氧化还原
电池(电)
阴极
化学工程
过电位
动力学
电解质
化学
铝
扩散
熔盐
相(物质)
材料科学
电化学
无机化学
电极
热力学
有机化学
物理化学
功率(物理)
物理
量子力学
工程类
作者
Jiashen Meng,Xuhui Yao,Xufeng Hong,Lujun Zhu,Zhitong Xiao,Yongfeng Jia,Fang Liu,Huimin Song,Yunlong Zhao,Quanquan Pang
标识
DOI:10.1038/s41467-023-39258-y
摘要
Conventional solid-to-solid conversion-type cathodes in batteries suffer from poor diffusion/reaction kinetics, large volume changes and aggressive structural degradation, particularly for rechargeable aluminium batteries (RABs). Here we report a class of high-capacity redox couples featuring a solution-to-solid conversion chemistry with well-manipulated solubility as cathodes-uniquely allowed by using molten salt electrolytes-that enable fast-charging and long-lived RABs. As a proof-of-concept, we demonstrate a highly reversible redox couple-the highly soluble InCl and the sparingly soluble InCl3-that exhibits a high capacity of about 327 mAh g-1 with negligible cell overpotential of only 35 mV at 1 C rate and 150 °C. The cells show almost no capacity fade over 500 cycles at a 20 C charging rate and can sustain 100 mAh g-1 at 50 C. The fast oxidation kinetics of the solution phase upon initiating the charge enables the cell with ultrafast charging capability, whereas the structure self-healing via re-forming the solution phase at the end of discharge endows the long-term cycling stability. This solution-to-solid mechanism will unlock more multivalent battery cathodes that are attractive in cost but plagued by poor reaction kinetics and short cycle life.
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