WO2014116064A1 - 산화철 나노입자의 제조 방법 - Google Patents

산화철 나노입자의 제조 방법 Download PDF

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Publication number
WO2014116064A1
WO2014116064A1 PCT/KR2014/000721 KR2014000721W WO2014116064A1 WO 2014116064 A1 WO2014116064 A1 WO 2014116064A1 KR 2014000721 W KR2014000721 W KR 2014000721W WO 2014116064 A1 WO2014116064 A1 WO 2014116064A1
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Prior art keywords
aqueous solution
iron oxide
negative electrode
iron
nanoparticles
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Ceased
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PCT/KR2014/000721
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English (en)
French (fr)
Korean (ko)
Inventor
이명기
박성빈
강성중
정왕모
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LG Chem Ltd
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LG Chem Ltd
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Priority to BR112015009488A priority Critical patent/BR112015009488B8/pt
Priority to JP2015545386A priority patent/JP6003008B2/ja
Priority to CN201480002846.7A priority patent/CN104755429B/zh
Priority to EP14743358.5A priority patent/EP2891629B1/en
Priority to IN2883DEN2015 priority patent/IN2015DN02883A/en
Priority to US14/248,479 priority patent/US9755231B2/en
Publication of WO2014116064A1 publication Critical patent/WO2014116064A1/ko
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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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
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
    • H01M4/521—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of iron for aqueous cells
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G49/00—Compounds of iron
    • C01G49/02—Oxides; Hydroxides
    • C01G49/06—Ferric oxide [Fe2O3]
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82B—NANOSTRUCTURES FORMED BY MANIPULATION OF INDIVIDUAL ATOMS, MOLECULES, OR LIMITED COLLECTIONS OF ATOMS OR MOLECULES AS DISCRETE UNITS; MANUFACTURE OR TREATMENT THEREOF
    • B82B1/00—Nanostructures formed by manipulation of individual atoms or molecules, or limited collections of atoms or molecules as discrete units
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82B—NANOSTRUCTURES FORMED BY MANIPULATION OF INDIVIDUAL ATOMS, MOLECULES, OR LIMITED COLLECTIONS OF ATOMS OR MOLECULES AS DISCRETE UNITS; MANUFACTURE OR TREATMENT THEREOF
    • B82B3/00—Manufacture or treatment of nanostructures by manipulation of individual atoms or molecules, or limited collections of atoms or molecules as discrete units
    • 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
    • H01M4/24—Electrodes for alkaline accumulators
    • H01M4/248—Iron electrodes
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/01—Particle morphology depicted by an image
    • C01P2004/03—Particle morphology depicted by an image obtained by SEM
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/30—Particle morphology extending in three dimensions
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/60—Particles characterised by their size
    • C01P2004/62—Submicrometer sized, i.e. from 0.1-1 micrometer
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00—Physical properties of inorganic compounds
    • C01P2006/40—Electric properties
    • 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
    • H01M2004/021—Physical characteristics, e.g. porosity, surface area
    • 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
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
    • H01M4/523—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron for non-aqueous cells
    • 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
    • H01M4/621—Binders
    • H01M4/622—Binders being polymers
    • 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
    • H01M4/624—Electric conductive fillers
    • H01M4/625—Carbon or graphite
    • 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
    • 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
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]

