阴极
电解质
相间
电化学
阳极
钾
电极
储能
化学
化学工程
材料科学
工程类
有机化学
物理化学
生物
量子力学
遗传学
物理
功率(物理)
作者
Ying Mo,Wang Zhou,Kexuan Wang,Kuikui Xiao,Yuqing Chen,Zixing Wang,Pei Tang,Peitao Xiao,Yuxuan Gong,Shi Chen,Peng Gao,Jilei Liu
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-01-18
卷期号:8 (2): 995-1002
被引量:33
标识
DOI:10.1021/acsenergylett.2c02659
摘要
Controlling the interfacial chemistries of the cathode and anode in potassium ion full-cells is critically important for better K+ storage; however, the correlation between cathode electrolyte interphase (CEI) and solid electrolyte interphase (SEI) and its effect on electrochemical performance is poorly understood, not mention their rational matchup. In this study, an electrochemical modification strategy has been employed for the tailored design of both the CEI on a K2Fe[Fe(CN)6] (KFeHCF) surface and the SEI on a graphite (Gr) surface. The optimized matchup between CEI and SEI realized a good rate and cycling performance in KFeHCF/Gr full-cells, which is attributed to the presence of a robust, homogeneous, and conductive SEI that contains chemically stable PEO (−(CH2CH2O)n−) and K2CO3. Our results not only promoted fundamental understanding of interfacial chemistry on K+ storage, but also provided rational design strategy to realize enhanced efficiency and durability of potassium ion full-cells, which can also be extended to other energy storage systems.
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