Bimetallic MOF-derived manganese-cobalt composite oxide as high-performance zinc-ion batteries cathode

IF 2.6 4区 化学 Q3 ELECTROCHEMISTRY
Bingzhe Ma, Youfeng Zhang, Yaping Feng, Sikai Wang, Yinling Wang, Wenzhu Zhang
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Abstract

The designing cathode materials of aqueous zinc-ion batteries (AZIBs) with high performance is significant challenges in the development of AZIBs. Metal–organic frameworks (MOFs) are considered prime candidates for cathode modification and high-performance cathode materials. Herein, a two-step hydrothermal method was employed to fabricate a bimetallic metal–organic framework MnCo-MOF on carbon cloth. The resulting precursor was calcined to produce a cathode composite MnCo2O4. As a cathode for AZIBs, MnCo2O4/CC exhibited an average specific capacity of 280.6 mAh/g. Upon completion of the cycle at a current density of 0.2 A/g, the specific capacity measured 275.1 mAh/g (retaining 98% of its initial capacity), while maintaining a coulombic efficiency of approximately 98.5%. The excellent cycling performance, superior specific capacity, and superb coulombic efficiency are ascribed to the concerted influence of the polymetallic ions. The micro and nano scale interconnected block structure of MnCo2O4 facilitates interaction between electrode substance and the electrolyte. This research broadens the selection of cathode material and offers valuable guidance for designing high-performance cathode materials for AZIBs.

Abstract Image

作为高性能锌离子电池阴极的双金属 MOF 衍生锰钴复合氧化物
设计具有高性能的锌离子水电池(AZIBs)阴极材料是开发 AZIBs 的重大挑战。金属有机框架(MOFs)被认为是阴极改性和高性能阴极材料的主要候选材料。本文采用两步水热法在碳布上制备了双金属金属有机框架 MnCo-MOF。所得到的前驱体经过煅烧生成了阴极复合材料 MnCo2O4。作为 AZIBs 的阴极,MnCo2O4/CC 的平均比容量为 280.6 mAh/g。在 0.2 A/g 的电流密度下完成循环后,比容量达到 275.1 mAh/g(保持了初始容量的 98%),同时库仑效率保持在约 98.5%。卓越的循环性能、超强的比容量和超高的库仑效率归功于多金属离子的协同作用。MnCo2O4 的微纳米级互连块状结构促进了电极物质与电解质之间的相互作用。这项研究拓宽了阴极材料的选择范围,为设计 AZIBs 的高性能阴极材料提供了宝贵的指导。
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来源期刊
CiteScore
4.80
自引率
4.00%
发文量
227
审稿时长
4.1 months
期刊介绍: The Journal of Solid State Electrochemistry is devoted to all aspects of solid-state chemistry and solid-state physics in electrochemistry. The Journal of Solid State Electrochemistry publishes papers on all aspects of electrochemistry of solid compounds, including experimental and theoretical, basic and applied work. It equally publishes papers on the thermodynamics and kinetics of electrochemical reactions if at least one actively participating phase is solid. Also of interest are articles on the transport of ions and electrons in solids whenever these processes are relevant to electrochemical reactions and on the use of solid-state electrochemical reactions in the analysis of solids and their surfaces. The journal covers solid-state electrochemistry and focusses on the following fields: mechanisms of solid-state electrochemical reactions, semiconductor electrochemistry, electrochemical batteries, accumulators and fuel cells, electrochemical mineral leaching, galvanic metal plating, electrochemical potential memory devices, solid-state electrochemical sensors, ion and electron transport in solid materials and polymers, electrocatalysis, photoelectrochemistry, corrosion of solid materials, solid-state electroanalysis, electrochemical machining of materials, electrochromism and electrochromic devices, new electrochemical solid-state synthesis. The Journal of Solid State Electrochemistry makes the professional in research and industry aware of this swift progress and its importance for future developments and success in the above-mentioned fields.
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