WO2017206299A1 - 一种锂离子电池改性石墨负极材料的制备方法 - Google Patents

一种锂离子电池改性石墨负极材料的制备方法 Download PDF

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WO2017206299A1
WO2017206299A1 PCT/CN2016/091734 CN2016091734W WO2017206299A1 WO 2017206299 A1 WO2017206299 A1 WO 2017206299A1 CN 2016091734 W CN2016091734 W CN 2016091734W WO 2017206299 A1 WO2017206299 A1 WO 2017206299A1
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graphite
powder
nickel
preparing
lithium
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田东
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田东
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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/362—Composites
    • H01M4/366—Composites as layered products
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/58—Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
    • H01M4/583—Carbonaceous material, e.g. graphite-intercalation compounds or CFx
    • H01M4/587—Carbonaceous material, e.g. graphite-intercalation compounds or CFx for inserting or intercalating light metals
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/628—Inhibitors, e.g. gassing inhibitors, corrosion inhibitors
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M2004/026—Electrodes composed of, or comprising, active material characterised by the polarity
    • H01M2004/027—Negative electrodes
    • Y—GENERAL 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
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries

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  • the invention belongs to the technical field of lithium ion battery anode materials, and particularly relates to a preparation method of a lithium ion battery modified graphite anode material.
  • Lithium-ion batteries have been widely used in portable electronic devices such as notebook computers, mobile phones, and medical microelectronic devices because of their high energy density and excellent cycle performance.
  • problems to be solved if applied to a wider field such as large fixed energy storage devices and electric vehicles.
  • These issues include how to further increase the energy density of lithium-ion batteries, enhance the matching between battery packs, reduce the attenuation of capacity during cycling, improve the safety during operation, broaden the normal operating temperature range, enhance the reliability of materials, and reduce Production costs, etc.
  • a major breakthrough in lithium-ion batteries is the innovation of electrode materials and electrolytes. The goal is to find alternatives that are superior to current commercial materials and electrochemical processes that occur during the process of replacement. It is in principle consistent with the current lithium-ion battery used. Therefore, research on the anode material of lithium ion batteries is very necessary.
  • the graphite anode materials currently used commercially have the advantages of low lithium insertion/deintercalation potential, suitable reversible capacity, abundant resources, and low price, and are ideal anode materials for lithium ion batteries.
  • its theoretical specific capacity is only 372 mAh/g, which limits the further improvement of the specific energy of lithium-ion batteries and cannot meet the needs of the increasingly high-energy portable mobile power sources.
  • SEI solid electrolyte membrane
  • the solid electrolyte membrane is formed by reacting an electrolyte, a negative electrode material, and lithium ions, and irreversibly consuming lithium ions, which is a major factor in forming an irreversible capacity.
  • the second is that the electrolyte is easily embedded in the lithium ion intercalation process.
  • the electrolyte is reduced, and the resulting gas product causes the graphite sheet to peel off.
  • the graphite sheet peels off and a new interface is formed, resulting in further SEI formation, irreversible capacity increase, and circulation. The stability is degraded.
  • the resin material and the graphite have poor affinity, so they are pyrolyzed carbon material and graphite.
  • the carbon material obtained by pyrolysis of the resin is low in yield and brittle.
  • the volatile matter in the pyrolysis process of the resin is high, the specific surface area is high, the adhesion of the resin is strong, and the coated particles are easily bonded. Together, it is easy to cause damage to the coating layer when pulverized after heat treatment.
  • the pitch pyrolysis carbon has a smaller specific surface area than the resin pyrolytic carbon coated graphite, and affinity with graphite. If the structure is firmer, the asphalt coating will be deformed by melting during the heating process. If the amount is too much, the coated graphite particles will be bonded to each other. If the amount is too small, the coating will be uneven, and the heating process will be easy to expand. , affecting the electrical properties of graphite.
