Oxygen Vacancies Boosting Lithium-Ion Diffusion Kinetics of Lithium Germanate for High-Performance Lithium Storage

被引:28
|
作者
Li, Long [1 ]
Meng, Tao [2 ]
Wang, Jie [1 ]
Mao, Baoguang [1 ]
Huang, Jingbin [1 ]
Cao, Minhua [1 ]
机构
[1] Beijing Inst Technol, Sch Chem & Chem Engn, Key Lab Cluster Sci,Minist Educ China, Beijing Key Lab Photoelect Electrophoton Convers, Beijing 100081, Peoples R China
[2] Hebei Agr Univ, Coll Sci, Baoding 071001, Peoples R China
基金
中国国家自然科学基金;
关键词
lithium germanate; oxygen vacancies; lithium storage; electronic conductivity; activation energy; diffusion kinetics; ANODE MATERIAL; RATE CAPABILITY; ALUMINA MEMBRANES; HIGH-CAPACITY; SURFACE; NANOPARTICLES; BATTERIES; REDUCTION; SODIUM; OXIDES;
D O I
10.1021/acsami.1c04200
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Oxygen vacancies play a positive role in optimizing the physical and chemical properties of metal oxides. In this work, we demonstrated oxygen vacancy-promoted enhancement of Li-ion diffusion kinetics in Li2GeO3 nanoparticle-encapsulated carbon nanofibers (denoted as Li2GeO3-x/C) and accordingly boosted lithium storage. The introduction of the oxygen vacancies in Li2GeO3-x/C can enhance electronic conductivity and evidently decrease activation energy of Li-ion transport, thus resulting in evidently accelerated Li-ion diffusion kinetics during the lithiation/delithiation process. Thus, the Li2GeO3-x/C nanofibers exhibit an exceptionally large discharge capacity of 1460.5 mA h g(-1) at 0.1 A g(-1), high initial Coulombic efficiency of 81.3%, and excellent rate capability. This facile and efficient strategy could provide a reference for injecting the oxygen vacancies into other metal oxides for high-performance anode materials.
引用
收藏
页码:24804 / 24813
页数:10
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