阳极
锂(药物)
材料科学
电化学
插层(化学)
X射线光电子能谱
假电容
傅里叶变换红外光谱
电极
法拉第效率
化学工程
无机化学
化学
超级电容器
内分泌学
物理化学
工程类
医学
作者
Rong Long,Gulian Wang,Zhong-Li Hu,Pengfei Sun,Li Zhang
出处
期刊:Rare Metals
[Springer Nature]
日期:2020-08-20
卷期号:40 (6): 1366-1372
被引量:18
标识
DOI:10.1007/s12598-020-01502-5
摘要
Lithium-ion batteries (LIBs) have been used to power various electric devices and store energy, but their toxic components by using inorganic materials generally cause serious environmental issues when disused. Recently, environmentally friendly and naturally abundant organic compounds have been adopted as promising electrode materials for next-generation LIBs. Herein, a new organic anode electrode based on sodium citrate is proposed, which shows gradually activated electrochemical behavior and delivers a high reversible capacity of 776.8 mAh·g−1 after 1770 cycles at a current density of 2 A·g−1. With the aid of the electrochemical characterization, Fourier-transform infrared (FTIR) and X-ray photoelectron spectroscopy (XPS) analysis, the lithium uptake mechanism of sodium citrate-based anodes is identified to be a combination of three-electron lithiation/delithiation and fast Li+ intercalation/deintercalation processes, in which Faradaic reactions could offer a theoretical contribution of 312 mAh·g−1 and intercalation pseudocapacitance would provide extra capacity. This work demonstrates the great potential for developing high-capacity organic electrodes for LIBs in future.
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