作者
Akira Kano,Takashi Okano,Nobuhiko Hojo,Simon Ito,Masahisa Fujimoto,Kensuke Nakura
摘要
Recently the demand for rechargeable batteries with high capacity, high power, long life, high reliability, and low cost has been increasing. While Li-ion batteries offer the highest energy density among present battery technologies, the higher cost and insufficient resources of lithium is a bottleneck to enabling their wider use. Na-ion batteries, where sodium acts as the current carrier, are attractive alternatives to Li-ion batteries because of the lower cost and abundance of sodium. However, the energy density of Na-ion batteries is still lower than that of Li-ion batteries, therefore the development of the active materials achieving a higher energy density is eagerly anticipated. For anode materials in Na-ion batteries, a non-graphitized carbon, such as hard carbon, is well-studied in contrast to Li-ion batteries, where graphite is usually used as the anode material. The capacity of non-graphitized carbon in Na-ion batteries is reported to be 200 - 300 mAh/g [1,2]. In Na-ion insertion process, it is proposed that Na-ions are inserted between stacked graphenes in the higher potential above ca. 0.2 V vs. Na+/Na, and then nano-pores are filled during electrochemical reaction in the lower potential region [1,2]. In our previous research, we focused on the effect of the pore structure of carbons, and found a linear relationship between the reversible capacity in the range of 0.2 - 0 V vs. Na+/Na and the closed pore volume of non-graphitized carbons. This result suggests that Na-ion could be inserted reversibly into the closed pore of non-graphitized carbons, and thus the non-graphitized carbon with large closed pore volume is a promising anode material for higher capacity Na-ion batteries [3]. In this study, we synthesized a new carbon material with a large closed pore volume using the carbon sources including a pore-forming agent as the starting material. It has the closed pore volume of 0.49 cc/g and its discharge capacity reached 438mAh/g. [1] D. A. Stevens et al, J. Electrochem. Soc., 148 (2001) A803 [2] S.Komaba et al, ACS Appl. Mater. Interfaces, 3 (2011) 4165 [3] A. Kano et al, 228th ECS meetings, (2015) 221