Abstract
The cathode material of Li1.1Co0.02La0.01Mn2O4 was successfully synthesized by the method of co-precipitation followed by a solid state reaction.In the sintering temperature range of 700~850 ℃,X-ray diffraction(XRD) results showed a single phase of each material and the increase of crystallization degree,and scanning electron microscopic(SEM) images indicated that the particle size increased and the specific surface area decreased,respectively,with increasing the sintering temperature.Due to its lower polarization resistance,the Co and La co-doped lithium-rich lithium manganate(sintered at 800 ℃) positive electrodes showed the most promising electrochemical performance.The capacity retention after 50 cycles reached 98.5%.
Keywords
lithium-ion battery, LiMn2O4, co-doped, La-doped, electrochemical performance
Publication Date
2009-02-28
Online Available Date
2009-02-28
Revised Date
2009-02-28
Received Date
2009-02-28
Recommended Citation
Da-qiao ZHOU.
Preparation and Performance of Co and La Co-doped Li-rich Lithium Manganate[J]. Journal of Electrochemistry,
2009
,
15(1): 74-78.
DOI: 10.61558/2993-074X.1958
Available at:
https://jelectrochem.xmu.edu.cn/journal/vol15/iss1/17
References
[1]Wu Y P,Dai X B,Ma J Q,et al.Applications and op-erating in lithium battery[M].Beijing:Chemical Indus-try Press,2004,168-170.
[2]Tabuchi M,Masqueller C.Characterizatin of Li1-δMn2-2δO4defect spinal material by their phase transitin,magnetic and electrochemical properties[J].J PowerSource,1997,68:623-628.
[3]Gurnmow R J,Kock A.Improved capacity retention inrechargeable 4V lithium-manganese oxides cell[J].Solid State Ionics,1992,69:59-73.
[4]Pasquier A D,Blyr A,Courjia P.Mechanism for limit-ed 55℃storage performance of Li1.05Mn1.95O4elec-trodes[J].J Elechtrochem Soc,1999,146:428-436.
[5]Nakai I,Shiraishi Y,Nishika W.Development of a newin suit cell for X-ray absorption fine structure analysis ofthe electrochemical reaction in rechargeable battery andits application to lithium battery material Li1+yMn2-yO4[J].Spectrochemica Acta(Part B),1999,54(1):143-149.
[6]Song D,Ikuta H,Uchida T.The spinel phases Li AlyMn2-yO4(y=0,1/12,1/9,1/6,1/3)and Li(Al,M)1/6O4(M=Cr,Co)as the cathode for rechargeablelithium batteries[J].Solid State Ionics,1999,117:151-156.
[7]Yao Y C,Dai Y N.Reasons and solutions for capacityfading of spinel LiMn2O4[J].Materials Review,2005,19:1-4.
[8]Zhao S X,Yan X M,Liu H X,at el.The structuralstability of S-M(M=Al,Co)co-doped spinelLiMn2O4cathode materials[J].Acta Physico-ChimicaSinica,2004,03:233-236.
[9]Liu Y X,Peng Z D,Hu G R,at el.Influence of do-ping rare-earth on electrochemical performance of spinelLiMn2O4[J].Battery Bimonthly,2002,32:191-193.
[10]Thacheray M M,David W I F.Lithium insertion intomanganese spinels[J].Mac Res Bull,1983,18:46.
[11]Amatucci G G,Schmutz C N,Blyr A.Materials′effects on the elevated and room temperature perform-ance of C/LiMn204Li-ion batteries[J].J PowerSource,1997,69:11-25.
[12]Feng C Q,Tang H,Zhang K L,et al.Synthesis con-ditions and oxygen station of non-stoichiometry spinalphase(LixMn1.93Y0.02O4)for lithium ion battery appli-cations[J].Mater Chem Phys,2003,80(3):573-576.
[13]Ahn D S,Song MY.Variations of the electrochemicalproperties of LiMn2O4with synthesis conditions[J].JElectrochem Soc,2000,147:874-879.
[14]Aurbach D,Langzam J.The correlation between sur-face chemistry,surface morphology,and cyclic effi-ciency of lithium electrodes in a few polar aprotic sys-tems[J].J Electrochem Soc,1989,136:3198-3205.
[15]Shen C H,Liu R S,Gundakaram R,et al.Effect ofdoping Co in LiMn2O4[J].J Power Sources,2001,102(1~2):21-28.
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