Three-Dimensional Cobalt Phosphide Nanowire Arrays as Negative Electrode Material for Flexible Solid-State Asymmetric Supercapacitors
Despite the great progress that has been accomplished in supercapacitors, the imbalance of the development of positive and negative electrode materials still remains a critical issue to achieve high energy density; therefore, exploring high-performance negative electrode materials is highly desirabl...
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Published in | ACS applied materials & interfaces Vol. 9; no. 20; pp. 16986 - 16994 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Chemical Society
24.05.2017
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Subjects | |
Online Access | Get full text |
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Summary: | Despite the great progress that has been accomplished in supercapacitors, the imbalance of the development of positive and negative electrode materials still remains a critical issue to achieve high energy density; therefore, exploring high-performance negative electrode materials is highly desirable. In this article, three-dimensional cobalt phosphide (CoP) nanowire arrays were synthesized on a carbon cloth and were utilized as a binder-free supercapacitor negative electrode. The as-synthesized CoP nanowire arrays presented a high capacitance of 571.3 mF/cm2 at a current density of 1 mA/cm2. By using CoP nanowire arrays as the negative electrode and MnO2 nanowire arrays as the positive electrode, a flexible solid-state asymmetric supercapacitor has been fabricated and has exhibited excellent electrochemical performance, such as a high energy density of 0.69 mWh/cm3 and a high power density of 114.2 mW/cm3. In addition, the solid-state asymmetric supercapacitor shows high cycle stability with 82% capacitance retention after 5000 charge/discharge cycles. This work demonstrates that CoP is a promising negative electrode material for high-performance supercapacitor applications. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1944-8244 1944-8252 1944-8252 |
DOI: | 10.1021/acsami.7b01109 |