CN100403587C - 一种掺杂层状锂离子电池正极材料及其制备方法 - Google Patents

一种掺杂层状锂离子电池正极材料及其制备方法 Download PDF

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CN100403587C
CN100403587C CNB2005100315572A CN200510031557A CN100403587C CN 100403587 C CN100403587 C CN 100403587C CN B2005100315572 A CNB2005100315572 A CN B2005100315572A CN 200510031557 A CN200510031557 A CN 200510031557A CN 100403587 C CN100403587 C CN 100403587C
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黄可龙
唐爱东
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Central South University
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Abstract

一种掺杂层状锂离子电池正极材料LiMn0.5-xNi0.5-xMo2xO2及其制备方法,属于能源材料技术领域。本发明将掺杂原料Ni、Mn、Mo以化学计量比混合均匀,溶于水或乙醇中;加入柠檬酸溶液搅拌,加入化学计量锂盐溶液,反应得到Li、Ni、Mn、Mo前驱体;在空气气氛中于300~600℃将得到前驱体的进行预分解;于700~1100℃高温煅烧预分解产物,合成得到层状LiNi0.5-xMn0.5-xMo2xO2材料。本发明采用溶胶-凝胶法制备前驱体,使各反应物能达到原子、分子级水平的混合程度,在空气中焙烧前驱体不需要控制气氛,合成工艺简单,生产成本低,采用本发明获得的层状锂离子电池正极材料,结构稳定,充放电比容量高,循环稳定性好。

Description

一种掺杂层状锂离子电池正极材料及其制备方法
技术领域
一种掺杂层状锂离子电池正极材料LiMn0.5-xNi0.5-xMo2xO2及其制备方法,属于能源材料技术领域。
背景技术
锂离子二次电池以其高能量密度、低自放电率和高电压,自20世纪90年代问世以来,被广泛用于现代通讯、空间技术、信息技术、国防等高科技领域,被誉为高效的“绿色能源”。目前市场广泛使用的锂离子电池正极材料LiCoO2价格贵、容量低(130~140mAh/g)、污染大,难以满足日益增长的二次电池的要求,因此提高锂离子电池正极材料的比容量和稳定性,降低成本,是目前改善锂离子电池性能的重要研究方向。LiNiO2与LiMnO2以价格便宜、污染小作为一种目前商用的LiCoO2正极材料的替代材料正逐渐成为锂离子电池研究与开发的热点。但LiNiO2合成条件苛刻,需严格控制合成中的氧气气氛,循环稳定性差,易引起安全问题等,其商业化应用进程一直较缓慢。具有层状结构的LiMnO2放电容量可达190mAh/g以上,是一种具有极大发展前景的正极材料,层状锂锰氧化物LiMnO2属于热力学亚稳态,起骨架支撑作用的Mn3+极不稳定;一方面,在Li+嵌入与脱出过程中易发生Mn3+向更稳定的高价态变化,使晶体结构畸变,向热力学稳定相尖晶石相转变,另一方面,由于高自旋Mn3+(t2g 3eg 1)引起的Jahn-Teller畸变,使得氧的排列发生畸变,难以形成理想的立方紧密堆积,从而严重地影响了其结构稳定性和电化学稳定性。
发明内容
为了简化生产工艺,以锰氧八面体为骨架改善LiNiO2层状的结构,减少阳离子混排及非计量比产物的生成,提高材料的结构稳定性,获得高容量、高循环稳定性的锂离子电池正极材料,本发明提供一种LiNi0.5-xMn0.5-xMo2xO2电池正极材料及其合成方法。
本发明提供的锂离子电池正极材料,其化学分子式为LiNi0.5-xMn0.5-xMo2xO2,其中0≤x≤0.05。
本发明提供的锂离子电池正极材料的合成方法包括以下步骤:
根据锂离子电池正极材料的分子式,将掺杂原料Ni、Mn、Mo以化学计量比混合均匀,溶于水或乙醇中;加入0.1~3.0mol/L的柠檬酸溶液,搅拌,使形成的溶液充分混合均匀,得掺杂原料混合液;
根据化学计量在掺杂原料混合液中加入锂盐溶液,搅拌,使各原料发生反应后形成均匀的混合溶液,用氨水或乙二胺溶液调PH=7~11,于70~90℃恒温24h,得到Li、Ni、Mn、Mo前驱体;
在空气气氛中于300~600℃将得到前驱体的进行预分解;在空气气氛中于700~1100℃高温煅烧预分解产物,合成得到层状LiNi0.5-xMn0.5-xMo2xO2材料。
本发明采用溶胶-凝胶法制备前驱体,使各反应物能达到原子、分子级水平的混合程度,在空气中焙烧前驱体不需要控制气氛,合成工艺简单,生产成本低,采用本发明获得的层状锂离子电池正极材料LiMn0.5-xNi0.5-xMo2xO2,结构稳定,充放电比容量高,循环稳定性好。
附图说明
图1:锂离子电池正极材料LiNi0.475Mn0.475Mo0.05O2的X射线衍射图;
图2:锂离子电池正极材料LiNi0.475Mn0.475Mo0.05O2的高倍率扫描电镜图;
图3:锂离子电池正极材料LiNi0.475Mn0.475Mo0.05O2的首次充放电循环曲线图。
具体实施方式
以下通过实施例进一步说明本发明。
实施例1:
将0.0475mol镍盐,0.0475mol锰盐,0.005mol钼盐溶于水中,使其混合均匀;将0.1mol柠檬酸配制2mol/L的柠檬酸溶液,加入上述原料混合液中,不断搅拌,使形成的溶液充分混合均匀;称量0.1mol锂盐溶解于水中加入到上述的均匀溶液中,不断搅拌,用氨水溶液调PH=9,于80℃恒温24h得到前驱体;在空气气氛中400℃将得到前驱体的进行预分解,冷却后研磨;在空气气氛中于900℃高温煅烧预分解产物合成得到的层状LiNi0.475Mn0.475Mo0.05O2材料。XRD衍射结果表明900℃合成得到的LiNi0.475Mn0.475Mo0.05O2化合物具有层状α-NaFeO2结构,结晶完整,呈单一相,无任何杂质峰出现。
将制得的正极活性物质、乙炔黑和聚四氟乙烯(PTFE)粘结剂按一定的比例(85∶10∶5)充分混合均匀,在容器中80-100℃下干燥24h消除水分后,涂于不锈钢网上,用油压机在20Kpa的压力下压成厚度均匀的正极膜。以金属锂片为负极,电解液为含1mol/LLiPF6的EC∶DMC∶EMC/1∶1∶1(w/w)混合溶液,水份含量小于9.34ppm,游离酸HF含量小于2.55ppm。在惰性气体手套箱内组装模拟电池,手套箱操作系统为高纯Ar气氛,水与氧的含量均小于1ppm,组装好的模拟电池在室温25℃或高温55℃下进行测试。用电池程控测试仪检测充放电容量及循环稳定性,采用恒流充、恒流放的模式,充放电电流均为28mA/g,充放电电压范围为2.5-4.6V。
测试结果表明,首次充放电容量分别为233mAh/g,180mAh/g,循环20次后充放电容量别分为185mAh/g,180mAh/g,充放电效率为97.2%图3为LiNi0.475Mn0.475Mo0.05O2的首次充放电循环曲线图。
实施例2:
将0.0475mol镍盐,0.0475mol锰盐,0.005mol钼盐溶于乙醇中,使其混合均匀;采用0.1mol柠檬酸配制2mol/L的柠檬酸乙醇溶液,加入上述原料混合液中,不断搅拌,使形成的溶液充分混合均匀;称量0.1mol锂盐溶解于乙醇中加入到上述的均匀溶液中,不断搅拌,用氨水或乙二胺溶液调PH=8,于80℃恒温24h得到前驱体;在空气气氛中400℃将得到前驱体的进行预分解,冷却后研磨;在空气气氛中于900℃高温煅烧预分解产物合成得到的层状LiNi0.475Mn0.475Mo0.05O2材料。XRD衍射结果表明900℃合成得到的LiNi0.475Mn0.475Mo0.05O2化合物具有六方层状结构,结晶完整,呈单一相,无任何杂质峰出现。
测试结果表明,首次充放电容量分别为210mAh/g,180mAh/g,循环20次后充放电容量分别为170mAh/g,165mAh/g,充放电效率为97%。

