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Enhanced reversibility and electrochemical performances of mechanically alloyed Cu 3 P achieved by Fe addition
Cu 3 P is a potential anode material for lithium-ion batteries with its comparable gravimetric capacity, but several times higher volumetric capacity (4732 mA h cm −3 ) than graphite. However, the cycling stability of Cu 3 P is poor at low discharge potentials and high current densities. In this wor...
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Published in: | RSC advances 2016, Vol.6 (32), p.26800-26808 |
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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: | Cu
3
P is a potential anode material for lithium-ion batteries with its comparable gravimetric capacity, but several times higher volumetric capacity (4732 mA h cm
−3
) than graphite. However, the cycling stability of Cu
3
P is poor at low discharge potentials and high current densities. In this work, Fe addition is employed as a simple strategy to modulate the composition and phase constitution of Cu
3
P nanopowders synthesized by wet mechanical alloying, and thereby to tune the electrochemical performance of the anode. The addition of Fe results in a composite constitute containing Cu
3
P as the major phase and some other minor phases including Cu, α-Fe and FeP, which are combinationally determined by X-ray diffraction, energy dispersive X-ray spectroscopy and Mössbauer spectroscopy. Electrochemical tests reveal that both the cycling stability and the rate capability of the electrodes are improved by Fe addition. The Cu
3
P electrode with 10% Fe addition shows the best cell performance, with the capacity being remarkably improved by over 100%, from 82 mA h g
−1
to 178 mA h g
−1
after 50 cycles at 0.75C between 2.0 V and 0.5 V
vs.
Li/Li
+
. The improvement of the electrochemical performance is engendered by a synergetic effect of the microstructure change of the powders and the presence of Fe-related minor phases, leading to increased electronic conductivity as well as enhanced electrochemical reversibility of the electrode. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/C6RA01637E |