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可充电水系铝有机电池

Rechargeable Aqueous Aluminum Organic Batteries.

作者信息

Chen Jiangchun, Zhu Qiaonan, Jiang Li, Liu Rongyang, Yang Yan, Tang Mengyao, Wang Jiawei, Wang Hua, Guo Lin

机构信息

School of Chemistry, Beijing Advanced Innovation Center for Biomedical Engineering, Beihang University, Beijing, 100191, China.

College of Optical and Electronic Technology, Jiliang University, Hangzhou, 310018, China.

出版信息

Angew Chem Int Ed Engl. 2021 Mar 8;60(11):5794-5799. doi: 10.1002/anie.202011144. Epub 2021 Jan 28.

Abstract

Aqueous aluminum-ion batteries (AABs) are regarded as promising next-generation energy storage devices, and the current reported cathodes for AABs mainly focused on inorganic materials which usually implement a typical Al ions (de)insertion mechanism. However, the strong electrostatic forces between Al and the host materials usually lead to sluggish kinetics, poor reversibility and inferior cycling stability. Herein, we employ an organic compound with redox-active moieties, phenazine (PZ), as the cathode material in AABs. Different from conventional inorganic materials confined by limited lattice spacing and rigid structure, the flexible organic molecules allow a large-size Al-complex co-intercalation through reversible redox active centers (-C=N-) of PZ. This co-intercalation behavior can effectively reduce desolvation penalty, and substantially lower the Coulombic repulsion during the ion (de)insertion process. Consequently, this organic cathode exhibits a high capacity and excellent cyclability, which exceeds those of most reported electrode materials for AABs. This work highlights the anion co-intercalation chemistry of redox-active organic materials, which is expected to boost the development of high-performance multivalent-ion battery systems.

摘要

水系铝离子电池(AABs)被视为很有前景的下一代储能装置,目前报道的用于AABs的阴极主要集中在无机材料上,这些无机材料通常采用典型的铝离子(脱)嵌入机制。然而,铝与主体材料之间的强静电力通常会导致动力学迟缓、可逆性差和循环稳定性不佳。在此,我们采用一种具有氧化还原活性部分的有机化合物吩嗪(PZ)作为AABs的阴极材料。与受限于有限晶格间距和刚性结构的传统无机材料不同,柔性有机分子允许通过PZ的可逆氧化还原活性中心(-C=N-)进行大尺寸铝配合物的共嵌入。这种共嵌入行为可以有效降低去溶剂化损失,并显著降低离子(脱)嵌入过程中的库仑排斥力。因此,这种有机阴极表现出高容量和优异的循环性能,超过了大多数报道的用于AABs的电极材料。这项工作突出了氧化还原活性有机材料的阴离子共嵌入化学,有望推动高性能多价离子电池系统的发展。

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