Synthesis and electrochemical characterization of Mg–Al co-doped Li-rich Mn-based cathode materials
Li-rich layered oxide cathodes suffer from poor rate capability, decayed voltage and inferior cycling stability. In this work, we propose a novel synergistic strategy to improve the electrochemical performance of Li-rich Li 1.2 Mn 0.54 Ni 0.13 Co 0.13 O 2 by the co-doping of magnesium and aluminium....
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Veröffentlicht in: | New journal of chemistry 2019, Vol.43 (30), p.12004-12012 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Li-rich layered oxide cathodes suffer from poor rate capability, decayed voltage and inferior cycling stability. In this work, we propose a novel synergistic strategy to improve the electrochemical performance of Li-rich Li
1.2
Mn
0.54
Ni
0.13
Co
0.13
O
2
by the co-doping of magnesium and aluminium. X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), energy dispersive spectrometry (EDS) mapping, X-ray photoelectron spectroscopy (XPS) measurements and electrochemical tests have been performed for analyzing and observing the characteristics and electrochemical properties of the as-prepared materials. The co-doping of Mg and Al materials delivers a larger initial reversible capacity of 271.9 mA h g
−1
, an improved cycling stability with 81.61% capacity retention after 100 cycles and an excellent rate capability of 119.8 mA h g
−1
at 5C. These significant improvements in electrochemical performances are possibly ascribed to the fact that tiny amounts of Mg and Al ions doped into the transition-metal layer help to enlarge the lithium slab spacing, leading to a reduced barrier of Li
+
during the intercalation–deintercalation process and enhanced rate capability. Meanwhile, the co-doping of Mg and Al not only inhibits the formation of oxygen vacancies, but also decreases cation mixing, which hinders the undesirable phase transformation from layered to spinel-like phases during cycling. |
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ISSN: | 1144-0546 1369-9261 |
DOI: | 10.1039/C9NJ01539F |