Structural and dielectric studies of LiNiPO4 and LiNi0.5Co0.5PO4 cathode materials for lithium-ion batteries

被引:38
作者
Babu, K. Vijaya [1 ]
Devi, L. Seeta [2 ]
Veeraiah, V. [2 ]
Anand, K. [3 ,4 ]
机构
[1] Andhra Univ, Adv Analyt Lab, Visakhapatnam, Andhra Pradesh, India
[2] Andhra Univ, Dept Phys, Visakhapatnam, Andhra Pradesh, India
[3] Sri Krishna Devaraya Univ, Dept Instrumentat, Anantapur, Andhra Pradesh, India
[4] Sri Krishna Devaraya Univ, USIC, Anantapur, Andhra Pradesh, India
来源
JOURNAL OF ASIAN CERAMIC SOCIETIES | 2016年 / 4卷 / 03期
关键词
Cathode materials; XRD; FTIR; Dielectric modulus; ELECTRICAL-PROPERTIES; PHOSPHO-OLIVINES; CONDUCTIVITY; TRANSPORT; LIMPO4; FE; CO; IMPEDANCE; LIFEPO4; LICOPO4;
D O I
10.1016/j.jascer.2016.05.001
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Olivine-type LiNiPO4 has been considered as a most competitive positive electrode active material for lithium-ion batteries. In the present paper, the LiNiPO4 and Co-doped LiNi0.5Co0.5PO4 are synthesized by solid-state reaction method under air atmosphere. All the X-ray diffraction peaks of both the compounds are indexed and it is found that the samples are well crystallized in orthorhombic olivine structure belonging to the space group Pnma. The crystallite size is calculated from the Scherrer formula and it is found to be 6.918 and 4.818nm for pure and doped samples, respectively. The surface morphology and grain sizes of the materials are investigated through scanning electron microscope. Presence of preferred local cation environment is understood from Fourier transform infrared spectroscopy (FTIR) studies. The conductivity and dielectric analysis of the samples are carried out at different temperatures and frequencies using the complex impedance spectroscopy technique. The electrical conductivity of LiNi0.5Co0.5PO4 is higher than that of pure LiNiPO4. (C) 2016 The Ceramic Society of Japan and the Korean Ceramic Society. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:269 / 276
页数:8
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