电解质
碳酸乙烯酯
电池(电)
电化学
阴极
材料科学
化学工程
离子
锂(药物)
储能
电极
化学
物理化学
有机化学
热力学
工程类
内分泌学
物理
功率(物理)
医学
作者
Jiaxin Zheng,Yuyang Hou,Yandong Duan,Xiaohe Song,Yi Wei,Tongchao Liu,Jiangtao Hu,Hua Guo,Zengqing Zhuo,Lili Liu,Zheng Chang,Xiaowei Wang,Danylo Zherebetskyy,Yanyan Fang,Yuan Lin,Kang Xu,Lin‐Wang Wang,Yuping Wu,Feng Pan
出处
期刊:Nano Letters
[American Chemical Society]
日期:2015-08-25
卷期号:15 (9): 6102-6109
被引量:98
标识
DOI:10.1021/acs.nanolett.5b02379
摘要
LiFePO4 has long been held as one of the most promising battery cathode for its high energy storage capacity. Meanwhile, although extensive studies have been conducted on the interfacial chemistries in Li-ion batteries,1-3 little is known on the atomic level about the solid-liquid interface of LiFePO4/electrolyte. Here, we report battery cathode consisted with nanosized LiFePO4 particles in aqueous electrolyte with an high charging and discharging rate of 600 C (3600/600 = 6 s charge time, 1 C = 170 mAh g(-1)) reaching 72 mAh g(-1) energy storage (42% of the theoretical capacity). By contrast, the accessible capacity sharply decreases to 20 mAh g(-1) at 200 C in organic electrolyte. After a comprehensive electrochemistry tests and ab initio calculations of the LiFePO4-H2O and LiFePO4-EC (ethylene carbonate) systems, we identified the transient formation of a Janus hydrated interface in the LiFePO4-H2O system, where the truncated symmetry of solid LiFePO4 surface is compensated by the chemisorbed H2O molecules, forming a half-solid (LiFePO4) and half-liquid (H2O) amphiphilic coordination environment that eases the Li desolvation process near the surface, which makes a fast Li-ion transport across the solid/liquid interfaces possible.
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