Claims (1)

1.一种锂离子电池正极材料的制备方法,该正极材料的化学分子式为LiNi0.5-xMn0.5-xMo2xO2,其中0<x≤0.05,其特征在于:将掺杂原料Ni、Mn、Mo以化学计量比混合均匀,溶于水或乙醇中;加入0.1~3.0mol/L的柠檬酸溶液,搅拌,使形成的溶液充分混合均匀,得掺杂原料混合液;
根据化学计量在掺杂原料混合液中加入锂盐溶液,搅拌,反应后用氨水或乙二胺溶液调pH=7~11,于70~90℃恒温24h,得到Li、Ni、Mn、Mo前驱体;
在空气气氛中于300~600℃将得到的前驱体进行预分解;在空气气氛中于700~1100℃高温煅烧预分解产物。
CNB2005100315572A 2005-05-20 2005-05-20 一种掺杂层状锂离子电池正极材料及其制备方法 Expired - Fee Related CN100403587C (zh)

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CN103474643A (zh) * 2013-09-28 2013-12-25 山东润峰集团新能源科技有限公司 一种链形富锂锰基固溶体正极材料的制备方法
CN105154980B (zh) * 2015-06-19 2017-08-11 福州大学 一种锂电池正极材料及其制备方法

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001048842A1 (en) * 1999-12-29 2001-07-05 Kimberly-Clark Worldwide, Inc. Nickel-rich and manganese-rich quaternary metal oxide materials as cathodes for lithium-ion and lithium-ion polymer batteries
CN1326232A (zh) * 2000-05-25 2001-12-12 中国科学院成都有机化学研究所 一种锂离子电池锂锰氧化物正极材料的制备方法
US20020076613A1 (en) * 2000-12-15 2002-06-20 Lee Jai Young Method for surface treatment of layered structure oxide for positive electrode in lithium secondary battery
CN1484336A (zh) * 2002-08-21 2004-03-24 三洋电机株式会社 非水电解质蓄电池
WO2004107480A2 (en) * 2003-05-28 2004-12-09 National Research Council Of Canada Lithium metal oxide electrodes for lithium cells and batteries

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001048842A1 (en) * 1999-12-29 2001-07-05 Kimberly-Clark Worldwide, Inc. Nickel-rich and manganese-rich quaternary metal oxide materials as cathodes for lithium-ion and lithium-ion polymer batteries
CN1326232A (zh) * 2000-05-25 2001-12-12 中国科学院成都有机化学研究所 一种锂离子电池锂锰氧化物正极材料的制备方法
US20020076613A1 (en) * 2000-12-15 2002-06-20 Lee Jai Young Method for surface treatment of layered structure oxide for positive electrode in lithium secondary battery
CN1484336A (zh) * 2002-08-21 2004-03-24 三洋电机株式会社 非水电解质蓄电池
WO2004107480A2 (en) * 2003-05-28 2004-12-09 National Research Council Of Canada Lithium metal oxide electrodes for lithium cells and batteries

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