HIGH CAPACITY HARD CARBON MATERIALS COMPRISING EFFICIENCY ENHANCERS

• US 20160344030A1
• Filed: 06/12/2014
• Published: 11/24/2016
• Est. Priority Date: 06/12/2013
• Status: Abandoned Application

• Current Assignee: Group14 Technologies Inc.
• Original Assignee: EnerG2 Technologies, Incorporated
• Inventors: Sakshaug, Avery, Kron, Benjamin E., Thompkins, Leah A., Geramita, Katharine, McAdie, Aaron, Costantino, Henry R., Feaver, Aaron M.
• Application Number:
  US14/897,828
• Publication Number:
  US 20160344030A1
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: C08L 61/14 Modified phenol-aldehyde condensates
• CPC Class Codes: H01G 11/26 characterised by their structure, e.g. multi-layered, porosity or surface features
• CPC Class Codes: H01G 11/32 Carbon-based
• CPC Class Codes: H01G 11/62 characterised by the solute, e.g. salts, anions or cations therein
• 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 2004/021 Physical characteristics, e.g. porosity, surface area
• CPC Class Codes: H01M 2004/027 Negative electrodes
• CPC Class Codes: H01M 4/02 Electrodes composed of, or comprising, active material
• CPC Class Codes: H01M 4/133 Electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx
• CPC Class Codes: H01M 4/1393 of electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx
• CPC Class Codes: H01M 4/362 Composites
• CPC Class Codes: H01M 4/587 for inserting or intercalating light metals
• CPC Class Codes: Y02E 60/10 Energy storage using batteries
• CPC Class Codes: Y02T 10/70 Energy storage systems for electromobility, e.g. batteries

Abstract

The present application is directed to hard carbon materials. The hard carbon materials find utility in any number of electrical devices, for example, in lithium ion batteries. Methods for making the disclosed carbon materials are also disclosed.

Claims

1. A carbon material comprising a surface area of less than 50 m²/g, between 5% and 20% phosphorous by weight relative to total weight of all components in the carbon material and a specific lithium uptake capacity of greater than 1.4:

6.

2. The carbon material of claim 1, wherein the specific surface area is less than 25 m2/g.

3. The carbon material of claim 2, wherein the specific surface area is less than 10 m2/g.

4. The carbon material of claim 1, wherein the carbon material comprises between 5% and 410% phosphorous by weight relative to total weight of all components in the carbon material.

5. The carbon material of claim 1, wherein the carbon material comprises between 410% and 20% phosphorous by weight relative to total weight of all components in the carbon material.

6. The carbon material of claim 1, wherein the carbon material comprises a total pore volume from 0.001 to 0.1 cm3/g.

7. The carbon material of claim 1, wherein the carbon material comprises a tap density from 0.3 to 0.9 g/cm3.

9. The carbon material of claim 1, wherein the first cycle efficiency of a lithium based energy storage device is greater than 80% when the carbon material is incorporated into an electrode of the lithium based energy storage device.

13. The carbon material of claim 1, wherein at least 80% of the total pore volume comprises pores less than 100 nm in diameter.

14. The carbon material of claim 1, wherein at least 50% of the total pore volume comprises pores less than 1 nm in diameter.

15. The carbon material of claim 1, wherein the total concentration of all elements having an atomic number from 11 to 92, excluding phosphorous, is below 200 ppm as measured by proton induced X-ray emission.

24. The carbon material of claim 1, wherein the carbon material comprises less than 10% crystallinity.

25. The carbon material of claim 1, wherein the carbon material comprises an La ranging from 20 nm to 30 nm as determined by RAMAN spectroscopy analysis.

29. The carbon material of claim 1, wherein the carbon material has a ratio of intercalation storage to pore storage ranging from 2:

1 to 1;

2.

31. The carbon material of claim 1, wherein the carbon material comprises a lithium plating potential between −

5 mV and −

15 mV versus lithium metal.

