Shi Hongen, Chen Yanjun, Li Jiahao, Guo Li
School of Materials Science and Engineering, North University of China, Taiyuan 030051, China; Institute of Advanced Energy Materials and Systems, North University of China, Taiyuan 030051, China.
School of Materials Science and Engineering, North University of China, Taiyuan 030051, China; Institute of Advanced Energy Materials and Systems, North University of China, Taiyuan 030051, China.
J Colloid Interface Sci. 2023 Dec 15;652(Pt A):195-207. doi: 10.1016/j.jcis.2023.08.067. Epub 2023 Aug 11.
NaV(PO) (NVP), possessing good ionic conduction properties and high voltage plateau, has been deemed as the most prospective material for sodium ion batteries. However, the weak intrinsic electronic conductivity has hindered its further commercialization. Herein, an ingenious strategy of Bi substitution at V site in NVP system is proposed. The ionic radius of Bi is slightly larger than that of V, which can further expand the crystal structure inside the NVP, thus accelerating the migration of Na. Meanwhile, the appropriate amount of carbon coating and carbon nanotubes (CNTs) enwrapping construct an effective three-dimensional network, which provides a conductive framework for electronic transfer. Furthermore, the introduction of CNTs also inhibit the agglomeration of active grains during the sintering process, reducing the particle size and shortening the diffusion path of Na. Comprehensively, the conductivity, ionic diffusion ability and structural stability of the modified NaVBi(PO)/C@CNTs (0 ≤ x ≤ 0.05) sample are significantly improved. The NaVBi(PO)/C@CNTs sample obtains a reversible capacity of 97.8 mAh g at 12C and maintains a value of 80.6 mAh g after 9000 ultra-long cycles. As for the super high rate at 80C, it exhibits a high capacity of 84.34 mAh g and retains a capacity of 73.34 mAh g after 6000 cycles. The superior electrochemical performance is derived from the enhancement of the crystal structure by Bi doping and the highly conductive network consisting of carbon coating layers and enwrapped CNTs.
NaV(PO)(NVP)具有良好的离子传导性能和高电压平台,被认为是钠离子电池最具前景的材料。然而,其固有的电子电导率较弱,阻碍了它的进一步商业化。在此,提出了一种在NVP体系中V位点进行Bi取代的巧妙策略。Bi的离子半径略大于V,这可以进一步扩展NVP内部的晶体结构,从而加速Na的迁移。同时,适量的碳包覆和碳纳米管(CNTs)包裹构建了一个有效的三维网络,为电子转移提供了导电框架。此外,CNTs的引入还抑制了烧结过程中活性颗粒的团聚,减小了粒径并缩短了Na的扩散路径。综合来看,改性后的NaVBi(PO)/C@CNTs(0≤x≤0.05)样品的电导率、离子扩散能力和结构稳定性都得到了显著提高。NaVBi(PO)/C@CNTs样品在12C时获得了97.8 mAh g的可逆容量,在9000次超长循环后保持在80.6 mAh g。至于在80C的超高倍率下,它表现出84.34 mAh g的高容量,在6000次循环后仍保留73.34 mAh g的容量。优异的电化学性能源于Bi掺杂对晶体结构的增强以及由碳包覆层和包裹的CNTs组成的高导电网络。