Nitrogen-doped Li4Ti5O12 nanosheets with enhanced lithium storage properties

N-doped Li4Ti5O12 nanosheets (NLTO) have been prepared by a simple hydrothermal reaction with further heat treatment at low temperature (500 °C) under NH3 atmosphere. The effects of the Nitrogen on structure and electrochemical performance are extensively studied. XRD results show that nitrogen dopi...

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Published inJournal of power sources Vol. 266; pp. 150 - 154
Main Authors Wang, Baofeng, Wang, Junsheng, Cao, Jie, Ge, Honghua, Tang, Yufeng
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 15.11.2014
Elsevier
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Abstract N-doped Li4Ti5O12 nanosheets (NLTO) have been prepared by a simple hydrothermal reaction with further heat treatment at low temperature (500 °C) under NH3 atmosphere. The effects of the Nitrogen on structure and electrochemical performance are extensively studied. XRD results show that nitrogen doping does not change the Li4Ti5O12 (LTO) crystal structure. TEM and SEM results indicate the as-synthesized NLTO has an irregular nano-sheet-like structure with a size of 50–200 nm, which results in short Li+ diffusion paths and rapid charge transfer reactions due to the high electrode–electrolyte interface area. Galvanostatic charge–discharge tests show that NLTO exhibits a higher rate capability of 151.8 mAh g−1 at 10 C than that of LTO (139.1 mAh g−1 at 10 C), suggesting that N-doping is beneficial to the improvement in high-rate capability of the Li4Ti5O12 nanosheets. •N-doped Li4Ti5O12 was prepared by hydrothermal route and following sintering in NH3.•N-doped Li4Ti5O12 has nanosheets structure.•Synergistic effect of N-doping and nanostructure leads to high rate performance.•N-doped Li4Ti5O12 shows improved cycle stability and specific capacity at high rate.
AbstractList N-doped Li4Ti5O12 nanosheets (NLTO) have been prepared by a simple hydrothermal reaction with further heat treatment at low temperature (500 °C) under NH3 atmosphere. The effects of the Nitrogen on structure and electrochemical performance are extensively studied. XRD results show that nitrogen doping does not change the Li4Ti5O12 (LTO) crystal structure. TEM and SEM results indicate the as-synthesized NLTO has an irregular nano-sheet-like structure with a size of 50–200 nm, which results in short Li+ diffusion paths and rapid charge transfer reactions due to the high electrode–electrolyte interface area. Galvanostatic charge–discharge tests show that NLTO exhibits a higher rate capability of 151.8 mAh g−1 at 10 C than that of LTO (139.1 mAh g−1 at 10 C), suggesting that N-doping is beneficial to the improvement in high-rate capability of the Li4Ti5O12 nanosheets. •N-doped Li4Ti5O12 was prepared by hydrothermal route and following sintering in NH3.•N-doped Li4Ti5O12 has nanosheets structure.•Synergistic effect of N-doping and nanostructure leads to high rate performance.•N-doped Li4Ti5O12 shows improved cycle stability and specific capacity at high rate.
Author Wang, Junsheng
Cao, Jie
Ge, Honghua
Tang, Yufeng
Wang, Baofeng
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  organization: CAS Key Laboratory of Materials for Energy Conversion and State Key Laboratory of High Performance Ceramics and Super Fine Microstructure, Shanghai Institute of Ceramics, CAS, Shanghai 200050, China
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Keywords Lithium ion batteries
Anode material
Lithium titanate oxide
Doping
Ternary compound
Nanosheet
Anode
Lithium Oxides
Doped materials
Secondary cell
Nanostructure
Nitrogen addition
Electrode material
Titanium Oxides
Lithium Titanates
Lithium oxide
Language English
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Snippet N-doped Li4Ti5O12 nanosheets (NLTO) have been prepared by a simple hydrothermal reaction with further heat treatment at low temperature (500 °C) under NH3...
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SubjectTerms Anode material
Applied sciences
Direct energy conversion and energy accumulation
Doping
Electrical engineering. Electrical power engineering
Electrical power engineering
Electrochemical conversion: primary and secondary batteries, fuel cells
Exact sciences and technology
Lithium ion batteries
Lithium titanate oxide
Materials
Title Nitrogen-doped Li4Ti5O12 nanosheets with enhanced lithium storage properties
URI https://dx.doi.org/10.1016/j.jpowsour.2014.05.009
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