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双金属 CoNi 基沸石咪唑骨架与碳纳米管的集成纳米结构作为高性能电化学超级电容器。

The intergrated nanostructure of bimetallic CoNi-based zeolitic imidazolate framework and carbon nanotubes as high-performance electrochemical supercapacitors.

机构信息

Henan Provincial Key Laboratory of Surface and Interface Science, Zhengzhou University of Light Industry, Zhengzhou 450002, China.

College of Environmental Science and Engineering, Donghua University, Shanghai 201620, China.

出版信息

J Colloid Interface Sci. 2022 Feb 15;608(Pt 2):1257-1267. doi: 10.1016/j.jcis.2021.10.089. Epub 2021 Oct 24.

DOI:10.1016/j.jcis.2021.10.089
PMID:34739989
Abstract

In this study, a series of one-dimensional (1D)/two-dimensional (2D) heterostructure hybrids were fabricated through the in situ growth of a Co and Ni bimetallic zeolitic imidazolate framework (CoNi-ZIF) around N-doped carbon nanotubes (N-CNTs). The hybrids were further exploited as effective supercapacitor materials. The N-CNTs were prepared by carbonizing a mixture of glucose and the melamine-cyanuric acid complex at a high temperature (900 °C) under N atmosphere and applied as the template for the in situ synthesis of CoNi-ZIF nanosheets (NSs). The 1D N-CNTs in the hybrids can act as the high-way for charge transfer to boost the faradaic reactions. Changing the usage of metal precursors not only provided abundant redox reaction sites in 2D CoNi-ZIF NSs but also modulated the microstructures and chemical components of the hybrids. The integration of the features of N-CNTs and CoNi-ZIF NSs can result in a synergistic effect between N-CNTs and CoNi-ZIF NSs. Therefore, the obtained CoNi-ZIFs and N-CNTs hybrid (CoNi-ZIF@N-CNT) exhibited superior electrochemical capacitive performance. Comparison revealed that the CoNi-ZIF@N-CNT-2 hybrid, which was prepared with a 1:1 mass ratio of Co(NO)·6HO and Ni(NO)·6HO, displayed the largest specific capacitance of 1118F g at 1 A g, which was higher than the capacitance of most reported metal-organic framework (MOF)-based supercapacitor electrodes. Moreover, the asymmetric supercapacitor based on the CoNi-ZIF@N-CNT-2 electrode exhibited a high energy density of 51.1 Wh kg at the power density of 860.1 W kg and good cycle stability. This work can provide a facile and effective way for the fabrication of heterostructured 1D/2D nanostructures based on 2D MOFs for advanced energy storage.

摘要

在这项研究中,通过在氮掺杂碳纳米管(N-CNTs)周围原位生长 Co 和 Ni 双金属沸石咪唑酯骨架(CoNi-ZIF),制备了一系列一维(1D)/二维(2D)异质结构杂化物。这些杂化物进一步被开发为有效的超级电容器材料。N-CNTs 通过在 N 气氛下将葡萄糖和三聚氰胺-均三嗪复合物的混合物在高温(900°C)碳化制备,并用作原位合成 CoNi-ZIF 纳米片(NSs)的模板。杂化物中的 1D N-CNTs 可以作为电荷转移的高速通道,以促进法拉第反应。改变金属前体的使用不仅在二维 CoNi-ZIF NSs 中提供了丰富的氧化还原反应位点,而且还调节了杂化物的微结构和化学成分。N-CNTs 和 CoNi-ZIF NSs 的特性的集成可以导致 N-CNTs 和 CoNi-ZIF NSs 之间的协同效应。因此,所获得的 CoNi-ZIF 和 N-CNTs 杂化物(CoNi-ZIF@N-CNT)表现出优异的电化学电容性能。比较表明,用 Co(NO)·6HO 和 Ni(NO)·6HO 的 1:1 质量比制备的 CoNi-ZIF@N-CNT-2 杂化物在 1 A g 下具有 1118F g 的最大比电容,高于大多数报道的金属-有机骨架(MOF)-基于超级电容器电极的电容。此外,基于 CoNi-ZIF@N-CNT-2 电极的非对称超级电容器在 860.1 W kg 的功率密度下具有 51.1 Wh kg 的高能量密度和良好的循环稳定性。这项工作为基于二维 MOF 的异质结构 1D/2D 纳米结构的制备提供了一种简单有效的方法,可用于先进的储能。

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