期刊文献+

LiNi_(0.5)Mn_(1.5)O_4高电压正极材料的制备及性能研究 被引量:6

Synthesis and property of the high-voltage cathode material LiNi_(0.5)Mn_(1.5)O_4
在线阅读 下载PDF
导出
摘要 采用液相共沉淀法制备镍锰复合碳酸盐前驱体,650℃煅烧后生成的镍锰复合氧化物与Li2CO3混合,在空气中于750~900℃下煅烧10h,600℃退火10h得到LiNi0.5Mn1.5O4。采用XRD、SEM和恒电流充放电测试等对样品进行了表征。SEM结果表明,合成温度对LiNi0.5Mn1.5O4的表面形貌及粒径有较大影响;XRD结果表明,合成的样品均为纯的立方尖晶石结构。电化学测试结果表明,800℃合成的样品在室温下具有较好的电化学性能:0.1、1、2、4C首次放电容量分别130.24、129.47、115.5、108.05mAh/g,且大倍率下具有较好的循环性能。 LiNi0.5Mn1.5O4 spinel has been prepared by a composite carbonate process, and the effects of calcination temperature on the physical properties and electroche-mical performance of the samples have been investigated. The results of XRD and scanning electron microscopy (SEM) showed that as calcination temperature increa-ses , the grain sizes of the samples is obviously increase. It was found that the samples calcined at 800℃ present good electrochemical performance. Between 3.5-4. 9V versus Li, it delivered 130.24,129.47,115.5, 108.05mAh/g at 0. 1,1, 2,4C rates respectively. And it showed good cycle performance under high current density.
出处 《功能材料》 EI CAS CSCD 北大核心 2009年第6期933-935,939,共4页 Journal of Functional Materials
基金 国家重点基础研究发展计划(973计划)资助项目(2007CB613607)
关键词 LINI0.5MN1.5O4 高电压 正极材料 LiNi0.5Mn1.5O4 high voltage cathode material
  • 相关文献

参考文献19

二级参考文献45

  • 1W.H. Tian, K. Ohishi and M. Nemoto 1)Department of Materials Physics and Chemistry, University of Science and Technology Beijing, Beijing 100083, China,2)Department of Materials Science and Engineering, Faculty of Engineering 36, Kyushu University, Fuk.PRECIPITATION HARDENING IN B2-ORDERED NiAl BY Ni_(2)AlTi COMPOUND[J].Acta Metallurgica Sinica(English Letters),2001,14(5):313-318. 被引量:7
  • 2方海升,王志兴,李新海,尹周澜,郭华军,彭文杰.Li_2CO_3、NiO和电解MnO_2合成高容量LiNi_(0.5)Mn_(1.5)O_4及其表征(英文)[J].无机化学学报,2006,22(2):311-315. 被引量:6
  • 3Amine K, Tukamoto H, Yasuda H, et al. J. Power Sources,1997,68:604-608.
  • 4Zhong Q, Bonakdarpour A, Zhang M, et al. J. Electrochem.Soc, 1997,144(1):205-213.
  • 5Ohzuku T, Takeda S, Iwanaga M. J. Power Sources, 1999,81-82:90-94.
  • 6Idemoto Y, Narai H, Koura N. J. Power Sources, 2003,119-121:125-129.
  • 7Kim J H, Myung S T, Sun Y K. Electrochim Acta, 2004,49:219-227.
  • 8Wu X, Kim S B. J. Power Sources, 2002,109:53-57.
  • 9Alcantara R, Jaraba M, Lavela P, et al. Electrochim Acta,2002,47:1829-1835.
  • 10Lee Y S, Sun Y K, Ota S, et al. Electrochem Commun, 2002,4(12):989-994.

共引文献138

同被引文献53

  • 1王洪,祝纶宇,陈鸣才.表面包覆改性尖晶石锰酸锂正极材料[J].电源技术,2007,31(3):239-241. 被引量:11
  • 2季勇,王志兴,尹周澜,郭华军,彭文杰,李新海.正极材料LiNi_(0.5)Mn_(1.5)O_4的合成及性能[J].无机化学学报,2007,23(4):597-601. 被引量:13
  • 3Yi T F, Zhu Y R, Zhu R S. Density fun- ctional theory study of lithium intercalation for 5 V LiNi0.5Mn1.5O4 cathode materials [J]. Solid State Ionics,179 , (2008).
  • 4Fang X, Lu Y, Ding N, Feng X Y, Liu C, Chen C H. Electrochemical properties of nano- and micro-sized LiNi0.sMn1.5O4 synthesized via thermal decomposition of a ternary eutectic Li Ni Mn acetate [J]. Electrochim Acta, 2010, 55(7).
  • 5Liu G Q, Wang Y J, Qi L, Li W, Synthesis and electrochemical performance of LiNi0.5Mn1.5O4 spinel compound[J]. Electrochim Acta, 2005, 50(12).
  • 6Chen Z Y, Zhu H L, Ji S, Vladimir L, Zhang J L, Zhu W. Performance of LiNi0.5Mn1.5O4 prepared by solid-state reaction[J]. J. Power Sources, 2009, 189(2).
  • 7Lcantara R, Jaraba M, Lavela P. Optimizing preparation conditions for 5 V electrode performance, and structural changes in Li2-xNi0.5Mn1.5O4 spinel [J]. Electrochim Acta, 2002,47(11).
  • 8Zhong Q M, Arman B, Zhang M J. Synthesis and electrochemistry of LiNixMn2-xO4 [J ] .J Electro- them Soe , 1997 , 144(1).
  • 9Feng X Y, Shen C, Fang X, Chen C H. Synthesis of LiNi0.5Mn1.5O4 by solid-state reaction with improved electrochemical performance [J]. Journal of Alloys and Compounds, 2011, 50(9).
  • 10Zhang X F, Liu J, Yu H Y, Yang G L, Wang J W, Yu Z J, Xie H M, Wang R S. Enhanced electro- chemical performances of LiNi0.5Mn1.5O4 spinel via ethylene glycol-assisted synthesis [J]. Electrochimica Acta, 2010, 55(11).

引证文献6

二级引证文献20

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