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Rational design of cobalt-nickel double hydroxides for flexible asymmetric supercapacitor with improved electrochemical performance

机译:电化学性能改善柔性非对称超级电容器钴镍双氢氧化物的理性设计

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Rational design of micro-nano morphology and suitable crystalline structure are highly desired for metal hydroxides to achieve overall high-performance in the advanced electrodes for flexible supercapacitors. Herein, a novel wisteria flower-like microstructure of cobalt-nickel double hydroxide (CoNi-DH) is suc-cessfully constructed on carbon cloth (CC) using an in-situ hydrolysis-induced exchange process between hydroxide ions and organic ligands of the Co-MOF in four different kinds of solutions containing Ni2+. The as-prepared wisteria flower-like microstructure grown on CC shows vertically aligned arrays with high specific area and abundant active sites, which not only guarantee the CoNi-DH active materials to be thoroughly exposed in the electrolyte, resulting in highly effective pseudocapacitive energy storage, but also are beneficial to rapid and reversible redox kinetics and thus give rise to high-rate capability. In addition, compared to Ni(NO3)(2), NiCl2, and Ni(CH3COO)(2) solutions, the Ni2SO4 solution is found to facilitate the formation of the most regular morphology and the largest interlayer spacing on (003) plane of the layered nickel hydroxide phase in the resultant CoNi-DH. As a result, the optimal CoNi-DH-S@CC (CoNi-DH prepared in Ni2SO4) serves as an advanced electrode to show high-rate capability (only 13% Cs decay after a 15-fold current elevation) and a superior specific capacity (C-s) of 929.4 C g(-1), which remarkably exceeds those of CoNi-DH-N (823.1 C g(-1), in Ni(NO3)(2)), CoNi-DH-Cl (798.4 C g(-1), in NiCl2), CoNi-DH-C (803.8 C g(-1), in Ni(CH3COO)(2)), and other similar metal hydroxides. Moreover, with this CoNi-DH-S electrode as the positive electrode, the as-prepared asymmetric supercapacitor (ASC) delivers an impressive capacity of 204.8 C g(-1), a superior energy density of 42.5 Wh kg(-1), and satisfactory cycle life (81.5% reservation after 7500 cycles). As a proof-of-concept application, a quasi-solid-state ASC is further successfully fabricated based on the CoNi-DH-S electrode to exhibit encouraging application potential. (C) 2020 Elsevier Inc. All rights reserved.
机译:为了在柔性超级电容器的先进电极中实现整体高性能,金属氢氧化物迫切需要合理设计微纳形貌和合适的晶体结构。本文采用原位水解诱导交换法,在四种不同的含镍溶液中,在碳布(CC)上成功构建了钴镍双氢氧化物(CoNi-DH)的紫藤花状微观结构。在CC上生长的紫藤花状微结构显示出垂直排列的阵列,具有高比表面积和丰富的活性位点,这不仅保证了CoNi DH活性材料在电解液中彻底暴露,导致高效的假电容储能,但也有利于快速和可逆的氧化还原动力学,从而提高速率能力。此外,与Ni(NO3)(2)、NiCl2和Ni(CH3COO)(2)溶液相比,发现Ni2SO4溶液有助于在生成的CoNi DH中的层状氢氧化镍相的(003)平面上形成最规则的形态和最大的层间间距。因此,最佳的CoNi-DH-S@CC(在Ni2SO4中制备的CoNi-DH)是一种先进的电极,显示出高的速率容量(电流升高15倍后,Cs仅衰减13%)和优越的比容量(C-s)929.4 Cg(-1),显著超过CoNi-DH-N(823.1 Cg(-1)、in-Ni(NO3)(2))、CoNi-DH-Cl(798.4 Cg(-1)、in-NiCl2)、CoNi-DH-C(803.8 Cg(-1)、in-Ni(CH3COO)(2))和其他类似的金属氢氧化物。此外,以这种CoNi-DH-S电极作为正极,制备的不对称超级电容器(ASC)提供了令人印象深刻的204.8 cG(-1)容量、42.5 Wh-kg(-1)的高能量密度和令人满意的循环寿命(7500次循环后81.5%的保留)。作为概念验证应用,基于CoNi-DH-S电极进一步成功制备了准固态ASC,展示了令人鼓舞的应用潜力。(C) 2020爱思唯尔公司版权所有。

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