Hydrothermal synthesis of Ni@C core–shell composites with high capacitance
•Ni@C core–shell composites were prepared by a simple hydrothermal method.•Ni@C composites exhibit good electrochemical performance for supercapacitors.•The composite displays the highest specific capacitance of 530Fg−1 at 1Ag−1.•An uniform carbon layer is very important for achieving a high electro...
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Published in | Journal of alloys and compounds Vol. 575; pp. 152 - 157 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Kidlington
Elsevier B.V
25.10.2013
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | •Ni@C core–shell composites were prepared by a simple hydrothermal method.•Ni@C composites exhibit good electrochemical performance for supercapacitors.•The composite displays the highest specific capacitance of 530Fg−1 at 1Ag−1.•An uniform carbon layer is very important for achieving a high electrochemical performance.
Ni@C core–shell composites with different crystal structures were synthesized by chemical reduction of nickel (II) acetate tetrahydrate using ethylene glycol as reducing agent and sodium citrate as a carbon source, followed by annealing at different temperatures in the nitrogen atmosphere. X-ray diffraction analysis indicates that the crystal structure of Ni is dependent on the annealing temperatures. At 250°C, both face-centered cubic and hexagonal closed-packed (hcp) phases of Ni coexist in the Ni@C composites, whereas there is only hcp phase Ni observed as being annealed at 300°C. The synthesized Ni@C composites were applied as electrode materials for supercapacitors and exhibited superior electrochemical performances. Especially, the electrode annealed at 250°C displays the highest specific capacitance of 530Fg−1 in 2MKOH solution at a current density of 1Ag−1. In addition, the synthesized Ni@C composite electrodes also show excellent rate capability and cycle stability, presenting the promising potential as electrode material for supercapacitors. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2013.04.010 |