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Understanding of the Li-insertion process in a phosphate based electrode material for lithium ion batteries
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Lasri, Karima
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Univ Cent Florida, NanoSci Technol Ctr, Orlando, FL 32816 USA
Univ Cent Florida, Dept Phys, Orlando, FL 32816 USA Cadi Ayyad Univ, Fac Sci & Technol, LCME, Av A El Khattabi,PB 549, Marrakech, Morocco

Dahbi, Mouad
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Mohammed VI Polytech Univ, Mat Sci & Nanoengn, Lot 660 Hay Moulay Rachid, Ben Guerir, Morocco Cadi Ayyad Univ, Fac Sci & Technol, LCME, Av A El Khattabi,PB 549, Marrakech, Morocco

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Tetard, Laurene
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Univ Cent Florida, NanoSci Technol Ctr, Orlando, FL 32816 USA
Univ Cent Florida, Dept Phys, Orlando, FL 32816 USA Cadi Ayyad Univ, Fac Sci & Technol, LCME, Av A El Khattabi,PB 549, Marrakech, Morocco

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机构:
[1] Cadi Ayyad Univ, Fac Sci & Technol, LCME, Av A El Khattabi,PB 549, Marrakech, Morocco
[2] Univ Cent Florida, NanoSci Technol Ctr, Orlando, FL 32816 USA
[3] Univ Cent Florida, Dept Phys, Orlando, FL 32816 USA
[4] Mohammed VI Polytech Univ, Mat Sci & Nanoengn, Lot 660 Hay Moulay Rachid, Ben Guerir, Morocco
关键词:
Li-ion batteries;
Anode material;
Nasicon structure;
Phosphate;
Energy storage;
ANODE MATERIALS;
ELECTROCHEMICAL PERFORMANCE;
NEGATIVE ELECTRODE;
NA-ION;
NASICON;
LITI2(PO4)(3);
INTERCALATION;
SPECTROSCOPY;
COMPOSITES;
MECHANISMS;
D O I:
10.1016/j.jpowsour.2019.226803
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:
Being considered as a high Li-ion mobility material, Nasicon structured Li1.5Fe0.5Ti1.5(PO4)(3) phosphate material was synthesized via sol-gel route and electrochemically tested as electrode material for lithium-ion batteries. The material was tested in half-lithium electrochemical cells, within two voltage windows, 1.5-3.0 V and 0.5-3.0 V, and delivered first discharge capacities of 129 mAh/g and 567 mAh/g, respectively. Raman spectroscopy was used to confirm the material's structure before and during cycling. In addition, a comparative study of the electrochemical performance by the use of two different binders (PVDF and CMC), was conducted and showed a significant change in the electrochemical performance due to the change of the binder. Electrochemical impedance spectroscopy was used to evidence the electrodes' interface changes during cycling.
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