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Designing High-Capacity, Lithium-Ion Cathodes Using X-ray Absorption Spectroscopy
We have taken advantage of the element specific nature of X-ray absorption spectroscopy to elucidate the chemical and structural details of a surface treatment intended for the protection of high-capacity cathode materials. Electrochemical data have shown that surface treatments of 0.5Li2MnO3•0.5LiC...
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Published in: | Chemistry of materials 2011-12, Vol.23 (24), p.5415-5424 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | We have taken advantage of the element specific nature of X-ray absorption spectroscopy to elucidate the chemical and structural details of a surface treatment intended for the protection of high-capacity cathode materials. Electrochemical data have shown that surface treatments of 0.5Li2MnO3•0.5LiCoO2 (Li1.2Mn0.4Co0.4O2) with an acidic solution of lithium–nickel-phosphate significantly improves electrode capacity, rate, and cycling stability. XAS data reveal that the surface treatment results in a modification of the composite structure itself, where Ni2+ cations, intended to be present in a lithium–nickel-phosphate coating, have instead displaced lithium in the transition metal layers of Li2MnO3-like domains within the 0.5Li2MnO3•0.5LiCoO2 structure. X-ray diffraction data show the presence of Li3PO4, suggesting that phosphate ions from the acidic solution are responsible for lithium extraction and nickel insertion with the formation of vacancies and/or manganese reduction for charge compensation. Furthermore, we show that the above effects are not limited to lithium–nickel-phosphate treatments. The studies described are consistent with a novel approach for synthesizing and tailoring the structures of high-capacity cathode materials whereby a Li2MnO3 framework is used as a precursor for synthesizing a wide variety of composite metal oxide insertion electrodes for Li-ion battery applications. |
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ISSN: | 0897-4756 1520-5002 |
DOI: | 10.1021/cm2026703 |