Patent Grant
8846135
The invention relates to a process for the preparation of conductive carbon layers on powdered supports, suitable in particular for electrode layers in lithium batteries.
A process for the preparation of carbon layers by pyrolysis of organic compounds or polymers on powdered ceramic supports is known. “A new method of coating powdered supports with conductive carbon films” (M. Molenda, R. Dziembaj, Z. Piwowarska, M. Drozdek, J. Therm. Anal. Cal., 88, 2007, 503-506) discloses a process for the preparation of conductive carbon layers by pyrolysis of polyacrylonitrile deposited on Al2O3 grains. According to the process, radical polymerization of acrylonitrile in an aqueous Al2O3 suspension was carried out, followed by controlled pyrolysis of the such-obtained precursor, under argon atmosphere, at 400-800° C. for 12 h. Similarly, pyrolysis of poly(N-vinylformamide) (PNVF) deposited on powdered Al2O3 by wet impregnation from an aqueous solution was performed in “Direct Preparation of Conductive Carbon Layer (CCL) on Alumina as a Model System for Direct Preparation of Carbon Coated Particles of the Composite Li-Ion Electrodes” (M. Molenda, R. Dziembaj, M. Drozdek, E. Podstawka, L. M. Proniewicz, Solid State Ionics 179, 2008, 197-201).
In the case of conductive carbon layers intended for lithium batteries, the layers should be characterized by sufficient electrical conductivity, as well as easy transport of lithium ions through the layer during charging and discharging. At the same time, they should exhibit possibly low contact surface area with an electrolyte to suppress formation of a SEI (Solid-Electrolite Interphase) layer. Electrical properties of a carbon layer are improved with increase of pyrolysis temperature, however given limited thermal stability of electrode materials in reductive conditions it is required that the pyrolysis process is carried out at the lowest temperature possible. Carbon layers obtained by pyrolysis of a PNVF precursor did not exhibit sufficiently high electrical conductivity and possessed a high specific surface area.
The process for the preparation of carbon layers on powdered supports comprises dissolving hydrophilic polymer (PH) at a level of 85 to 99.9% by weight in water, adding pyromellitic acid (PMA) or pyromellitic dianhydride (PMDA) at a level of 0.1-15% by weight, followed by adding to the mixture a powdered support at a level of 1-99% by weight. The suspension is concentrated and dried, and then the prepared composite precursor is subjected to pyrolysis at 300-1500° C.
Preferably, the hydrophilic polymer is poly(N-vinylformamide), polyacrylamide or N-vinylformamide-acrylamide copolymers
Preferably, the powdered support comprises metal oxides, lithium and transition metal silicates and polysilicates, lithium and transition metal phosphates and polyphosphates, germanates, vanadates, metals and metal alloys, metal nitrides and silicon.
Most preferably, the powdered support comprises Al2O3, LiMn2O4, Li1-xMn2-2xO4 (0≦x≦0.33), LiMn2O4-ySy (0≦y≦0.25), LiFePO4, LiMxFe1-xPO4 (M=V, Mn, Co, Ni, Cu; 0≦x≦1), Li2MSiO4 (M=V, Mn, Fe, Co, Ni, Cu), LiMSiO4 (M=V, Mn, Fe, Co, Ni, Cu), LiCoO2, LiMxCO1-xO2 (M=V, Fe, Co, Ni, Cu; 0≦x≦1), LiMn1/3CO1/3Ni1/3O2, Sn, SnO, SnO2, tin alloys, Si.
Preferably, the pyrolysis is carried out in inert conditions, preferably under inert gas atmosphere, most preferably argon, nitrogen or helium atmosphere.
Preferably, the pyrolysis is carried out in weakly reducing conditions.
Preferably, the pyrolysis is carried out under vacuum.
In the process of the invention, it was unexpectedly found that adding pyromellitic acid (PMA) or pyromellitic dianhydride (PMDA) to the hydrophilic polymer composition significantly enhances electrical properties of prepared carbon layers and at the same time allows decreasing temperature of the pyrolysis process.
