Cobalt-free Li-rich high-capacity cathode material for lithium-ion cells synthesized through sol–gel method and its electrochemical performance
Lithium-rich layered cathode materials are regarded as promising candidates for lithium-ion batteries (LIBs) due to their high specific capacity and superior energy density. The present work adopts a citric acid-assisted sol–gel method to synthesize cobalt-free Li-rich Li 1.17 Ni 0.34 Mn 0.5 O 2 cat...
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Veröffentlicht in: | Ionics 2022-11, Vol.28 (11), p.5005-5014 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Lithium-rich layered cathode materials are regarded as promising candidates for lithium-ion batteries (LIBs) due to their high specific capacity and superior energy density. The present work adopts a citric acid-assisted sol–gel method to synthesize cobalt-free Li-rich Li
1.17
Ni
0.34
Mn
0.5
O
2
cathode material for lithium-ion batteries. The crystal structure and surface morphology were studied by X-ray diffraction (XRD) and field-emission scanning electron microscopy (FE-SEM), respectively. The electrochemical performance was evaluated by charge–discharge cycling tests and cyclic voltammetry (CV). The as-synthesized cathode exhibits a well-ordered layered structure consisting of LiMO
2
and Li
2
MnO
3
phases. When subjected to charge–discharge cycle at C/10 rate in the voltage window of 2.0–4.8 V, the Li
1.17
Ni
0.34
Mn
0.5
O
2
cathode exhibited charge and discharge capacities of 320.8 and 242.4 mAh g
−1
, respectively, with an irreversible capacity of 78.4 mAh g
−1
and coulombic efficiency of 75.6%, in the initial cycle. Cycling studies showed capacity retention of 91.6 % at C/10 after 100 cycles and 85 % at 1C after 150 cycles. Moreover, the material also possesses an excellent rate performance. Thus, the Li-rich cobalt-free cathode material presented here exhibits good specific capacity, rate capability, and cycle life, making it a promising candidate for low cost and high energy density lithium-ion cells. |
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ISSN: | 0947-7047 1862-0760 |
DOI: | 10.1007/s11581-022-04725-x |