法拉第效率
材料科学
电化学
阳极
电解质
锂(药物)
电极
锐钛矿
化学工程
扩散
兴奋剂
二氧化钛
假电容器
离子
无定形固体
纳米技术
复合材料
化学
光电子学
超级电容器
医学
生物化学
物理
有机化学
物理化学
光催化
工程类
热力学
内分泌学
催化作用
作者
Qiang He,Zhonggui Sun,Xingwang Shi,Weiwei Wu,Jiagao Cheng,Renfu Zhuo,Zhiya Zhang,Jun Wang
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2021-01-14
卷期号:35 (3): 2717-2726
被引量:22
标识
DOI:10.1021/acs.energyfuels.0c03580
摘要
Titanium dioxide (TiO2) is proposed as a promising anode material for lithium-ion batteries (LIBs) due to its highly stable structure and slight side reaction at the electrode/electrolyte interface. The low specific capacity and slow Li-ion diffusion kinetics are the major bottlenecks for the actual application of TiO2. It is thus important to exploit viable pathways to enhance the electrochemical performance and understand the corresponding mechanisms. In this work, high-quality amorphous TiO2 (TO) and anatase TiO2 (cTO) film electrodes are employed to investigate the bulk electrochemical performance by minimizing the surface contribution. At the same time, nitrogen (N) doping is performed for further comparison. The results show that TO has a relatively lower specific capacity than cTO. However, N-doped TO (TON) presents a specific capacity more than 4 times higher than TO and 3 times higher than cTO. TON also exhibits a significantly improved initial Coulombic efficiency (ICE) and a relatively higher Li-ion diffusion coefficient. Our study shows that the superior electrochemical performance of TON is correlated to the synergistic effects of the bulk pseudocapacitor and battery characteristics.
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