Facile synthesis of mesoporous TiNb2O7/C microspheres as long-life and high-power anodes for lithium-ion batteries

被引:37
|
作者
Yang, Yan [1 ]
Yue, Yang [2 ]
Wang, Lin [1 ]
Cheng, Xinfeng [1 ]
Hu, Yingtao [1 ]
Yang, Zhi-zheng [3 ]
Zhang, Ruixue [1 ]
Jin, Bo [3 ]
Sun, Ruixue [1 ]
机构
[1] Nanyang Normal Univ, Coll Chem & Pharmaceut Engn, Engn Technol Res Ctr Henan Prov Solar Catalysis, Nanyang 473061, Peoples R China
[2] Henan Agr Univ, Coll Sci, Zhengzhou 450001, Peoples R China
[3] Jilin Univ, Sch Mat Sci & Engn, Nanling Campus,5988 Renmin St, Changchun 130025, Peoples R China
基金
中国国家自然科学基金;
关键词
Lithium-ion battery; Anode material; TiNb2O7; Amorphous carbon; HIGH-RATE-CAPABILITY; HIGH-PERFORMANCE ANODE; SUPERIOR PERFORMANCE; ENERGY-STORAGE; ANATASE TIO2; CYCLE-LIFE; FRAMEWORK; NETWORK; VACUUM; OXIDES;
D O I
10.1016/j.ijhydene.2020.02.214
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The unique ReO3 crystallographic shear structure of TiNb2O7 has enabled its application as anode material for lithium-ion batteries, in which the lattice parameter and volume change of TiNb2O7 are often negligible during lithium-ion insertion/extraction. However, several intrinsic problems of TiNb2O7, including low electronic and ionic conductivity, can restrict its application significantly. In this study, carbon-coated mesoporous TiNb2O7 microspheres are fabricated through a simple solvothermal reaction. By combining the advantages of both the amorphous carbon and mesoporous structure, TiNb2O7/C composite exhibits superior lithium storage performance, with higher rate capability (200 mAh g(-1) at 30 C) and cyclability (191 mAh g(-1) at 10 C after 500 cycles). The improved performance is due mainly to the high pseudocapacitance and low charge transfer resistance obtained from the mesoporous structure and amorphous carbon layer. The study provides a new way of constructing TiNb2O7 for ultra-fast storage devices, demonstrating great potential for application in power batteries. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:12583 / 12592
页数:10
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