Flower-like nickel-cobalt hydroxides converted from phosphites for high rate performance hybrid supercapacitor electrode materials

Flower-like nickel-cobalt hydroxides converted from phosphites for high rate performance hybrid supercapacitor electrode materials
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DOI:
10.1016/j.electacta.2016.05.213
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发表时间:
2016-08-20
影响因子:
6.6
通讯作者:
Liu, Chenguang
Liu, Chenguang
中科院分区:
材料科学2区
文献类型:
--
作者:
Gou, Jianxia;Xie, Shengli;Liu, Chenguang

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Ni-Co氢氧化物作为混合超级电容器的电极材料已被广泛研究。在这项工作中,我们报告了一种有效的方法来显着提高镍钴氢氧化物的倍率性能,通过工程的双通道结构和调整钴的价态,这是通过一个简单的在适合的化学处理亚磷酸盐实现。在20 A g(-1)时,得到的花状Ni-Co氢氧化物电极的比电容为1425 F g(-1),是1 A g(-1)时1698 F g(-1)的83.9%。在10A·g ~(-1)电流密度下循环4000次后,其效率为80.6%。此外,在组装的水性不对称超级电容器中,使用Ni-Co氢氧化物作为正极材料和活性炭作为负极材料,在801.2W kg(-1)的功率密度下实现了40.1Wh kg(-1)的能量密度。我们的研究表明,化学处理引起形态和相变,并诱导部分Co-2转化为更导电的Co 3+状态。而其电化学性能与钴的微观结构和价态有着密切的关系。(C)2016爱思唯尔有限公司版权所有
Ni-Co hydroxides have been extensively studied as electrode materials for hybrid supercapacitors. In this work, we report an effective method to significantly improve the rate performance of Ni-Co hydroxides through engineering the dual-channel structure and tuning the valence state of Cobalt, which is realized through a facile in suit chemical treatment of phosphites. The specific capacitance of the obtained flower-like Ni-Co hydroxide electrode is 1425 F g(-1) at 20 A g(-1), which is 83.9% of 1698 F g(-1) at 1 A g(-1). Simultaneously, a moderate cycling stability with an efficiency of 80.6% after cycling 4000 times at a current density of 10 A g(-1) is obtained. Moreover, an energy density of 40.1 Wh kg(-1) at a power density of 801.2 W kg(-1) has been achieved in an assembled aqueous asymmetric supercapacitor, using Ni-Co hydroxide as positive electrode material and activated carbon as negative electrode material. Our study shows that the chemical treatment evokes morphology and phase transformation and induces partial Co-2 conversion to a more conductive Co3+ state. And the electrochemical performance has a significant relationship with the microstructure and valence state of Cobalt. (C) 2016 Elsevier Ltd. All rights reserved.