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D. Arumugam, G. Paruthimal Kalaignan, P. Manisankar
Solid State Ionics 179 (2010) 580 – 586
Sameh Hamzawy
Alagr Raj Paulraj
MESC9
Outline
 Introduction
 Experiment
 Results and discussion
 Conclusion
 Introduction
Advantages Disadvantages
LiCoO2 High specific capacity High cost
Better cyclic performance Toxicity
LiMn2O4 Inexpensive, relatively. Poor cycle performance
at high temperature.
Environmentally Capacity fading
Lithium-ion batteries have gained increasing importance
as power sources due to their high working voltage, low
self discharge rate, and long life.
 Reducing the amount of Mn3+ in LiMn2O4  improve
the cyclability of the materials.
 Substitute Mn by some metal species such as :
LiNixMn2−xO4, LiCoxMn2 −xO, LiLaxMn2 −xO4 ????
Experiment:
Spinel LiLaxMn2 – xO4 ,where x=0.00, 0.01, 0.03, 0.05
and 0.10 were synthesized by sol-gel method.
Results and discussion
X-ray diffraction pattern of the spinel LiMn2 O4 and
lanthanum substituted LiLaxMn2− x O 4 powders
prepared by sol – gel technique at 900 °C.
 Single phase
diffraction patterns for
the 5 samples
 Cubic spinel structure
 The intensity of the
diffraction peaks are
enhanced after doping,
indicating large crystal
size.
Lattice parameters, unit cell volume, and intensity ratios of spinel
LiLaxMn2 – xO4 , (x=0.00 to 0.10) cathode materials.
Increasing lanthanum doping , increases the lattice parameters
More lattice space for Li intercalation and deintercalation
Prevent lattice shrinking during the deintercalation
SEM image of LiMn2O4 and lanthanum substituted LiLaxMn2 – xO4 powders synthesized
at 900 °C. a) LiMn2 O4, b) LiLa0.01Mn1.99O4 , c) LiLa0.03Mn1.97O4 , d) LiLa0.05Mn1.95O4 and
e) LiLa0.10Mn1.90O4.
Raj’s part
Raman Spectroscopy
 Local symmetrical
properties
 Sensitive to the
short range
environment of
cations and the
coordinated oxygen
ions.
Galvanostatic charge/discharge studies
Cycling was done
between 2.75V to 4.5
V @ .1c Current
density
Two plateaus one
at4.05 &another 4.15
Cyclic Voltammetery
LiMn2O4
LiLa0.01Mn1.99O4
LiLa0.05Mn1.95O4
LiLa0.10Mn1.90O4
Life Cycle Test
LiMn2O4
LiLa0.05Mn1.95O4
Rate capability of LiLa0.05Mn1.95O4
C Rate Intial
stage
capacity
(mAh/g)
Capacity
After 50
cycles
(mAh/g)
.1c 127 115
.5 129 112
1 119 106
2 112 103
5 102 87
Conclusion
 The LiLa x Mn 2 − x O 4 (x=0.00, 0.01, 0.03, 0.05 ,0.10)
cathode materials were synthesized by low T sol-gel
method.
 single phase structure was conformed by XRD and
Raman ,Higher dopant level impurity phases were
present
 LiLa0.05Mn1.95O4 has excellent capacity retention.
Thank you

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Cathode materials for rechargeable lithium ion batteries

  • 1. D. Arumugam, G. Paruthimal Kalaignan, P. Manisankar Solid State Ionics 179 (2010) 580 – 586 Sameh Hamzawy Alagr Raj Paulraj MESC9
  • 2. Outline  Introduction  Experiment  Results and discussion  Conclusion
  • 3.  Introduction Advantages Disadvantages LiCoO2 High specific capacity High cost Better cyclic performance Toxicity LiMn2O4 Inexpensive, relatively. Poor cycle performance at high temperature. Environmentally Capacity fading Lithium-ion batteries have gained increasing importance as power sources due to their high working voltage, low self discharge rate, and long life.
  • 4.  Reducing the amount of Mn3+ in LiMn2O4  improve the cyclability of the materials.  Substitute Mn by some metal species such as : LiNixMn2−xO4, LiCoxMn2 −xO, LiLaxMn2 −xO4 ???? Experiment: Spinel LiLaxMn2 – xO4 ,where x=0.00, 0.01, 0.03, 0.05 and 0.10 were synthesized by sol-gel method.
  • 5. Results and discussion X-ray diffraction pattern of the spinel LiMn2 O4 and lanthanum substituted LiLaxMn2− x O 4 powders prepared by sol – gel technique at 900 °C.  Single phase diffraction patterns for the 5 samples  Cubic spinel structure  The intensity of the diffraction peaks are enhanced after doping, indicating large crystal size.
  • 6. Lattice parameters, unit cell volume, and intensity ratios of spinel LiLaxMn2 – xO4 , (x=0.00 to 0.10) cathode materials. Increasing lanthanum doping , increases the lattice parameters More lattice space for Li intercalation and deintercalation Prevent lattice shrinking during the deintercalation
  • 7. SEM image of LiMn2O4 and lanthanum substituted LiLaxMn2 – xO4 powders synthesized at 900 °C. a) LiMn2 O4, b) LiLa0.01Mn1.99O4 , c) LiLa0.03Mn1.97O4 , d) LiLa0.05Mn1.95O4 and e) LiLa0.10Mn1.90O4.
  • 9. Raman Spectroscopy  Local symmetrical properties  Sensitive to the short range environment of cations and the coordinated oxygen ions.
  • 10. Galvanostatic charge/discharge studies Cycling was done between 2.75V to 4.5 V @ .1c Current density Two plateaus one at4.05 &another 4.15
  • 13. Rate capability of LiLa0.05Mn1.95O4 C Rate Intial stage capacity (mAh/g) Capacity After 50 cycles (mAh/g) .1c 127 115 .5 129 112 1 119 106 2 112 103 5 102 87
  • 14. Conclusion  The LiLa x Mn 2 − x O 4 (x=0.00, 0.01, 0.03, 0.05 ,0.10) cathode materials were synthesized by low T sol-gel method.  single phase structure was conformed by XRD and Raman ,Higher dopant level impurity phases were present  LiLa0.05Mn1.95O4 has excellent capacity retention.