氟
阴极
材料科学
化学工程
频道(广播)
纳米技术
计算机科学
工艺工程
化学
环境科学
物理化学
有机化学
电信
工程类
作者
Keyi Chen,Meng Lei,Zhenguo Yao,Yongjian Zheng,Jiulin Hu,Chuanzhong Lai,Chilin Li
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2021-11-03
卷期号:7 (45): eabj1491-eabj1491
被引量:97
标识
DOI:10.1126/sciadv.abj1491
摘要
Conversion-type iron fluoride is a promising alternative cathode to intercalation oxides because of its higher energy density. However, its intrinsic solid-solid conversion is sluggish during repeated splitting and rebonding of metal-fluorine moieties. Here, we propose a solid-liquid conversion mechanism to activate the fluorine transport kinetics of iron oxyfluorides enabled by fluoride anion receptor of tris(pentafluorophenyl)borane (TPFPB). TPFPB promotes the dissociation of inert lithium fluoride and provides a facile fluorine transport channel at multiphase interfaces via the formation of solvated F− intermediate therein. The construction of solid-liquid channel with fluorinated cathode electrolyte interface is the key for the achievement of FeO0.3F1.7 and FeO0.7F1.3 in terms of sustaining conversion reaction (with an energy efficiency approaching 80%) and high-rate performance (with reversible capacity of 320 mAh/g at 2 A/g). The cathode energy densities can reach 1100 Wh/kg for FeO0.3F1.7 and 700 Wh/kg for FeO0.7F1.3 under the power densities of 220 and 4300 W/kg, respectively.
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