Carbon material, method for producing same, and use for same

1. A carbon material, being a non-flaky carbon material, wherein a ratio between a peak intensity I110 of (110) plane and a peak intensity I004 of (004) plane of a graphite crystal determined by a powder XRD measurement, I110/I004, is 0.10 or more and 0.35 or less; an average circularity is 0.80 or more and 0.95 or less; an average interplanar spacing d002 of (002) plane by an X-ray diffraction method is 0.337 nm or less; and a total pore volume of pores having a diameter of 0.4 μm or less measured by a nitrogen gas adsorption method is 25.0 μl/g or more and 40.0 μl/g or less; and by observing optical structures in a cross-section of the carbon material, when areas of the optical structures are accumulated from a smallest structure in an ascending order, SOP represents an area of an optical structure whose accumulated area corresponds to 60% of a total area of all the optical structures; when the structures are counted from a structure of a smallest aspect ratio in an ascending order, AROP represents an aspect ratio of a structure which ranks at a position of 60% in a total number of all the structures; and when D50 represents a median diameter in a volume-based cumulative particle size distribution by laser diffraction method, SOP, AROP and D50 satisfy the following relationships:

1.5 ≤AROP ≤6.0 and

0.2× D 50≤( SOP×AROP ) 1/2 <2× D 50.

2. The carbon material as claimed in claim 1 , wherein the carbon material has a D50 value of 1 μm or more and 30 μm or less.

3. The carbon material as claimed in claim 1 , whose BET specific surface area is 3.0 m 2 /g or more and 9.0 m 2 /g or less.

4. The carbon material as claimed in claim 1 , whose R value (ID/IG) as being an intensity ratio between a peak intensity (ID) of a peak in a vicinity of 1350 cm −1 and a peak intensity (IG) of a peak in a vicinity of 1580 cm −1 measured by Raman spectroscopy spectra is 0.08 or more and 0.18 or less.

5. A method for producing the carbon material as claimed in claim 1 , comprising a process of graphitizing particles with D50 of 10 μm or less obtained by pulverizing a coke having a thermal history of 1,000° C. or less by heating at 2,400° C. to 3,600° C., and a process of bringing the pulverized particles into contact with an oxygen gas during heating, wherein, by observing optical structures in a cross-section of the coke, when areas of the optical structures are accumulated from a smallest structure in an ascending order, an area of an optical structure whose accumulated area corresponds to 60% of a total area of all the optical structures is 50 to 5,000 μm 2 ; and when the optical structures are counted from a structure of a smallest aspect ratio in an ascending order, an aspect ratio of a structure which ranks at a position of 60% in a total number of all the structures is 1.5 or more and 6 or less.

6. The method for producing a carbon material as claimed in claim 5 , wherein the process of bringing the pulverized particles into contact with an oxygen gas is conducted at a time of heating in the process of graphitization.

7. The method for producing a carbon material as claimed in claim 5 , wherein the process of bringing the pulverized particles into contact with an oxygen gas is conducted at a time of cooling after the process of graphitization.

8. The method for producing a carbon material as claimed in claim 5 , wherein the process of bringing the pulverized particles into contact with an oxygen gas is conducted in a separate heating treatment after completion of the graphitization process.

9. A carbon material for a battery electrode, comprising the carbon material claimed in claim 1 .

10. A paste for an electrode comprising the carbon material for a battery electrode claimed in claim 9 and a binder.

11. An electrode for a lithium battery comprising the formed body of the paste for an electrode claimed in claim 10 .

12. A lithium-ion secondary battery comprising the electrode claimed in claim 11 as a constituting element.

13. A method for producing an electrode for a lithium battery, comprising a process of applying the paste for an electrode claimed in claim 10 on a current collector followed by drying and compressing at a pressure of 1 to 3 t/cm 2 .