Lithium ferrite (Li0.5Fe2.5O4): synthesis, structural, morphological and magnetic evaluation for storage

被引:25
|
作者
Ahmad, Mukhtar [1 ]
Shahid, Muhammad [1 ]
Alanazi, Yousef Mohammed [2 ]
Rehman, Atiq Ur [3 ]
Asif, Muahmmad [1 ]
Dunnill, Charles W. [4 ]
机构
[1] COMSATS Univ Islamabad, Dept Phys, Lahore Campus, Lahore 54000, Pakistan
[2] King Saud Univ, Coll Engn, Chem Engn Dept, Riyadh, Saudi Arabia
[3] Riphah Int Univ, Dept Phys, Lahore Campus, Lahore, Pakistan
[4] Energy Safety Inst ESRI, Swansea Univ Bay Campus, Swansea SA1 8EN, SA, Wales
关键词
Lithium-ion batteries; Lithium ferrites; Structural parameter; Magnetic properties; CV measurements; COBALT FERRITE; SATURATION; NICKEL;
D O I
10.1016/j.jmrt.2022.03.113
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Lithium ferrite Li0.5Fe2.5O4 has been synthesized by the use of the solegel technique. X-ray diffractometer (XRD) has been employed to confirm the crystal structure of spinel ferrites. No impurity peaks are detected in XRD graph, which confirms single phase crystal structure. The evaluation of grain size and analysis of external surface morphology of synthesized lithium ferrites has been done by scanning electron microscope (SEM). Average grain size was about equal to 131 nm. Energy dispersive x-ray spectra showed all the elements were present in required proportions. Magnetic characteristics such as saturation magnetization (M-s), remanence (M-r), and coercive force (H-c) have been measured from MH loops. Saturation magnetization has been measured to be 43.69 emu/by law of approach to saturation. The coercivity value lies in the range of few hundred Oersted which is vital condition for electromagnetic materials. Cyclic Voltammetry (CV) measurements were made, to know about the electrochemical performance of the material. CV results show that with the increase in scan rate specific capacitance decreases and the area of the loop increases which is promising for the formation of super capacitors and lithium-ion batteries (LIB's). (C) 2022 The Author(s). Published by Elsevier B.V.
引用
收藏
页码:3386 / 3395
页数:10
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