  • the present invention discloses a method for preparing a lithium ion battery modified graphite anode material, wherein the anode material of the lithium ion battery is a composite material having a core-shell structure, which can effectively solve the above technical problems.
  • a lithium ion battery anode material is a core-shell structure
  • the core layer is graphite
  • the middle layer is metal nickel
  • the pyrolytic carbon is the outermost layer.
  • the introduction of metallic nickel effectively improves the rate performance, and at the same time acts to isolate the graphite powder from direct contact with the electrolyte, thereby preventing the graphite layer from peeling off and pulverizing caused by co-insertion of lithium ions and electrolyte. , greatly improving the cycle performance and rate performance of graphite as a negative electrode material for lithium ion batteries during charge and discharge.
  • a preparation method of a lithium ion battery modified graphite anode material the specific preparation steps are as follows:
  • the material obtained in the step 5 is pulverized and sieved to obtain a powder having a particle diameter D50 of 5 to 30 ⁇ m, that is, a graphite/Ni/C composite material having a core-shell structure of the present invention.
  • m (graphite): m (Ni) 100: (5 to 10)
  • the particle diameter D50 of the graphite powder is between 5 and 30 nm
  • the compound of nickel is chlorinated.
  • nickel, nickel sulfate, and nickel nitrate is a mixture of two or more of nickel, nickel sulfate, and nickel nitrate.
  • the drying temperature in the step (3) is 40 to 60 ° C, and the time is 12 to 24 hours.
  • the carbon formed in the pyrolysis process of the organic resin is subjected to the carbothermal reduction method, and the temperature and time of the thermal reduction are controlled, so that the shell layer of the core-shell structure is composed of graphite and a simple substance of metal, and the carbon source is heat. After the solution, an amorphous carbon layer coated polymer is formed.
  • the graphite powder is used as the core and the metallic nickel is the shell layer, which constitutes the core-shell structure inside the anode material of the lithium ion battery, and the outer surface is covered with a carbon layer, thereby improving the graphite powder as the lithium ion battery.
  • the cycle performance and rate performance of the anode material during charge and discharge process make the graphite matrix composite material have excellent cycle and rate performance;
  • the graphite/Ni/C alloy composite material is prepared by adopting the technical scheme of the invention, and the composite material is a core-shell structure and the graphite powder is used as a core layer of a metal nickel.
  • the introduction of nickel effectively improves the rate performance, and acts as a barrier to the direct contact between the graphite powder and the electrolyte, effectively avoiding the formation of unstable SEI film on the surface of the graphite powder.
  • the carbon layer on the surface increases the electrical properties of the composite. The role.
  • Example 1 is a graph showing the first charge and discharge of the material of Example 1.
  • Example 2 is a graph showing a rate discharge curve of the material of Example 1.
  • a preparation method of a lithium ion battery modified graphite anode material the preparation steps are as follows:
  • the material obtained in the step 5 is pulverized and sieved to obtain a powder having a particle diameter D50 of 5 to 30 ⁇ m, that is, a graphite/Ni/C composite material having a core-shell structure of the present invention.
  • PVDF polyvinylidene fluoride
  • NMP N-methylpyrrolidone
  • the charge-discharge voltage is 0-2.0V, and the charge-discharge rate is 0.5C.
  • the measured result is that the first discharge capacity is 357.6mAh/g, and the first efficiency is 94.3.
  • the first charge-discharge curve is shown in Figure 1.
  • a preparation method of a lithium ion battery modified graphite anode material the preparation steps are as follows:
  • the material obtained in the step 5 is pulverized and sieved to obtain a powder having a particle diameter D50 of 5 to 30 ⁇ m, that is, a graphite/Ni/C composite material having a core-shell structure of the present invention.
  • the first discharge capacity was 354.3 mAh/g, and the first efficiency was 95.2.
  • a 1%, 5C, 10C, 15C current rate discharge test was performed, and the measured result was a 5C/1C retention rate of 96.3%, a 10C/1C retention rate of 94.6%, and a 15C/1C retention rate of 91.1%.

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  • Electrochemistry (AREA)
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  • Engineering & Computer Science (AREA)
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Abstract

一种锂离子电池改性石墨负极材料的制备方法，以石墨粉为核，金属镍为壳层，组成锂离子电池负极材料内部的核壳结构，外表面为碳层包覆。本方法利用有机树脂热解过程中形成的碳，采用碳热还原法，金属镍的引入有效的提高了倍率性能，同时起到隔离石墨粉与电解液直接接触的作用，从而防止了锂离子与电解液的共插所引起的石墨层剥落与粉化，大大改善了石墨作为锂离子电池负极材料在充放电过程中的循环性能和倍率性能。另一方面表面的碳层起到了增加了复合材料导电性的作用。