Definitions

  • the present invention relates to a method for producing iron oxide nanoparticles. Specifically, the present invention relates to a method for producing iron oxide nanoparticles, iron oxide nanoparticles prepared by the method and a negative electrode material comprising the same.
  • Secondary batteries are categorized into a positive electrode, a negative electrode, an electrolyte, and a separator.
  • the most influential part of the battery may be the positive electrode and the negative electrode in which the electrochemical reaction takes place.
  • the metal oxide has a disadvantage in that capacity decreases and cycle efficiency decreases during the charging / discharging process when the particle size is large (> 1 ⁇ m)
  • researches for making metal oxide particles into nanometer sizes through various chemical synthesis have been made. It is going on.
  • the conventional method for synthesizing iron oxide nanoparticles has to maintain a difficult synthetic environment (inert atmosphere), use expensive high-purity raw materials, and the particles obtained by ultrasonic irradiation are not uniform, crystallinity is also poor and its application The range is narrow and the ultrasonic irradiation time also takes a long time there is a problem that mass production is impossible.
  • the present invention can be mass-produced by simple process conditions, and provides a method for producing iron oxide nanoparticles with low capacity loss even during several charge / discharge processes.
  • the present invention provides iron oxide nanoparticles prepared by the above method and a negative electrode material including the same.
  • the present invention also provides a cathode for an electrochemical device made of the anode material and an electrochemical device having the same.
  • the method of the present invention it is possible to control the particle size and particle size distribution of the powder in an economical and simple manufacturing process, and to produce iron oxide nanoparticles with low capacity loss even in several charge / discharge processes.
  • 1 and 2 are electron micrographs (SEM) of iron oxide nanoparticles prepared by the method of the present invention.
  • Figure 3 is a comparison graph measuring the capacity of the secondary battery prepared in Example 1 and Comparative Example 1.
  • the iron chloride (FeCl 3 ) aqueous solution may be 2M to 3M concentration
  • the sodium hydroxide (NaOH) aqueous solution may be 5M to 6M concentration
  • the sodium sulfate (Na 2 SO 4 ) aqueous solution may be 0.5M to 1M, specifically 0.6M concentration.
  • the iron chloride aqueous solution when the iron chloride aqueous solution is 2M or less or 3M or more, a metal oxide having a particle size of 1 ⁇ m or more may be synthesized.
  • the concentration of the sodium hydroxide aqueous solution is 6M or more, the pH of the aqueous solution to be synthesized increases the problem that the metal oxide is not synthesized.
  • the concentration of the sodium sulfate solution is 1M or more, there is a problem that a metal oxide of a uniform form is not produced.
  • an aqueous sodium phosphate (Na 2 PO 4 ) solution may be used instead of the aqueous sodium sulfate (Na 2 SO 4 ) solution.
  • the iron chloride aqueous solution sodium hydroxide aqueous solution: sodium sulfate aqueous solution may be mixed in a ratio of 10: 9: x (where x is 0 ⁇ x ⁇ 1) as a volume ratio.
  • reaction step may be carried out under conditions of 90 to 150 hours, specifically about 90 to 100 hours at atmospheric pressure at 100 to 105 °C, specifically 102 °C.
  • the method of the present invention may further comprise the step of cooling, drying and then cooling the solid product obtained after the reaction is completed. At this time, the washing is sequentially washed with water and ethanol.
  • the present invention can obtain iron oxide nanoparticles whose particle size and particle shape are uniformly controlled by the method of the present invention.
  • the particle size (diameter) of the obtained iron oxide nanoparticles may be 500nm to 1 ⁇ m. If the particle size of the iron oxide nanoparticles are further refined to less than 500nm, or more than 1 ⁇ m, there is a disadvantage that the capacity retention rate and cycle efficiency rapidly decrease during the charging and discharging process.
  • the particle shape of the iron oxide nanoparticles may be an oval of approximately round shape.
  • the iron oxide nanoparticles having controlled particle size and particle shape can be manufactured using only the simple manufacturing process, and a secondary battery having a low capacity loss can be manufactured even in several charge / discharge processes. .
  • the present invention can provide a negative electrode material including the iron oxide nanoparticles.
  • the negative electrode material may further include a conductive material, a binder or a filler, in addition to the iron oxide nanoparticles.
  • the iron oxide nanoparticles are added in 40 to 65% by weight based on the total weight of the negative electrode material. If the content of the iron oxide nanoparticles is less than 40% by weight, there is a disadvantage that high capacity can not be implemented, and if the content of the iron oxide nanoparticles is more than 65% by weight, cycle stability due to the disadvantage that electrode peeling occurs from the first two cycles. There is a problem that can not be implemented.