32. The carbon material of claim 1, wherein the carbon material exhibits less than 10% capacity decrease when the current density is raised from an initial value to 40 times the initial value.

38. The carbon material of claim 1, wherein the carbon material comprises graphite, and the carbon material exhibits end of life evidenced by a voltage (V) vs Li/Li+ of 5% of maximum voltage at a depth of discharge of 75%>

or less.

42. The carbon material of claim 38, wherein the graphite content ranges from 80 to 85%.

43. An electrode comprising a binder and the carbon material of claim 1.

44. An electrical energy storage device comprising:

a) at least one anode comprising the electrode of claim 43;

b) at least one cathode comprising a metal oxide; and

c) an electrolyte comprising lithium ions;

wherein the electrical energy storage device has a first cycle efficiency of at least 70% and a reversible capacity of at least 200 mAh/g with respect to the mass of the hard carbon material present in the device.

50. The electrical energy storage device of claim 44, wherein the electrical energy storage device has a gravimetric capacity of greater than 500 mAh/g based on total mass of active material in the electrical energy storage device.

52. The electrical energy storage device of claim 44, wherein the electrical energy storage device has a ratio of intercalation storage to pore storage ranging from 2:

1 to 1;

2.

8. (canceled)

10-12. -12. (canceled)

16-23. -23. (canceled)

26-28. -28. (canceled)

30. (canceled)

33-37. -37. (canceled)

39-41. -41. (canceled)

45-49. -49. (canceled)

51. (canceled)

53. (canceled)

54. A co-polymer gel comprising an epoxy containing phenolic-aldehyde co-polymer, the co-polymer gel comprising phosphorous-containing cross links, a phosphorous content of at least 1% by mass of the dry weight of the co-polymer and an optional solvent.

55-64. -64. (canceled)

65. A method for preparing a condensation polymer gel, the method comprising:

a) forming crosslinked polymer gel particles having a volume average particle size ranging from 0.01 to 25 mm from an epoxy containing phenolic-aldehyde co-polymer in an optional solvent system; and

b) crosslinking the polymer gel particles with a dopant phosphorous containing compound under conditions sufficient to associate at least 1% by mass of the dry weight of the co-polymer of the dopant phosphorous containing compound to bind covalently with the co-polymer gel.

66. (canceled)

67. A method for preparing a condensation polymer gel, the method comprising:

a) forming crosslinked polymer gel particles having a volume average particle size ranging from 0.01 to 25 mm from an epoxy containing phenolic-aldehyde co-polymer in an optional solvent system; and

b) crosslinking the polymer gel particles with a dopant nitrogen-containing compound under conditions sufficient to associate at least 1% by mass of the dry weight of the co-polymer of the dopant nitrogen-containing compound to bind covalently with the co-polymer gel.

68-69. -69. (canceled)

70. A carbon material prepared by a process comprising:

1) polymerizing one or more polymer precursors to obtain a polymer gel; and

2) pyrolyzing the polymer gel to obtain the carbon material, wherein a nitrogen containing substance is contacted with the polymer gel during polymerization of the one or more polymer precursors, the nitrogen containing substance is contacted with the polymer gel after polymerization of the polymer gel, the nitrogen containing compound is contacted with the carbon material or polymer gel during pyrolysis or the nitrogen containing compound is contacted with the carbon material after pyrolysis or combinations thereof.

71. A carbon material prepared by a process comprising:

1) polymerizing one or more polymer precursors to obtain a polymer gel; and

2) pyrolyzing the polymer gel to obtain the carbon material, wherein a phosphorous containing substance is contacted with the polymer gel during polymerization of the one or more polymer precursors, the phosphorous containing substance is contacted with the polymer gel after polymerization of the polymer gel, the phosphorous containing compound is contacted with the carbon material or polymer gel during pyrolysis or the phosphorous containing compound is contacted with the carbon material after pyrolysis or combinations thereof.