Exploring the capacitance of a novel nickel fluoride hydroxide nanomaterial in aqueous solutions

IF 2.4 4区 化学 Q3 CHEMISTRY, PHYSICAL
Ionics Pub Date : 2024-08-14 DOI:10.1007/s11581-024-05760-6
Yanli Zhang, Liangliang Dong, Li Wang, Qiang Zhang, Xiangming He
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Abstract

The pursuit of an electrode material that is electrochemically active in aqueous solutions and possesses both high energy density and abundant resources is critical for the development of aqueous hybrid capacitors, which are integral to clean energy storage systems. In this study, we introduce for the first time a novel nickel compound with two anions, displaying a high theoretical energy density—the Ni4OHF7 nanomaterial. We provide a comprehensive analysis of its structure and its electrochemical performance in alkaline aqueous solutions. The Ni4OHF7 nanomaterial is found to be composed of particles approximately 20 nm in size. The electrochemical behavior of Ni4OHF7 in alkaline aqueous solution is mediated by redox reactions occurring between Ni4+ and Ni3+, as well as between Ni3+ and Ni2+. The electrochemical mechanism is primarily diffusion-controlled faradic intercalation process. The study delves into the impact of charge–discharge regulations. Notably, the voltammetric specific capacitance reaches 84.5 F g −1 at a scan rate of 0.03 V s −1, while the discharge specific capacitance is as high as 1128.3 F g −1 at a current density of 1 A g −1. The voltammetric specific capacitance initially increases along with cycling before diminishing and ultimately stabilizes at approximately 30 F g −1 at a scan rate of 0.1 V s −1. The decline in capacitance is attributed to the progressive increase of the charge transfer resistance. The assembled activated carbon (AC)/Ni4OHF7 hybrid capacitor exhibits superior energy and power densities (103.0 Wh kg −1, 7560.7 W kg −1).

Abstract Image

探索新型氟化氢镍纳米材料在水溶液中的电容量
寻求一种在水溶液中具有电化学活性、同时具有高能量密度和丰富资源的电极材料,对于开发清洁能源存储系统不可或缺的水基混合电容器至关重要。在本研究中,我们首次介绍了一种具有两种阴离子、理论能量密度高的新型镍化合物--Ni4OHF7 纳米材料。我们对其结构及其在碱性水溶液中的电化学性能进行了全面分析。我们发现 Ni4OHF7 纳米材料由大小约为 20 纳米的颗粒组成。Ni4OHF7 在碱性水溶液中的电化学行为是由 Ni4+ 和 Ni3+ 之间以及 Ni3+ 和 Ni2+ 之间发生的氧化还原反应介导的。电化学机制主要是扩散控制的法拉第插层过程。研究深入探讨了充放电规律的影响。值得注意的是,在 0.03 V s -1 的扫描速率下,伏安比电容达到 84.5 F g -1 ,而在 1 A g -1 的电流密度下,放电比电容高达 1128.3 F g -1 。伏安比电容最初会随着循环而增加,然后减小,最终稳定在扫描速率为 0.1 V s -1 时的约 30 F g -1 左右。电容下降的原因是电荷转移电阻逐渐增大。组装后的活性炭(AC)/Ni4OHF7 混合电容器具有出色的能量密度和功率密度(103.0 Wh kg -1 和 7560.7 W kg-1)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ionics
Ionics 化学-电化学
CiteScore
5.30
自引率
7.10%
发文量
427
审稿时长
2.2 months
期刊介绍: Ionics is publishing original results in the fields of science and technology of ionic motion. This includes theoretical, experimental and practical work on electrolytes, electrode, ionic/electronic interfaces, ionic transport aspects of corrosion, galvanic cells, e.g. for thermodynamic and kinetic studies, batteries, fuel cells, sensors and electrochromics. Fast solid ionic conductors are presently providing new opportunities in view of several advantages, in addition to conventional liquid electrolytes.
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