Synthesis method for carbon material based on LixM1-yM'(XO4)n

• US 7,285,260 B2
• Filed: 09/21/2001
• Issued: 10/23/2007
• Est. Priority Date: 09/26/2000
• Status: Expired due to Term

• Current Assignee: CNRS, Hydro-Quebec (Province of Québec), Universite De Montreal, L'
• Original Assignee: CNRS, Hydro-Quebec (Province of Québec), Universite De Montreal, L'
• Inventors: Ravet, Nathalie, Gauthier, Michel, Armand, Michel, Magnan, Jean-Francois
• Primary Examiner(s): Langel; Wayne A.
• Application Number:
  US10/362,764
• Publication Number:
  US 20040086445A1
• Time in Patent Office: 2,223 Days
• Field of Search: 423/306, 423/311, 423/327.1, 423/326, 423/331, 423/332, 423/518, 423/544, 423/554, 423/556, 423/555, 429/231.95
• US Class Current: 423/306
• CPC Class Codes: C01B 17/96 Methods for the preparation of sulfates in general particular individual sulfates, see the relevant groups of subclasses C01B - C01G, according to the cation
• CPC Class Codes: C01B 25/37 Phosphates of heavy metals
• CPC Class Codes: C01B 25/45 containing plural metal, or metal and ammonium
• CPC Class Codes: C01B 33/20 Silicates persilicates C01B15/14 ; containing aluminium C01B33/26
• CPC Class Codes: C01P 2004/03 obtained by SEM
• CPC Class Codes: C01P 2004/04 obtained by TEM, STEM, STM or AFM
• CPC Class Codes: C01P 2004/50 Agglomerated particles
• CPC Class Codes: C01P 2004/80 Particles consisting of a mixture of two or more inorganic phases
• CPC Class Codes: H01G 11/02 using combined reduction-oxidation reactions, e.g. redox arrangement or solion
• CPC Class Codes: H01G 11/46 Metal oxides
• CPC Class Codes: H01G 11/50 specially adapted for lithium-ion capacitors, e.g. for lithium-doping or for intercalation
• CPC Class Codes: H01G 11/86 specially adapted for electrodes carbonisation or activation of carbon for the manufacture of electrodes H01G11/34
• CPC Class Codes: H01M 10/052 Li-accumulators
• CPC Class Codes: H01M 10/0525 Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
• CPC Class Codes: H01M 4/136 Electrodes based on inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy
• CPC Class Codes: H01M 4/366 as layered products
• CPC Class Codes: H01M 4/485 of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy H01M4/505, H01M4/525 take precedence
• CPC Class Codes: H01M 4/525 of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
• CPC Class Codes: H01M 4/5825 Oxygenated metallic salts or polyanionic structures, e.g. borates, phosphates, silicates, olivines
• CPC Class Codes: H01M 4/625 Carbon or graphite
• CPC Class Codes: Y02E 60/10 : Energy storage using batteries
• CPC Class Codes: Y02E 60/13 : Energy storage using capacitors
• CPC Class Codes: Y10T 428/2982 : Particulate matter [e.g., sphere, flake, etc.]
• CPC Class Codes: Y10T 428/2991 : Coated
• CPC Class Codes: Y10T 428/30 : Self-sustaining carbon mass or layer with impregnant or other layer

Abstract

Method of synthesis for a material made of particles having a core and a coating and/or being connected to each other by carbon cross-linking, the core of these particles containing at least one compound of formula Li_xM_1−yM′_y(XO₄)_n, in which x,y and n are numbers such as 0≦x≦2, 0≦y≦0.6 and 1≦n≦1.5, M is a transition metal, M′ is an element with fixed valency, and the synthesis is carried out by reaction and bringing into equilibrium the mixture of precursors, with a reducing gaseous atmosphere, in such a way as to bring the transition metal or metals to the desired valency level, the synthesis being carried out in the presence of a source of carbon called carbon conductor, which is subjected to pyrolysis. The materials obtained have excellent electrical conductivity as well as very improved chemical activity.

