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One for two" strategy to prepare MOF-derived NiCo2S4 nanorods grown on carbon cloth for high-performance asymmetric supercapacitors and efficient oxygen evolution reaction
被引:72
|作者:
Wang, Di
[1
]
Tian, Liyong
[1
]
Huang, Jieyu
[1
]
Li, Dawei
[1
]
Liu, Jingyan
[1
]
Xu, Yang
[1
]
Ke, Huizhen
[2
]
Wei, Qufu
[1
,2
]
机构:
[1] Jiangnan Univ, Key Lab Ecotext, Minist Educ, Wuxi 214122, Jiangsu, Peoples R China
[2] Minjiang Univ, Fujian Key Lab Novel Funct Text Fibers & Mat, Fuzhou 350108, Fujian, Peoples R China
基金:
国家重点研发计划;
中国国家自然科学基金;
关键词:
Hierarchical structure;
Asymmetric supercapacitors;
Oxygen evolution reaction;
Metal-organic frameworks;
Transition metal sulfides;
METAL-ORGANIC FRAMEWORKS;
NITROGEN-DOPED CARBON;
NI FOAM;
NANOSHEET ARRAYS;
NANOTUBE ARRAYS;
BIFUNCTIONAL ELECTROCATALYST;
NANOWIRE ARRAYS;
HYDROGEN;
ELECTRODES;
REDUCTION;
D O I:
10.1016/j.electacta.2020.135636
中图分类号:
O646 [电化学、电解、磁化学];
学科分类号:
081704 ;
摘要:
Metal-organic frameworks (MOFs) have recently emerged as promising hierarchical structured porous materials for high-performance energy storage and conversion devices due to their unique tunable structure and excellent porosity. Herein, we reported a "one for two" strategy to prepare NiCo2S4 nanorods directly grown on carbon cloth (NiCo2S4@CC) via a simply modified MOFs-derived approach for high-performance asymmetric supercapacitors and efficient oxygen evolution reaction (OER). As an electrode for asymmetric supercapacitors, the NiCo2S4@CC electrode showed excellent electrochemical performance with high specific capacitance and good rate capability. The asymmetric supercapacitor using NiCo2S4@CC as a cathode electrode and N-doped porous carbon nanosheets grown on the CC (NC@CC ) as an anode electrode achieved a superior energy density and power density and a long cycle life. Furthermore, the NiCo2S4@CC exhibited a notable electrocatalytic activity as an electrocatalyst for OER. The remarkable electrochemical performance of as-prepared NiCo2S4@CC could be mainly attributed to its hierarchical structure, sufficient active sites and low metal-anion bond energy after sulfuration reaction. This work could provide an unprecedented opportunity to fabricate functional materials under rational design for various applications. (C) 2020 Elsevier Ltd. All rights reserved.
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