2010
DOI: 10.1016/j.jpowsour.2010.01.058
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Electrochemical and structural studies of LiCo1/3Mn1/3Fe1/3PO4 as a cathode material for lithium ion batteries

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Cited by 29 publications
(19 citation statements)
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“…Mn, Co, Ni are displayed in Fig. 3b [9,[27][28][29][30]. The decrease in capacity of LiFePO 4 upon increasing the doping concentration of cations is due to formation of defect cluster in the system while the cell voltage increased from 3.5 to 4.7 V. Thus the interstitial defect induces electrostatic interactions between the defect regions that lead to agglomerated defect clusters, which restrict the Li + mobility resulting in poor capacity retention [21].…”
Section: (B) Defects Due To Doping In M Sitementioning
confidence: 99%
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“…Mn, Co, Ni are displayed in Fig. 3b [9,[27][28][29][30]. The decrease in capacity of LiFePO 4 upon increasing the doping concentration of cations is due to formation of defect cluster in the system while the cell voltage increased from 3.5 to 4.7 V. Thus the interstitial defect induces electrostatic interactions between the defect regions that lead to agglomerated defect clusters, which restrict the Li + mobility resulting in poor capacity retention [21].…”
Section: (B) Defects Due To Doping In M Sitementioning
confidence: 99%
“…Change in cell voltage and specific capacity on different metal ion complex [9,[28][29]. Intensity / a.u.…”
Section: Summary and Overviewmentioning
confidence: 99%
“…The olivine compounds LiMPO 4 contain tetrahedral "anion" structure units (PO 4 ) 3-with strong covalent bonding, generating oxygen octahedral occupied by other M metal ions. The PO 4 unit tends to reduce the covalency of the M -O bond, modifying the redox potential for the M 2+ / 3+ couple and thus producing a practical voltage while lithium insertion and re-insertion occurs [7][8]. Among the LiMPO 4 reported in the literature [7][8][9][10], lithium iron phosphate (LiFePO 4; [7]) and lithium manganese phosphate (LiMnPO 4 ; [10]) have been recognised as promising cathode material for rechargeable battery applications.…”
Section: Introductionmentioning
confidence: 99%
“…The PO 4 unit tends to reduce the covalency of the M -O bond, modifying the redox potential for the M 2+ / 3+ couple and thus producing a practical voltage while lithium insertion and re-insertion occurs [7][8]. Among the LiMPO 4 reported in the literature [7][8][9][10], lithium iron phosphate (LiFePO 4; [7]) and lithium manganese phosphate (LiMnPO 4 ; [10]) have been recognised as promising cathode material for rechargeable battery applications. This is mainly because a large reversible capacity of 164 mAh/g was achieved over a wide composition range of Li 1-y Mn y PO 4 and Li 1-y Fe y PO 4 , even at Mn & Fe contents as high as y = 0.75 [11].…”
Section: Introductionmentioning
confidence: 99%
“…However, its low electronic conductivity [12] and low diffusion coefficient of Li + [13] hinder its commercial applications. At present, various approaches, such as carboncoating [14,15], metal-doping [16][17][18][19][20], and particle-size minimizing [21][22][23][24], have been tried to tackle these problems. So far, a number of literatures [25][26][27][28][29] have been reported that metal-doping (Co 2+ , Cr 3+ , Ti 4+ , V 5+ , Al 3+ , Na + , Ni + , Mg 2+ , Nd 3+ ) can improve the electrochemical performance of LiFePO 4 significantly.…”
Section: Introductionmentioning
confidence: 99%