A Cobalt-Free Li(Li0.17Ni0.17Fe0.17Mn0.49)O2 Cathode with More Oxygen-Involving Charge Compensation for Lithium-Ion Batteries

被引:27
作者
Wei, Hezhuan [1 ]
Cheng, Xiaolu [2 ]
Fan, Hongwei [1 ]
Shan, Qian [1 ]
An, Shengli [1 ]
Qiu, Xinping [2 ]
Jia, Guixiao [1 ]
机构
[1] Inner Mongolia Univ Sci & Technol Baotou, Sch Met & Mat, Inner Mongolia 014010, Peoples R China
[2] Tsinghua Univ, Dept Chem, Key Lab Organ Optoelect & Mol Engn, Beijing 100084, Peoples R China
关键词
density functional calculations; iron; lithium; oxygen; redox chemistry; IMPROVED ELECTROCHEMICAL PERFORMANCE; POSITIVE ELECTRODE MATERIAL; HIGH-ENERGY DENSITY; ANIONIC REDOX; LAYERED OXIDES; LI; FE; LI2MNO3; PARTICIPATION; STABILITY;
D O I
10.1002/cssc.201900241
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
High-energy-density and low-cost lithium-ion batteries are sought to meet increasing demand for portable electronics. In this study, a cobalt-free Li(Li0.17Ni0.17Fe0.17Mn0.49)O-2 (LNFMO) cathode material is chosen, owing to the reversible anionic redox couple O2-/O-. The aim is to elucidate the Fe-substitution function and oxygen redox mechanism of experimentally synthesized Li(Li0.16Ni0.19Fe0.18Mn0.46)O-2 by DFT. The redox processes of cobalt-containing Li(Li0.17Ni0.17Co0.17Mn0.49)O-2 (LNCMO) are compared with those of LNFMO. Redox couples including Ni2+/Ni3+/Ni4+, Fe3+/Fe4+ or Co3+/Co4+, and O2-/O- are found, confirmed by a X-ray photoelectron spectroscopy, and explained by redox competition between O and transition metals. In LNFMO and LNCMO, O ions with an Li-O-Li configuration readily participate in oxidation, and the most active O ions are coordinated to Mn4+ and Li+. Oxidation of O in LNCMO is triggered earlier, along with that of Co. Fe substitution activates O ions, contributes additional oxygen redox charge compensation of 0.44 e per formula unit, avoids concentrated accumulation of oxygen oxidation, and improves structural stability. This work provides new scope for designing cobalt-free, low-cost, and higher-energy-density cathode materials for Li-ion batteries.
引用
收藏
页码:2471 / 2479
页数:9
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