Study on structure and electrochemical properties of carbon-coated monoclinic Li3V2(PO4)3 using synchrotron based in situ X-ray diffraction and absorption

被引:41
|
作者
Yoon, Jeongbae [1 ]
Muhammad, Shoaib [1 ]
Jang, Donghyuk [1 ]
Sivakumar, N. [2 ]
Kim, Jaeyoon [1 ]
Jang, Won-Hee [3 ]
Lee, Yun-Sung [3 ]
Park, Young-Uk [4 ]
Kang, Kisuk [4 ]
Yoon, Won-Sub [1 ]
机构
[1] Sungkyunkwan Univ, Dept Energy Sci, Suwon 440746, Gyeonggi Do, South Korea
[2] Kookmin Univ, Sch Adv Mat Engn, Seoul 136702, South Korea
[3] Chonnam Natl Univ, Fac Appl Chem Engn, Kwangju 500757, South Korea
[4] Seoul Natl Univ, Dept Mat Sci & Engn, Seoul 151744, South Korea
基金
新加坡国家研究基金会;
关键词
Lithium battery; Cathode materials; Lithium vanadium phosphate; In situ XRD; In situ XAS; LITHIUM VANADIUM PHOSPHATE; CATHODE MATERIAL; ION BATTERIES; PERFORMANCE; COMPOSITE; ELECTRODE; LIFEPO4;
D O I
10.1016/j.jallcom.2013.03.188
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
Monoclinic Li3V2(PO4)(3), is a highly promising cathode material for lithium-ion rechargeable batteries. It has good ion mobility and high lithium capacity due to its ability to reversibly extract all three lithium ions. Here, we present, a systematic investigation of phase transitions and volume variations that occur during lithium extraction from the carbon-coated monoclinic phase of Li3V2(PO4)(3) by synchrotron based in situ X-ray diffraction and X-ray absorption spectroscopy. This monoclinic Li3V2(PO4)(3) illustrates complex behavior of four successive two-phase transitions upon extraction of all three lithium ions between 3.0 and 4.8 V vs. Li/Li+. Each XRD pattern of the intermediate compositions can be fully indexed in the monoclinic space group P2(1)/n, with net volume reduction of 6.47%. In situ V K-edge XANES in combination with study of structural parameters is applied to find the vanadium valence state at plateau regions, which highlights the variations in electrochemical potential constraining to extraction of lithium ion from different crystal sites. (C) 2013 Elsevier B. V. All rights reserved.
引用
收藏
页码:76 / 81
页数:6
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