CN103700817A - LiV3O8 和LiNi0.4Co0.2Mn0.4O2共混改性锂电池正极材料的制备方法 - Google Patents

LiV3O8 和LiNi0.4Co0.2Mn0.4O2共混改性锂电池正极材料的制备方法 Download PDF

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CN103700817A
CN103700817A CN201310697587.1A CN201310697587A CN103700817A CN 103700817 A CN103700817 A CN 103700817A CN 201310697587 A CN201310697587 A CN 201310697587A CN 103700817 A CN103700817 A CN 103700817A
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邢青青
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JIANGSU KING LITHIUM CELL CO Ltd
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/48Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/52Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
    • H01M4/525Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/48Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/485Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/48Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/50Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese
    • H01M4/505Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Abstract

本发明涉及锂电池正极材料的制造,具体是一种LiV3O8和LiNi0.4Co0.2Mn0.4O2共混改性锂电池正极材料的制备方法。本发明的方法包括以下步骤:a.正极材料LiV3O8的制备;b.三元正极LiNi0.4Co0.2Mn0.4O2的制备;c.将正极材料LiV3O8和LiNi0.4Co0.2Mn0.4O2按照3:7 的质量比在三维锥混机内混合;在马弗炉内烧结,在480-500℃预烧2h;650-675℃烧结4h;在800-825℃烧结6h,并在此温度保温8h;后随炉自然冷却,破碎,最后制得共混材料(LiV3O8和LiNi0.4Co0.2Mn0.4O2)。本发明通过三元材料与LiV3O8的共混改性,能够获得高压实密度的正极材料,经检测,可以有效提高容量性能。

