Zhou Tao, Chen Yanjun
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 Oct 26;654(Pt B):1163-1176. doi: 10.1016/j.jcis.2023.10.124.
The inherent poor ionic and electronic conductivity and relatively low capacity seriously limit the development of NaV(PO) (NVP). Currently, Y substitution is proposed for the first time and corresponding Y-doped NVP samples are successfully synthesized by traditional solid phase method. By replacing V (0.64 Å) of Y (0.9 Å) with large ionic radius, the transport channel of Na is expanded, accelerating the migration rate of Na. Meanwhile, the strong Y-O chemical bond reinforces the crystal structure of NVP and improves its stability. It is worth noting that Y reacts with slightly excess Na during the sintering process to form a new conductive phase NaYO coated on the surface of NVP particles. NaYO possesses excellent semiconductor properties and can form a double conductive construction together with the amorphous carbon layer to improve the kinetics of NVP system. Moreover, the unique heterojunction could be generated between the boundaries of NaV(PO)-NaYO, further elevating the ionic conductivity. According to the investigations of ex-situ XRD and in-situ EIS, NaYO can provide active Na, participating in the electrochemical process to supply extra reversible capacity. Comprehensively, the optimized NVP-Y0.07/C releases a high capacity of 125.2 mAh/g at 0.1 C, far exceeding the theoretical value of NVP (117.6 mAh/g). Even at 60 C, a high specific capacity of 94.2 mAh g can be achieved. When cycled at 250 C, it maintains 85.5 % after 2000 cycles. Besides, the assembled NVP-Y0.07/C//hard carbon full cell can deliver a reversible value of 118.2 mAh/g, suggesting the superior practical application potentials.
固有的离子和电子导电性差以及相对较低的容量严重限制了NaV(PO)(NVP)的发展。目前,首次提出Y取代,并通过传统固相法成功合成了相应的Y掺杂NVP样品。通过用大离子半径的Y(0.9 Å)取代V(0.64 Å),扩大了Na的传输通道,加快了Na的迁移速率。同时,强Y-O化学键增强了NVP的晶体结构并提高了其稳定性。值得注意的是,Y在烧结过程中与略微过量的Na反应,形成包覆在NVP颗粒表面的新导电相NaYO。NaYO具有优异的半导体性能,可与非晶碳层一起形成双导电结构,以改善NVP体系的动力学。此外,在NaV(PO)-NaYO的边界之间可产生独特的异质结,进一步提高离子电导率。根据非原位XRD和原位EIS的研究,NaYO可以提供活性Na,参与电化学过程以提供额外的可逆容量。综合来看,优化后的NVP-Y0.07/C在0.1 C下释放出125.2 mAh/g的高容量,远远超过NVP的理论值(117.6 mAh/g)。即使在60 C时,也可实现94.2 mAh/g的高比容量。在250 C下循环时,2000次循环后仍保持85.5%。此外,组装的NVP-Y0.07/C//硬碳全电池可提供118.2 mAh/g的可逆值,表明其具有优异的实际应用潜力。