  • the conductive material is typically added in an amount of 1 to 30% by weight based on the total weight of the negative electrode material.
  • a conductive material is not particularly limited as long as it has conductivity without causing chemical change in the battery, and examples thereof include graphite such as natural graphite and artificial graphite; Carbon blacks such as carbon black, acetylene black, Ketjen black, channel black, furnace black, lamp black and summer black; Conductive fibers such as carbon fibers and metal fibers; Metal powders such as carbon fluoride powder, aluminum powder and nickel powder; Conductive whiskeys such as zinc oxide and potassium titanate; Conductive metal oxides such as titanium oxide; Conductive materials such as polyphenylene derivatives and the like can be used.
  • the binder is a component that assists the bonding of the iron oxide nanoparticles and the conductive material and the current collector, and is usually added in an amount of 1 to 30% by weight based on the total weight of the negative electrode material.
  • binders include polyvinylidene fluoride, polyvinyl alcohol, carboxymethyl cellulose (CMC), starch, hydroxypropyl cellulose, regenerated cellulose, polyvinylpyrrolidone, tetrafluoroethylene, polyethylene, Polypropylene, ethylene-propylene-diether polymer (EPDM), sulfonated EPDM, styrene butylene rubber, fluorine rubber, various copolymers, and the like.
  • the filler is optionally used as a component for inhibiting the expansion of the electrode, and is not particularly limited as long as it is a fibrous material without causing chemical change in the battery, for example, olefin polymers such as polyethylene, polypropylene; Fibrous materials, such as glass fiber and carbon fiber, are used.
  • the present invention can provide a negative electrode for an electrochemical device, the negative electrode material is applied on the current collector.
  • the negative electrode may be prepared by dissolving the negative electrode material of the present invention in a solvent to make a slurry, applying the same on a negative electrode current collector, and then drying and rolling the negative electrode material.
  • the negative electrode current collector is not particularly limited as long as it has conductivity without causing chemical changes in the battery.
  • the negative electrode current collector may be made of at least one of stainless steel, nickel, copper, titanium, and alloys thereof. And generally has a thickness of 3 ⁇ m to 500 ⁇ m.
  • the present invention can provide an electrochemical device composed of a negative electrode including the negative electrode material, a positive electrode, a separator, and a nonaqueous electrolyte.
  • the electrochemical device may be a lithium secondary battery.
  • the electrochemical device may be manufactured according to a conventional method.
  • the solid product was cooled and washed sequentially with water and ethanol.
  • the product was then dried in a vacuum drier to obtain iron oxide nanoparticles (particle size: 500 nm) (see FIG. 2).
  • the slurry was prepared by mixing the iron oxide nanoparticles, the conductive agent (Super-P) and the binder (KF 1100) prepared above in a weight ratio of 65:10:25 (g), and the slurry was coated on a copper current collector and then 120 It was dried for 12 hours or more in a vacuum oven at °C.
  • the counter electrode was made of lithium metal, and a coin-type half cell was prepared using 1 M LiPF 6 / ethylene carbonate (EC): ethyl methyl carbonate (EMC) (volume ratio 1: 1) as an electrolyte. It was.
  • the slurry was prepared by mixing the iron oxide nanoparticles, the conductive agent (Super-P) and the binder (KF 1100) prepared in Example 1-1 in a weight ratio of 40:30:30 (g), and the slurry was used as a copper current collector. After coating on and dried in a vacuum oven at 120 °C for more than 12 hours.
  • the counter electrode used lithium metal, and a coin-shaped half cell was prepared using 1 M LiPF 6 / ethylene carbonate (EC): ethyl methyl carbonate (EMC) (volume ratio 1: 1) as an electrolyte.
  • EC ethylene carbonate
  • EMC ethyl methyl carbonate
  • a slurry was prepared by mixing 50 nm iron oxide nanoparticles, a conductive agent (Super-P), and a binder (KF 1100) prepared by a general method in a 65:10:25 weight ratio (g), and the slurry was added to a copper current collector. After coating was dried for 12 hours or more in a vacuum oven at 120 °C.
  • the counter electrode used lithium metal, and a coin-shaped half cell was prepared using 1 M LiPF 6 / ethylene carbonate (EC): ethyl methyl carbonate (EMC) (volume ratio 1: 1) as an electrolyte.
  • EC ethylene carbonate
  • EMC ethyl methyl carbonate
  • Performance evaluation of the secondary battery prepared in Example 1, Example 2 and Comparative Example 1 was performed as follows. The batteries were charged and discharged at 10 th in a charge / discharge region of 2.0 to 0.005 V (vs. Li / Li +), with a current density of 0.1C. Their initial charge and discharge efficiency results are shown in Table 1 below. In addition, the charge and discharge results using the battery of Example 2 is shown in the graph of FIG.
  • Example 1 Example 2 Comparative Example 1 1 th cycle Discharge capacity 1318 mAh / g 1460 mAh / g 1481 mAh / g Charge capacity 1008 mAh / g 1027 mAh / g 750 mAh / g 2 th cycle Discharge capacity 1004 mAh / g 1044 mAh / g 841 mAh / g Charge capacity 963 mAh / g 993 mAh / g 312 mAh / g 10 th cycle capacity 904 mAh / g 894 mAh / g 62 mAh / g Capacity retention rate 93.8% 92.3% 19.9%

