Thermodynamic and kinetic analysis for carbothermal reduction process of CoSb alloy powders used as anode for lithium ion batteries
► Carbothermal reduction mechanism of Co 4O 3–Sb 2O 3–C system was clarified based on thermodynamic calculation and kinetic analysis. ► Actually required carbon amount for carbothermal reduction process was suggested. ► Pure CoSb powder was prepared via carbothermal reduction process, which shows hi...
Saved in:
Published in | Journal of alloys and compounds Vol. 509; no. 28; pp. 7657 - 7661 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Kidlington
Elsevier B.V
14.07.2011
Elsevier |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | ► Carbothermal reduction mechanism of Co
4O
3–Sb
2O
3–C system was clarified based on thermodynamic calculation and kinetic analysis. ► Actually required carbon amount for carbothermal reduction process was suggested. ► Pure CoSb powder was prepared via carbothermal reduction process, which shows high electrochemical performance as anode for lithium ion battery.
Thermodynamic calculation and kinetic analysis were performed on the carbothermal reduction process of Co
3O
4–Sb
2O
3–C system to clarify the reaction mechanism and synthesize pure CoSb powder for the anode material of secondary lithium-ion batteries. The addition of carbon amount and thus the purity of CoSb powders were critical to the electrochemical property of CoSb anode. It was revealed that in an inert atmosphere, Co
3O
4 was preferentially reduced to CoO, followed by the reduction of Sb
2O
3 and CoO. CO
2 was the gas product for the reduction of Co
3O
4 and Sb
2O
3, while CO was the gas product for that of CoO. Based on the analysis result, pure CoSb powder without any oxides and residual carbon was synthesized, which showed a higher specific capacity and a lower initial irreversible capacity loss, compared to CoSb sample with residual carbon. This work can be a reference for other carbothermal reduction systems. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2011.04.143 |