Description

一种锂离子电池改性石墨负极材料的制备方法 技术领域
本发明属于锂离子电池负极材料技术领域，具体涉及一种锂离子电池改性石墨负极材料的制备方法。
背景技术
锂离子电池以其具有高的能量密度和优异的循环性能已经被广泛地应用于笔记本电脑、移动电话、医学微电子设备等便携式电子设备中。但是，如果要应用到更加广阔的领域例如大型固定能量储存装置和电动汽车仍然存在很多需要解决的问题。这些问题包括如何进一步增加锂离子电池能量密度、增强电池组之间的匹配、减小循环过程中容量的衰减、提高工作过程中的安全性、拓宽正常工作温度范围、增强材料的可靠性、降低生产成本等。现在，业内普遍认为锂离子电池方面的重大突破是对电极材料和电解液部分进行革新，目标是找到性能优于目前商业化使用材料的替代物并且替代物在工作过程中所发生的电化学过程要与目前所使用的锂离子电池原理上保持一致。因此，对锂离子电池负极材料的研究是非常有必要的。
目前商业化使用的石墨类负极材料，具有较低的锂嵌入/脱嵌电位、合适的可逆容量且资源丰富、价格低廉等优点，是比较理想的锂离子电池负极材料。但其理论比容量只有372mAh/g，因而限制了锂离子电池比能量的进一步提高，不能满足日益发展的高能量便携式移动电源的需求。同时，石墨作为负极材料时，在首次充放电过程中在其表面形成一层固体电解质膜(SEI)。固体电解质膜是电解液、负极材料和锂离子等相互反应形成，不可逆地消耗锂离子，是形成不可逆容量的一个主要的因素；其二是在锂离子嵌入的过程中，电解质容易与其共嵌在迁出的过程中，电解液被还原，生成的气体产物导致石墨片层剥落，尤其在含有PC的电解液中，石墨片层脱落将形成新界面，导致进一步SEI形成，不可逆容量增加，同时循环稳定性下降。碳材料作为锂离子电池负极材料依然存在充放电容量低、初次循环不可逆损失大、溶剂分子共插层和制备成本高等缺点，这些也是在目前锂离子电池研究方面所需解决的关键问题。
目前对石墨的包覆改性处理中，均只单独包覆树脂类硬炭前躯体或者是沥青类软炭前躯体。中国专利CN101604743A和CN1224251A等采用树脂类作为包覆材料，主要优点是树脂在低温下流动性好，不仅能包覆表面，而且很容易通过石墨内的微孔渗入到石墨颗粒内部，对提高石墨颗粒的振实密度和电子电导率有益，还可以通过加热、引入催化剂或紫外线照射 等方法固化，树脂热解过程中不会熔化变形，也不会产生明显膨胀，但也存在一些问题，主要有：树脂类材料和石墨的亲和力较差，因此他们热解得到的炭材料和石墨结合不牢固，由树脂热解得到的炭材料得率偏低，具有脆性，树脂热解过程中挥发份多，比表面积偏高，树脂的粘结力较强，易于造成包覆颗粒粘接在一起，热处理后粉碎时易造成包覆层的破坏。以上这些问题，影响了树脂包覆石墨材料的循环效率、循环稳定性和石墨电极的压缩性。
中国专利CN96198348.5和CN03120199.6等，采用沥青、石油焦油、煤焦油或它们的混合物包覆石墨，沥青热解炭比树脂热解炭包覆石墨的比表面积小，和石墨的亲合性要好，结构更牢固，但沥青包覆在加热过程中因熔化而变形，用量过多也易造成包覆石墨颗粒的相互粘接，用量过少易造成包覆不均匀，并且加热过程中易于膨胀，影响石墨的电性能。
发明内容
