Effect of concentration of dextrose-derived hard carbon anode on the electrochemical performance for sodium-ion batteries

被引:2
|
作者
Chakraborty, Rupan Das [1 ]
Pani, Tapan K. [1 ]
Martha, Surendra K. [1 ]
机构
[1] Indian Inst Technol Hyderabad, Dept Chem, Sangareddy 502284, Telangana, India
关键词
Dextrose-derived hard carbon; Anode; Sodium-ion battery; Electrochemical performance; Diffusion studies; STORAGE; CATHODE; NANOSPHERES; ELECTRODES; INSERTION; SURFACE; DESIGN;
D O I
10.1007/s10008-024-06136-6
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Hard carbons (HCs) are widely used as anode materials for sodium-ion batteries due to their availability, ease of synthesis, and low cost. HCs can store Na ions between stacked sp2-layers of carbon and micropores. In this work, hard carbons are synthesized from 1 M, 2 M, 3 M, 4 M, and 5 M dextrose solutions by hydrothermal synthesis followed by high-temperature calcination at 1100 degrees C in an argon atmosphere. Among all hard carbons derived from different concentrations of dextrose solutions, hard carbon derived from 3 M dextrose solution delivers superior electrochemical performance compared to other hard carbons. Hard carbon derived from 3 M dextrose solution (DHC-3 M) provides an initial reversible capacity of 273 mAh g-1 with a capacity retention of 82% at the end of 100 charge-discharge cycles at 30 mA g-1. Further, high-rate charge-discharge cycling at 200 mA g-1 shows an initial capacity of 200 mAh g-1 and retains over 61% capacity at the end of 500 cycles. The improved capacity of DHC-3 M is due to the higher d-spacing value and more disorderness, which improve the plateau region capacity due to the intercalation of Na+ in the carbon matrix. Besides, 3 M dextrose-derived hard carbons are less agglomerated than other concentrations and show less charge transfer resistance before and after cycling, resulting in improved electrochemical performance.
引用
收藏
页码:1829 / 1840
页数:12
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