Description

LiV3O8 和LiNi0.4Co0.2Mn0.4O2共混改性锂电池正极材料的制备方法
技术领域
本发明涉及锂电池正极材料的制造,具体是一种LiV3O8和LiNi0.4Co0.2Mn0.4O2共混改性锂电池正极材料的制备方法。
背景技术
LiV3O8和三元材料均被用于锂电池的正极材料,材料压实密度较低,限制了材料容量性能的提高。
发明内容
本发明所要解决的技术问题是,提供一种压实密度高、容量性能好的LiV3O8和LiNi0.4Co0.2Mn0.4O2共混改性锂电池正极材料的制备方法。
本发明的方法包括以下步骤:
a.正极材料Li V3O8的制备,具体步骤为
a-1.按照所需摩尔比将NH4VO3和电池级碳酸锂分别于玛瑙研钵中研细后,放入三维锥混机内混合均匀,在90-100℃真空干燥箱中干燥12-15h;再将其研磨3-4h;
a-2.将研磨后的物料放入马弗炉内烧结,先在480-500℃预烧2h;后在700-740℃烧结5h;在800-850℃烧结7h,同时在此温度保温8h;后随炉自然冷却;破碎得到纳米级LiV3O8正极材料;
b.三元正极LiNi0.4Co0.2Mn0.4O2的制备,具体步骤为
b-1.将Ni(NO3)2·6H2O,Co(NO3)2·6H2O,Mn(NO3)2·6H2O按照2:1:2的摩尔比例配置成金属离子溶液,其中金属离子的总量是2mol/L;配置2mol/L的NaOH溶液,后将这两种溶液在50℃反应,在反应过程中,用氨水调节pH在9-11范围内;反应完毕后,继续陈化18-20h,将沉淀物质洗涤、烘干后,研磨即得三元前躯体(Ni0.4Co0.2Mn0.4)(OH)2
b2.将上述所制的三元前躯体(Ni0.4Co0.2Mn0.4)(OH)2和电池级碳酸锂按照M/Li=1:1.02的摩尔比在三维锥混机内混合使其达到混合均匀,M为三元总含量;混合后的物料放入马弗炉内烧结,先在480-500℃预烧3h;在700-735℃烧结6h;在850-875℃烧结8h;在900-920℃烧结10h,并在此温度保温10h;后随炉自然冷却、破碎,过200目筛,最后制的三元正极材料LiNi0.4Co0.2Mn0.4O2
c.将正极材料LiV3O8和LiNi0.4Co0.2Mn0.4O2按照3:7的质量比在三维锥混机内混合;在马弗炉内烧结,在480-500℃预烧2h;650-675℃烧结4h;在800-825℃烧结6h,并在此温度保温8h;后随炉自然冷却,破碎,最后制得共混材料(LiV3O8和LiNi0.4Co0.2Mn0.4O2)。
本发明通过三元材料与LiV3O8的共混改性,能够获得高压实密度的正极材料,经检测,可以有效提高容量性能。
具体实施方式
本发明实施例的方法包括以下步骤:
a.正极材料Li V3O8的制备,具体步骤为
a-1.按照所需摩尔比将NH4VO3和电池级碳酸锂分别于玛瑙研钵中研细后,放入三维锥混机内混合均匀,用时2h,在100℃真空干燥箱中干燥15h;再将其研磨4h;
a-2.将研磨后的物料放入马弗炉内烧结,先在500℃预烧2h;后在740℃烧结5h;在850℃烧结7h,同时在此温度保温8h;后随炉自然冷却;破碎过200目筛。得到纳米级LiV3O8正极材料;
b.三元正极LiNi0.4Co0.2Mn0.4O2的制备,具体步骤为
b-1.将Ni(NO3)2·6H2O,Co(NO3)2·6H2O,Mn(NO3)2·6H2O按照2:1:2的摩尔比例配置成金属离子溶液,其中金属离子的总量是2mol/L;配置2mol/L的NaOH溶液,后将这两种溶液在50℃反应,在反应过程中,用氨水调节pH在9-11范围内;反应完毕后,继续陈化20h,将沉淀物质洗涤4次,放置真空干燥箱烘干后,研磨即得三元前躯体(Ni0.4Co0.2Mn0.4)(OH)2
b2.将上述所制的三元前躯体(Ni0.4Co0.2Mn0.4)(OH)2和电池级碳酸锂按照M/Li=1:1.02的摩尔比在三维锥混机内混合使其达到混合均匀,M为三元总含量;混合后的物料放入马弗炉内烧结,先在500℃预烧3h;在735℃烧结6h;在875℃烧结8h;在920℃烧结10h,并在此温度保温10h;后随炉自然冷却、破碎,过200目筛,最后制的三元正极材料LiNi0.4Co0.2Mn0.4O2
c.将正极材料LiV3O8和LiNi0.4Co0.2Mn0.4O2按照3:7的质量比在三维锥混机内混合4h。;在马弗炉内烧结,在500℃预烧2h;675℃烧结4h;在825℃烧结6h,并在此温度保温8h;后随炉自然冷却,破碎,过筛。最后制得共混材料(LiV3O8和LiNi0.4Co0.2Mn0.4O2)。
本发明实施例制得的材料物化指标:
采用固相烧结法制备共混材料其平均粒度在8.50-10.5之间,液氮吸附法测的共混材料比表面积为0.43m2/g。
干粉压实密度
条件:在30Mpa压力下,保压时间为6min。检测结果如下表。
测试项目 1 2 3 平均值
LiNi0.4Co0.2Mn0.4O2 3.65 3.64 3.64 3.64
Li V3O8 3.86 3.87 3.86 3.86
共混材料 3.78 3.77 3.77 3.77
从上表可知,LiNi0.4Co0.2Mn0.4O2和LiV3O8两者混合产品共烧制备的材料的干粉压实密度处于较好水平。
产品测试数据:
正极配方活性物质:SP:PVDF=96.0:2.0:2.0(固含量67%);
负极配方石墨:CMC:SP:SBR=94.0:2.0:1.5:2.5(固含量48%);
电解液型号:TC-E2011027;
全电池测试数据:0.2C首次放电比容量≥193mAh/g;
全电池倍率数据如下表:
Figure BDA0000440266180000031
从上表可以看出,共混材料在1C的放电倍率为96.8%,2C放电倍率为92.5%。

Claims (1)