针对以上技术问题，本发明公开了一种锂离子电池改性石墨负极材料的制备方法，所述锂离子电池负极材料为具有核-壳结构的复合材料，能有效的解决上述技术问题。
对此，本发明采用的技术方案为：一种锂离子电池负极材料为核-壳结构，所述核层为石墨，中间层为金属镍，热解碳为最外层。
采用此技术方案，金属镍的引入有效的提高了倍率性能，同时起到隔离石墨粉与电解液直接接触的作用，从而防止了锂离子与电解液的共插所引起的石墨层剥落与粉化，大大改善了石墨作为锂离子电池负极材料在充放电过程中的循环性能和倍率性能。
一种锂离子电池改性石墨负极材料的制备方法，具体制备步骤如下：
(1)制备摩尔溶度为0.1～3mol/L的镍的化合物水溶液，然后称取一定量的石墨粉加入溶液，不断搅拌得到混合溶液；
(2)在混合溶液中加入碱性溶液，镍产生沉淀，得到Ni(OH)2附着在石墨粉表面的混合溶液；
(3)将步骤2制得的含沉淀的混合溶液离心分离、烘干，得到石墨/Ni(OH)2固体粉末；
(4)将石墨/Ni(OH)2固体粉末加入到有机树脂的无水乙醇溶液中搅拌1～2小时，然后在50～70℃下不断搅拌至蒸干得到固体粉末；
(5)将上述固体粉末在氮气气氛下，以5～20℃/min的升温速率，加热至800-950℃，并保温1～4h，然后降温至室温；
(6)将步骤5中得到的材料进行粉碎并过筛，得到粒径D50介于5～30μm的粉体，即本发明具有核-壳结构的石墨/Ni/C复合材料。
其中，步骤(1)中石墨和镍的质量比为m(石墨):m(Ni)＝100：(5～10)，石墨粉的粒径D50介于5～30nm，镍的化合物为氯化镍、硫酸镍、硝酸镍中一种或两种以上的混合。
其中，步骤(2)中的碱性溶液为氢氧化钠、氢氧化钾、氨水中的一种，溶度为0.1～1mol/L，加入的量为n(OH-):n(Ni)＝(2～2.2)：1。
其中，步骤(3)中的烘干温度为40～60℃，时间为12～24小时。
其中，步骤(4)中有机树脂为环氧树脂、酚醛树脂或糠醛树脂中一种或两种以上，树脂与石墨粉的重量比为m(树脂)：m(石墨)＝(5～10)：100。
采用此技术方案，利用有机树脂热解过程中形成的碳，采用碳热还原法，通过控制热还原的温度和时间，使得核-壳结构的壳层由石墨和金属单质组成，碳源为热解后形成无定型碳层包覆的聚合物。
与现有技术相比，本发明的有益效果为：
第一，采用本发明的技术方案，以石墨粉为核，金属镍为壳层，组成锂离子电池负极材料内部的核壳结构，外表面为碳层包覆，改善了石墨粉作为锂离子电池负极材料在充放电过程中的循环性能和倍率性能，使石墨基复合材料具有优异的循环和倍率性能；
第二，采用本发明的技术方案，制备石墨/Ni/C合金复合材料过程，复合材料为核壳结构且以石墨粉为核、金属镍的壳层。镍的引入有效的提高了倍率性能，对石墨粉与电解液直接接触起到隔离的作用，有效避免石墨粉表面不稳定SEI膜的形成，另一方面表面的碳层增加了复合材料的电性的作用。
附图说明
图1为实施例1的材料的首次充放电曲线图。
图2为实施例1的材料的倍率放电曲线图。
具体实施方式
下面结合具体实施例，对本发明的较优的实施例作进一步的详细说明。
实施例1
一种锂离子电池改性石墨负极材料的制备方法，其制备步骤如下：
(1)称取氯化镍2g，制备溶度为0.5mol/L的氯化镍水溶液，按照m(石墨):m(Ni)＝100：5的比例，加入18.1g的石墨粉，不断搅拌得到混合溶液；
