Electrochemical performance and thermal stability of Li1.18Co0.15Ni0.15Mn0.52O2 surface coated with the ionic conductor Li3VO4

被引:129
作者
Fu, Qiang [1 ]
Du, Fei [1 ]
Bian, Xiaofei [1 ]
Wang, Yuhui [1 ]
Yan, Xiao [1 ]
Zhang, Yongquan [1 ]
Zhu, Kai [1 ]
Chen, Gang [1 ,2 ]
Wang, Chunzhong [1 ,2 ]
Wei, Yingjin [1 ]
机构
[1] Jilin Univ, Coll Phys, Minist Educ, Key Lab Phys & Technol Adv Batteries, Changchun 130012, Peoples R China
[2] Jilin Univ, State Key Lab Superhard Mat, Changchun 130012, Peoples R China
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
CATHODE MATERIAL; POSITIVE ELECTRODE; THIN-FILMS; LITHIUM; CAPACITY; DETERIORATION; OXIDATION; BEHAVIOR; CELLS; XPS;
D O I
10.1039/c4ta00189c
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
Li1.18Co0.15Ni0.15Mn0.52O2 cathode material was prepared by the sol-gel method. The material was coated with the ionic conductor Li3VO4 via direct reaction with NH4VO3 at 350 degrees C. The Li3VO4 coated material had a higher ordered hexagonal layered structure, and less Li+/Ni2+ cation mixing. The surface of the coated material was composed of Li3VO4 polycrystals, which were impregnated into the bulk of the active material. The surface coating protected the material from contact with CO2 in the air, thus inhibiting the formation of an Li2CO3 layer. Electrochemical studies showed that the Li3VO4 surface coating improved the activation of Mn4+ ions, resulting in a high discharge capacity. It also prohibited the growth of a solid electrolyte interface film, and facilitated the charge transfer reactions at the electrode/electrolyte interface, thus improving the rate capability and cycle stability of the material. DSC analysis of the fully charged electrode showed that the temperature of the exothermic peak increased from 205.2 degrees C to 232.8 degrees C, and that the amount of heat that was released was reduced from 807.5 J g(-1) to 551.0 J g(-1), highlighting the improved thermal stability of the material after coating with Li3VO4.
引用
收藏
页码:7555 / 7562
页数:8
相关论文
共 47 条
[11]   Layered Li(Li0.2Ni0.15+0.5zCo0.10Mn0.55-0.5z)O2-zFz cathode materials for Li-ion secondary batteries [J].
Kang, SH ;
Amine, K .
JOURNAL OF POWER SOURCES, 2005, 146 (1-2) :654-657
[12]   Electrochemical performance of Li[LixNi(1-3x)/2Mn(1+x)/2]O2 cathode materials synthesized by a sol-gel method [J].
Kim, JH ;
Sun, YK .
JOURNAL OF POWER SOURCES, 2003, 119 :166-170
[13]   AlF3-coated Li(Li0.17Ni0.25Mn0.58)O2 as cathode material for Li-ion batteries [J].
Li, G. R. ;
Feng, X. ;
Ding, Y. ;
Ye, S. H. ;
Gao, X. P. .
ELECTROCHIMICA ACTA, 2012, 78 :308-315
[14]   Origin of deterioration for LiNiO2 cathode material during storage in air [J].
Liu, HS ;
Zhang, ZR ;
Gong, ZL ;
Yang, Y .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2004, 7 (07) :A190-A193
[15]   Functional surface modifications of a high capacity layered Li[Li0.2Mn0.54Ni0.13Co0.13]O2 cathode [J].
Liu, Jun ;
Manthiram, Arumugam .
JOURNAL OF MATERIALS CHEMISTRY, 2010, 20 (19) :3961-3967
[16]   Synthesis and characterization of LiNi1-x-yCoxMnyO2 as the cathode materials of secondary lithium batteries [J].
Liu, ZL ;
Yu, AS ;
Lee, JY .
JOURNAL OF POWER SOURCES, 1999, 81 :416-419
[17]   Layered cathode materials Li[NixLi(1/3-2x/3)Mn(2/3-x/3)]O2 for lithium-ion batteries [J].
Lu, ZH ;
MacNeil, DD ;
Dahn, JR .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2001, 4 (11) :A191-A194
[18]   Synthesis, structure, and electrochemical behavior of Li[NixLi1/3-2x/3Mn2/3-x/3]O2 [J].
Lu, ZH ;
Beaulieu, LY ;
Donaberger, RA ;
Thomas, CL ;
Dahn, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2002, 149 (06) :A778-A791
[19]   Understanding the anomalous capacity of Li/Li[NixLi(1/3-2x/3)Mn(2/3-x/3]O2 cells using in situ X-ray diffraction and electrochemical studies [J].
Lu, ZH ;
Dahn, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2002, 149 (07) :A815-A822
[20]   Lack of cation clustering in Li[NixLi1/3-2x/3Mn2/3-x/3]O2 (0<x≤1/2) and Li[CrxLi(1-x)/3Mn(2-2x)/3]O2 (0<x<1) [J].
Lu, ZH ;
Chen, ZH ;
Dahn, JR .
CHEMISTRY OF MATERIALS, 2003, 15 (16) :3214-3220