期刊文献+

共沉淀法制备LiNi_(0.5)Mn_(1.5)O_4正极材料及其性能 被引量:5

Performance of LiNi_(0.5)Mn_(1.5)O_4 cathode material synthesized by coprecipitation method
下载PDF
导出
摘要 采用共沉淀法制备镍锰复合氢氧化物沉淀,然后与LiOH·H_2O混合,空气中800℃煅烧18h,并500℃短时间退火处理5h得到高电压正极材料LiNi_(0.5)Mn_(1.5)O_4。通过X射线衍射光谱法(XRD),扫描电子显微镜法(SEM)和恒电流充放电测试对样品的物相、形貌和电化学性能进行了表征。合成的LiNi_(0.5)Mn_(1.5)O_4具有立方尖晶石结构,结晶性良好,颗粒粒径均匀,为200~300nm。电化学测试表明:样品存在4.7V附近的电压平台,在0.5C的较大放电电流下,首次充电容量为141.0 mAh/g,首次放电容量为122.9 mAh/g,80次循环后样品的容量保持率为97.7%,且经过活化后每个循环的库仑效率都超过了98%,具有极其优秀的循环稳定性和充放电的可逆性。 The composite hydroxid of nickel and manganese was prepared by the coprecipitation method.LiNi0.5)Mn1.5O4 was synthesised by firing the mixture of the prepared composite hydroxid and LiOH- H2O at 800℃ for 18 h and then annealing at 500 ℃ for 5 h in air.The phase,morphology and electrochemical properties of the sample were characterized by XRD,SEM and constant current charge-discharge tests. The synthesized LiNi0.5)Mn1.5O4belonging to cubic phase was a spinel structure with clearly defined shape and particle size of 200-300 nm. Electrochemical tests show that the synthesized LiNi0.5)Mn1.5O4 presents only one plateau near 4.7 V and the charge and discharge capacity are 141.0 mAh/g and 122.9 mAh/g, respectively. After 80 cycles, the capacity retention rate of the sample discharged at 0.5 C is 97.7%. And its coulombic efficiency of every cycle is above 98.5% through activation. The prepared LiNi0.5)Mn1.5O4has very excellent cycle stability and charge-discharge reversibility.
出处 《电源技术》 CAS CSCD 北大核心 2010年第7期644-646,共3页 Chinese Journal of Power Sources
关键词 正极材料 LiNi0.5)Mn1.5O4 共沉淀法 电化学性能 cathode maertial LiNi0.5)Mn1.5O4 coprecipitation method electrochemistry performance
  • 相关文献

参考文献10

  • 1陈召勇,肖劲,朱华丽,刘业翔.不同原料对Li-Ni-Mn-O5V正极材料的结构和性能的影响[J].无机化学学报,2005,21(9):1417-1421. 被引量:3
  • 2WU X L,SEUNG B K.Improvement of electrochemical propertie of LiNi0.5Mn15O4 spinel[J].Journal of Power Sources,2002,109: 53- 57.
  • 3XU H Y, XIE S, DING N, et al.Improvement of electrochemical properties of LiNi0.5Mn1.5O4 spinel prepared by radiated polymer gel method[J]. Electrochimica Acta, 2006, 51: 4352-4357.
  • 4徐宁,刘国强,曾潮流,吴维.锂离子蓄电池正极材料LiNi_(0.5)Mn_(1.5)O_4的合成[J].电源技术,2003,27(B05):213-216. 被引量:2
  • 5MYUNG S T, KOMABA S, KUMAGAI N, et al. Nano-crystalline LiNi0.5Mn1.5O4 synthesized by emulsion drying method [J]. Electrochimica Acta, 2002, 47: 2543-2549.
  • 6KIM J H,MYUNG S T,SUN Y K.Molten salt synthesis of LiNi0.5- Mn1.5O4 spinel for 5 V class cathode material of Li-ion secondary battery[J]. Electrochimica Acta, 2004, 49: 219-227.
  • 7WEN L, LU Q, XU G X. Molten salt synthesis of spherical LiNi0.5- Mn1.5O4 cathode materials [J].Electrochimica Acta,2006,51 : 4388- 4392.
  • 8YU L H, CAO Y L, YANG H X, et al.Synthesis and electrochemical properties of highvoltage LiNi0.5Mn1.5O4 electrode material for Li-ion batteries by the polymer-pyrolysis method[J]. J Solid State Eleetrochem, 2006, 10: 283-287.
  • 9PARK S H, SUN Y K. Synthesis and electrochemical properties of 5 V spinel LiNi0.5Mn1.5O4 cathode materials prepared by ultrasonic spray pyrolysis method[J]. Electrochimica Acta, 2004, 50:431-434.
  • 10ZHONG Q, BONAKDARPOUR A, ZHANG M, et al. Synthesis and electrochemistry of LiNixMn2- xO4[J]. J Electrochem Soc, 1997, 144(1): 205-213.

二级参考文献19

  • 1AMINE K, TUKAMOTO H, YASUDA H, et al. A new threevoltage spinel LiNi0.4 Mn1.5O4 for secondary lithium batteries [ J ]. J Electrochem Soc, 1996,143 : 1 607.
  • 2SIGLA C, GLIYOMARD D, VEBAERE A, et al. Poaitive electrode materials with high operating voltage for lithium batteries:LiCryMn2- y (0≤y≤1) [J ]. Solid State Ionies, 1995, 81 : 167.
  • 3AMINE K, TUKAM(YFO H, YASUDA H, et al. Preparation and ectrochemical investigation of LiMn2-xMexO4 (Me = Ni, Fe and x= 0.5, 1 ) cathode material for secondary lithium batteries [ J ]. J Electrochem Soc, 1997, 68: 604.
  • 4EIN-EIL Y, SHARON H L, MARIA A R. LiCuxMn2-xO4(0.1≤x≤0.5): A new class of cathode materials Li batteries[J]. J Electrochem Soc, 1998,145:3 383.
  • 5ZHONG Qi-ming, ARMAN B, ZHANG Mei-jie, et al. Synthesis and electroehemistry of LiNixMn2-xO4 [J ]. J Electrochem Soc,1997,144 : 205.
  • 6Alcantara R, Jaraba M, Lavela P, et al. J. Electrochem. Soc.,2004,151:53-58.
  • 7Caballero A, Hernan L, Melero M, et al. J. Electrochem.Soc., 2005,152:6-12.
  • 8Sang H, Yang K, Electrochimica Acta, 2004,50:431-434.
  • 9Xia Y, Zhou H, Yoshio M, J. Electrochem. Soc., 1997,144:2593-2600.
  • 10Dong H, Seung M, J. Electrochem. Soc., 1997,144:3342-3347.

共引文献3

同被引文献137

引证文献5

二级引证文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部