(2)向上述混合溶液中缓慢加入0.5mol/L的氨水溶液，共61.7ml，生成沉淀，得到Ni(OH)2附着在石墨粉表面的混合溶液；
(3)将步骤2制得的含沉淀的混合溶液离心分离、烘干，得到石墨/Ni(OH)2固体粉末；
(4)称取1.5g酚醛树脂溶于无水乙醇，在加入步骤3中的固体粉末，搅拌1～2小时后，然后在50～70℃下不断搅拌至蒸干得到固体粉末；
(5)将上述固体粉末在氮气气氛下，以5℃/min的升温速率，加热至900℃，并保温4h，然后降温至室温；
(6)将步骤5中得到的材料进行粉碎并过筛，得到粒径D50介于5～30μm的粉体，即本发明具有核-壳结构的石墨/Ni/C复合材料。
为检验本发明方法制备的负极材料的性能，用半电池测试方法进行测试，用以上负极材料：乙炔黑：PVDF(聚偏氟乙烯)＝93：3：4(重量比)，加适量NMP(N-甲基吡咯烷酮)调成浆状，涂布于铜箔上，经真空110℃干燥8小时制成负极片；以金属锂片为对电极，电解液为1mol/L LiPF6/EC+DEC+DMC＝1：1：1，聚丙烯微孔膜为隔膜，组装成电池。充放电电压为0～2.0V，充放电速率为0.5C，测得结果为首次放电容量为357.6mAh/g，首次效率为94.3，首次充放电曲线图见附图1。
同时，进行1C、5C、10C、15C电流的倍率放电测试，测得结果为5C/1C保持率为97.8％，10C/1C保持率为95.1％，15C/1C保持率为92.5％，倍率放电曲线图见附图2。
实施例2
一种锂离子电池改性石墨负极材料的制备方法，其制备步骤如下：
(1)称取NiSO4·6H2O化合物10g，制备溶度为0.5mol/L的氯化镍水溶液，按照m(石墨):m(Ni)＝100：10的比例，加入22.32g的石墨粉，不断搅拌得到混合溶液；
(2)向上述混合溶液中缓慢加入1mol/L的氢氧化钠溶液，共78ml，生成沉淀，得到Ni(OH)2附着在石墨粉表面的混合溶液；
(3)将步骤2制得的含沉淀的混合溶液离心分离、烘干，得到石墨/Ni(OH)2固体粉末；
(4)称取1.3g环氧树脂溶于无水乙醇，在加入步骤3中的固体粉末，搅拌1～2小时后，然后在50～70℃下不断搅拌至蒸干得到固体粉末；
(5)将上述固体粉末在氮气气氛下，以10℃/min的升温速率，加热至950℃，并保温3h，然后降温至室温；
(6)将步骤5中得到的材料进行粉碎并过筛，得到粒径D50介于5～30μm的粉体，即本发明具有核-壳结构的石墨/Ni/C复合材料。
采用实施例1同样的测试方法，测得结果为首次放电容量为354.3mAh/g，首次效率为95.2，。同时，进行1C、5C、10C、15C电流的倍率放电测试，测得结果为5C/1C保持率为96.3％，10C/1C保持率为94.6％，15C/1C保持率为91.1％。
以上显示和描述了本发明的基本原理、主要特征及本发明的优点。本行业的技术人员应该了解，本发明不受上述实施例的限制，上述实施例和说明书中描述的只是说明本发明的 原理，在不脱离本发明精神和范围的前提下，本发明还会有各种变化和改进，这些变化和改进都落入要求保护的本发明范围内。本发明的要求保护范围由所附的权利要求书及其等效物界定。

