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构型熵策略增强结构稳定性实现了铝电池的稳健阴极。

Configurational Entropy Strategy Enhanced Structure Stability Achieves Robust Cathode for Aluminum Batteries.

作者信息

Kang Rongkai, Zhang Dongmei, Du Yiqun, Sun Chenyi, Zhou Wei, Wang Han, Wan Jiaqi, Chen Guowen, Zhang Jianxin

机构信息

Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials (Ministry of Education), School of Materials Science and Engineering, Shandong University, Jinan, 250061, China.

School of Materials Science and Engineering, Qingdao University of Science and Technology, Qingdao, 266042, China.

出版信息

Small. 2024 Feb;20(5):e2305998. doi: 10.1002/smll.202305998. Epub 2023 Sep 19.

DOI:10.1002/smll.202305998
PMID:37726243
Abstract

Rechargeable aluminum batteries (RABs) are an emerging energy storage device owing to the vast Al resources, low cost, and high safety. However, the poor cyclability and inferior reversible capacity of cathode materials have limited the enhancement of RABs performance. Herein, a high configurational entropy strategy is presented to improve the electrochemical properties of RABs for the first time. The high-entropy (Fe, Mn, Ni, Zn, Mg) O cathode exhibits an ultra-stable cycling ability (109 mAh g after 3000 cycles), high specific capacity (268 mAh g at 0.5 A g ), and rapid ion diffusion. Ex situ characterizations indicate that the operational mechanism of (Fe, Mn, Ni, Zn, Mg) O cathode is mainly based on the redox process of Fe, Mn, and Ni. Theoretical calculations demonstrate that the oxygen vacancies make a positive contribution to adjusting the distribution of electronic states, which is crucial for enhancing the reaction kinetics at the electrolyte and cathode interface. These findings not only propose a promising cathode material for RABs, but also provide the first elucidation of the operational mechanism and intrinsic information of high-entropy electrodes in multivalent ion batteries.

摘要

可充电铝电池(RABs)由于铝资源丰富、成本低且安全性高,是一种新兴的储能装置。然而,正极材料较差的循环稳定性和可逆容量限制了RABs性能的提升。在此,首次提出一种高组态熵策略来改善RABs的电化学性能。高熵(Fe、Mn、Ni、Zn、Mg)O正极表现出超稳定的循环能力(3000次循环后为109 mAh g)、高比容量(在0.5 A g时为268 mAh g)和快速的离子扩散。非原位表征表明,(Fe、Mn、Ni、Zn、Mg)O正极的运行机制主要基于Fe、Mn和Ni的氧化还原过程。理论计算表明,氧空位对调整电子态分布有积极贡献,这对于增强电解质与正极界面处的反应动力学至关重要。这些发现不仅为RABs提出了一种有前景的正极材料,还首次阐明了多价离子电池中高熵电极的运行机制和内在信息。

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