2D Mesoporous Nanomesh from N-Doped Carbon-Encapsulated V2O3 Nanowires as an Anode for Lithium-Ion Batteries

被引:22
作者
Liu, Chang Sheng [1 ]
Ye, Xi [1 ]
Zhou, BoYu [1 ]
Zeng, Xin Qian [1 ]
Xu, Jun [1 ,3 ]
Xu, Qing Chi [1 ]
Li, Jianfeng [2 ]
机构
[1] Xiamen Univ, Fujian Prov Key Lab Soft Funct Mat, Res Inst Biomimet & Soft Matter, Dept Phys, Xiamen 361005, Peoples R China
[2] Xiamen Univ, MOE Key Lab Spectrochem Anal & Instrumentat, State Key Lab Phys Chem Solid Surfaces, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
[3] Xiamen Univ, Shenzhen Res Inst, Shenzhen 518057, Peoples R China
基金
中国国家自然科学基金;
关键词
HYDROTHERMAL SYNTHESIS; RECENT PROGRESS; PERFORMANCE; NANOPARTICLES; NANOMATERIALS; FRAMEWORKS; ELECTRODE; OXIDE;
D O I
10.1021/acs.jpcc.0c06899
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
Vanadium (III) oxide nanomaterials have been investigated and considered as potential anode materials for Li-ion batteries (LIBs). Fabrication of two-dimensional (2D) mesoporous nanomeshes from carbon-encapsulated V2O3, though is technically challenging, can further enhance its electrochemical performances due to the shortening of the Li+-ion diffusion distance, the highly conductive pathway for electrons, and the tremendous increase of surface areas. In this paper, an ice-templated assembly approach is utilized to fabricate a 2D mesoporous nanomesh from N-doped carbon-encapsulated V2O3 (V2O3@N-C Nm). The V2O3@N-C Nm anode exhibits a highly reversible capacity of similar to 651 mA h g(-1) at a current density of 200 mA g(-1) over 100 cycles, which is 2.5 times and 1.3 times higher than those of V2O3 Nm and V2O3@N-C nanocomposite (V2O3@N-C Nc), respectively. The superior electrochemical performances of V2O3@N-C Nm are mainly due to its unique nanomesh nanostructure, which facilitates the lithiation/delithiation process, alleviates structural collapse, enhances electrical conductivity, and provides efficient diffusion channels.
引用
收藏
页码:24073 / 24080
页数:8
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