Dong Haodi, Liu Changcheng, Huang Que, Sun Zhihua, Liang Taixin, Fan Chunfang, Chen Yanjun
School of Environment and Safety Engineering, North University of China, Taiyuan 030051, Shanxi, People's Republic of China; Institute of Advanced Energy Materials and Systems, North University of China, Taiyuan 030051, Shanxi, People's Republic of China.
School of Environment and Safety Engineering, North University of China, Taiyuan 030051, Shanxi, People's Republic of China; Institute of Advanced Energy Materials and Systems, North University of China, Taiyuan 030051, Shanxi, People's Republic of China.
J Colloid Interface Sci. 2024 Aug;667:371-384. doi: 10.1016/j.jcis.2024.04.105. Epub 2024 Apr 16.
The poor structural stability and conductivity of NaV(PO) (NVP) have been serious limitations to its development. In this paper, Sc is selected to replace partial site of V which can enhance its ability to bond with oxygen, forming the ScO octahedral unit, resulting in improved structural stability and better kinetic properties for the NVP system. Moreover, due to the larger ionic radius of Sc compared to V, moderate Sc substitution can support the crystal framework as pillar ions and expand the migration channels for de-intercalation of Na, thus efficiently promoting ionic conductivity. The introduction of polyacrylonitrile (PAN) to provide an N-doped porous carbon substrate is another key aspect. The low-cost carbon resource of PAN can induce a beneficial nitrogen-doped carbon skeleton with defects, enhancing electronic conductivity at the interface to reduce the polarization phenomenon. The established pore structure can serve as a buffer for unit cell deformation caused by Na migration. Furthermore, the enlarged specific surface area provides more active sites for electrolyte infiltration, improving the material utilization rate. The after cycling X-ray Diffraction/scanning electron microscope (XRD/SEM) further confirms the stabilized porous carbon skeleton and improved crystal stability of Sc-3 material. Ex-situ XRD analysis shows that the crystal volume change in the Sc-3 cathode is relatively slight but reversible during the charge/discharge process, indicating that Sc doping plays a crucial role in stabilizing the unit cell structure. The hybrid Sc/VO and PO units jointly build a strong bone structure to resist stress and weaken deformation. Accordingly, the optimized Sc-3 sample reveals an initial capacity of 115.9 mAh/g at 0.1C, with a capacity retention of 78.6 % after 2000 cycles at 30C. The Sc-3//CHC full battery can release a capacity of 191.3 mAh/g at 0.05C, accompanied by successful illumination, showcasing its promising practical applications.
NaV(PO)(NVP)较差的结构稳定性和导电性一直是其发展的严重限制因素。本文选择Sc取代部分V位点,这可以增强其与氧结合的能力,形成ScO八面体单元,从而提高NVP体系的结构稳定性和更好的动力学性能。此外,由于Sc的离子半径比V大,适度的Sc取代可以作为支柱离子支撑晶体骨架,并扩大Na脱嵌的迁移通道,从而有效提高离子导电性。引入聚丙烯腈(PAN)以提供N掺杂的多孔碳基底是另一个关键方面。PAN这种低成本的碳资源可以诱导形成具有缺陷的有益氮掺杂碳骨架,增强界面处的电子导电性以减少极化现象。所建立的孔结构可以作为由Na迁移引起的晶胞变形的缓冲。此外,增大的比表面积为电解质渗透提供了更多活性位点,提高了材料利用率。循环后的X射线衍射/扫描电子显微镜(XRD/SEM)进一步证实了Sc-3材料稳定的多孔碳骨架和改善的晶体稳定性。非原位XRD分析表明,Sc-3正极在充放电过程中的晶体体积变化相对较小但可逆,这表明Sc掺杂在稳定晶胞结构中起着关键作用。Sc/VO和PO混合单元共同构建了一个强大的骨架结构来抵抗应力并减弱变形。因此,优化后的Sc-3样品在0.1C时的初始容量为115.9 mAh/g,在30C下经过2000次循环后容量保持率为78.6%。Sc-3//CHC全电池在0.05C时可释放191.3 mAh/g的容量,并伴有成功的照明,展示了其有前景的实际应用。