Zhang Chenrui, Shang Jingrui, Dong Huilong, Ang Edison Huixiang, Tai Linlin, Aizudin Marliyana, Wang Xuhong, Geng Hongbo, Gu Hongwei
School of Materials Engineering, Changshu Institute of Technology, Changshu, Jiangsu, 215500, China.
Natural Sciences and Science Education, National Institute of Education, Nanyang Technological University, Singapore 637616, Singapore.
Nanoscale. 2021 Nov 11;13(43):18322-18331. doi: 10.1039/d1nr05708a.
In comparison with lithium-ion batteries, sodium-ion batteries (SIBs) have been proposed as an alternative for large-scale energy storage. However, finding an anode material that can overcome the sluggish electrochemical reaction kinetics and fast capacity fading caused by large volume expansion during cycling is problematic. In this study, the intercalation technique for nitrogen-doped carbon layers is implemented for the molybdenum disulfide (MoS/NC) structure to improve the rate and cycling stability of SIBs by increasing the diffusion rate of sodium ions and mitigating excessive volume structural expansion. The as-synthesized MoS/NC anode has a high discharge specific capacity of 546 mA h g at 1 A g after 160 cycles, as well as a high rate and stable cycle performance of 406 mA h g at 10 A g after 1000 cycles. Upon coupling with a high-voltage NaV(PO)OF cathode, the sodium-ion full battery displays high specific energies of 78.57 W h kg and 49.70 W h kg at specific powers of 193.76 W kg and 3756.80 W kg, respectively, with commercialization potential demonstrated.
与锂离子电池相比,钠离子电池(SIBs)已被提议作为大规模储能的替代方案。然而,找到一种能够克服循环过程中由于大体积膨胀导致的缓慢电化学反应动力学和快速容量衰减的负极材料是个难题。在本研究中,通过增加钠离子的扩散速率并减轻过度的体积结构膨胀,对二硫化钼(MoS₂/NC)结构实施了氮掺杂碳层的插层技术,以提高钠离子电池的倍率性能和循环稳定性。合成的MoS₂/NC负极在1 A g下经过160次循环后具有546 mA h g的高放电比容量,以及在10 A g下经过1000次循环后具有406 mA h g的高倍率和稳定循环性能。与高压Na₃V₂(PO₄)₃F正极耦合后,钠离子全电池在比功率分别为193.76 W kg和3756.80 W kg时,分别显示出78.57 W h kg和49.70 W h kg的高比能量,展现出商业化潜力。