Molecular and Morphological Engineering of Organic Electrode Materials for Electrochemical Energy Storage

材料科学 原设备制造商 有机自由基电池 纳米技术 分子工程 储能 电解质 电化学 电极 电池(电) 计算机科学 化学 功率(物理) 物理化学 物理 操作系统 量子力学
作者
Zhenzhen Wu,Qirong Liu,Yang Pan,Hao Chen,Qichun Zhang,Sheng Li,Yongbing Tang,Shanqing Zhang
出处
期刊:Electrochemical energy reviews [Springer Science+Business Media]
卷期号:5 (S1) 被引量:54
标识
DOI:10.1007/s41918-022-00152-8
摘要

Abstract Organic electrode materials (OEMs) can deliver remarkable battery performance for metal-ion batteries (MIBs) due to their unique molecular versatility, high flexibility, versatile structures, sustainable organic resources, and low environmental costs. Therefore, OEMs are promising, green alternatives to the traditional inorganic electrode materials used in state-of-the-art lithium-ion batteries. Before OEMs can be widely applied, some inherent issues, such as their low intrinsic electronic conductivity, significant solubility in electrolytes, and large volume change, must be addressed. In this review, the potential roles, energy storage mechanisms, existing challenges, and possible solutions to address these challenges by using molecular and morphological engineering are thoroughly summarized and discussed. Molecular engineering, such as grafting electron-withdrawing or electron-donating functional groups, increasing various redox-active sites, extending conductive networks, and increasing the degree of polymerization, can enhance the electrochemical performance, including its specific capacity (such as the voltage output and the charge transfer number), rate capability, and cycling stability. Morphological engineering facilitates the preparation of different dimensional OEMs (including 0D, 1D, 2D, and 3D OEMs) via bottom-up and top-down methods to enhance their electron/ion diffusion kinetics and stabilize their electrode structure. In summary, molecular and morphological engineering can offer practical paths for developing advanced OEMs that can be applied in next-generation rechargeable MIBs. Graphical abstract

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