Exploring the optimal posttreatment strategy for boosting the electrochemical performances of a new bimetal–organic framework-based supercapacitor

IF 6.1 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Frontiers Pub Date : 2024-10-24 DOI:10.1039/d4qi02314e
Xinwen Dou, Mingyue Liu, Tian Cao, Chan Wang, Yingjie Zhang, Yuhang Jia, Qiang Ju, Zhenlan Fang
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Abstract

Metal–organic frameworks (MOFs) have attracted great interest owing to their potential application in electrochemical energy storage. However, the poor conductivity, low structural stability and specific capacitance of pristine MOFs are their critical limitations for practical applications in energy storage devices. To solve these issues, different methods of posttreatments have been applied for MOFs to get their derivations, which are expected to exhibit unique porous structures, fascinating morphology and different chemical compositions, conductivity, stability as well as fasinating electrochemical behaviors. Nevertheless, to the best of our knowledge, the systematic investigations on the effects of different posttreatment methods on electrochemical behaviors of MOF derivatives have never been reported. Here, we have synthesized a series of new monometallic and bimetallic Ni/Co-MOF with varied ratio of Ni to Co ions through self-assembly of metal ions and terephthalic acid (BDC). Four different types of posttreatment methods including sulfidation, carbonization, oxidation, and hydroxylation have been applied in the bimetallic Ni/Co-MOF with the ratio of Ni to Co equaling to 2:1 (Ni2Co1-MOF) due to its best electrochemical behavior among these MOF precursors, and the generated MOF derivatives are named as Ni2Co1-S, Ni2Co1-C, Ni2Co1-O and Ni2Co1-OH, respectively. The obtained optimized Ni2Co1-S-140-6 electrode shows the highest specific capacitance (1500 F g−1 at 1 A g−1), the best conductivity (Rs = 2.38Ω), excellent rate capability (73.3%) and the highest cycle stability (88.2% retention after 5000 cycles) in relation to that of Ni2Co1-C, Ni2Co1-O and Ni2Co1-OH electrodes, demonstrating that sulfidation is the best posttreatment strategy. Moreover, an aqueous asymmetric supercapacitor (A-ASC), assembled by the cathode of Ni2Co1-S-140-6 and the anode of PPy in-situ growing on acid-etched carbon cloth (AECC), exhibits a wide voltage window (1.7V), competitive energy density of 147 Wh kg–1 at the power density of 845 W kg–1 and ideal long-term stability with specific capacitance retention of 75.9% after 5000 cycles at 10 A g–1. This work offers full view of postsynthetic strategies of MOFs for developing high-performance electrochemical energy storage devices.
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探索提高基于双金属有机框架的新型超级电容器电化学性能的最佳后处理策略
金属有机框架(MOFs)因其在电化学储能方面的潜在应用而备受关注。然而,原始 MOFs 的导电性差、结构稳定性低和比电容小是它们在储能设备中实际应用的关键限制因素。为了解决这些问题,人们对 MOFs 采用了不同的后处理方法,以获得其衍生物,这些衍生物有望表现出独特的多孔结构、迷人的形态、不同的化学成分、导电性、稳定性以及迷人的电化学行为。然而,据我们所知,有关不同后处理方法对 MOF 衍生物电化学行为影响的系统研究还从未报道过。在此,我们通过金属离子与对苯二甲酸(BDC)的自组装,合成了一系列新型单金属和双金属 Ni/Co-MOF,其中 Ni 和 Co 离子的比例各不相同。由于在这些 MOF 前体中 Ni 与 Co 的比例为 2:1(Ni2Co1-MOF)的双金属 Ni/Co-MOF 的电化学性能最好,因此对其进行了四种不同的后处理方法,包括硫化、碳化、氧化和羟基化,生成的 MOF 衍生物分别命名为 Ni2Co1-S、Ni2Co1-C、Ni2Co1-O 和 Ni2Co1-OH。与 Ni2Co1-C、Ni2Co1-O 和 Ni2Co1-OH 电极相比,优化后的 Ni2Co1-S-140-6 电极具有最高的比电容(1 A g-1 时为 1500 F g-1)、最佳的电导率(Rs = 2.38Ω)、出色的速率能力(73.3%)和最高的循环稳定性(5000 次循环后保持率为 88.2%),表明硫化是最佳的后处理策略。此外,由 Ni2Co1-S-140-6 阴极和酸蚀刻碳布(AECC)上原位生长的 PPy 阳极组装而成的水性非对称超级电容器(A-ASC)具有宽电压窗口(1.7V),在功率密度为 845 W kg-1 时具有 147 Wh kg-1 的竞争能量密度,并且具有理想的长期稳定性,在 10 A g-1 条件下循环 5000 次后比电容保持率为 75.9%。这项工作为开发高性能电化学储能器件提供了全面的 MOFs 后合成策略。
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
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
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