LU601996B1 - Method of preparing an amorphous moo2-x@c composite material - Google Patents
Method of preparing an amorphous moo2-x@c composite materialInfo
- Publication number
- LU601996B1 LU601996B1 LU601996A LU601996A LU601996B1 LU 601996 B1 LU601996 B1 LU 601996B1 LU 601996 A LU601996 A LU 601996A LU 601996 A LU601996 A LU 601996A LU 601996 B1 LU601996 B1 LU 601996B1
- Authority
- LU
- Luxembourg
- Prior art keywords
- amorphous
- composite material
- ethanol
- preparing
- precursor
- Prior art date
Links
Classifications
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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
- 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
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/05—Preparation or purification of carbon not covered by groups C01B32/15, C01B32/20, C01B32/25, C01B32/30
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G39/00—Compounds of molybdenum
- C01G39/02—Oxides; Hydroxides
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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
- H01M4/362—Composites
- H01M4/366—Composites as layered products
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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
- H01M4/483—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides for non-aqueous cells
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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
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
- H01M4/624—Electric conductive fillers
- H01M4/625—Carbon or graphite
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- 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
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- 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
- C01P2004/04—Particle morphology depicted by an image obtained by TEM, STEM, STM or AFM
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/80—Particles consisting of a mixture of two or more inorganic phases
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- 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
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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
- H01M2004/021—Physical characteristics, e.g. porosity, surface area
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Composite Materials (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Battery Electrode And Active Subsutance (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Claims (7)
1. Verfahren zur Herstellung eines amorphen MoO2,@C-Verbundmaterials, dadurch gekennzeichnet, dass Phosphomolybdänsäure als Molybdänquelle und Pyrrol als Kohlenstoffquelle verwendet werden, umfassend folgende Schritte: S1: Lösen von Phosphomolybdänsäure in Ethanol, um eine Phosphomolybdänsäure-Ethanollösung herzustellen; anschließend Lösen von 2-Methylimidazol in einem anderen Teil Ethanol, um eine 2-Methylimidazol-Ethanollösung zu bilden, und dann Hinzufügen zu der Phosphomolybdänsäure-Ethanollösung; dann Stehenlassen der gemischten Lösung und Sammeln des resultierenden Mo-MI-Vorläufers durch Zentrifugieren; S2: Dispergieren der in S1 erhaltenen Mo-MI-Vorläufer-Nanokugeln in entionisiertem Wasser, gefolgt von Rühren; dann tropfenweises Hinzufügen einer Pyrrol-Lôsung und kontinuierliches Rühren in einem Eiswasserbad; anschließend Durchführen einer Zentrifugation, um einen mit Polypyrrol beschichteten Mo-MI-Vorläufer (Mo-MI@PPy) zu erhalten, gefolgt von einer Vakuumtrocknung des Vorläufers bei 60°C für 24 Stunden; und S3: Unterziehen des getrockneten Mo-MI@PPy-Vorläufers einer Pyrolyse bei 450°C für 2 Stunden unter einer Stickstoffatmosphéare, wodurch ein amorphes MoO2x@C-Verbundmaterial erhalten wird.
2. Verfahren zur Herstellung des amorphen MoO2x@C-Verbundmaterials nach Anspruch 1, dadurch gekennzeichnet, dass in S1 ein Verhältnis von Phosphomolybdänsäure zu Ethanol 0,06 mmol: 100 mL beträgt.
3. Verfahren zur Herstellung des amorphen MoO2,@C-Verbundmaterials nach Anspruch 1, dadurch gekennzeichnet, dass in S1 ein Verhältnis von 2-Methylimidazol zu Ethanol 12,0 mml: 100 mL.
4. Verfahren zur Herstellung des amorphen MoO2x@C-Verbundmaterials nach 6041996 Anspruch 1, dadurch gekennzeichnet, dass in S1 eine Reinheit des Ethanols 99,7 % betragt.
5. Verfahren zur Herstellung des amorphen MoO2,@C-Verbundmaterials nach Anspruch 1, dadurch gekennzeichnet, dass in S2 ein Verhältnis von Mo-MI-Nanokugeln zu entionisiertem Wasser 50 mg: 50 mL.
6. Verfahren zur Herstellung des amorphen MoO2x@C-Verbundmaterials nach Anspruch 1, dadurch gekennzeichnet, dass in S2 eine Menge des verwendeten Pyrrols 100 pL beträgt.
7. Verfahren zur Herstellung des amorphen MoO2,@C-Verbundmaterials nach Anspruch 1, dadurch gekennzeichnet, dass in S2 die Mo-MI-Nanokugeln in entionisiertem Wasser dispergiert und 1 h lang gerührt werden, gefolgt von der tropfenweisen Zugabe von 100 pl Pyrrol-Lôsung und Rühren für 2 h in einem Eiswasserbad.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202411627840.0A CN119528219A (zh) | 2024-11-14 | 2024-11-14 | 一种非晶态MoO2-x@C复合材料的制备方法 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LU601996B1 true LU601996B1 (en) | 2025-12-10 |
Family
ID=94704717
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU601996A LU601996B1 (en) | 2024-11-14 | 2025-06-10 | Method of preparing an amorphous moo2-x@c composite material |
Country Status (2)
| Country | Link |
|---|---|
| CN (1) | CN119528219A (de) |
| LU (1) | LU601996B1 (de) |
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2024
- 2024-11-14 CN CN202411627840.0A patent/CN119528219A/zh active Pending
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2025
- 2025-06-10 LU LU601996A patent/LU601996B1/en active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| CN119528219A (zh) | 2025-02-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Patent granted |
Effective date: 20251210 |