溶剂化
电解质
法拉第效率
阳极
电化学
阴极
相间
化学物理
材料科学
电极
金属
离子
无机化学
化学
化学工程
物理化学
有机化学
生物
冶金
工程类
遗传学
作者
Chutao Wang,Zongqiang Sun,Бо Лю,Lin Liu,Xiaoting Yin,Qing Hou,Jingmin Fan,Jiawei Yan,Ruming Yuan,Mingsen Zheng,Quanfeng Dong
标识
DOI:10.1038/s41467-024-50751-w
摘要
Constructing powerful anode/cathode interphases by modulate ion solvation structure is the principle of electrolyte design. However, the methodological and theoretical design principles of electrolyte/solvation structure and their effect on electrochemical performance are still vague. Here, we propose a cationic weakly coordinating-intervention strategy for modulating the Na+ solvation sheathes and constructing robust anode/cathode interphases in sodium-metal batteries. Unlike the local highly concentrated electrolytes, 1,2-difluorobenzene can weakly coordinate with Na+ thus transforming the solvation structure into Na+-anion-incorporated structures and strengthening anode/cathode interphases formation by combining with salt decomposition. Furthermore, the correlations between the electrode interface properties and solvation structure are revealed, which can be tuned by the weakly coordination. Ultimately, the modulated electrolyte achieves 97.5% Coulombic efficiency for 600 cycles in Na‖Cu cells at 1 mA cm−2 and a beneficial lifetime (2500 h) in Na‖Na cells. Meanwhile, Na‖PB cells have achieved long-term operation at 4.8 V, along with operation at wide temperatures. Here, authors propose a weakly coordinating-intervention strategy to modulate the Na+ solvation sheath and construct a robust interphase in sodium-metal batteries. Correlation between electrode interface properties and solvation structure is also stated.
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