Net-structured Co3O4/C nanosheet array with enhanced electrochemical performance toward lithium storage
•Co3O4/C nanosheet array on nickel foam was synthesized by hydrothermal method, followed by magnetron sputtering of a carbon layer.•The Co3O4/C nanosheet array electrode delivers an initial discharge capacity of 1340.4mAhg−1 at 0.1C.•After 100 cycles, the capacity retention of the Co3O4/C is 88.8% o...
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Published in | Materials research bulletin Vol. 51; pp. 112 - 118 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Ltd
01.03.2014
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Subjects | |
Online Access | Get full text |
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Summary: | •Co3O4/C nanosheet array on nickel foam was synthesized by hydrothermal method, followed by magnetron sputtering of a carbon layer.•The Co3O4/C nanosheet array electrode delivers an initial discharge capacity of 1340.4mAhg−1 at 0.1C.•After 100 cycles, the capacity retention of the Co3O4/C is 88.8% of its initial discharge capacity.•The enhanced electrochemical performances are attributed to the porous nanosheet array and the thin carbon layer coated on Co3O4 nanosheets.
Freestanding Co3O4/C nanosheet array growing directly on nickel foam substrate was synthesized using a hydrothermal approach, followed by a direct current magnetron sputtering of a thin carbon layer. The Co3O4 nanosheets with thicknesses of 10–20nm are interconnected with each other, forming a highly open net-structure. The Co3O4/C nanosheet array electrode delivers an initial discharge capacity of 1340.4mAhg−1 at 0.1C, and maintains a high specific capacity of 912.1mAhg−1 at room temperature and can still remain 88.8% of its initial discharge capacity at 55°C at 1C after 100 cycles. The enhanced electrochemical performances are attributed to the porous nanosheet array and the thin carbon layer coated on Co3O4 nanosheets, which cannot only facilitate Li+ and electron transportation in the electrode, but also improve its structure stability during cycling. |
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ISSN: | 0025-5408 1873-4227 |
DOI: | 10.1016/j.materresbull.2013.11.043 |