假电容
材料科学
化学工程
碳二亚胺
扩散
动力学
电化学
微晶
电池(电)
基质(水族馆)
离子
纳米技术
化学
化学物理
电极
物理化学
热力学
冶金
高分子化学
有机化学
量子力学
功率(物理)
物理
海洋学
超级电容器
工程类
地质学
作者
Jiayin Li,Rong Wang,Penghui Guo,Xing Liu,Yunfei Hu,Zhanwei Xu,Yijun Liu,Liyun Cao,Jianfeng Huang,Koji Kajiyoshi
出处
期刊:ACS Nano
[American Chemical Society]
日期:2021-04-12
卷期号:15 (4): 6410-6419
被引量:58
标识
DOI:10.1021/acsnano.0c08314
摘要
Iron carbodiimide (FeNCN) belongs to a type of metal compounds with a more covalent bonding structure compared to common transition metal oxides. It could provide possibilities for various structural designs with improved charge-transfer kinetics in battery systems. Moreover, these possibilities are still highly expected for promoting enhancement in rate performance of sodium (Na)-ion battery. Herein, oriented FeNCN crystallites were grown on the carbon-based substrate with exposed {010} faces along the [001] direction (O-FeNCN/S). It provides a high Na-ion storage capacity with excellent rate capability (680 mAh g–1 at 0.2 A g–1 and 360 mAh g–1 at 20 A g–1), presenting rapid charge-transfer kinetics with high contribution of pseudocapacitance during a typical conversion reaction. This high rate performance is attributed to the oriented morphology of FeNCN crystallites. Its orientation along [001] maintains preferred Na-ion diffusion along the two directions in the entire morphology of O-FeNCN/S, supporting fast Na-ion storage kinetics during the charge/discharge process. This study could provide ideas toward the understanding of the rational structural design of metal carbodiimides for attaining high electrochemical performance in future.
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