Claims

1. A method for the synthesis of a compound of the formula Li_xM₁₋

yM′

_y(XO₄)_n, wherein x, y and n are numbers such that 0≦

x≦

2, 0≦

y≦

0.6, and 1≦

n≦

1.5, M is a transition metal or a mixture of transition metals in the first line of the periodic table, M′

is an element with fixed valency selected from the group consisting of Mg²⁺, Ca²⁺, Al³⁺, Zn²⁺, and combinations thereof and X is S, P or Si, comprising;

bringing into equilibrium in a reaction medium, in the required proportions, a mixture comprising the following precursors;

a) a source of M, wherein at least one part of the transition metal or metals that constitute M are in an oxidation state greater than that of the transition metal or metals in the final compound Li_xM<sub>1−

y</sub>M′

_y(XO₄)_n;

b) a source of an element M′

;

c) a compound that is a source of lithium; and

optionally,

d) a compound that is a source of X,

wherein the sources of elements M, M′

, Li and X are introduced, in whole or in part, in the form of compounds having more than one source element, and

wherein the synthesis is carried out by reaction and bringing into equilibrium, in the absence of carbon or in the presence of an amount of carbon insufficient or too inert kinetically to realize the reduction of a metal salt that constitutes M, in the proportions required, the mixture of the precursors a) to d) and by reduction, with a reducing gaseous atmosphere, to bring the transition metal or metals to the desired degree of valency.

2. The method according to claim 1, wherein the source of M is also the source of X, the source of M′

is also the source of X, the source of lithium is also the source of X, or the source of X is also the source of lithium.

3. The method according claim 1, wherein bringing the mixture of precursors a) to d) into equilibrium is carried out in the form of an intimate or homogeneous mixture.

4. The method according to claim 1, wherein the source of M is a compound comprising a transition metal or mixture of transition metals selected from the group consisting of iron, manganese, cobalt, nickel, vanadium, titanium, chromium, and copper.

5. The method according to claim 4, wherein the source of M is a compound in a state of oxidation from 3 to 7.

6. The method according to claim 4, wherein the source of M is a compound selected from the group consisting of iron (III) oxide, magnetite, manganese dioxide, di-vanadium pentoxide, trivalent iron phosphate, trivalent iron nitrate, trivalent iron sulfate, iron hydroxyphosphate, lithium hydroxyphosphate, trivalent iron sulfate, trivalent iron nitrate, and mixtures thereof.

7. The method according to claim 1, wherein the source of lithium is a compound selected from the group consisting of lithium oxide, lithium hydroxide, lithium carbonate, neutral phosphate Li₃PO₄, acid phosphate LiH₂PO₄, lithium orthosilicates, lithium metasilicates, lithium polysilicates, lithium sulfate, lithium oxalate, lithium acetate, and mixtures thereof.

8. The method of synthesis according to claim 7, wherein the source of lithium is lithium carbonate of the formula Li₂CO₃.

9. The method according to claim 1, wherein the source of X is selected from the group consisting of sulfuric acid, lithium sulfate, phosphoric acid, phosphoric acid esters, neutral phosphate Li₃PO₄, acid phosphate LiH₂PO₄, monoammonium phosphate, diammonium phosphate, trivalent iron phosphate, manganese and ammonium phosphate (NH₄MnPO₄), silica, lithium silicates, alkoxysilanes and partial hydrolysis products thereof, and mixtures thereof.

