Facile one-step synthesis of nanocomposite based on carbon nanotubes and Nickel-Aluminum layered double hydroxides with high cycling stability for supercapacitors

被引:36
作者
Bai, Caihui [1 ]
Sun, Shiguo [1 ]
Xu, Yongqian [1 ]
Yu, Ruijin [1 ]
Li, Hongjuan [1 ]
机构
[1] Northwest A&F Univ, Coll Sci, Yangling 712100, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Layered double hydroxides; Carbon nanotubes; Nanocomposite; Supercapacitor; Homogeneous precipitation; Specific capacitance; MICROWAVE-ASSISTED SYNTHESIS; HIGH-PERFORMANCE; OXIDE COMPOSITE; LDH; ELECTRODES; FABRICATION; CAPACITANCE; NANOSHEETS;
D O I
10.1016/j.jcis.2016.07.001
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nickel-Aluminum Layered Double Hydroxide (NiAl-LDH) and nanocomposite of Carbon Nanotubes (CNTs) and NiAl-LDH (CNTsiNiAl-LDH) were prepared by using a facile one-step homogeneous precipitation approach. The morphology, structure and electrochemical properties of the as-prepared CNTsiNiAl-LDH nanocomposite were then systematically studied. According to the galvanostatic charge-discharge curves, the CNTsiNiAl-LDH nanocomposite exhibited a high specific capacitance of 694 F g(-1) at the 1 A g(-1). Furthermore, the specific capacitance of the CNTs/NiAl-LDH nanocomposite still retained 87% when the current density was increased from 1 to 10 A g(-1). These results indicated that the CNTsiNiAl-LDH nanocomposite displayed a higher specific capacitance and rate capability than pure NiAl-LDH. And the participation of CNTs in the NiAl-LDH composite improved the electrochemical properties. Additionally, the capacitance of the CNTs/NiAl-LDH nanocomposite kept at least 92% after 3000 cycles at 20 A g(-1), suggesting that the nanocomposite exhibited excellent cycling durability. This strategy provided a facile and effective approach for the synthesis of nanocomposite based on CNTs and NiAI-LDH with enhanced supercapacitor behaviors, which can be potentially applied in energy storage conversion devices. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:57 / 62
页数:6
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