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Nanotechnology (AREA)
  • Manufacturing & Machinery (AREA)
  • Battery Electrode And Active Subsutance (AREA)
  • Secondary Cells (AREA)
  • Compounds Of Iron (AREA)
PCT/KR2014/000721 2013-01-25 2014-01-24 산화철 나노입자의 제조 방법 Ceased WO2014116064A1 (ko)

Priority Applications (6)

Application Number Priority Date Filing Date Title
BR112015009488A BR112015009488B8 (pt) 2013-01-25 2014-01-24 Método de preparação de nanopartículas de óxido de ferro (iii), nanopartículas de óxido de ferro (iii), material para anodo, anodo e dispositivo eletroquímico
JP2015545386A JP6003008B2 (ja) 2013-01-25 2014-01-24 酸化鉄ナノ粒子の製造方法
CN201480002846.7A CN104755429B (zh) 2013-01-25 2014-01-24 氧化铁纳米粒子的制备方法
EP14743358.5A EP2891629B1 (en) 2013-01-25 2014-01-24 Method of producing iron oxide nanoparticles
IN2883DEN2015 IN2015DN02883A (OSRAM) 2013-01-25 2014-01-24
US14/248,479 US9755231B2 (en) 2013-01-25 2014-04-09 Method of preparing iron oxide nanoparticles

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR1020130008784A KR101560441B1 (ko) 2013-01-25 2013-01-25 산화철 나노입자의 제조 방법
KR10-2013-0008784 2013-01-25

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US14/248,479 Continuation US9755231B2 (en) 2013-01-25 2014-04-09 Method of preparing iron oxide nanoparticles

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WO2014116064A1 true WO2014116064A1 (ko) 2014-07-31

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US (1) US9755231B2 (OSRAM)
EP (1) EP2891629B1 (OSRAM)
JP (1) JP6003008B2 (OSRAM)
KR (1) KR101560441B1 (OSRAM)
CN (1) CN104755429B (OSRAM)
BR (1) BR112015009488B8 (OSRAM)
IN (1) IN2015DN02883A (OSRAM)
WO (1) WO2014116064A1 (OSRAM)

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CN105152223A (zh) * 2015-07-23 2015-12-16 南通万宝实业有限公司 一种用于制备硬磁体的精细颗粒磁性氧化铁粉制备方法

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CN104966839A (zh) * 2015-07-15 2015-10-07 山东大学 一种锂电池负极材料改性方法
KR101823362B1 (ko) 2016-09-12 2018-01-31 한국기초과학지원연구원 산화철 나노입자 제조방법 및 이에 의해 제조된 산화철 나노입자
CA3041293A1 (en) 2016-10-21 2018-04-26 Nantenergy, Inc. Corrugated fuel electrode
CN106582670B (zh) * 2016-12-22 2020-04-07 中国工程物理研究院材料研究所 一种锡掺杂氧化铁介晶纳米粒子及其制备方法和应用方法
KR102066641B1 (ko) * 2017-09-15 2020-01-15 주식회사 엘지화학 수도커패시터용 음극 활물질의 제조 방법
KR101966239B1 (ko) 2017-10-25 2019-04-08 한국기초과학지원연구원 막대형 산화철 입자 및 이의 제조방법
KR101983046B1 (ko) 2017-11-08 2019-05-29 한국기초과학지원연구원 이차전지용 음극활물질, 그 제조방법 및 이를 포함하는 리튬이차전지
US11611115B2 (en) 2017-12-29 2023-03-21 Form Energy, Inc. Long life sealed alkaline secondary batteries
WO2020023912A1 (en) 2018-07-27 2020-01-30 Form Energy Inc. Negative electrodes for electrochemical cells
US12294086B2 (en) 2019-07-26 2025-05-06 Form Energy, Inc. Low cost metal electrodes
CN111204816A (zh) * 2020-01-13 2020-05-29 华东理工大学 一种二氧化硅包覆三氧化二铁的复合材料及其制备方法
KR20240101037A (ko) 2022-12-23 2024-07-02 한국전자기술연구원 산화철 나노입자 및 그의 제조방법
WO2024209262A1 (en) 2023-12-04 2024-10-10 Feirahi Farzaneh PRODUCING MODIFIED IRON NANOPARTICLES WITH CHITINASE AND β-GLUCANASE ENZYMES USING ACACIA NILOTICA EXTRACT
CN118791050B (zh) * 2024-07-09 2025-10-14 北京科技大学 一种碱金属掺杂氧化铁制备高容量锂离子电池负极材料的方法

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EP2891629A1 (en) 2015-07-08
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CN104755429A (zh) 2015-07-01
EP2891629B1 (en) 2017-12-20
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US9755231B2 (en) 2017-09-05
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