10. The method according to claim 9, wherein the source of X is anhydrous or hydrated ferric phosphate.

11. The method according to claim 1, wherein at least one compound of the formula Li_xM₁₋

yM′

_y(XO₄)_n, is a compound of the formula LiFePO₄;

LiFe<sub>1−

s</sub>Mn_sPO₄, wherein 0≦

s≦

0 9, LiFe<sub>1−

y</sub>Mg_yPO₄;

LiFe<sub>1−

y</sub>Ca_yPO₄, wherein, 0≦

y≦

0.3;

LiFe<sub>1−

s−

y</sub>Mn_sMg_yPO₄, wherein 0≦

s≦

1 and 0≦

y≦

0.2;

Li_1+xFeP<sub>1−

x</sub>Si_xO₄, wherein 0≦

x≦

0.9;

Li_1+xFe<sub>1−

s</sub>Mn_sP<sub>1−

x</sub>Si_xO, wherein 0≦

s≦

1;

Li_1+zFe<sub>1−

s−

z</sub>Mn_sP<sub>1−

z</sub>S_zO₄, wherein 0≦

s≦

1, 0≦

z≦

0.2;

Li_1+2qFe<sub>1−

s−

q</sub>Mn_sPO₄, wherein 0≦

s≦

1 and 0≦

q≦

0.3;

Li_1+rFe<sub>1−

s</sub>Mn_s(S_1rP_rO₄)_1,5, wherein 0≦

r≦

1 and 0≦

s,t≦

1 or Li_0,5+uFe<sub>1−

t</sub>Tit(PO₄)_1,5, wherein 0≦

t≦

1 and 0≦

u≦

1.5.

12. The method according to claim 1, wherein the compound of formula Li_xM₁₋

yM′

_y(XO₄)_n, has an olivine or Nasicon structure.

13. The method according to claim 1, wherein reduction is obtained by the action of a gaseous reducing atmosphere able to reduce the oxidation state of a metallic ion of M to the level required for the composition of the compound without reducing the oxidation state of a metallic ion of M to the neutral metallic state.

14. The method according to claim 13, wherein the gaseous reducing atmosphere comprises hydrogen or a gas that is capable of generating hydrogen under the synthesis conditions, ammonia or a substance capable of generating ammonia under the synthesis conditions or carbon monoxide, and wherein the hydrogen, ammonia, or carbon monoxide gas is used in a pure state or in a mixture, and, optionally, in the presence of water vapor, carbon dioxide, or a neutral gas.

15. The method according to claim 14, wherein the gaseous reducing atmosphere comprises a mixture of CO/CO₂, H₂/H₂O, NH₃/H₂O, or a mixture thereof, generating an oxygen equilibrium pressure less than or equal to that determined by the transition metal at the state of oxidation corresponding to precursors a) to d) introduced to form the compound Li_xM₁₋

yM′

_y(XO₄)_n, but greater than that corresponding to the reduction of any one of the transition elements present in a metallic state, insuring the thermodynamic stability of Li_xM<sub>1−

y</sub>M′

_y(XO₄)_n, in the reaction mixture, independent of reaction time of the synthesis.

16. The method according to claim 14, wherein the gaseous reducing atmosphere comprises a mixture of CO/CO₂, H₂/H₂O, NH₃/H₂O, or a mixture thereof, generating an oxygen equilibrium pressure that is less than or equal to that determined by one of the transition metals present in Li_xM₁₋

yM′

_y(XO₄)_n, wherein the synthesis temperature is between 200°

C. and 1200°

C., and wherein contact time between the reaction mixture and the gaseous reducing atmosphere is between 2 minutes and 5 hours.

17. The method according to claim 15, wherein the gaseous reducing atmosphere is obtained by decomposition, in a vacuum or in an inert atmosphere, of an organic compound or a mixture of organic compounds comprising at least hydrogen and oxygen, bound chemically, and wherein pyrolysis of the organic compound or mixture of organic compounds generates carbon monoxide, a mixture of carbon dioxide and monoxide, hydrogen, or a mixture of hydrogen and water vapor to carry out the reduction leading to formation of the compound Li_xM₁₋

yM′

_y(XO₄)_n.

18. The method according to claim 15, wherein the gaseous reducing atmosphere is obtained by partial oxidation by oxygen or air, of a hydrocarbon or sacrificial carbon, optionally in the presence of water vapor, at a temperature of between 400°

C. and 1200°

C. to facilitate formation of carbon monoxide or hydrogen or of a mixture of carbon monoxide and hydrogen.

19. The method according to claim 1, wherein the value of x in Li_xM₁₋

yM′

_y(XO₄)_n is chosen so as to insure thermodynamic control and/or rapid kinetics of the reduction by permitting selection of gaseous reducing atmospheres that are easily accessible by simple mixture of gases or by reforming of simple organic molecules.

