Zheng Fan, Zhichao Hou, Wenqiang Lu, Hongbao Zheng, Nan Chen, Mingguang Yao, Chunzhong Wang, Heng Jiang, Dong Zhang, Fei Du
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引用次数: 0
摘要
锰离子水电池(AMIBs)因其卓越的理论容量、出色的安全性和成本效益而越来越受到关注。然而,有关适合 AMIB 的阴极材料的研究并不多,而且这些材料中的锰离子存储机制也没有得到深入研究。此外,现有阴极材料的电化学性能仍不理想。本文设计并合成了 Ag0.11V2O5 作为阴极材料,并首次将置换/插层反应机制引入锰离子存储。Ag0.11V2O5 在 5 A g-¹ 的条件下循环 1200 次后,容量保持率达到 90.3%,在 20 A g-¹ 的条件下实现了 100.01 mAh g-¹ 的高速率性能。这种令人印象深刻的电化学性能归功于该反应,它提供了更多的 Mn2+ 储存位点,并在电极内生成了高导电性的 Ag。这项研究提出了一种实现高容量 AMIB 的新方法。
Combination Displacement/Intercalation Reaction of Ag0.11V2O5 Cathode Realizes Efficient Manganese Ion Storage Properties
Aqueous manganese-ion batteries (AMIBs) are becoming more noticeable because of their excellent theoretical capacity, outstanding safety profile, and cost-effectiveness. However, there aren't many studies on cathode materials appropriate for AMIBs, and the manganese-ion storage mechanisms within these materials have not been thoroughly investigated. Furthermore, the electrochemical performance of existing cathode materials remains suboptimal. Here, Ag0.11V2O5 is designed and synthesized as the cathode material and introduces the combination displacement/intercalation reaction mechanism to the manganese ion storage for the first time. Ag0.11V2O5 demonstrates a capacity retention of 90.3% after 1200 cycles at 5 A g⁻¹ and achieves a high rate performance of 100.01 mAh g⁻¹ at 20 A g⁻¹. This impressive electrochemical performance is attributed to the reaction, which provides more Mn2+ storage sites and generates highly conductive Ag within the electrode. This study presents a novel approach to achieving high-capacity AMIBs.
期刊介绍:
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