In the process of the invention, pyromellitic acid or the anhydride thereof takes the role of a promoter which structuralizes graphitization of the polymer during pyrolysis, rather than being a layer-making factor—its pyrolysis does not lead to obtaining a carbonizate, but decomposition is complete. The planar structure of the molecule of pyromellitic acid or an anhydride thereof accelerates seeding and forming graphene layers, which facilitate two-dimensional crystallization of a graphite-like material. Additionally, pyromellitic acid or the anhydride thereof is thought to facilitate organization of hydrophilic polymer on the surface of the powdered support already at the impregnation step. It was unexpectedly found that the carbon layers originating from pyrolysis of the hydrophilic polymer composition with PMA or PMDA are closely adjacent and tightly cover grains of the support. At the same time the layers are not continuous by nature, having mesopores of a mean size of about 32-35 Å. Such modification of the carbon layer of the composite is particularly beneficial when employed as electrode layers in lithium batteries, since it protects well cathode material against reaction with the electrolyte and simultaneously secures unhampered diffusion of lithium ions through mesopores of the carbon layer.
In the process of the invention the composition of a carbon precursor (the water-soluble hydrophilic polymer) with a promoter which structuralizes graphitization of the polymer (PMA or PMDA) allows obtaining of the carbon layer with very good dispersion of carbon material and expected physicochemical properties, such as thickness, tightness and porosity. In particular, suitable electrical conductivity (>10−4 Scm−1) of the carbon layer prepared at above 400° C. can be obtained in the process.
Preferably the process proceeds entirely in aqueous environment and the precursors employed are non-toxic, which makes the technology safe and environmentally friendly.
The process of the invention can be employed for obtaining electrode composites (both cathodes and anodes) for lithium batteries. Electrode composites produced by the process of the invention are characterized by better electrical properties and increased chemical stability, that improves operational safety of lithium batteries. The process of the invention can also be employed for preparing composite adsorbents of defined surface morphology obtained from suitable inorganic supports.
The subject-matter of the invention is described in more detail in the following working examples.
10 g of freshly distilled N-vinylformamide (98%) was dissolved in 66 g of deionized water pre-treated with argon for about 30 minutes. The reaction was placed on a water bath and warmed to 35° C. under argon atmosphere. 1.9092 g of AIBA initiator (2,2′-azobis(2-methylpropionamidinyl) dichloride) was then added and the reaction was kept at 60° C. for 2 h. Poly(N-vinylformamide) thus obtained was air-dried for 24 h at 110° C.
0.625 g of dry poly-N-vinylformamide and 0.0329 g pyromellitic acid was dissolved in 12.5 cm3 of deionized water. 0.375 g LiMn2O3.95S0.05 was then added and the contents stirred for 15 minutes. The homogenous mixture formed was kept at 90° C. with continuous stirring for about 2 h to evaporate and concentrate it to a viscosity precluding sedimentation of the suspension. The composite precursor formed was transferred to a teflon container and air-dried for 24 h at 90° C.
The dried precursor was crumbled and pyrolyzed at 400° C. under argon atmosphere (99.999%), for 12 h. This yielded a carbon layer characterized by electrical conductivity of 7.4·10−6 S/cm at 25° C. and electrical conductivity activation energy Ea=0.34 eV. Carbon content in the composite determined by TPO method was 27.6%.
0.7 g of dry poly(N-vinylformamide) and 0.04 g of pyromellitic acid were dissolved in 14.1 cm3 of deionized water. 1.0 g of LiMn2O4 spinel was then added and the mixture stirred for 15 minutes. The homogenous mixture formed was kept at 90° C. with continuous stirring for about 2 h to evaporate and concentrate it to the viscosity precluding sedimentation of the suspension. The composite precursor formed was transferred to a teflon container and air-dried for 24 h at 90° C.
The dried precursor was crumbled and pyrolyzed at 400° C., under argon atmosphere (99.999%) for 12 h. This yielded a composite comprised of the LiMn2O4 support coated by a carbon layer, characterized by the electrical conductivity of 3.3·10−6 S/cm at 25° C. and the electrical conductivity activation energy Ea=0.37 eV. Specific surface area of the composite as determined by BET isotherm method was 5.5 m2/g, and carbon content in the composite was 20.3% (determined by TPO method).