Claims (5)

  1. 一种锂离子电池改性石墨负极材料的制备方法，其特征包括以下步骤：
    (1)制备摩尔溶度为0.1～3mol/L的镍的化合物水溶液，然后称取一定量的石墨粉加入溶液，不断搅拌得到混合溶液；
    (2)在混合溶液中加入碱性溶液，镍产生沉淀，得到Ni(OH)2附着在石墨粉表面的混合溶液；
    (3)将步骤2制得的含沉淀的混合溶液离心分离、烘干，得到石墨/Ni(OH)2固体粉末；
    (4)将石墨/Ni(OH)2固体粉末加入到有机树脂的无水乙醇溶液中搅拌1～2小时，然后在50～70℃下不断搅拌至蒸干得到固体粉末；
    (5)将上述固体粉末在氮气气氛下，以5～20℃/min的升温速率，加热至800-950℃，并保温1～4h，然后降温至室温；
    (6)将步骤5中得到的材料进行粉碎并过筛，得到粒径D50介于5～30μm的粉体，即本发明具有核-壳结构的(石墨/Ni)C复合材料。
  2. .根据权利要求1中所述的一种锂离子电池改性石墨负极材料的制备方法，其特征是：步骤(1)中石墨和镍的质量比为m(石墨):m(Ni)＝100：(5～10)，石墨粉的粒径D50介于5～30nm，镍的化合物为氯化镍、硫酸镍、硝酸镍中一种或两种以上的混合。
  3. 根据权利要求1中所述的一种锂离子电池改性石墨负极材料的制备方法，其特征是：步骤(2)中的碱性溶液为氢氧化钠、氢氧化钾、氨水中的一种，溶度为0.1～1mol/L，加入的量为n(OH-):n(Ni)＝(2～2.2)：1。
  4. 根据权利要求1中所述的一种锂离子电池改性石墨负极材料的制备方法，其特征是：步骤(3)中的烘干温度为40～60℃，时间为12～24小时。
  5. 根据权利要求1中所述的一种锂离子电池改性石墨负极材料的制备方法，其特征是：步骤(4)中有机树脂为环氧树脂、酚醛树脂或糠醛树脂中一种或两种以上，树脂与石墨粉的重量比为m(树脂)：m(石墨)＝(5～10)：100。
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112928259A (zh) * 2021-02-09 2021-06-08 凯博能源科技有限公司 石墨材料及其制备方法和应用
CN114094106A (zh) * 2021-11-23 2022-02-25 山东大学 一种聚磷酸铵改性石墨负极材料及其制备方法和应用
CN114335538A (zh) * 2021-12-24 2022-04-12 陕西煤业化工技术研究院有限责任公司 一种石墨负极材料及其制备方法及一种锂电池
CN114335462A (zh) * 2021-12-24 2022-04-12 陕西煤业化工技术研究院有限责任公司 一种用于低温的石墨负极材料及其制备方法及一种锂电池
CN116589280A (zh) * 2023-07-14 2023-08-15 长沙中瓷新材料科技有限公司 一种石墨匣钵的制备方法

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107507971A (zh) * 2017-08-29 2017-12-22 湖南格兰博智能科技有限责任公司 一种硅基负极材料、制备方法和锂离子电池
CN112786887A (zh) * 2021-01-14 2021-05-11 广东凯金新能源科技股份有限公司 一种高温用石墨负极材料及其制备方法
CN114890414B (zh) * 2022-06-27 2024-03-08 广东邦普循环科技有限公司 一种废旧电池中石墨材料的回收利用方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1224251A (zh) * 1997-12-26 1999-07-28 中国科学院化学研究所 一种锂离子电池碳负极材料及其制备方法
US6395427B1 (en) * 1999-11-04 2002-05-28 Samsung Sdi Co., Ltd. Negative active material for rechargeable lithium battery and method of preparing same
CN103545521A (zh) * 2012-07-11 2014-01-29 长沙永力新能源科技有限公司 一种特殊壳层结构石墨基碳负极复合材料及制备方法

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1224251A (zh) * 1997-12-26 1999-07-28 中国科学院化学研究所 一种锂离子电池碳负极材料及其制备方法
US6395427B1 (en) * 1999-11-04 2002-05-28 Samsung Sdi Co., Ltd. Negative active material for rechargeable lithium battery and method of preparing same
CN103545521A (zh) * 2012-07-11 2014-01-29 长沙永力新能源科技有限公司 一种特殊壳层结构石墨基碳负极复合材料及制备方法

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112928259A (zh) * 2021-02-09 2021-06-08 凯博能源科技有限公司 石墨材料及其制备方法和应用
CN112928259B (zh) * 2021-02-09 2022-05-24 中创新航技术研究院(江苏)有限公司 石墨材料及其制备方法和应用
CN114094106A (zh) * 2021-11-23 2022-02-25 山东大学 一种聚磷酸铵改性石墨负极材料及其制备方法和应用
CN114094106B (zh) * 2021-11-23 2023-08-11 山东大学 一种聚磷酸铵改性石墨负极材料及其制备方法和应用
CN114335538A (zh) * 2021-12-24 2022-04-12 陕西煤业化工技术研究院有限责任公司 一种石墨负极材料及其制备方法及一种锂电池
CN114335462A (zh) * 2021-12-24 2022-04-12 陕西煤业化工技术研究院有限责任公司 一种用于低温的石墨负极材料及其制备方法及一种锂电池
CN116589280A (zh) * 2023-07-14 2023-08-15 长沙中瓷新材料科技有限公司 一种石墨匣钵的制备方法
CN116589280B (zh) * 2023-07-14 2023-10-03 长沙中瓷新材料科技有限公司 一种石墨匣钵的制备方法

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