20. The method according to claim 1, wherein thermal processing comprising the formation reaction of Li_xM₁₋

yM′

_y(XO₄)_n, reduction, and pyrolysis is carried out by heating to a temperature between 500°

C. and 1100°

C.

21. The method according to claim 20, wherein maximum temperature of thermal processing is between 500°

C. and 800°

C.

22. The method according to claim 1, wherein the temperature and time of the synthesis are chosen as a function of the nature of the transition metal or metals, wherein the temperature is a minimum temperature at which the gaseous reducing atmosphere reduces the transition metal or metals to an oxidation state in the compound Li_xM₁₋

yM′

_y(XO₄)_n and below a temperature leading to a reduction of the transition metal or metals to the metallic state or an oxidation of the carbon resulting from pyrolysis of the organic substance, and wherein the time is less than a time leading to the reduction of the transition metal or metals to the metallic state or an oxidation of the carbon resulting from pyrolysis or the organic substance.

23. The method according to claim 22, wherein the compound Li_xM_1-yM′

_y(XO₄)_n is LiMPO₄ and wherein the amount of carbon conductor after pyrolysis is between 0.1% and 10% by mass in comparison to the mass of the compound LiMPO₄.

24. The method according to claim 1, wherein the compound of formula Li_xM₁₋

yM′

_y(XO₄)_n is LiFePO₄.

25. The method according to claim 24, wherein the source of iron is selected from the group consisting of iron phosphates, iron oxyphosphates, iron hydroxyphosphates, iron oxides and lithium oxides, and mixtures thereof, and wherein at least part of the iron is in oxidation state III.

26. The method according to claim 24, wherein the source of lithium is selected from the group consisting of lithium phosphate, lithium dihydrogenophosphate, lithium carbonate, lithium acetate and lithium hydroxide, and mixtures thereof.

27. The method according to claim 24, wherein the source of phosphorus is ammonium phosphate, orthophosphoric acid, metaphosphoric acid, pyrophosphoric acid, or phosphorus pentoxide.

28. The method according to claim 1, wherein the reduction is carried out in a reactor used for preparing the mixture of precursors or in a different reactor.

29. A method of synthesis of a material made of particles,

wherein the particles comprise a core and a coating and/or are connected to each other by cross-linking, wherein the core comprises at least one compound of the formula Li_xM₁₋

yM′

_y(XO₄)_n, wherein x, y and n are numbers such that 0≦

x≦

2, 0≦

y≦

0.6, and 1≦

n≦

1.5, M is a transition metal or a mixture of transition metals from the first line of the periodic table, M′

is an element with fixed valency selected from the group consisting of Mg²⁺, Ca²⁺, Al³⁺, Zn²⁺ and combinations thereof and X is 5, P or Si, wherein the coating comprises carbon connecting at least two particles to each other, and wherein the cross-linking comprises carbon connecting at least two particles to each other, the method comprising bringing into equilibrium in a reaction medium, in the proportions required, a mixture comprising the following precursors;

a) a source of M, wherein at least part of the transition metal or metals that constitute M are in an oxidation state greater than that of the metal in the final compound Li_xM<sub>1−

y</sub>M′

_y(XO₄)_n;

b) a source of an element M′

;

c) a compound that is a source of lithium; and

optionally,

d) a compound that is a source of X;

wherein the sources of the elements M, M′

, Li and X are introduced, in whole or in part, in the form of compounds having more than one source element, and

wherein the synthesis is carried out by reaction and bringing into equilibrium, in the absence of carbon or in the presence of an amount of carbon insufficient or too inert kinetically to realize the reduction of a metal salt that constitutes M, in the proportions required, the mixture of precursors a) to d) with a gaseous reducing atmosphere, in such a way as to bring the transition metal or metals to the desired degree of valency,

wherein the synthesis is carried out in the presence of an organic substance as a source of carbon conductor, and

wherein the synthesis leads to the material by a pyrolysis step for the carbon conductor after or simultaneously with preparing the mixture of the precursors and reduction of the mixture obtained.