1.87045 g of dry (175° C./24 h) lithium nitrate (V) LiNO3 was dissolved in 70 cm3 of deionized water in a sealed glass vessel under the stream of argon (99.999%, 20 dm3/h). 13.25465 g of manganese (II) acetate hydrate Mn(CH3COO)2·4H2O (Aldrich 99.99%) was added to the solution. Once the substrates dissolved, 10 ml of 25% NH3 aq was added dropwise until pH=10 was reached. The salmon-colored mixture (a sol) was left to condense for 24 h with continuous stirring and heating at about 100° C. in argon atmosphere (99.999%, 20 dm3/h). The gel formed was transferred to a melting pot and air-dried at 90° C. for 48 h.
The dried xerogel precursor was crumbled and air-calcined at 300° C. (with heating rate of 1° C./min) for 24 h, followed by 6 h at 650° C. (with heating rate of 5° C./min).
The LiMn2O4 spinel obtained was characterized by electrical conductivity of 1.2·10−4 S/cm at 25° C. and electrical conductivity activation energy Ea=0.34 eV. Specific surface area of the spinel as determined by BET isotherm method was 6.1 m2/g.
0.8084 g of dry poly(N-vinylformamide) prepared as in Example 1 and 0.0365 g of pyromellitic dianhydride were dissolved in 10 cm3 of deionized water. 1 g of Al2O3 was then added and the mixture stirred for 30 minutes. The homogenous mixture formed was kept at 90° C. with continuous stirring for about 3 h to evaporate and concentrate it to a viscosity precluding sedimentation of the suspension. The composite precursor formed was transferred to a teflon container and air-dried for 24 h at 90° C.
The dried precursor was crumbled and pyrolyzed at 550° C. in argon atmosphere (99.999%), for 6 h. This yielded a carbon layer characterized by electrical conductivity of 8.1·10−4 S/cm at 25° C. Carbon content in the composite determined by TPO method was 13.5%.
Example 1 was followed, with corresponding change of parameters for the following samples:
For materials of the C/Li—Mn—O—S type prepared according to Example 1 and Example 4, carbon content and surface morphology were estimated and studied. The estimated carbon content was determined based on pyrolysis of a 11% PMA and 89% PNVF precursor not deposited on a support. The actual carbon content was determined by temperature-programmed TPO oxidation, as disclosed in “A new method of coating powdered supports with conductive carbon films” (M. Molenda, R. Dziembaj, Z. Piwowarska, M. Drozdek, J. Therm. Anal. Cal., 88, 2007, 503-506). The determination was made with EGA-TGA/DTG/SDTA techniques on Mettler-Toledo 851e thermoanalyzer coupled with Thermostar Balzers quadrupole spectrometer. The measurements were performed in the air stream of 80 ml/min at the temperature range of 30-1000° C. with a heating rate of 5° C./min. The surface morphology was studied by BET isotherm method. Specific surface area measurements were carried out under the pressure of 5.7·10−7 Pa on Micrometrics ASAP 2010 sorptiometer. The samples were degassed at 200-250° C. for 2 h under the pressure of 0.260.4 Pa. The results obtained are presented in Table 1.
The actual carbon content was greater than the estimated amount for all composites. This can prove a beneficial influence of pyromellitic acid or pyromellitic dianhydride on pyrolysis mechanism of the precursor deposited on support grains. The increase of carbon percentage on the support surface enhances its dispersion without local aggregation.
Characteristics of the obtained adsorption isotherms suggests the presence of pores in the form of microcracks and inter-grain splits. At the same time, pore size indicates the presence of mesopores of the very narrow and uniform diameter distribution in the range of 32-35 Å.
| Number | Date | Country | Kind |
|---|---|---|---|
| 385908 | Aug 2008 | PL | national |
This application is a continuation of PCT/PL2009/000081, filed on Aug. 13, 2009, which claims priority to PL Application No. PL385908, filed on Aug. 19, 2008, the contents of each being incorporated herein by reference.
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| Number | Date | Country | |
|---|---|---|---|
| 20110151112 A1 | Jun 2011 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/PL2009/000081 | Aug 2009 | US |
| Child | 13027787 | US |
