材料科学
电解质
熔盐
电池(电)
电化学
盐(化学)
离子液体
溶解
阴极
储能
锂(药物)
冶金
化学工程
无机化学
电极
有机化学
催化作用
工程类
物理
化学
医学
功率(物理)
物理化学
量子力学
内分泌学
作者
Kang Han,Xinying Qiao,Xuanpeng Wang,Meng Huang,Zhenhang Zhong,Qi Zhang,Chaojiang Niu,Jiashen Meng,Liqiang Mai
出处
期刊:Nano Energy
[Elsevier]
日期:2024-10-01
卷期号:129: 110085-110085
标识
DOI:10.1016/j.nanoen.2024.110085
摘要
Aluminum-organic batteries (AIBs) have gained significant popularity for large-scale energy storage due to their abundance of aluminum reserves, cost-effectiveness, and environmental friendliness. However, the current aluminum-organic batteries primarily relied on ionic liquid electrolytes suffer from slow reaction kinetics and limited cycle life. Herein, we report a novel and efficient aluminum-organic battery that addresses these limitations by utilizing a molten salt electrolyte and designing a strongly interacting organic cathode. By enhancing π-π stacking interactions, we induced a transition in commercial PTCDA (Perylene-3,4,9,10-tetracarboxylic dianhydride) molecules from the β-phase to the highly interactive α-phase, known as PA450. This transformation not only stabilizes the structure of the PA450 electrode, preventing dissolution in the molten salt electrolyte, but also significantly improves electron conductivity. The Al||PA450 molten salt battery demonstrates exceptional electrochemical performance, exhibiting a high reversible capacity of 135 mAh g–1 and outstanding cyclability for up to 2000 cycles at 10 A g−1. Additionally, the structural rearrangement and ion transport properties induced by the co-intercalation of Al3+ and AlCl2+ were studied are investigated. This work provides deep insights into the unique characteristics of organic materials for ultrafast energy storage in molten salt electrolytes.
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