Crystal Structure, Physical Properties, and Electrochemistry of Copper Substituted LiFePO4 Single Crystals
Source abstract
Abstract
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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Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Chemical Synthesis and Characterization
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Chemistry and Materials, Binghamton University, Binghamton 13902, New York, United States
Department of Geology, Moscow State University, Moscow 119991, Russia
Department of Chemistry, Stony Brook University, Stony Brook 11794, New York, United States
Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States
Department of Chemistry, University of Tennessee, Knoxville, Tennessee 37996, United States
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