1.一种LiV3O8 和LiNi0.4Co0.2Mn0.4O2共混改性锂电池正极材料的制备方法,其特征是:包括以下步骤,
a.正极材料Li V3O8的制备,具体步骤为
a-1.按照所需摩尔比将NH4VO3和电池级碳酸锂分别于玛瑙研钵中研细后,放入三维锥混机内混合均匀,在90-100℃真空干燥箱中干燥12-15h;再将其研磨3-4h;
a-2.将研磨后的物料放入马弗炉内烧结,先在480-500℃预烧2h;后在700-740℃烧结5h;在800-850℃烧结7h,同时在此温度保温8h;后随炉自然冷却;破碎得到纳米级LiV3O8正极材料;
b.三元正极LiNi0.4Co0.2Mn0.4O2的制备,具体步骤为
b-1.将Ni(NO3)2·6H2O,Co(NO3)2·6H2O,Mn(NO3)2·6H2O按照2:1:2的摩尔比例配置成金属离子溶液,其中金属离子的总量是2mol/L;配置2mol/L的NaOH溶液,后将这两种溶液在50℃反应,在反应过程中,用氨水调节pH在9-11范围内;反应完毕后,继续陈化18-20h,将沉淀物质洗涤、烘干后,研磨即得三元前躯体(Ni0.4Co0.2Mn0.4)(OH)2
b2.将上述所制的三元前躯体(Ni0.4Co0.2Mn0.4)(OH)2和电池级碳酸锂按照M/Li=1:1.02的摩尔比在三维锥混机内混合使其达到混合均匀,M为三元总含量;混合后的物料放入马弗炉内烧结,先在480-500℃预烧3h;在700-735℃烧结6h;在850-875℃烧结8h;在900-920℃烧结10h,并在此温度保温10h;后随炉自然冷却、破碎,过200目筛,最后制的三元正极材料LiNi0.4Co0.2Mn0.4O2
c.将正极材料LiV3O8和LiNi0.4Co0.2Mn0.4O2按照3:7  的质量比在三维锥混机内混合;在马弗炉内烧结,在480-500℃预烧2h;650-675℃烧结4h;在800-825℃烧结6h,并在此温度保温8h;后随炉自然冷却,破碎,最后制得共混材料(LiV3O8和LiNi0.4Co0.2Mn0.4O2)。
CN201310697587.1A 2013-12-18 2013-12-18 LiV3O8 和LiNi0.4Co0.2Mn0.4O2共混改性锂电池正极材料的制备方法 Pending CN103700817A (zh)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104701533A (zh) * 2015-02-11 2015-06-10 江苏科捷锂电池有限公司 523三元材料共混改性正极材料的制备方法
CN111193016A (zh) * 2020-01-09 2020-05-22 上海应用技术大学 用钒离子和钠离子共同取代的三元正极材料及其制备方法
WO2024011454A1 (zh) * 2022-07-13 2024-01-18 宁德时代新能源科技股份有限公司 电池包和用电装置

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1750299A (zh) * 2005-09-09 2006-03-22 贵州新材料矿业发展有限公司 一种锂二次电池正极材料及其制备方法
CN102651471A (zh) * 2011-02-22 2012-08-29 富士重工业株式会社 正极活性物质、使用该正极活性物质的锂离子蓄电设备及其制造方法

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1750299A (zh) * 2005-09-09 2006-03-22 贵州新材料矿业发展有限公司 一种锂二次电池正极材料及其制备方法
CN102651471A (zh) * 2011-02-22 2012-08-29 富士重工业株式会社 正极活性物质、使用该正极活性物质的锂离子蓄电设备及其制造方法

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
杨辉等: "一种锂离子电池正极纳米材料LiV3O8的制备和性能", 《无机材料学报》 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104701533A (zh) * 2015-02-11 2015-06-10 江苏科捷锂电池有限公司 523三元材料共混改性正极材料的制备方法
CN111193016A (zh) * 2020-01-09 2020-05-22 上海应用技术大学 用钒离子和钠离子共同取代的三元正极材料及其制备方法
WO2024011454A1 (zh) * 2022-07-13 2024-01-18 宁德时代新能源科技股份有限公司 电池包和用电装置

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