30. The method according to claim 29, wherein the carbon present in the material, in the form of coating and cross-linking, adheres intimately to the particles of the material resulting in an electronic conductivity of the material that is greater than that of a material comprising corresponding non-coated particles.

31. The method according to claim 29, wherein the addition of carbon conductor is carried out after the synthesis of Li_xM₁₋

yM′

_y(XO₄)_n.

32. The method according to claim 29, wherein the addition of carbon conductor is carried out simultaneously with the synthesis of Li_xM₁₋

yM′

_y(XO₄)_n.

33. The method according to claim 29, wherein the reaction parameters of the kinetics of the reduction by the gaseous reducing atmosphere are chosen such that the carbon conductor does not participate in a significant way in the reduction process.

34. The method according to claim 33, wherein the reaction parameters of flow and composition of the gaseous reducing atmosphere, temperature, and contact time, are chosen such that the carbon conductor does not participate in a significant way in reduction and wherein the temperature of reaction is less than 900°

C. and contact time is less than 5 hours.

35. The method according to claim 29, wherein the organic substance that is the source of carbon conductor is selected such that the particles of the material obtained after the pyrolysis step essentially have the form and granulometric distribution of the precursors of the reaction.

36. The method according to claim 29, wherein the organic substance that is the source of the carbon conductor is selected from the group consisting of polymers and oligomers containing a carbon skeleton, simple carbohydrates and polymers, and aromatic hydrocarbons.

37. The method according to claim 36, wherein the organic substance that is the source of carbon conductor is chosen so as to leave a deposit of carbon conductor on the surface (coating) of the solid particles that constitute the material and/or between these solid particles, carbon bridges (cross-linking), at the time of pyrolysis.

38. The method according to claim 37, wherein the organic substance that is the source of carbon conductor comprises at least one of the compounds selected from the group consisting of polyethylene, polypropylene, glucose, fructose, sucrose, xylose, sorbose, starch, cellulose and cellulose esters, block polymers of ethylene and ethylene oxide, and polymers of furfuryl alcohol.

39. The method of synthesis according to claim 29, wherein the source of the carbon conductor contains, in the same compound or in the mixture that comprises the source, oxygen and hydrogen that are bound chemically and from which pyrolysis locally releases carbon monoxide and/or carbon dioxide and/or hydrogen and water vapor that contributes to creating locally the gaseous reducing atmosphere for synthesis of the material Li_xM₁₋

yM′

_y(XO₄)_n.

40. The method according to claim 29, wherein the source of carbon conductor is added to the reaction mixture at the start or in the course of the mixture of precursors a) to d).

41. The method according to claim 40, wherein the amount of carbon conductor in the reaction medium is between 0.1% and 25%, inclusively, of the total mass of the reaction mixture.

42. The method according to claim 29, wherein the organic substance that is the source of carbon conductor is dispersed in processing an intimate mixture of precursors a) to d) by agitating, mechanical grinding, by ultrasonic homogenizing, optionally in the presence of a liquid, or by spray-drying of a solution, suspension, or emulsion of one or more of precursors a) to d).

43. The method according to claim 29, wherein the material obtained has a conductivity that is greater than 10⁻

8 S.cm<sup>−

1</sup>, when measured on a sample of powder compacted at 100 Kg.cm<sup>−

2</sup>.

44. A method of synthesis according claim 29, wherein the core of the particles of the material essentially comprises a compound of formula Li_xM₁₋

yM′

_y(XO₄)_n and the amount of carbon conductor for coating and/or cross-linking in the material comprises between 0.2% and 5%, inclusively, in comparison to the mass of material obtained at the time of synthesis.