Spherical pristine LiMn2O4 and Ni doped LiNixMn2-xO4 (x=0.1, 0.2, 0.3, 0.4, 0.5) cathode materials for lithium ion battery with high first cycle discharge capacity and excellent cycle performance were synthesized using the solution-combustion technique. XRD
analysis revealed peak shift towards higher angle and lattice shrink as a result of Ni doping. CSAFM result confirms LiNi0.5Mn1.5O4
provides higher current of 10nA than pristine LiMn2O4 of 0.05nA. The EIS result displays that small Ni content (x=0.1, 0.2) doping
reduced the impedances of pristine LiMn2O4. The composition LiNi0.1Mn1.9O4 exhibits higher capacity and better cycleability than
other Ni content compositions. Charge/discharge cycling result shows that Ni substitution substantially improved the capacity retention of LiMn2O4. All Ni doped LiNixMn2-xO4 (x= 0.1, 0.2, 0.3,0.4, 0.5) compositions are able to retain 99% of their respective first cycle discharge capacities, whereas LiMn2O4 retains only 60% of its first cycle discharge capacity of 122 mAh/g after 50 cycles.
Reference:
Kebede, M, Kunjuzwa, N, Ozoemena, K and Mathe, M. 2013. Synthesis and Electrochemical Properties of Ni Doped Spinel LiNixMn2-xO4 (0 ≤ x ≤ 0.5) Cathode Materials for Li-Ion Battery. ECS Transactions, vol. 50(4), pp 1-14
Kebede, M. A., Kunjuzwa, N., Ozoemena, K., & Mathe, M. K. (2013). Synthesis and Electrochemical Properties of Ni Doped Spinel LiNixMn2-xO4 (0 ≤ x ≤ 0.5) Cathode Materials for Li-Ion Battery. http://hdl.handle.net/10204/7410
Kebede, Mesfin A, N Kunjuzwa, K Ozoemena, and Mahlanyane K Mathe "Synthesis and Electrochemical Properties of Ni Doped Spinel LiNixMn2-xO4 (0 ≤ x ≤ 0.5) Cathode Materials for Li-Ion Battery." (2013) http://hdl.handle.net/10204/7410
Kebede MA, Kunjuzwa N, Ozoemena K, Mathe MK. Synthesis and Electrochemical Properties of Ni Doped Spinel LiNixMn2-xO4 (0 ≤ x ≤ 0.5) Cathode Materials for Li-Ion Battery. 2013; http://hdl.handle.net/10204/7410.
Copyright: 2013 Electrochemical Society. This is an OA journal. The journal authorizes the publication of the information herewith contained. Published in ECS Transactions, vol. 50(4), pp 1-14