceptibility and orders antiferromagnetically at 48 K. The magnetic moments are aligned along [010] as in LiFePO 4 . The optical measurements indicate that the dark brown color originates from interionic d-d transitions. A part of the lithium ions can be cycled in an electrochemical cell, corresponding to the oxidation/reduction of the iron ions. An onset of a second electrochemical process is observed at about 4.1 V, tentatively attributed to the removal of Li ions from the Fe site. The first principles calculations indicate above 5 V redox potential for the Cu 2+ /Cu 3+ pair in the olivine structure, much higher than experimentally observed. The diffusion coefficient is determined from galvanostatic intermittent titration data, as part of the delithiation process proceeds as a single-phase reaction in this disordered compound.
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Upreti et al. (2011) studied this question.
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