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基于金属有机框架设计三金属硫化物空心纳米笼作为超级电容器的电极材料

Design of trimetallic sulfide hollow nanocages from metal-organic frameworks as electrode materials for supercapacitors.

作者信息

Zhao Xueyan, Bi Qiong, Yang Cui, Tao Kai, Han Lei

机构信息

School of Materials Science & Chemical Engineering, Ningbo University, Ningbo, Zhejiang 315211, China.

Institute of Drug Discovery Technology, Ningbo University, Ningbo, Zhejiang 315211, China.

出版信息

Dalton Trans. 2021 Nov 2;50(42):15260-15266. doi: 10.1039/d1dt02819g.

DOI:10.1039/d1dt02819g
PMID:34633015
Abstract

Transition metal sulfides (TMSs) are the most used electrode materials for supercapacitors (SCs). However, they still suffer from unsatisfactory electrochemical properties. Designing a hollow mixed TMS nanostructure with a well-defined chemical composition and shape is an effective strategy to tackle this issue, yet remains challenging. Herein, using a bimetallic zeolitic imidazolate framework (Zn-Co-ZIF) with various Zn/Co ratios as the template, a series of trimetallic sulfide (Ni-Zn-Co-S) hollow nanocages were successfully prepared by sequential nickel nitrate etching, co-precipitation and vulcanization. As an electrode material for a three-electrode SC in an aqueous alkaline electrolyte, the Ni-Zn-Co-S-0.25 electrode achieves an ultra-high specific capacitance of 1930.9 at 1 A g with a good rate performance (64.5% at 10 A g). In order to further prove the advantage of the as-prepared Ni-Zn-Co-S-0.25 material, it was assembled into an asymmetric energy storage device using an activated carbon (AC) anode. The Ni-Zn-Co-S-0.25//AC cell exhibits an outstanding energy storage capability (32.8 W h kg at 864.8 W kg) with a splendid cyclic life (retaining ∼92.2% of the initial capacitance after 10 000 cycles). The excellent electrochemical performance of Ni-Zn-Co-S-0.25 is ascribed to the merits of the trimetallic sulfide hollow nanocage , good electronic conductivity, a large active surface area, fast charge transfer, rich redox reactions and the synergic effect of different metal ions.

摘要

过渡金属硫化物(TMSs)是超级电容器(SCs)中使用最多的电极材料。然而,它们的电化学性能仍不尽人意。设计具有明确化学成分和形状的中空混合TMS纳米结构是解决这一问题的有效策略,但仍具有挑战性。在此,以具有不同Zn/Co比的双金属沸石咪唑框架(Zn-Co-ZIF)为模板,通过依次进行硝酸镍蚀刻、共沉淀和硫化,成功制备了一系列三金属硫化物(Ni-Zn-Co-S)中空纳米笼。作为碱性水电解质中三电极SC的电极材料,Ni-Zn-Co-S-0.25电极在1 A g时实现了1930.9的超高比电容,具有良好的倍率性能(在10 A g时为64.5%)。为了进一步证明所制备的Ni-Zn-Co-S-0.25材料的优势,将其与活性炭(AC)负极组装成不对称储能装置。Ni-Zn-Co-S-0.25//AC电池表现出出色的储能能力(在864.8 W kg时为32.8 W h kg),具有出色的循环寿命(10000次循环后保留约92.2%的初始电容)。Ni-Zn-Co-S-0.25优异的电化学性能归因于三金属硫化物中空纳米笼的优点、良好的电子导电性、大的活性表面积、快速的电荷转移、丰富的氧化还原反应以及不同金属离子的协同效应。

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