Study of the local structure of LiNi0.33+δMn0.33+δCo0.33-2δO2 (0.025 ≤ δ ≤ 0.075) oxides

被引:39
作者
Ben-Kamel, K. [3 ]
Amdouni, N. [3 ]
Mauger, A. [2 ]
Julien, C. M. [1 ]
机构
[1] Univ Paris 06, Lab Electrolytes Colloides & Syst Analyt PECSA, F-75005 Paris, France
[2] Univ Paris 06, IMPMC, F-75005 Paris, France
[3] Univ Tunis El Manar, UR Phys Chim Mat Solides, Tunis 1060, Tunisia
关键词
Transition-metal oxides; Layered compounds; Local structure; Sol-gel; HRTEM; X-RAY-ABSORPTION; LINI0.5MN0.5O2 CATHODE MATERIAL; LITHIUM COBALT OXIDES; LI-ION BATTERIES; ELECTROCHEMICAL PROPERTIES; ELECTRODE MATERIALS; POSITIVE ELECTRODE; NMR; OPTIMIZATION; LICOO2;
D O I
10.1016/j.jallcom.2012.03.018
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
A series of oxides of the composition LiNiy+delta Mny+delta Coy-2 delta O2 (y = 0.33; delta = 0.025, 0.05, 0.075) were synthesized using the sol-gel method assisted by citric acid as chelating agent. The resulting nano-sized particles crystallize with a layered structure in the rhombohedral system. They exhibit an ordered rock-salt alpha-NaFeO2-type structure (R (3) over barm space group) having an interlayer spacing close to 0.47 nm. Long- and short-range structural properties were characterized using several techniques such as X-ray diffraction (XRD), Raman scattering (RS), Fourier transform infrared (FTIR) and Li-7 magic angle spinning (MAS) NMR spectroscopy, high-resolution transmission electron microscopy (HRTEM) and energy dispersive analysis of X-rays (EDAX). Rietveld refinements of the XRD diagrams and NMR resonance integration show that the concentration of Ni2+ ions located onto Li-3b sites is lower than 3% for the three samples. HRTEM images show layered structure without dislocations. The role of the cobalt is investigated quantitatively. The results show that the increasing cobalt content induces better crystallinity, smaller cation mixing, and a change of particles morphology, from octahedron-to spherical-like shape with size in the range 200-350 nm. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:91 / 98
页数:8
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