Facile synthesis of NiAl layered double hydroxide nanoplates for high-performance asymmetric supercapacitor

JOURNAL OF ALLOYS AND COMPOUNDS

卷:721

Article

Li, Lei¹  Hui, Kwan San²  Hui, Kwun Nam³  Xia, Qixun¹  Fu, Jianjian¹  Cho, Young-Rae¹ 

[1] Pusan Natl Univ, Sch Mat Sci & Engn, San 30 Jangjeon Dong, Busan 609735, South Korea

[2] Univ East Anglia, Sch Math, Norwich NR4 7TJ, Norfolk, England

[3] Univ Macau, Inst Appl Phys & Mat Engn, Ave Univ, Macau, Peoples R China

关键词: Layered double hydroxide;    Nanoplates;    Ultrathin;    Graphene;    Asymmetric supercapacitor;   

DOI  :  10.1016/j.jallcom.2017.06.062

来源: Elsevier

【 摘 要 】

NiAl layered double hydroxide (NiAl-LDH) is a promising electrode material for supercapacitor owing to its versatility in compositions, high theoretical capacitance, environmental benignity, and low cost. However, capacity fading of NiAl-LDH hinders its application in energy storage. Herein, we develop a facile hydrothermal approach to synthesize NiAl-LDH nanoplates (H-NiAl-LDH) possessing high elec-trochemical activity and desirable morphology to improve ion diffusion kinetics and reduce charge transfer resistance, leading to enhanced specific capacitance compared to pristine NiAl-LDH (P-NiAl-LDH) grown by co-precipitation method. Scanning electron microscopy shows that the H-NiAl-LDH are as thin as similar to 30 nm with a mean lateral dimension of 150 nm. The H-NiAl-LDH electrode delivers remarkably high specific capacitance of 1713.2 F g(-1) at 1 A g(-1) and good cycling ability of 88% capacitance retention over 5000 cycles compared to only 757.1 F g(-1) at 1 A g(-1) and 76.4% of the P-NiAl-LDH. An asymmetric supercapacitor (ASC) is assembled using H-NiAl-LDH and graphene as positive and negative electrodes, respectively. The ASC operating at 1.4 V delivers a high specific capacitance of 125 F g(-1) at 1 A g(-1) with a high energy density of 34.1 Wh kg(-1) at a power density of 700 W kg(-1) and outstanding cyclic stability of 91.8% capacitance retention after 5000 cycles. (C) 2017 Published by Elsevier B.V.

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