Sun Yong-Gang, Hu Yu, Dong Li, Zhou Ting-Ting, Qian Xiang-Yu, Zhang Fa-Jia, Shen Jia-Qi, Shan Zhi-Yang, Yang Li-Ping, Lin Xi-Jie
School of Chemistry & Chemical Engineering, Yancheng Institute of Technology, Yancheng 224051, China.
School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing 100083, China.
Nanomaterials (Basel). 2025 Mar 10;15(6):423. doi: 10.3390/nano15060423.
Layered sodium trititanate (NaTiO) is a promising anode material for sodium-ion batteries due to its suitable charge/discharge plateaus, cost-effectiveness, and eco-friendliness. However, its slow Na diffusion kinetics, poor electron conductivity, and instability during cycling pose significant challenges for practical applications. To address these issues, we developed a template-free method to synthesize NaTiO-C hollow microspheres. The synthesis began with polymerization-induced colloid aggregation to form a TiO-urea-formaldehyde (TiO-UF) precursor, which was then subjected to heat treatment to induce inward crystallization, creating hollow cavities within the microspheres. The hollow structure, combined with a conductive carbon matrix, significantly enhanced the cycling performance and rate capability of the material. When used as an anode, the NaTiO-C hollow microspheres exhibited a high reversible capacity of 188 mAh g at 0.2C and retained 169 mAh g after 500 cycles. Additionally, the material demonstrated excellent rate performance with capacities of 157, 133, 105, 77, 62, and 45 mAh g at current densities of 0.5, 1, 2, 5, 10, and 20C, respectively. This innovative approach provides a new strategy for developing high-performance sodium-ion battery anodes and has the potential to significantly advance the field of energy storage.
层状钛酸钠(NaTiO)因其合适的充放电平台、成本效益和环境友好性,是一种很有前景的钠离子电池负极材料。然而,其缓慢的钠离子扩散动力学、较差的电子导电性以及循环过程中的不稳定性,给实际应用带来了重大挑战。为了解决这些问题,我们开发了一种无模板方法来合成NaTiO-C中空微球。合成过程始于聚合诱导胶体聚集,形成TiO-脲醛(TiO-UF)前驱体,然后对其进行热处理以诱导向内结晶,在微球内部形成中空腔。这种中空结构与导电碳基质相结合,显著提高了材料的循环性能和倍率性能。当用作负极时,NaTiO-C中空微球在0.2C时表现出188 mAh g的高可逆容量,500次循环后仍保留169 mAh g。此外,该材料在电流密度分别为0.5、1、2、5、10和20C时,表现出优异的倍率性能,容量分别为157、133、105、77、62和45 mAh g。这种创新方法为开发高性能钠离子电池负极提供了一种新策略,并有潜力显著推动储能领域的发展。