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用于具有改善电化学性能的柔性不对称超级电容器的钴镍双氢氧化物的合理设计。

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

作者信息

Wu Yatao, Chen Hao, Lu Yingzhuo, Yang Jin, Zhu Xinqiang, Zheng Yu, Lou Gaobo, Wu Yitian, Wu Qiang, Shen Zhehong, Pan Zhenghui

机构信息

School of Engineering, Zhejiang A&F University, Hangzhou 311300, PR China.

School of Engineering, Zhejiang A&F University, Hangzhou 311300, PR China; School of Materials Science and Engineering, Zhejiang University, Hangzhou 310027, PR China.

出版信息

J Colloid Interface Sci. 2021 Jan 1;581(Pt B):455-464. doi: 10.1016/j.jcis.2020.08.013. Epub 2020 Aug 6.

Abstract

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 successfully 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 Ni. 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(NO), NiCl, and Ni(CHCOO) solutions, the NiSO 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 NiSO) serves as an advanced electrode to show high-rate capability (only 13% C decay after a 15-fold current elevation) and a superior specific capacity (C) of 929.4 C g, which remarkably exceeds those of CoNi-DH-N (823.1 C g, in Ni(NO)), CoNi-DH-Cl (798.4 C g, in NiCl), CoNi-DH-C (803.8 C g, in Ni(CHCOO)), 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, a superior energy density of 42.5 Wh kg, 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.

摘要

为使金属氢氧化物在柔性超级电容器的先进电极中实现整体高性能,对其微纳形态和合适的晶体结构进行合理设计至关重要。在此,通过在含镍的四种不同溶液中,利用氢氧根离子与钴基金属有机框架(Co-MOF)的有机配体之间的原位水解诱导交换过程,在碳布(CC)上成功构建了一种新型的紫藤花状氢氧化钴镍(CoNi-DH)微观结构。制备的生长在CC上的紫藤花状微观结构呈现出垂直排列的阵列,具有高比表面积和丰富的活性位点,这不仅保证了CoNi-DH活性材料在电解质中充分暴露,从而实现高效的赝电容储能,而且有利于快速和可逆的氧化还原动力学,进而产生高倍率性能。此外,与硝酸镍(Ni(NO))、氯化镍(NiCl)和醋酸镍(Ni(CHCOO))溶液相比,发现硫酸镍(NiSO)溶液有助于在所得CoNi-DH中,在层状氢氧化镍相的(003)面上形成最规则的形态和最大的层间距。结果,最优的CoNi-DH-S@CC(在NiSO中制备的CoNi-DH)作为先进电极表现出高倍率性能(电流提高15倍后仅13%的电容衰减)和929.4 C g的优异比电容(C),显著超过CoNi-DH-N(在Ni(NO)中为823.1 C g)、CoNi-DH-Cl(在NiCl中为798.4 C g)、CoNi-DH-C(在Ni(CHCOO)中为803.8 C g)以及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)具有204.8 C g的可观电容、42.5 Wh kg的优异能量密度和令人满意的循环寿命(7500次循环后保留81.5%)。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,展现出令人鼓舞的应用潜力。

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